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Description

To lead, implement and report on process/cleaning validation projects. To lead equipment/ Controlled Temperature Units (CTU's) qualification studies. To provide support to all other validation activities. Assert a high level of technical expertise across a range of different equipment/processes/products qualification/validation.

TECHNICAL APPLICATION

· Validation documentation - drafting, reviewing and approving validation documentation.

· To lead the execution of equipment/CTU qualification, Container Closure Integrity (CCI) and Filter validation programs

· To lead cleaning validation and process validation programs

· Accountable for scheduling, tracking, reporting and achieving project deadlines

· To lead cycle development of equipment sterilization/ depyrogenation/ cleaning cycles.

· Input into the core aspects of Manufacturing and Cleaning SOP's.

· Participation in the development of continuous improvement programs

· Actively contribute to project teams.

· Lead and co-ordinate the execution of the re-qualification program.

· Mentoring junior validation engineers.

· Conducting and participating in Risk assessments.

Assist in ensuring that any compliance/training issues both internal and site wide, are critically evaluated and highlighted as appropriate.

INFORMATION GATHERING AND DATA ANALYSIS

· Performing data analysis and determining conclusions reached.

· Make informed decisions / recommendations around conclusions reached from data analysis.

Signing off and approving protocols, reports, change controls and process deviations.

COMPLIANCE

· Understanding and applying industry specific compliance standards/regulations to all Qualification/Validation activities.

Participates in internal and external audits and inspections.

Qualifications

B.Sc. /B.A. degree required (science, engineering or other technical field preferred)

· Experience in IMB/FDA environment advantageous.

· Strong technical writing and communication skills

· Ability to close items to completion.

· Ability to pay high level of detail and QA data to very high standard

· Ability to develop high technical aptitude in products/processes

· Demonstrated leadership, interpersonal, technical aptitude, and problem solving skills.

· Strong team skills, including ability to co-ordinate various departments to support validation programs.

· Project Management skills.

· Must be flexible and able to manage multiple priorities.

· Must be goal-oriented and able to prioritize and manage risks.

*LI-SC1

Job
: Engineering Generic

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Validation-Engineer-Job/1703538/170353817035382012-06-15Merck/MSDEngineering Genericfull-timeUSDstarting0BSIreland
Description

This role will be part of the process team starting up and providing on going technical support to the filling processes at our Vaccines & Biologics Formulation / Fill facility in Carlow. The successful candidate will be responsible for providing process and technical support to selected sterile processing operations, ongoing support of manufacturing processes and support for the introduction of new products. Also responsible for analytical and engineering studies associated with the development of new components, products, processes, systems, and facilities.

Key Responsibilities:

· Represent function on multi-disciplinary teams tasked with start-up, qualification, validation, new product introduction and ongoing process / product support. This will involve team leadership, technical input and execution of planned work.

· Support and execute process related investigations and work across functions to produce robust corrective actions

· Lead / Work on projects using lean and statistical tools to drive continuous improvement. Projects may range from Kaizen events to large multi-disciplinary projects

· Protocol & Report generation in support of the introduction of new product / processes

· Generation of Design of Experiments (DoE) to support robust transfer of new products to the Carlow site in line with LSS principles

· Support on the manufacturing floor and technology operations laboratory studies for shakedown, process development and engineering batches

· Tech support during routine manufacturing operations

Key Attributes

· Experience of Sterile fill processes and equipment

· Strong technical focus to develop and execute project plans

· Excellent experience of process improvements.

· Knowledge of Information Technology and automated production systems

· Experience in producing and reviewing documents such as process descriptions and PFDs is essential

· Strong communications skills

· Experience of participating and leading multidisciplinary teams

· Collaborative and inclusive approach to work

· Detail orientated

Qualifications

Experience

· Minimum of 2 yrs experience in biotechnology/pharmaceutical industry in a production/process role with considerable experience in sterile filling processes.

· A history of partnering with groups across an organization.

· Experience with automated production systems such as Distributed Control Systems (DCS) and PLCs

· Lean Six Sigma and / or Operations Excellence experience is desirable

Education

· Bsc. in Engineering, Science or similar discipline

Job
: Process Engineering

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/Process-City-Process-Engineer-Job-AR/1756989/175698917569892012-06-15Merck/MSDProcess Engineeringfull-timeUSDstarting0BSIreland
Description

Merck Sharp & Dohme - where patients come first

Merck Sharp & Dohme Biologics (Ireland) Ltd. is a subsidiary of Merck & Co. Inc., New Jersey, USA, one of the leading healthcare companies in the world.

Located on the periphery of Carlow Town, Merck Sharp & Dohme Biologics (Ireland) Ltd. is our latest Irish facility, joining existing Merck Sharp & Dohme operations in Tipperary and Dublin. The vaccines, biologics and other products we will formulate in our new Carlow facility could ultimately be used by millions of people across the world.

We are now seeking applications from energetic, motivated and innovative people interested in becoming part of this exciting new phase in our global development. Working with likeminded individuals, you will join a growing dynamic team in a newly constructed, contemporary environment. Successful applicants in each of the positions outlined here will make an important contribution to our overall operations in Carlow, Ireland and worldwide.

This role is one of our exciting job opportunities right now:

Quality Assurance Specialist

This position reports to the QA Lead and will be part of the Quality Organisation at Carlow.

Key Responsibilities:

* Support deviation and a typical close out and initiating/following up on corrective and preventative actions
* Support quality related customer complaint investigations and trending activities
* Support the development and implementation of improved quality reporting measures
* Aid the implementation of the Quality Management System
* Promote continuous improvement of the Quality Management System
* Provide support and advice during cross functional investigations / projects and as required
* Provide direct support during customer and regulatory audits
* Conduct self inspections and external audits as appropriate
* Provide training in all aspects of Quality Management Systems and GMP
* Support the review of all batch related documentation
* Carry out Annual Product Reviews
* Write/Review Quality department SOPs
Initiate/ Maintain Quality Department Metrics

Qualifications

* 7+ years experience of working in a similar Quality Assurance related role in the Pharmaceutical Industry
* Knowledge of EU/US quality related pharmaceutical regulations
* Experience of conducting quality based investigations and root cause analysis

Education

* Degree in Science or related discipline

Job
: Quality Operations

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Quality-QA-Specialist-Job-GA/1733755/173375517337552012-06-15Merck/MSDQuality Operationsfull-timeUSDstarting0BSIreland
Description

Responsible and accountable for supporting all Automation and IT components of the process. On-floor support of manufacturing activities.

Active participation in the Tier process and proactively resolving technical issues before they impact the business priorities.

Ensure supply of high quality product through ensuring equipment and system availability; maximize performance through continuous process improvement initiatives and other relevant project support.

Ensure compliance with, implementation and maintenance updates of local Carlow specific SOP's and technical documentation eg. Change Management, Problem Incident Management.

Ensure's adherence with Merck IT standards. Following business processes in the execution and support of A&IT systems in Carlow.

Required to comply with Merck Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.

Participate effectively in writing/revising/ rolling out accurate operational procedures, training documents and maintenance procedures for various IPT systems; ensure all work is carried out in line with same.

Responsible for supporting a culture of Continuous Improvement by deploying Merck Six Sigma tools within MMDIT on projects such as: problem solving, standardization, reducing cycle time, Lean principles within the process.

Work collaboratively to drive a safe and compliant culture in Carlow.

o Extensive technical and operational expertise in one of more of the following disciplines:

o Computer Systems Validation

o MIS Systems

o Business Systems

o Manufacturing Execution Systems

o Instrumentation/Automation & Control

o BMS / SCADA / DCS Systems

o Control System/Shopfloor Integration

o Financial Systems / Inventory Management Systems / SAP

o Proficiency in Microsoft Office and job related computer applications required

o Understanding of mechanical/electrical/pneumatic processes

o Equipment and process validation

o Pharmaceutical and Biotechnology manufacturing processes

o Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices

o Report, standards, policy writing skills required

o Knowledge, and ideally application, of industry standard training documentation systems/methods

o Lean Six Sigma Methodology experience desired

Job
: Engineering

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Carlow-Systems-Engineer-Job/1858701/185870118587012012-06-15Merck/MSDEngineeringfull-timeUSDstarting0BSCarlow, Leinster, IE
Description

The establishment of the EMEA SBS Centre is part of MSD's strategy to create a multi-function, multi-lingual organization to support MSD at a regional level. The EMEA SBS Centre will support business transactions in the areas of Finance, Accounting and Managed Services such as travel and meetings.

We are now recruiting for key talent for our new SBS centre.

Description:

Reporting to the Service Team Manager or Supervisor, the Finance Analyst, is responsible for providing commercial services, in order to cash (OTC) areas such as billing, Accounts receivables (AR) and collections.

The primary activities that you will be performing include:

* Executing the transactions required and the services as defined in the OtC area.
* Supporting the launch of SAP across major markets in Europe.
* Partnering with key stakeholders (Finance, Sales Procurement, etc) to ensure that all transactional activity is properly recorded and compliant with country statutory and tax requirements.
* Seek out opportunities for streamlining and rendering service delivery more efficiently, and participates in special projects to support Shared Business Services objectives.
* Resolve related issues pertaining to OTC and an understanding of when, how and where to escalate cases as required to meet defined service levels.
* Additional responsibilities to support a new organization in Europe as required.

Qualifications

Education:

* Bachelors Degree required.
* Business Level fluency (oral and written) in Italian or German required.

Preferred:

* A minimum of 2 years of demonstrated work experience within the General accounting and or PtP shared services area.
* Experience working in an organization providing services across multiple markets or geographies.
* A minimum of one year of experience working with SAP.
* High degree of integrity and personal ethics in implementing corporate policies and procedures
* Effective team player with collaborative focus
* Must be able to work in a fast-paced, dynamic environment, under pressure, and with a high degree of professionalism
* Must be comfortable in an environment of changing technologies and processes, and demonstrate flexibility in adjusting to new ways of working
* Experience working in a SOX404 environment.
* Strong oral and written communication skills.
* Flexible work arrangements will be considered based on business needs.

Job
: Customer Contact Center

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 3

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Contact-ItalianGerman-Order-to-Cash-Finance-Analyst-Job-NV-89825/1366982/136698213669822012-06-15Merck/MSDCustomer Contact Centerfull-timeUSDstarting0BSIreland
Description

The QC Lead Technicain shall carry out most of his/her duties in the Quality Control Laboratory and the primary tasks and responsibilities of the position are as follows.

· Working as directed by Quality Manager according to Company safety policies, cGMP and cGLP.

· Formulating weekly work schedules with the Quality Manager and ensuring that these schedules are communicated and followed.

· Checking raw materials, in-process and finished product work.

· Trending of raw materials, in-process, finished product results.

· Ensuring results are recorded in a timely and accurate fashion.

· Reviewing analyst documentation and ensuring Right First Time KPIs are achieved.

· Issuing monthly / annual reports to the Quality Manager

· Ensuring that all Quality Systems within the department are adhered to on a daily basis.

· Trouble-shooting within the QC Department and providing technical assistance / support to other Departments within MSD Carlow

· Maintaining laboratory SOPs and specifications in a state of compliance.

· Assisting with out of specification investigations.

· Training of QC staff and regular review of training records.

· Involvement in QC equipment projects including purchasing and ensuing validation.

· Working on projects as detailed by Quality Manager

· Representing the QC Department on site/inter departmental projects.

· Performing any other activities as indicated by the Quality Manager.

Qualifications

The successful applicant will possess the following knowledge, skills, qualifications and experience.

* At least 6 years experience working within a cGLP environment (IMB and FDA approved).
* A minimum of 2 years supervisory (team leading a team of 3-5 analysts) experience within a lab environment with a proven track record of effectively scheduling & delegating Analysts' work.
* A BSc in a related discipline is a must.
* Extensive experience with Lab based techniques (Desired Level: Subject Matter Expert)
* Ability to critically review analytical data. Possessing excellent attention to detail is a must.
* Ability to advise, lead and manage a small team of analysts.
* Ability to trouble shoot, identify analytical issues and follow up with corrective actions.
Experience of preparing for regulatory audits.

Job
: Quality GMP Related

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Quality-QC-Lead-Technician-Job-GA/1703551/170355117035512012-06-15Merck/MSDQuality GMP Relatedfull-timeUSDstarting0BSIreland
Description

The successful candidate will be part of the Operations team (Integrated Process Team-IPT) providing support to the filling processes at our Vaccines Formulation / Fill facility in MSD Carlow.

Key Responsibilities

* The incumbent will be responsible for participating in C&Q and Validation activities to support start up by being and active member in our cross functional suite teams.
* Following Qualification and start up the role will include responsibility for the development of SOP's, routine operations and monitoring of production equipment using MES/DCS and PLC based systems.
* The Successful candidate will also be responsible for delivery of training, maintaining housekeeping, and 5S in all production areas while focusing on continuous process improvement using Lean Principles.
* This role will involve maintaining process equipment, completing preventative maintenance and equipment troubleshooting and repairs.
* Applicant should have previously demonstrated strong team skills, flexibility, motivation, ability to troubleshoot/problem solve, with a strong emphasis around safety and compliance practices.
* Applicants should actively support, participate and embrace an empowered team culture and have excellent communication skills
* Aseptic/Sterile Manufacturing experience required.

Qualifications

Education

* Applicants will have a Trade Qualification as Fitter / Electrician and minimum of five years experience in the biotech / pharmaceutical industry

Job
: Manuf./Operations Generic

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Production-Technician-Job-VA/1155628/115562811556282012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSIreland
Description

Merck Sharp & Dohme - where patients come first

Merck Sharp & Dohme Biologics (Ireland) Ltd. is a subsidiary of Merck & Co. Inc., New Jersey, USA, one of the leading healthcare companies in the world.

Located on the periphery of Carlow Town, Merck Sharp & Dohme Biologics (Ireland) Ltd. is our latest Irish facility, joining existing Merck Sharp & Dohme operations in Tipperary and Dublin. The vaccines, biologics and other products we will formulate in our new Carlow facility could ultimately be used by millions of people across the world.

We are now seeking applications from energetic, motivated and innovative people interested in becoming part of this exciting new phase in our global development. Working with likeminded individuals, you will join a growing dynamic team in a newly constructed, contemporary environment. Successful applicants in each of the positions outlined here will make an important contribution to our overall operations in Carlow, Ireland and worldwide.

This role is one of our exciting job opportunities right now:

Quality Assurance Specialist

This position reports to the QA Lead and will be part of the Quality Organisation at Carlow.

Key Responsibilities:

* Support deviation and a typical close out and initiating/following up on corrective and preventative actions
* Support quality related customer complaint investigations and trending activities
* Support the development and implementation of improved quality reporting measures
* Aid the implementation of the Quality Management System
* Promote continuous improvement of the Quality Management System
* Provide support and advice during cross functional investigations / projects and as required
* Provide direct support during customer and regulatory audits
* Conduct self inspections and external audits as appropriate
* Provide training in all aspects of Quality Management Systems and GMP
* Support the review of all batch related documentation
* Carry out Annual Product Reviews
* Write/Review Quality department SOPs
Initiate/ Maintain Quality Department Metrics

Qualifications

* 7+ years experience of working in a similar Quality Assurance related role in the Pharmaceutical Industry
* Knowledge of EU/US quality related pharmaceutical regulations
* Experience of conducting quality based investigations and root cause analysis

Education

* Degree in Science or related discipline

Job
: Quality Operations

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Quality-QA-Specialist-Job-GA/1157466/115746611574662012-06-15Merck/MSDQuality Operationsfull-timeUSDstarting0BSIreland
Description

The incumbent is responsible for the completion of financial, operational and/or

computer audits, integrated audits and process audits, and for the delivery of an audit

report that adds value to the business unit audited. Under the direction of the Client

Audit Director and/or the Auditor-in-Charge, the incumbent is responsible for the

effectiveness and efficiency of the audit that he/she is assigned to. You are responsible

for expediting all stages of the writing and review of reports, which accurately reflect

facts and recommendations of an objective appraisal of Merck operations. You will

maintain the highest standards of professionalism and independence in the execution of

your duties, always with the Company's best interests in mind. You will lead by personal

behavior and ethics that are also of the highest standard. The incumbent should embody

the Corporate Audit Group (CAG) values and vision, and is cognizant of the CAG

Policies and Procedures, and adheres to them and applies them.

Participate in achieving the Corporate Audit's annual audit plan according to

established schedules.

The primary role will be to lead small teams of auditors on

various assignments. Incumbent will be expected to lead complex, large and/or sensitive

audits with limited management supervision in addition to actively participating in the

audit and performing audit work. Incumbent will have overall responsibility for the

preparation and quality of workpapers for the team as defined in the CAG's Policies and

Procedures. Incumbent is expected to effectively partner and communicate with the

client, support groups, internal resources and external organizations.

Complete audit programs and workpapers within the parameters set forth for performing

audit work.

Use of Audit software is required to document audit findings, evaluations,

work programs, test results, evidential matter, and audit reports. The incumbent is

expected to meet deadlines as set forth by Corporate Audit's Polices and Procedures and

comply with established internal and external workpaper standards and procedures.

Apply elements of the Corporate Audit Group Vision and Values to assist in maintaining

a strong internal control environment throughout Merck.

Integrate and maintain both the

stewardship and consultative roles into all assignments. Follow the standards of conduct

defined for the profession and as defined in Corporate Audit's Policies and Procedures.

Participate in the assigned roles for specific projects and ensure the realization of the

specified results

. Support Corporate Audit management in the sharing of best practices

and establishment of a best practices database that will support line management in

enhancing the stewardship practices across geographical areas. Incumbent will

accomplish this by maintaining client relationships, completing tasks efficiently and

according to established milestones, encouraging positive team interactions and providing

progress reports.

Demonstrate proactive commitment to the "Know and Develop Yourself" principle of

Merck's leadership model

. When acting in a leadership capacity, demonstrate proactive

commitment to the "Know, Support and Develop Your People" principle of the Merck

leadership model.

Qualifications

Education Requirement:

•

BS/BA required preferably in Accounting or Finance.

Required:

•

Knowledge of audit methodology and internal controls.

•

A minimum of 3 years of prior internal audit and or public accounting and

or general accounting experience.

•

Willingness to travel within assigned regions/entities both domestically and

internationally to complete testing; estimated travel up that 40% of the time.

Preferred:

•

Excellent interpersonal skills, including the ability to interact effectively with

client/business process owners

•

Effective oral and written communication, computer, and time management skills

and the ability to work with limited supervision

•

Knowledge of SAP.

Job
: General Audit

Primary Location: IE-Leinster-Dublin
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Senior-Internal-Auditor-Job-L/1558421/155842115584212012-06-15Merck/MSDGeneral Auditfull-timeUSDstarting0BSDublin, Leinster, IE
Description

Responsible for implementing procedures and best practices supporting Merck's Supplier Development & Performance Management program, under the direction of the SD&PM Relationship Manager. The incumbent will exercise leadership in monitoring and maintaining Supplier compliance with worldwide regulatory requirements, current Good Manufacturing Practices (cGMPs), MMD Quality Manual, and pertinent legal and / or business contract requirements. Key responsibilities include leading Supplier Deviation investigations, evaluation and execution of Supplier Change Management, up-skilling Suppliers, and interfacing with MMD sites associated with Supplier issues within the region. The incumbent will assist the SD&PM Relationship Manager in calibrated Quality oversight and interfacing with Procurement and Technology colleagues.

The incumbent will possess Analytical, Scientific, Technical, Manufacturing, and / or Quality experiences in order to effectively administer and control Quality and Technical programs and projects needed to manage Suppliers, under the direction of the SD&PM Relationship Manager. Must understand worldwide regulatory requirements and cGMPs associated with materials supply.

Primary Roles include, but are not limited to:

* Travels up to 50% of the time, to and from Supplier sites and MMD sites within the region. Serves as the primary point of contact to Suppliers in the region.
* Responsible for coordination, oversight and communication on matters related to the cGMP status with the Suppliers.
* Acts as a liaison between Suppliers and internal Merck site personnel to resolve manufacturing, quality, technical, and supply issues and to facilitate proactive Quality improvements at the Supplier.
* Partners with SD&PM Quality, Procurement and Technology colleagues to provide efficient and effective solutions and Corrective Actions / Preventative Actions (CAPAs) to Supplier and / or site issue resolution, including Deviation Management, response to Supplier audit issues and customer complaints.
* Provides compliance input and support for implementation of analytical methodology and process development initiatives.
* Coordinates and evaluates Supplier- or Merck-initiated Change Control associated with materials supply. Provides support to the Suppliers to facilitate, qualify, and / or validate materials for new product introductions.
* Coordinates, communicates and oversees general technical matters pertaining to Suppliers, including optimization of component / material usage and upskilling Suppliers to provide improved materials and services.
Tracks and monitors Supplier operational and quality performance. Supports development and delivery of Supplier metrics and scorecards.

Qualifications

Education:

* BS/BA degree in Engineering, Science or Business

Required:

* Minimum 5 years experience in Quality, Technical, Manufacturing Operations, or related Business Operations working with products or processes.

Preferred:

* Demonstrated Quality, Technical and / or Manufacturing experience in the areas of chemical, pharmaceutical and / or vaccine manufacturing or packaging.
* Six Sigma Black Belt, Green Belt or Yellow Belt certification
* Experience conducting technical investigations
* Ability to develop and / or improve commercial relationships
* Knowledge of cGMPs, technical writing, data management collection and analysis
* Facilitates business negotiations in a professional manner
Works independently with all levels of the organization, and has demonstrated the following skills:
* Rapid / Disciplined decisions
* Acts with courage and candor
* Drives results
* Escalation of issues / concerns to management, as appropriate

Ability to Prioritize, Align and Simplify

Linde: *LI-LVG1

Job
: Qual Assurce - 3rd Party Manuf

Primary Location: NL-NH-Haarlem
Other Locations: Belgium, IT-25-Pavia, NL-NB-Oss
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Haarlem-Supplier-Development-&-Performance-Mngmt-Specialist-Job-NH/1851268/185126818512682012-06-15Merck/MSDQual Assurce - 3rd Party Manuffull-timeUSDstarting0BSHaarlem, NH, NL
Description

Department

Analytical Development and Validation (ADV) is a scientific Center of Excellence responsible for advanced analytical characterization of protein products. Over 60 highly trained professionals support development of commercial manufacturing processes, develop and validate quality control assays and perform complex analytical characterization and trouble-shooting. The in-depth expertise on analyses of proteins is crucial to the MSD network and is truly unique in the Netherlands.



You Provide leadership as an analytical manager of 4-5 scientists specialized in immunoassays and gel electrophoresis. Interface with groups that develop manufacturing methods for drug substance and drug product to optimize workflows. Perform critical evaluation of analytical output generated by the group. You act as an immunoassay subject matter expert within the Merck biotechnology network. Build an internal and external (industrial/academic) network to identify opportunities for innovation. You Identify new technologies that increase/improve the output of the group (e.g. high throughput assays). Identify scientific issues, develop solutions with stakeholders and implement solutions. Prepare and deliver oral and written technical reports for regulatory purposes.

Qualifications

Desired Skills & Experience

· PhD in analytical (bio) chemistry (or MSc with more than 5 years of relevant experience)

· In-depth experience with immunoassays (preferably to identify and characterize complex glycoproteins/antibodies)

· High scientific achievements/high degree of scientific credibility

· Excellent interpersonal and communication skills

· Strong results orientation and can-do mentality

· Fluent in English (Oral and written)

· Experience with assay automation (high throughput formats)

· Experience with gel electrophoresis, SPR (Biacore), Western blotting and/or substrate assays

· Knowledge of EU/US regulatory requirements

· Knowledgeable of laboratory safety guidelines

· Knowledgeable of statistical data evaluation

· Knowledgeable of late stage drug development

· Knowledgeable of Quality by Design principles

· Percentage in service 100

Information

For more information on the position please contact Corné Stroop, Section Head ADV; 0412 66 3140

Job
: Lab Technician

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Senior-Analytical-Scientist-%28groupleader%29-Job-NB/1855914/185591418559142012-06-15Merck/MSDLab Technicianfull-timeUSDstarting0BSOss, NB, NL
Description

Region/Country Marketing Learning Lead supports the identification of learning needs of the client, identifies appropriate learning solutions, and implements new and existing learning solutions that support the practice of marketing excellence with a specific focus on providing learning support to regional and / or country-level marketing and market access organizations in the Global Human Health division.

This is to include performance consulting to understand business learning needs, needs analyses, identifying program content, establishing training standards and protocols, designing program evaluations that measure learning gained and business impact, assessing future training direction/needs based on company goals and objectives, integrating advances in technology to enhance learning, supporting facilitation and delivery needs, serving as an expert resource on marketing process and practices and other related activities that meet the emerging needs of Global Human Health professionals.

* Works extensively with key stakeholders (Regional Marketing including Chief Marketing Officer and Marketing Excellence/Sales & Marketing Effectiveness professionals, Regional Market Access Leader, Country Leadership including Managing Directors/Country Managers/Business Unit Directors, Market Access Learning Lead and Brand/Customer Managers) to determine marketing capabilities and competencies that need to be developed.
* Develops client relationships, builds sponsorship, and ensures timely communication to meet client business outcomes
* Captures regional/country level input to inform the design and development of learning in support of global marketing initiatives
* Supports the implementation of associated learning for globally sponsored marketing and market access initiatives and customizes as necessary to meet local learning and execution needs.
* Develops, secures, maintains, and when appropriate serves as faculty for learning programs
* Facilitates the sharing of internal and external best marketing practices techniques and/or applications across the division.
* Performs periodic analyses on the performance and activities associated with learning initiatives.
* Supports marketing process/practice owners to realize adoption of marketing process and capabilities using effective learning methods.
* Performs administrative functions (e.g. management presentations) in a professional and timely fashion.
* Directs those activities intended to evaluate and measure learning results and impact relative to business and strategic objectives. .

Qualifications

Education Minimum Requirement:

* Bachelors Degree required
* Master's Degree preferred

Required Experience and Skills

* Minimum of three (3) years experience in either Marketing or in a Marketing Support function
* Minimum of seven (7) years Pharma or similar industry.
* Demonstrated leadership and project management skills critical.
* Strong commercial experience, well applied business & marketing acumen.
* Global business experience and cultural sensitivity
* Strong meeting and training facilitation skill in multi-cultural settings are essential.
* Knowledge of/experience in Performance Consulting techniques and Instructional Design highly desirable
* Demonstrated experience and skill in conducting performance and needs analysis and ability to summarize and communicate needs and recommendations to management at all levels verbally and in writing.
* Excellent interpersonal and communication skills required.
* Ability to effectively work on a project team, often from remote locations/virtually, with employees at all levels
* Good judgment, problem solving, decision making and follow up skills
* Ability to adapt to the changing needs of customers and the business

Desired Experience and Skills

* Experience in Learning strongly preferred
* Knowledge of/comfort with technology a plus
* Experience in marketing &/or market access learning a strong plus
* Ability to coach and counsel performance
* Multi-lingual skills desired

Experience with Marketing/Merck Marketing (e.g. SCOPE) as strong plus

*LI-DR1

Job
: Technical Training

Primary Location: CH-Lucerne
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Europe-Canada-Systems-Leader-Job-OK/1774610/177461017746102012-06-15Merck/MSDTechnical Trainingfull-timeUSDstarting0BSCH-Lucerne
Description

This role will be part of the process team starting up and providing on going technical support to the filling processes at our Vaccines & Biologics Formulation / Fill facility in Carlow. The successful candidate will be responsible for providing process and technical support to selected sterile processing operations, ongoing support of manufacturing processes and support for the introduction of new products. Also responsible for analytical and engineering studies associated with the development of new components, products, processes, systems, and facilities.

Key Responsibilities:

· Represent function on multi-disciplinary teams tasked with start-up, qualification, validation, new product introduction and ongoing process / product support. This will involve team leadership, technical input and execution of planned work.

· Support and execute process related investigations and work across functions to produce robust corrective actions

· Lead / Work on projects using lean and statistical tools to drive continuous improvement. Projects may range from Kaizen events to large multi-disciplinary projects

· Protocol & Report generation in support of the introduction of new product / processes

· Generation of Design of Experiments (DoE) to support robust transfer of new products to the Carlow site in line with LSS principles

· Support on the manufacturing floor and technology operations laboratory studies for shakedown, process development and engineering batches

· Tech support during routine manufacturing operations

Key Attributes

· Experience of Sterile fill processes and equipment

· Strong technical focus to develop and execute project plans

· Excellent experience of process improvements.

· Knowledge of Information Technology and automated production systems

· Experience in producing and reviewing documents such as process descriptions and PFDs is essential

· Strong communications skills

· Experience of participating and leading multidisciplinary teams

· Collaborative and inclusive approach to work

· Detail orientated

Qualifications

Experience

· Minimum of 2 yrs experience in biotechnology/pharmaceutical industry in a production/process role with considerable experience in sterile filling processes.

· A history of partnering with groups across an organization.

· Experience with automated production systems such as Distributed Control Systems (DCS) and PLCs

· Lean Six Sigma and / or Operations Excellence experience is desirable

Education

· Bsc. in Engineering, Science or similar discipline

Job
: Process Engineering

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 3]]>http://jobs.merck.com/job/Technology-Transfer-%28TT%29-Lead-ScientistEngineer-Job/1094575/109457510945752012-06-15Merck/MSDProcess Engineeringfull-timeUSDstarting0BSIreland
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This newly created position within the Merck Animal Health organization will be responsible for the development and leadership of the Poultry Species Research Team.

Responsibilities will include but are not limited the development of short and long-term business strategies designed to progress and achieve the business objectives of the Merck Animal Health organization in this business segment.

* Primary responsibility is for development of new vaccines with a global reach for their species (products registered in the US are currently marketed in over 50 different countries)
* Expectation to work closely with Sales/Marketing and Technical Veterinarians to build disease solutions that include vaccines and adjacent technologies (such as diagnostics)
* Has team of ~10 scientists directly reporting to position, but project team sizes can be as large as 30, due to utilization of global resources in matrix teams
* Expected to set vision for introduction of new technologies to address current un-met needs and new diseases as they emerge
* Will play a key role in mining technology and ideas through academic and third party collaborations and network

Qualifications

Education Minimum Requirements:

* DVM/VMD or Ph.D. in a Biological Sciences discipline

Required Skills and Experience:

* Minimum of 10 years poultry species R&D experience which includes the development of vaccines
* Experience must also include fluency with applicable federal government regulations and GLP, GCP and GMP standards.
* Excellent communication skills

* Able to lead diverse teams and drive decisions in the presence of complex choices

* Business Acumen - Understanding of competitor products and market needs to provide vision to be best-in-class

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003352.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-JE1

Job
: Biology-Discovery

Primary Location: US-NE-Elkhorn
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Head%2C-Poultry-Healthcare-Products-Research-Job-NE-68022/1460281/146028114602812012-06-15Merck/MSDBiology-Discoveryfull-timeUSDstarting0BSElkhorn, NE, US
Description

Implementation of the digestion of animal cell cultures on a scale from 100L-2000L with all associated preparatory work. Responsible for the training and the maintenance of the facilities. All works are subject to the cGMP guidelines and must be documentary wobbles accordingly.

Responsibilities

The primary activities include but are not limited to:

•Preparation, execution and evaluation of fermentations
•Performs independent analysis for process control necessary to process given by
•maintenance of the facilities used for fermentation and analysis and equipment
•Understands and follows the guidelines for cGMP by WAG and SP in their area
•Prepares, if necessary by the Engineer Controls & Compliance Biotech and the supervisor, GMP-relevant documents (eg, batch sheet's, SOP's, solution sheets, qualification documents).
•Performs skills independently after instructions from the supervisor or the Engineer Controls & Compliance by
• Appointed as necessary to chemicals and consumables required

Qualifications

Education:
Chemistry or biology lab technician, chemical technician

Skills Required:
cGMP experience, English,

Competencies:
Accurate and reliable work, willingness to work irregular hours including weekend work, teamwork, flexible, ready for new challenge

Job
: Biology-Discovery

Primary Location: CH-LU-Luzern
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-Technician-Fermentation-Job-LU/1848102/184810218481022012-06-15Merck/MSDBiology-Discoveryfull-timeUSDstarting0BSLuzern, LU, CH
Description

Department

Facilities Management (FM) operates and provides comprehensive facility en site services efficiently en effectively, in a safe and compliant manner, allowing clients to focus on their core business.



The Director Facility Management Manages all FM assets through a life cycle management model. You work closely together with the Director Contract Management to deliver the Hard Services through the integral facility management (IFM) provider required to keep buildings in the required state.

You develop replacement plans for assets. Assures compliance with regulatory and MSD requirements for Quality and Environmental Health and Safety (EHS).

You provide technical /facilities expert guidance to colleagues, clients and service providers. You are responsible for efficient occupation of buildings. Manages and develops a team of 12 specialists on building management. Leverages relationships by interfacing and influencing clients, Global Engineering and service providers to produce optimal result.

Is responsible for an annual capital budget of approximately 12 M Euro at the Moleneind site, a maintenance projects budget of 3 M Euro and an energy budget of approximately 11 M Euro.

Qualifications

Desired Skills & Experience

You have 15 + years experience in engineering/management, project engineering or production role at a major research lab or production facilities operation. 5+ experience years fully directing/managing maintenance/engineering services at a pharmaceutical manufacturing facility or significant lab facility. Strong leadership and interpersonal skills within a matrix management environment. 5-10 years managing third party service providers in facilities/engineering

Fluent verbally and in writing in English and Dutch. It is desirable to have experience in both line and staff responsibilities. Good interpersonal, leadership and negotiating skills, presentation, independence, creativity in problem solving and can-do mentality are required. Experience with Merck Sigma, presentation (Powerpoint), Computerized maintenance management system (CMMS) and financial analysis tools (Excel) is desirable.

Information

For more information on the position please contact Erik Meerwaldt, Sr Director Facilities Management; +31 412 662474

Job
: Facilities Management

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Director-Facilities-Management-Job-NB/1862513/186251318625132012-06-15Merck/MSDFacilities Managementfull-timeUSDstarting0BSOss, NB, NL
Description

The LSS Engineer will be part of the site LSS team, with primary responsibility for providing specific LSS tools and methods support for site tech transfer programs to help deliver stable, capable and robust products and manufacturing processes resulting in optimised Right First Time ( RFT ) performance upon commencement of commercial production.

The LSS engineer will work closely with the site product leads and tech transfer teams at all stages of the pipline/in-line transfer process as outlined in the ICH QbD philosophy and ensure the systematic management and analysis of product and process data during these stages.

The LSS engineer will also ensure the systematic use of risk management tools ( FMEA ) and quality improvement tools ( QFD ) during the tech transfer stages.

The LSS engineer will be responsible for providing data analysis and quality tool training and support to the tech transfer team members.

A secondary responsibility will be to support various site LSS initiatives as outlined in the site MPS roadmap.

Qualifications

Education :

Preferably degree qualified in Engineering, Science or Mathematics.

LSS Certification.

Ideal Experience :

Ideally, the successful candidate will have 5 years experience working in a pharmaceutical sterile liquid product form/fill facility on tech transfer projects from process development phase through to commercial production. The candidate will be familiar with the ICH QbD philosophy on the phases of product and process development and will have hands on experience of establishing systems within a MES environment to gather and analyse cycle/process development data and experience of using this data to characterise and optimise manufacturing processes. Alternatively, similar type new product introduction experience in a manufacturing environment.

Essential Experience :

Use of all of the following data analysis, problem solving and process improvement tools : Product and process FMEA's ; Design and analysis of DOE's including screening and fractional factorial designs ; Conducting process stability and capability studies with normal and non-normal data ; Conducting measurement system analysis studies for attribute and variable data ; implementing statistical process controls for attribute and variable data environments ; use of QFD ; expert use of statistical analysis software packages ; experience of implementing lean manufacturing principles in a manufacturing environment.

Skill & Capabilities:

-Ability to be self directed and also work effectively within teams.

-Ability to present and articulate data analysis findings which can be understood by all levels of the site

-Ability to deal with ambiguity and uncertainty and have strong personal resilience, and excellent organization skills.

-Demonstrate behaviours that foster an inclusive environment.
-Ability to influence without formal reporting lines.

Job
: OE/Six Sigma

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Sigma-LSS-Engineer-Tech-Transfer-Job/1487041/148704114870412012-06-15Merck/MSDOE/Six Sigmafull-timeUSDstarting0BSIreland
Description

This role will be part of the process team starting up and providing on going technical support to the filling processes at our Vaccines Formulation / Fill facility in Carlow

An engineering role focusing on vision and other automated inspection for in-line sterile products in syringes and vials. .

- Closely working with senior members of existing team and receiving on the job training.

- Provides process, equipment and operation knowledge on all relevant Inspection systems and qualification strategy.

- Assisting with delivery of the on-site Inspection program schedule and drive to meet schedule needs.

- Supports characterization of the process parameter ranges for products on the inspection equipment.

- Assisting completion of Knapp statistical baselines for oncoming Carlow products.

- Supports operations with ongoing inspection issues, process improvements and drives to root cause resolution.

- Lead and supports Quality functions with investigations, deviations, Quality notifications and AQLs.

- Supports establishment of statistical process control limits(PCL's) for inspection process reject rates.

- Support the preparation and manufacture of defective sample product to support qualification challenges

- Involvement in set-up (vision tuning) of automated inspection systems to meet production yield expectations and quality / regulatory standards

Qualifications

1-3 years experience in a processing engineering role in pharmaceutical, medical device or electronics Industry would be advantageous.

Strong technical writing and communication skills.

Strong computer literacy

Experience with automated process control systems would be an advantage (e.g. computerized equipment controls, OEM SCADA, HMI use etc.)

Lean Six Sigma and / or Operations Excellence experience is desirable

The candidate should be able to show evidence of process improvement accomplishments.

A history of partnering with groups across an organisation. The successful candidate for this role will need to partner with discipline such as IT, Operations and Quality to deliver robust processes

Comfortable working in a project environment with multiple schedule driven tasks and targets

Education:

Min Degree Qualified Engineering or Science related discipline.

1 - 3 years Industrial Experience in the pharmaceutical, medical device or electronics industries

Job
: Process Engineering

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Process-City-Process-Engineer-%28Inspection-Systems%29-Job-AR/1405510/140551014055102012-06-15Merck/MSDProcess Engineeringfull-timeUSDstarting0BSIreland
Description

SUMMARY OF POSITION

The position reports to Head Commercial and Market Access, dotted to General Manager.

The position will support and manage local pricing and reimbursement projects.

The position will be responsible with negotiations, relations and provide product value proposition support to stakeholders, payers and institutional administrative.

SPECIFICALLY:

* To assist in the development and implementation of reimbursement strategies for MSD products
* To assist in the development of product specific value based propositions and communication tools
* To monitor and report on competitive pricing actions and decisions.
* To monitor and report on reimbursement coverage of MSD and key competitive products.
* To request price actions.
* Work with headquarters and affiliate brand personnel, headquarters and affiliate finance personnel and headquarters and affiliate pricing and reimbursement personnel
* Monitor the literature in relation to Pharmacoeconomic publications that may have positive or negative implications for MSD's current and future products.
* Be aware of and work within company policies (Finance & HR) and industry guidelines (eg PhRMA, ISPOR,) and apply MSD Values in daily activities
* To develop planning for access initiatives in country operations
* Own the relation and communicate to NGO's, Payers, stakeholders, decision makers and main actors in reimbursement process.
* Implement and coordinate specific drivers to get access.
* Added value proposition development and communication to NGO's, Payers, stakeholders decision makers and main actors in reimbursement process.
* Work with institutional or national budget holders providing advise and support about financial efficiency and use internal data.
* Perform other functions and duties that may be assigned.

MAJOR ACTIVITIES OR RESPONSABILITIES

Market Access Landscape (60%)

- Identify Market Access barriers and opportunities along all brands.

- Development and implementation of Market Access strategies to improve and ensure patient access to treatments.

- Regional strategies implementation

Pricing Analysis (20%)

- support country price change requests

- analyze pricing levels according to Global Guidelines and maximize rentability

- Present and support local price actions to head quarter's teams.

Competitor Price Reviews (10%)

- analyze price level competition according with local market dynamics

- Creation and implementation of tools to support prices

Other activities to be defined accordingly (10%)

Qualifications

Educational Requirements

Minimum: Bachelors in Health Sciences or Bachelor of Finance, Marketing, Economics or Business Administration

Preferred: Masters or MBA

Professional Work Experience

Minimum: 3 to 5 years in the area

And

Demonstrated ability to develop and manage agency and Key opininion leaders relationship

Demonstrated ability to collaborate with international teams

Specific skills: Proficient in MS Office software

Advanced knowledge of MS Excel

Good written and verbal communication skills

Attention to detail

Demonstrated ability to work cross-functionally in pharmaceutical company environment

Job
: Account Management Generic

Primary Location: AR-Buenos Aires-Vicente López
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Vicente-L%C3%B3pez-Market-Access-Manager-Job/1895234/189523418952342012-06-15Merck/MSDAccount Management Genericfull-timeUSDstarting0BSVicente López, Buenos Aires, AR
Description

Afdeling:

De afdeling Quality Control Biotech bestaat uit twee laboratoria die enerzijds verantwoordelijk zijn voor de analyse van monsters uit de Biotech productieprocessen, en anderzijds voor de analyse van vrijgifte- en stabiliteitsmonsters van Biotech producten. De afdeling Quality Control heeft 18 medewerkers en maakt deel uit van het Biotech Quality Centre of Excellence. De afdeling werkt nauw samen met o.a. de productiefabrieken en met de analytische ontwikkelingsafdeling.

Functie

* Uitvoeren van analyses t.b.v. produktieproces controle en voor vrijgifte testen van de Biotechnologische produkten
* Rapporteren, verifiëren, valideren en evalueren van analytische resultaten
* Deelnemen aan van verbeter projecten
* Deelnemen aan trouble shooting activiteiten

Qualifications

Eisen

* HLO Analytische (Bio) Chemie of soortgelijke opleiding
* Minimaal 2 jaar relevante ervaring
* Ervaring met het analyseren van eiwit moleculen is vereist
* Ervaring met GMP is vereist
* Ervaring met analyse techniek Elisa is vereist
* Sterk in de nederlandse taal en redelijk in de engelse taal is vereist
* Goede communicatieve vaardigheden
* Resultaatgericht en een echte doe mentaliteit
* Min. 32 uur per week beschikbaar

Job
: Quality Lab Related

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Laboratorium-Specialist-Quality-Job-NB/1866482/186648218664822012-06-15Merck/MSDQuality Lab Relatedfull-timeUSDstarting0BSOss, NB, NL
Description

Global Engineering Services aims to be the best engineering organization within the best healthcare company. We exist to help MSD manufacture and deliver pharmaceutical, consumer, and animal health products to our customers by delivering extraordinary engineered business solutions. We espouse the following values:

* Safety and Compliance are Core Personal Values
* Honesty & Integrity in all We Do
* Trust and Respect for our People
* Customer Focused
* Foster Collaboration, Teamwork, Internally & Externally
* Inclusion is Core Value

Responsibilities

You are responsible for the scoping of a portfolio of around 150 small and middle scale facility and manufacturing projects at MSD sites in Oss. Activities range from business case verification, through concept design and implementation to ensure compliance with applicable Merck polices and standards. Projects may include all aspects of API, Pharmaceutical and Bio Pharmaceutical development production facilities. You will also act as a Subject Matter Expert for Electrical & Instrumentation, Controls.

Qualifications

Bachelor or Masters Degree in an Engineering discipline (preferably Electrical) combined with relevant experience in engineering of E&IC for project for e.g. Pharma, Energy or FMCG. You have at least four years of experience in Electrical, Instrumentation and/or Automation (PLC & SCADA systems and control hardware) in relation with Bio Pharmaceuticals and aseptic unit operations. Experience in governing EPCM contractors and process engineering is a preference. Fluent in English & Dutch. On occasion flexibility will be required with regards to travelling.

More information: Hans Hollebek, hans.hollebek@merck.com, tel. 0412-66 3486. Reference number: 11898HB

Job
: Engineering Generic

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Project-Engineer-Electrical-&-Instrumentation%2C-Control-Job-NB/1881751/188175118817512012-06-15Merck/MSDEngineering Genericfull-timeUSDstarting0BSOss, NB, NL
Description

MSD in Lucerne/Switzerland is a Swiss subsidiary of the successful global pharmaceutical company Merck & Co. Inc. with its headquarters in USA. Approx. 100'000 employees are currently working for us globally and we are showing strong growth.

Our Swiss operations include MSD International GmbH, Merck Sharp & Dohme-Chibret AG,Essex Chemie AG, Schering Plough Central East AG and Werthenstein BioPharma GmbH with currently 700 employees.

For our BioPharma Site Werthenstein in Schachen we are currently looking to fill the position for a

Criystallization Process Development Scientist

Task description:

The Merck/MSD Crystallization Lab (XLab) located at the WAG site in Schachen, Switzerland (outside of Lucerne) supports crystallization process development for all small molecules Active Pharmaceutical Ingredients (API) in the MSD pipeline."This group is seeking an individual contributor who will serve as a resident crystallization expert focused on assessing the commercial viability of identified crystal forms, developing crystallization/milling/filtration/drying processes, supporting crystallization process troubleshooting and technology transfers, and conducting technology development in the area of crystallization processing and API physical property control. The position involves interfacing with the Pharmaceutical Science and Process Chemistry groups through membership on cross-functional product and technology development teams. The subject matter expert will also be expected to develop, share, and facilitate use of best practices in laboratory experimentation and development.

The incumbent must be a highly productive, results-oriented individual able to develop original ideas or innovative approaches that make a major scientific or technical advancement to projects within the MSD pipeline. The position requires advanced technical knowledge in API process development; expert knowledge of kinetics, thermodynamics, and crystallization fundamentals; familiarity with standard crystallization diagnostic tools (for example, microscopy, FBRM, FTIR, etc.); and sound knowledge of related fields in pharmaceutical product development. Good communication (fluency in English) and interpersonal skills are also needed to collaborate on assigned projects and to coach, advice, train, and/or motivate non-reporting engineers and scientists. Experience on cross-functional teams, familiarity with Pharmaceutical Science needs with respect to bioavailability and formulation issue, and an ability to interpret physical measurements data are all prefe

Qualifications

Education Minimum Requirement:

* The position requires a Ph.D. in Chemical Engineering or Chemistry from an accredited college/university or B.S. and/or M.S. in Chemical Engineering or Chemistry from an accredited college/university
* Min. of 3 years of relevant work experience.

Required Experience and Skills:

* For BS/MS candidates, at least 3 years of relevant work experience is required, while for PhD candidates, relevant work experience is strongly preferred. Relevant work experience may include the following:

o Experience with process development, scale-up, and technology transfer, moving from laboratory to pilot plant and/or production scale.

· Demonstrated capability to develop and execute an experimental program to address issues of process robustness, productivity, and cost, integrating efforts with specialists in other technical disciplines.

· Demonstrated proficiency in balancing resource requirements within projects and among multiple assigned projects.

· Familiarity with fundamental crystallization concepts and experience with state-of-the art crystallization process development tools such as FBRM, FTIR, automated lab reactors, and physical characterization equipment (XRD, DSC, etc).

· Experience with chemical engineering-related technology development

Other Considerations:

· A European passport allowing for work authorization in Switzerland is required

· The candidates must be fluent in English (oral and written communication)

· The job will require travel in support of issue resolution and technology transfers in Supply. This is expected to constitute < 25% of the incumbent's time

· Relocation from within Europe will be provided

· The position is for a non-manager/individual contributor reporting into the head of the Chemical Process Development & Commercialization Crystallization Lab located in New Jersey, USA.

Are you interested in this very challenging and exciting role? Then please apply online and send us your profile for review.

Job
: Research Science Generic

Primary Location: CH-Lucerne
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Halley-Research-Station-Crystallization-Process-Development-Scientist-Job/1799253/179925317992532012-06-15Merck/MSDResearch Science Genericfull-timeUSDstarting0BSCH-Lucerne
Description

Summary of Responsibilities

Based in the EMEA Shared Business Service Centre in Dublin, the successful candidate will support the EMEA region the individual will be responsible for the development of reports using business intelligence technology and data available in SAP. The individual will be responsible for providing functional leaders with timely reports/analysis designed to support strategic and tactical decision making. Working closely with SBS stakeholders to understand business requirements, and translates these requirements into plans for delivery. A deep knowledge of SAP data models and specific data objects is required along with experience of business intelligence and reporting technology to design and deliver on reporting requirements. The scope of the reports may include various business performance measures such as process cycle times and volumes, as well segmentation, trending, clustering and forecasting analysis. The individual must perform quality control using various validation/verification techniques and documentation to ensure the reports work as intended. The individual is expected to participate as part of a community of similar roles supporting other SBS regions including the SBS Information Management Center of Excellence. As part of the community of practice, the incumbent is expected to share ideas and best practices. The individual needs to stay current with industry best practices in the uses of analytics and reports to create business opportunities and solve problems. The individual core responsibilities are in support of SBS EMEA, but may be involved with global initiatives

Primary Activities

· Engage SBS stakeholders to understand business goals and objectives

· Act in the capacity of a business analyst to identify and prioritize business reporting requirements

· Design and deliver business reports using SAP data and business intelligence technology (Spotfire)

· Test business reports to ensure quality

· Collaborate as a member of a global community of practice in order to learn and collectively advance the discipline

Qualifications

Qualifications

Bachelor's Degree or equivalent and at least 4 years of relevant work experience with demonstrated expertise in business analysis, business requirements development, report design and delivery, data architecture and/or data management. Their individual must have the ability to:

§ Effectively interact with MSD stakeholders to assess ideas and understand business reporting requirements

§ Understand the value of analytics and reports to provide insight and optimize business operations;

§ Translate reporting requirements into designs and deliver reports involving SAP ECC and BW data models, and business intelligence technology such as Spotfire;

§ Test reports to ensure they meet quality standards

§ Participate as a member of a community of practice to learn from others and share ideas.

The Individual must also demonstrate the following:

§ Deep knowledge of the data and SAP data models that supports

§ Strong ability to understand and visualize data relationships across data objects

§ Strong ability to produce solutions involving visualizations of business models

§ Direct experience with business intelligence reporting tools such as Cognos, SAP BI, Business Objects, Spotfire, etc.

§ Understanding of descriptive modeling and navigation techniques (segmentation, trend analysis, slide-and-dice, etc.)

§ Strong problem solving skills

§ Customer focus

§ Experience and orientation towards verification/validation/quality control

§ Results orientation

§ Excellent communication and interpersonal skills are required along with demonstrated experience working with cross-functional teams.

§ Sigma certification is desirable.

Job
: Business Consulting

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Business-Corner-Business-Financial-Analyst-Job-OH/1606560/160656016065602012-06-15Merck/MSDBusiness Consultingfull-timeUSDstarting0BSIreland
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Qualifications

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # DIR004167.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Channel Sales Generic

Primary Location: US-Minnesota
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Specialty-Representative-HIV-%28-MinneapolisMilwaukee%29-Job/1877978/187797818779782012-06-15Merck/MSDChannel Sales Genericfull-timeUSDstarting0BSUS-Minnesota
Description

Process - Maintenance Engineer / Instrumentation & Control

* Work with the maintenance team to ensure that Calibration program and Planned Maintenance are complete to the schedule.
* Participates in internal and external audits and inspections;
* Manage process / equipment improvements through completion of projects as required.
* Drive continuous improvement, perform root cause analysis on system failures and substandard equipment performance, using standard tools and methods, to resolve machine and system issues e.g. FMEA, Fishbone diagrams, 5 why's etc, all under aseptic/clean room conditions.
* Responsible for delivery of training, while focusing on continuous process improvement using Lean Principles.
* Troubleshoots equipment problems, identifies need for new equipment and/or modifications to existing equipment to optimize throughput and reduce process cycle times; Drive change through Change control
* Reduce maintenance costs and improve the overall equipment effectiveness by driving Total Productive Maintenance (TPM)
* Oversees coordination of resources to implement suggestions/ideas of merit;
* Serves as the point-of-contact for new equipment and/or modifications to existing equipment;
* Facilitates focus on continuous improvement activities utilizing six sigma and lean methology.
* Provides input review and approval for atypical , observation, and process capability investigations;
* Recognizes and investigates opportunities for financial savings and supports opportunities for financial savings by providing resources, expertise and project work; Participates in development of profit plan and budgets.

Drive continuous improvement and root cause analysis. Ensure planned Maintenance and calibration program are completed to the schedule.

Qualifications

* BS, BA Degree, Instrumentation and Control or equivalent required in Engineering, Science or related discipline.
* 5 + years of related work experience in a GMP manufacturing environment.
* Experience of managing Calibration and Maintenance systems.
* Experience in high speed manufacturing environment an advantage.
* Experience with HVAC, Autoclaves, SIP/CIP, Formulation an advantage.
* Applicant should have previously demonstrated strong team and communication skills, flexibility, motivation, ability to project manage, with a strong emphasis around safety and compliance practices.
* Applicants should actively support, participate and embrace an empowered team culture and have excellent communication skills

Job
: Production / Maintenance

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Carlow-Maintenance-Engineer-Job-L/1703555/170355517035552012-06-15Merck/MSDProduction / Maintenancefull-timeUSDstarting0BSCarlow, Leinster, IE
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Specialty Representative is a key member of the HIV Specialty Team and plays a critical role in supporting Merck's customer centric business model. He/she is responsible for working with the HIV Specialty Team to understand and identify Health Care Provider (HCP) customer needs, support pull-through activities relative to the customer strategy, and ensure that Merck is viewed as demonstrating value and better health outcomes to healthcare professionals and their patients.

The primary activities include:

* Communicates about product in a way that's meaningful and relevant to each individual customer; customizes discussions and client interactions based on understanding of customer's needs
* Engages in informed discussions about products with HCP customers - knowing when/how to seek and provide additional information
* Within select customer accounts acts as primary point of contact for customer, meet with key customers/personnel to understand practice structure, business model, key influencers Managed Care Organization (MCO), employers, state and local regulations)/network structure, customer needs and identifies business opportunities
* For select customer accounts/HCPs, coordinate with customer team to develop customer strategy - outlining strategy for interactions/ relationship, solutions and potential offerings for customer
* Partners with National Account Executives (NAEs) to maintain strong focus on Managed Care pull-through
* Shares learning and best-practices from one customer to help other customers meet their needs
* Demonstrates a focus on better health outcomes (beyond acquisition, considers the HCP and patient experience)
* Provides input into resource allocation decisions across customers
* Identifies and selects programs/services available in the library of Merck "resources" to address customer needs
* Works with solutions group (Headquarters - HQ) and/or Medical Account Executive (MAE) to develop and deliver relevant offerings that address desired customer needs
* Maintain current understanding of practice structure, business model, key influencers/ network structure and make information available to relevant stakeholders
* Collaborate and communicate effectively with extended "in-scope" customer team to ensure a consistent customer experience across Merck's divisions and functional areas; ensure integration with National Account Executive (NAE), Merck Vaccines (MV) personnel, Health Management Services (HMS) Manager, Solutions Consultant, Customer Strategies and Solutions (CSS), Regional Medical Director (RMD) and other key stakeholders to share key customer learning and support customer needs
* Outstanding in all competency areas (Account Management; External Market Focus; 1:1 Customer Interactions)
* Influences beyond their specific geography or product area

Territory covers the state of Alabama and may be based in Birmingham or Montgomery, Alabama.

May require (6) overnights per month.

Qualifications

Education:

* Required: BA/BS
* Preferred: MBA/MS

Required:

* Prior experience working in a scientific field or healthcare environment

* Previous sales experience

* Prior experience developing new business opportunities with existing customers

* Experience establishing new customer relationships, understanding of Merck products and therapeutic areas

* Consistent performer in most competency areas

* Valid Driver's License

Preferred:

* Prior consulting or customer service experience
* Experience developing and executing a plan for engaging customers and meeting customer needs
* Understanding of Headquarter operations
* Ability to analyze metrics to assess progress against objectives
* HIV Sales Experience

Job
: Channel Sales Generic

Primary Location: US-Alabama
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Specialty-Representative-HIV-%28Alabama%29-Job/1877980/187798018779802012-06-15Merck/MSDChannel Sales Genericfull-timeUSDstarting0BSUS-Alabama
Description

MSD in Lucerne/Switzerland is a Swiss subsidiary of the successful global pharmaceutical company Merck & Co. Inc. with its headquarters in USA. Approx. 100'000 employees are currently working for us globally and we are showing strong growth.

Our Swiss operations include MSD International GmbH, Merck Sharp & Dohme-Chibret AG, Essex Chemie AG, Schering Plough Central East AG and Werthenstein BioPharma GmbH with currently 700 employees.

We are currently expanding our international hub in Lucerne and are therefore looking for an

Administrative Assistant

Responsibilities:

· Responsible for performing administrative support tasks for executive level

· Scheduling executive appointments and meetings

· Calendar maintenance for executive level employees

· Answering/screening/routing telephone calls

· preparing expense reports

· preparing and editing executive presentations

· Making travel arrangements and organize events internally and externally

Qualifications

· Commercial education or equivalent (KV), higher level education highly preferred.

· Typically requires a minimum of 3 + years' experience as general administrative assistant

· Ability to communicate in English, both orally and in writing, German preferred

· Very strong Word, Excel and Powerpoint user

· Team oriented and flexible

· Optimistic and passionate

· Open to feedback & learning

Are you interested in working in a very international and fast growing area? We would like to offer this opportunity to young professionals who want to be part of this group with global responsibility.

If you are interested in this interesting role the please send us your profile for review.

Job
: Administrative Svcs Generic

Primary Location: CH-Lucerne
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Moenkopi-Administrative-Area-Administrative-Assistant-Job-AZ/1774611/177461117746112012-06-15Merck/MSDAdministrative Svcs Genericfull-timeUSDstarting0BSCH-Lucerne
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position will lead a group of scientists responsible for routine, early development (non-GMP) analytical support testing. A highly dynamic person with experience in lab automation and high throughput testing is required. The position requires lab management skills with regard to sample workflow, testing schedules, data reporting and personnel management. The position will interact with various customers such as the cell culture, purification, formulation and new technologies groups and therefore requires excellent interpersonal communication skills.

Qualifications

Minimum Education Required:

* A Ph.D. in chemistry, biochemistry, biology or related biological sciences with 3-6 years experience or an MS with 10-15 years experience or a BS with 12-16 years experience in the pharmaceutical industry, ideally with well characterized biologics, is required.

Minimum Skills and Experience Required:

* Previous laboratory supervisory experience is required
* Excellent written and verbal communication skills are required.
* Experience in a team based environment is critical.
* Experience in a GMP environment is a plus but is not critical.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003578.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Bio/Immuno Assay Development

Primary Location: US-NJ-Union
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Union-Principal-Scientist-Job-NJ-07083/1828434/182843418284342012-06-15Merck/MSDBio/Immuno Assay Developmentfull-timeUSDstarting0BSUnion, NJ, US
Description

La société Merck d'aujourd'hui est un chef de file mondial dans le domaine des soins de santé qui œuvre au bien-être du monde. Grâce à nos médicaments, vaccins, traitements biologiques, produits de santé grand public et de santé animale, nous collaborons avec nos clients et œuvrons dans plus de 140 pays à procurer des solutions de santé novatrices.

Notre capacité d'exceller dépend de l'intégrité, des connaissances, de l'imagination, des compétences, de la diversité et du travail d'équipe de personnes telles que vous. À titre de membres de notre équipe, vous aurez la chance de travailler avec des collègues talentueux et dévoués, tout en vous perfectionnant et en cheminant dans votre carrière.

Relevant de la Directrice, Réglementation, ses principales responsabilités sont:

* La préparation et à la présentation des dossiers de nos produits aux organismes de réglementation fédéraux;
* Réviser et évaluer la documentation relative aux essais cliniques, à la fabrication et au marketing;
* Conseiller, de manière opportune et professionnelle, les clients internes (services du marketing, de l'exploitation, des affaires juridiques, des affaires médicales) et externes (Santé Canada).

Exigences

* Possède un baccalauréat ou une maîtrise dans un domaine scientifique apparenté à la santé;
* A acquis 3 années d'expérience dans l'industrie pharmaceutique;
* Connaissance de la Loi sur les aliments et drogues et de son règlement d'application ainsi que du processus entourant l'élaboration d'un produit;
* Avoir un bon sens de l'organisation;
* Faire preuve de professionnalisme;
* Être capable de gérer plusieurs projets de front, avec des échéances serrées;
* Avoir un sens aigu des affaires;
* Être fin stratège et agir conséquemment;
* Avoir un solide jugement et de l'initiative;
* Être habile négociatrice, faire preuve de tact et de diplomatie;
* Se montrer efficace au sein d'une équipe;
* Être capable de s'exprimer facilement en français et en anglais, tant à l'oral qu'à l'écrit;
* Exigences linguistiques : Français et Anglais

Nos employés constituent la clé du succès de notre société. Nous faisons preuve d'engagement envers eux en offrant un programme de récompenses concurrentiel et enrichissant. Les avantages de Merck sont conçus de façon à soutenir la grande variété d'objectifs, de besoins et de styles de vie de nos employés et des nombreuses personnes qui comptent le plus dans leurs vies. Merck souscrit au principe de l'égalité d'accès à l'emploi et adopte fièrement la diversité sous tous ses aspects.

Représentants des firmes de recherche de candidats

Veuillez lire attentivement :

Merck n'accepte aucune aide non sollicitée de la part de firmes de recherche pour cette offre d'emploi. Nous vous prions de ne pas téléphoner ni envoyer de courriels. Tous les curriculum vitæ transmis par des firmes de recherche à un employé de Merck par courriel, Internet ou de quelque autre façon que ce soit sans détenir une entente écrite en vigueur pour ce poste, deviendront la propriété exclusive de Merck. Aucun paiement ne sera versé dans l'éventualité où un candidat serait embauché par Merck à la suite d'une recommandation ou autre méthode.

Poste
: Nom générique : Normes gouvernementales

Localisation principale: CA-QC-Montreal (Kirkland)

Statut de l'employé: Temporaire

Nombre de postes vacants: 1]]>http://jobs.merck.com/job/Montreal-TMP-Chef-de-projet%2C-Affaires-r%C3%A9glementaires-Produits-grand-public-%28mandat-temp_-15-Job-QC/1883045/188304518830452012-06-15Merck/MSDNom générique : Normes gouvernementalesfull-timeUSDstarting0BSMontreal, QC, CA
Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Logistic Manager

Responsible for the Product Supply, in order to ensure customer satisfaction;

Responsible for imports and exports procedures including customs clearance of products, raw and packaging materials, requested by the organization;

Responsible for warehousing and distribution activities, including transportation, inventory management , warehousing, and ensuring structures are in place to monitor the flow of products.

Duties, Responsibilites, Activities:

* Monitoring the quantity, cost and efficiency of the movement and storage of goods
* Responsible for the Product Supply, including import and export procedures, customs, warehousing and distribution, in order to assure the product availability according to business plans and effective inventory management.
* Maintains a safe work environment and ensures compliance with safety objectives and policies.
* Identifies and implements continual improvement initiatives to enhance the performance of the position, team, and company
* Monitors and assures employees and work area compliance, visibly demonstrates commitment, leads by example, seeks immediate resolution of safety and environmental matters/concerns by providing appropriate resources, conducts employee training/orientation as required and conducts/participates in incident investigations.

Qualifications

Education: Bachelor's Degree

Preferred Area of Study: Business Administration or International Business

Experience: 3+ years of experience as Logistics Manager preferred

Skills/Knowledge:

Good planning, time management and organization skills.

Good communication and interpersonal skills.

Ability to lead a team.

Ability to make presentations to cross departmental staff/teams.

Ability to train less experienced staff, ability to handle multiple tasks simultaneously, and excellent writing skills

Knowledge of English language at advanced level is required.

Proficiency in the use of Microsoft Office, Excel, PowerPoint and Project is required.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. MSD's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

*LI-KT1

Job
: Logistics

Primary Location: PA-Panamá-Panamá
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/Panam%C3%A1-Logistic-Manager-Job/1885955/188595518859552012-06-15Merck/MSDLogisticsfull-timeUSDstarting0BSPanamá, Panamá, PA
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


We are looking for a motivated individual who will implement glycoprotein analytical methods in support of strain, process and pre-clinical development. The position offers an opportunity to gain experience in a wide range of protein characterization techniques, including chromatographic separations, glycosylation analysis, peptide mapping, Western blotting, IEF and ELISA. The position also offers opportunities to make significant experimental and intellectual contributions to our ongoing efforts in characterization of the biological processes for glycoprotein production. Skills of glycosylation characterization techniques using HPLC, Mass Spectrometry and cell culture techniques would be a plus.

Qualifications

Minimum Education Required:

* A BS with 7 years of experience or MS degree with 5 years of experience in Biological Sciences/biochemistry or related field.

Minimum Skills and Experience Required:

* Laboratory experience with execution of biochemistry experiments; theoretical knowledge of microbiology and protein biochemistry.
* Effective oral and written communication skills
* Capable of working independently in designing experiments and generating data.
* Demonstrated ability to work in a team environment and experience with characterization of proteins.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MOL000279.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Molecular Discovery

Primary Location: US-NH-Lebanon
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Lebanon-Research-Biochemist-Job-NH-03756/1826382/182638218263822012-06-15Merck/MSDMolecular Discoveryfull-timeUSDstarting0BSLebanon, NH, US
Description

MSD in Lucerne/Switzerland is a Swiss subsidiary of the successful global pharmaceutical company Merck & Co. Inc. with its headquarters in USA. Approx. 100'000 employees are currently working for us globally and we are showing strong growth.

Our Swiss operations include MSD International GmbH, Merck Sharp & Dohme-Chibret AG, Essex Chemie AG, Schering Plough Central East AG and Werthenstein BioPharma GmbH with currently 700 employees.

We are growing our international commercial organization in Lucerne and are therefore recruiting for a position as

Global Late Lifecycle Management Leader, Diversified Brands

This new leader will be responsible for driving planning across markets and brands to mitigate the impact of the upcoming LOE "Loss of exclusivity" to Merck as much as possible. The leader in this role will establish a best in class industry approach, leveraging internal and external benchmarks, and build the necessary capabilities to implement this approach. They will develop the overall strategy, identify high revenue opportunities across the portfolio and markets, and for specific products work cross-functionally with the other Customer Business Line leaders, Global Brand Leaders, Regional Marketing Leaders, Diversified Brand Commercial Leads and with market teams to develop and implement tailored strategies for products.

Specific responsibilities will include:

* Develop and implement overall Merck LOE/LCM planning strategy, including gaining appropriate level of senior management engagement and sponsorship across organization (Global Human Health, Merck Research Laboratories, Merck Manufacturing Division, markets) to sustain implementation and drive anticipated revenues:
* Identify products and markets for focus
* Establish clear planning approaches to optimize for revenue and drive execution and engagement model across all stakeholders
* Drive implementation and execution, using a lean, fast and efficient resource model
* Establish new metrics to measure/track performance
* Develop deep understanding of the market dynamics of LOE transitions to lead optimization of Merck's portfolio performance for LOEs globally
*
Esablish strong knowledge and understanding of drivers of product performance in LOE transitions, included but not limited to market dynamics, therapeutic/disease area needs etcDevelop deep understanding of the market dynamics of LOE transitions to lead optimization of Merck's portfolio performance for LOEs globally

* Establish standard approaches to undertake comprehensive product performance assessments for the peri/post LOE period
Develop a broad toolkit of practical approaches (product and solution-based) for managing peri/post-LOE transitions
* Develop expertise on impact of various approaches
* Coordinate with internal and external experts in the field to supplement knowledge base
* Coordinate with key support functions across the company (medical/legal, regulatory, clinical, manufacturing, OR etc) to ensure appropriate resourcing in support of peri/post-LOE transitions for products
* Develop knowledge of and assess potential partners/suppliers in support of transition planning
* Implement change management program to implement this new LCM/LOE planning approach

Qualifications

* Bachelor Degree required
* A minimum of 20 years relevant experience in lifecycle management, marketing, market access / managed markets, or process/change management related role
* Well-developed interpersonal skills with experience in interacting with colleagues at various levels are required
* Deep knowledge and and experience with peri/post LOE transitions (planning and execution). Particular experience with US and EU desired
* Wide-ranging commercial/operational experience with proven-track record
* Solid knowledge of Merck products, sales & marketing, competition and the pharmaceutical industry
* Superior analytical, problem solving, judgment, interpersonal skills
* Process development, analysis and improvement experience/skills
* Strong leadership, communication and program management skills
* Innovative and able to invent and create opportunities, Self starter
* Superior written and oral communication skills
* Well-developed interpersonal skills with experience in interacting with colleagues at various levels are required

Job
: Marketing Program Management

Primary Location: CH-Lucerne
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Late-Lifecycle-Management-Leader-Job/1750650/175065017506502012-06-15Merck/MSDMarketing Program Managementfull-timeUSDstarting0BSCH-Lucerne
Description

Merck Sharp & Dohme-Chibret AG ist die Schweizer Niederlassung der Merck & Co., USA. Merck entwickelt, produziert und vertreibt weltweit innovative Medikamente und gehört international zu den führenden Pharmaunternehmen. Weltweit arbeiten ca. 100'000 Mitarbeiter für uns.

Die Schweizer Organisation beeinhaltet die Unternehmungen MSD International GmbH, Merck Sharp & Dohme-Chibret AG, Essex Chemie AG, Schering Plough Central East und Werthenstein BioPharma GmbH mit gesamthaft 700 Mitarbeitern.

Für die Werthenstein BioPharma in Schachen LU suchen wir zur Verstärkung des Teams im GMP/Comparator Labs per sofort oder nach Vereinbarung eine/n

Analytiker-/in

Aufgabenbereich:

· Organisation, Koordination sowie selbständige Durchführung aller analytischen Aktivitäten im Zusammenhang mit Stabilitätsstudien und Freigaben von pharmazeutischen Vergleichsprodukten

· Entwicklung, Validierung und Transfer von analytischen Methoden für die Freigabe und Stabilität von pharmazeutischen Vergleichsprodukten

· Unterstützung der Laboranten bei ihrer Arbeit

· Mitarbeit bei globalen Projekten

· Geräteverantwortung

Qualifications

· Akademiker/in (Hochschulabsolvent/in oder Fachhochschulabsolvent/in in Chemie oder parmazeutischer Analytik) mit praktischer Erfahrung in der instrumentellen Analytik Erfahrung in GMP-Richtlinien wünschenswert

· Sehr gute Englischkenntnisse

· Hohes Qualitätsbewusstsein und Sinn für eine effiziente Arbeitsweise

· Ausgeprägte Lernbereitschaft und Selbständigkeit

· Teamorientierte und offene Persönlichkeit

*LI-DR1

Job
: Clinical Research Generic

Primary Location: CH-Lucerne
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1

Shift (if applicable)
: 2nd

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Analytiker-in-Job/1881752/188175218817522012-06-15Merck/MSDClinical Research Genericfull-timeUSDstarting0BSCH-Lucerne
Description

Reporting to the Service Team Manager or Supervisor, the RtR (Record to Report) Finance Analyst, is responsible for providing commercial services, in either general accounting RtR areas such as fixed assets, intercompany, general ledger, bank, and transactional tax.

The primary activities that you will be performing include:

* Executing the transactions required and the services as defined in the RtR area.
* Supporting the launch of SAP across major markets in Europe.
* Partnering with key stakeholders (Finance, Sales Procurement, etc) to ensure that all transactional activity is properly recorded and compliant with country statutory and tax requirements.
* Seek out opportunities for streamlining and rendering service delivery more efficiently, and participates in special projects to support Shared Business Services objectives.
* Resolve related issues pertaining RtR and an understanding of when, how and where to escalate cases as required to meet defined service levels.
* Additional responsibilities to support a new organization in Europe as required.

Qualifications

Education:

* Bachelors Degree required.

Preferred:

* A minimum of 2 years of demonstrated work experience within the General accounting and or PtP shared services area.
* Experience working in an organization providing services across multiple markets or geographies.
* A minimum of one year of experience working with SAP.
* High degree of integrity and personal ethics in implementing corporate policies and procedures
* Effective team player with collaborative focus
* Must be able to work in a fast-paced, dynamic environment, under pressure, and with a high degree of professionalism
* Must be comfortable in an environment of changing technologies and processes, and demonstrate flexibility in adjusting to new ways of working
* Experience working in a SOX404 environment.
* Strong oral and written communication skills.
* Flexible work arrangements will be considered based on business needs.

Job
: Treasury Operations

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Record-to-Report-Finance-Analyst-Job-VA/1366985/136698513669852012-06-15Merck/MSDTreasury Operationsfull-timeUSDstarting0BSIreland
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

El Gerente de Asuntos Regulatorios es responsable de obtener de las autoridades venezolanas el registro sanitario necesario para la comercialización de los productos elaborados o importados por la Organización, así como garantizar el cumplimiento de los requerimientos sanitarios locales y las políticas de la Compañía para la comercialización de los productos de MSD Farmacéutica

PRINCIPALES RESPONSABILIDADES:

- Preparar las solicitudes de registro de nuevos productos, nuevas indicaciones y posologías de manera que cumplan con todas las regulaciones sanitarias locales, seleccionando, evaluando y organizando la documentación técnico-científica que se obtiene de Casa Matriz.
- Mantener actualizados los productos comercializados por la Empresa de acuerdo a las regulaciones sanitarias venezolanas y las políticas de registro de la Compañía.
- Obtener de las autoridades sanitarias la aprobación para realizar en Venezuela cada estudio de investigación clínica que se decida llevar a cabo con los productos, sometiendo la documentación y estudios requeridos.
- Hacer seguimiento al registro en Venezuela de las marcas de fábrica de la Compañía, necesarias para la comercialización de sus productos en el país y mantener actualizados los listados de las marcas disponibles.
- Revisar y aprobar conjuntamente con el Director Médico el arte final de todo el material promocional de los productos, de acuerdo a la política de mercadeo de la Compañía y a las condiciones del registro sanitario local.
- Supervisar y controlar al personal a su cargo asegurando que cumplan con las políticas y normas de la compañía.
- Participar en las reuniones de trabajo de las diferentes asociaciones relacionadas con la Industria Farmacéutica

Cualificaciones
Educación:

Profesional Farmacéutico.

Registrado en el Ministerio de Salud.

Miembro del Colegio de Farmacéuticos de Venezuela.

Registrado en el Instituto de Previsión Farmacéutica.

Experiencia:

5 años o más de experiencia laboral en el area regulatoria, de los cuales, 4 años o más desempeñándose como Gerente.

Idiomas:

Inglés (Nivel intermedio-avanzado).

Competencias:

Organización y planificación. Orientación al trabajo en equipo. Orientación a resultados. Toma de decisiones rápidas y disciplinadas, Candor y Coraje, impacto e influencia.

*LI-KT1

Puesto
: Asuntos regulatorios genéricos

Ubicación principal: VE-Caracas Capital District-Caracas
Tipo de acuerdo laboral: Fijo(a)
Viajes: Sí, un 15% del tiempo
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Caracas-Gerente-de-Asuntos-Regulatorios-Job/1835827/183582718358272012-06-15Merck/MSDAsuntos regulatorios genéricosfull-timeUSDstarting0BSCaracas, Caracas Capital District, VE
Description

Analytical Development and Validation (ADV) is a scientific Center of Excellence responsible for advanced analytical characterization of protein products. Over 60 highly trained professionals support development of commercial manufacturing processes, develop and validate quality control assays and perform complex analytical characterization and trouble-shooting. The in-depth expertise on analyses of proteins is crucial to the MSD network and is truly unique in the Netherlands.

You will validate, execute and transfer analytical methods for the quality control of protein products. You will implement analytical methods, provide (trouble-shooting) support to quality control laboratories and participate in (international) analytical teams. You wil act as a technical lead in QC methods and deliver technical reports for regulatory purposes.

Qualifications

You are an MSc (or BSc with > 5 years of lab experience) in (analytical) science with expert knowledge in chromatography and/or capillary electrophoresis .Demonstrated ability to independently plan and execute tasks. Knowledgeable of statistical data evaluation. Strong results orientation, can-do mentality, excellent interpersonal/communication skills and fluent in English.

Information

For more information about this role, please contact Gerben Wynia, Section Head ADV; 0412663013.

Job
: Lab Technician

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Analytical-Scientist-%28GMP%29-Job-NB/1840109/184010918401092012-06-15Merck/MSDLab Technicianfull-timeUSDstarting0BSOss, NB, NL
Beschreibung

Summary:

Durchführung von Fermentation mit tierischen Zellkulturen im Massstab von 100L -2000L mit allen dazu gehörenden Vorbereitungsarbeiten. Verantwortlich die Qualifizierung und den Unterhalt der Anlagen. Alle Arbeiten unterliegen den cGMP Richtlinien und müssen auch dementsprechend dokumenteiert werden.

Job Description and Responsibilities

The primary activities include but are not limited to:

* Vorbereitung, Durchführung und Nachbereitung von Fermentationen
* Führt die zur Prozesskontrolle nötigen Analysen selbständig nach gegebenen Verfahren durch
* Unterhalt der zur Fermentation und Analyse verwendeten Anlagen und Apparaturen
* Kennt und befolgt die Richtlinien für cGMP von WAG und SP in seinem Aufgabenbereich
* Erarbeitet, wenn nötig mit dem Engineer Controls & Compliance Biotech und dem Vorgesetzten, GMP relevante Dokumente (z.B. Batch Sheet's, SOP's, Solution Sheets, Qualifizierungs Unterlagen).
* Führt Qualifizierung nach Anweisungen des Vorgesetzten oder des Engineers Controls & Compliance selbständig durch
* Bestellt wenn notwendig Chemikalien und Verbrauchsmaterialien nach Bedarf

Qualifikationen

Education:

Chemie oder Biologie Laborant, Chemikant

Skills Required:

cGMP Erfahrung, Englisch,

Competencies required for the role (max. 5)

Exaktes und verlässliches Arbeiten, Bereitschaft für unregelmässige Arbeitszeit incl. Wochenendarbeit, Teamarbeit, flexibel, bereit für Neues

Job
: Biologie/Entdeckung

Primärer Standort: CH-LU-Luzern

Mitarbeiterstatus: Permanent

Anzahl offener Stellen: 1

Externes Job Ausschreibungsportal
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-Laborant-Fermentation-Job-LU/1848112/184811218481122012-06-15Merck/MSDBiologie/Entdeckungfull-timeUSDstarting0BSLU, CH
Description
La société Merck d'aujourd'hui est un chef de file mondial dans le domaine des soins de santé qui œuvre au bien-être du monde. Grâce à nos médicaments, vaccins, traitements biologiques, produits de santé grand public et de santé animale, nous collaborons avec nos clients et œuvrons dans plus de 140 pays à procurer des solutions de santé novatrices.

Notre capacité d'exceller dépend de l'intégrité, des connaissances, de l'imagination, des compétences, de la diversité et du travail d'équipe de personnes telles que vous. À titre de membres de notre équipe, vous aurez la chance de travailler avec des collègues talentueux et dévoués, tout en vous perfectionnant et en cheminant dans votre carrière.

Relevant de la Directrice, Réglementation, ses principales responsabilités sont:

- La préparation et à la présentation des dossiers de nos produits aux organismes de réglementation fédéraux;
- Réviser et évaluer la documentation relative aux essais cliniques, à la fabrication et au marketing;
- Conseiller, de manière opportune et professionnelle, les clients internes (services du marketing, de l'exploitation, des affaires juridiques, des affaires médicales) et externes (Santé Canada).

Exigences
- Possède un baccalauréat ou une maîtrise dans un domaine scientifique apparenté à la santé;
- A acquis 3 années d'expérience dans l'industrie pharmaceutique;
- Connaissance de la Loi sur les aliments et drogues et de son règlement d'application ainsi que du processus entourant l'élaboration d'un produit;
- Avoir un bon sens de l'organisation;
- Faire preuve de professionnalisme;
- Être capable de gérer plusieurs projets de front, avec des échéances serrées;
- Avoir un sens aigu des affaires;
- Être fin stratège et agir conséquemment;
- Avoir un solide jugement et de l'initiative;
- Être habile négociatrice, faire preuve de tact et de diplomatie;
- Se montrer efficace au sein d'une équipe;
- Être capable de s'exprimer facilement en français et en anglais, tant à l'oral qu'à l'écrit;
- Exigences linguistiques : Français et Anglais

Nos employés constituent la clé du succès de notre société. Nous faisons preuve d'engagement envers eux en offrant un programme de récompenses concurrentiel et enrichissant. Les avantages de Merck sont conçus de façon à soutenir la grande variété d'objectifs, de besoins et de styles de vie de nos employés et des nombreuses personnes qui comptent le plus dans leurs vies. Merck souscrit au principe de l'égalité d'accès à l'emploi et adopte fièrement la diversité sous tous ses aspects.

Représentants des firmes de recherche de candidats

Veuillez lire attentivement :

Merck n'accepte aucune aide non sollicitée de la part de firmes de recherche pour cette offre d'emploi. Nous vous prions de ne pas téléphoner ni envoyer de courriels. Tous les curriculum vitæ transmis par des firmes de recherche à un employé de Merck par courriel, Internet ou de quelque autre façon que ce soit sans détenir une entente écrite en vigueur pour ce poste, deviendront la propriété exclusive de Merck. Aucun paiement ne sera versé dans l'éventualité où un candidat serait embauché par Merck à la suite d'une recommandation ou autre méthode.

Poste
: Nom générique : Normes gouvernementales

Localisation principale: CA-QC-Montreal (Kirkland)
Statut de l'employé: Temporaire
Nombre de postes vacants: 1]]>http://jobs.merck.com/job/Montreal-%28Kirkland%29-TMP-Chef-de-projet%2C-Affaires-r%C3%A9glementaires-Produits-grand-public-%28mandat-temp_-15-Job/1883037/188303718830372012-06-15Merck/MSDNom générique : Normes gouvernementalesfull-timeUSDstarting0BSMontreal (Kirkland), Montreal (Kirkland), CA
Description

Afdeling

Facilities Management (FM) levert en draagt zorg voor een uitgebreid pakket van huisvesting en locatiediensten, zodat onze klanten zich kunnen concentreren op hun kerntaken. Wij doen dit effectief en efficiënt, op een veilige manier en conform wet- en regelgeving.

De Functie

Hoofdtaken en verantwoordelijkheden van de Engineer FM voor de sector Pharmaceutical Operations Oss (POO) zijn:

* Verantwoordelijk zijn voor het in goede staat houden van de gebouwen en gebouwgebonden installaties.
* Zorg dragen voor het in gekwalificeerde staat zijn en blijven van Good manufacturing practice (GMP) kritische utiliteiten.
* Het adresseren van klachten en (huisvestings)problemen van klanten.
* Aansturen van van dienstverleners/contractors aan bij wijzigingen en niet- gestandaardiseerd onderhoud.
* Leiding geven aan kleinere projecten op het gebied van huisvesting, gebouwen en gebouwgebonden installaties.
* Iinitiëren, plannen en laten uitvoeren van verhuizingen inclusief de toepassing van MSD policies ten behoeve van huisvesting.
* Beoordelen en verantwoordelijkheid nemen met betrekking tot veiligheid in onderhoudswerk en kleinere projecten.
* Bewaking kosten/budgetten voor wijzigingen en (kleinere) projecten.

Qualifications

Wij vragen

* Technische of Facility Management opleiding op MBO+ of HBO niveau
* Greenbelt in Lean Six Sigma is een sterke pré
* Minimaal drie jaar ervaring in een technische positie
* Uitstekende contactuele eigenschappen
* "Can do" mentaliteit
* Sterk ontwikkeld probleemoplossende vermogen
* Goede mondelinge en schriftelijke uitdrukkingsvaardigheid aangevuld met goed presentatievaardigheden
* Aantoonbare projectmanagement kwaliteiten
* Uistekend ontwikkeld servicegevoel

We bieden

Houd je ervan te worden uitgedaagd, steeds weer, dan is MSD een goede keuze als werkgever. We hebben uitstekende arbeidsvoorwaarden en je krijgt er alle mogelijkheden om je verder te ontwikkelen en door te groeien. MSD geeft je veel ruimte voor eigen initiatief en je krijgt veel verantwoordelijkheid.

Contact

Voor meer informatie over de functie kun je contact opnemen met Henk Alers, Manager FM POO, 0412 662143

Job
: Facilities Management

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Engineer-Facilities-Management-Job-NB/1885952/188595218859522012-06-15Merck/MSDFacilities Managementfull-timeUSDstarting0BSOss, NB, NL
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Performs microbiological testing on a variety of samples, including but not limited to, finished products, bulk sterile products and vaccines, excipients, and process utilities (i.e. water). Applies procedures as prescribed by quality standards and compendia. Prevalent procedures include tests such as sterility, LAL, bioburden, MLT (microbial limit testing), and microbial identifications.

Ensures test data is accurate and all work is performed right first time. Supports both drug substance and drug product manufacturing processes by providing critical microbiological support. Assists with Technical Service Requests and other special studies. Works with lab colleagues to ensure testing is completed in a timely manner, ensuring production and shipping timelines are met. Position will also be responsible for assisting with laboratory GMP activities by performing instrument calibrations (where appropriate), instrument troubleshooting, laboratory atypical result investigations, data auditing, and sample flow management.

Qualifications

Education Required:

* Bachelor's degree in chemistry, microbiology, biology or other science related field.

Required Experience:

* Minimum 1 year related work experience.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition QUA002945.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality Lab Related

Primary Location: US-VA-Elkton
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkton-Associate-Analyst-Job-VA-22827/1885956/188595618859562012-06-15Merck/MSDQuality Lab Relatedfull-timeUSDstarting0BSElkton, VA, US
Description

Coordinate production activities and support equipment, including MES and SAP based systems, to ensure optimum equipment uptime and target outputs. Equipment will include, yet is not limited to, parts washers, autoclaves, portable tank CIP/SIP/storage panels, Vial Washer, Depyro Tunnel, Debagger and filling machines.

Coordinate schedules, tasks and resources in IPT and cross functionally, including vendor management, communications, training, project work, audit/inspection duties.

Coordinate clean room cleaning, housekeeping and materials management in all production areas while focusing on continuous process improvement using Lean Principles

Manage equipment flow, including tracking soiled and clean hold times, proper labeling and inventory management of clean and sterile equipment using Kanbans and automated MES system to set QC status and expiry of sterile equipment.

Ensure process equipment is maintained including preventative maintenance, equipment troubleshooting and repairs to ensure continuous, reliable and repeatable operation of equipment. Effectively manage and schedule equipment shutdowns, ensuring resources are available, thereby minimizing downtown.
Ensure effective participation in writing/revising/ rolling out accurate operational procedures, training documents and maintenance procedures for various IPT systems; ensure all work is carried out in line with same.

Qualifications

o Leaving Certificate or equivalent required

o Diploma or higher preferred; ideally in a related discipline

o Experience and/or a particular skill set in their area of expertise that adds value to the business; ideally in a manufacturing, preferably GMP setting

Job
: Manuf./Operations Generic

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/production-lead-technican-Job-VA/1703543/170354317035432012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSCarlow, Leinster, IE
Description

Este puesto es responsable por la ejecución de las labores de manera que los registros de contabilidad sean realizados de acuerdo con los principios de contabilidad generalmente aceptados, y los sistemas y procedimientos establecidos por la empresa.

PRINCIPALES RESPONSABILIDADES

* Llevar la custodia, control de las cuentas por pagar y la revisión de los cheques emitidos.
* Análisis, revisión de las solicitudes de prestamos de autos.
* Hacer los registros necesarios de las transacciones contables en el sistema computarizado.
* Análisis y conciliación de activos fijos.
* Aplicar los controles, procedimientos y políticas requeridas en la sección de Cuentas por Pagar en acuerdo y bajo lo establecido por la empresa

Qualifications

Licenciatura en Contabilidad, Finanzas o Administración

Manejo avanzado en MS Office, AS400 y JDEdwards

Inglés intermedio (comprensión y escritura)

Conocimientos de las leyes locales y a nivel de Centro América y República Dominicana relacionadas.

Mínimo 2 a 3 años de experiencia en el área de contabilidad, manejo de notas de débito, ciclo contable completo.

Job
: General Accounting

Primary Location: PA-Panamá-Panamá
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/Panam%C3%A1-Asistente-Contable-Job/1763440/176344017634402012-06-15Merck/MSDGeneral Accountingfull-timeUSDstarting0BSPanamá, Panamá, PA
Description

Incumbent will provide Security Administration for all users of Human Resource data. This includes the transaction systems such as PeopleSoft, Time & Labor, LDS Reporting, myLEARNING, Training Information System, Severance Reporting tool, myPMP, Medgate, Cognos etc. The responsibilities include but are not limited to the following:

· Provide Human Resource (HR) Data Security support of all HR Systems in test and production environments for global locations

· Provide security support for rollout of all new HR applications

· Develop and programs that extract data from SQL to report, clarify and/or resolve security issues

· Develop and maintain associated documentation for supported systems and execute security schemes

· Provide support to the maintenance of the HR Security Web site content

· Audit and monitor use of systems, identifying problem areas as well as opportunities. Follow-up on questionable security violations and inform Manager of circumstances

· Manage records of security requests and associated additions/deletions/corrections daily to meet Merck compliancy requirements

· Manage tickets related to security requests according to service targets

· Analyze and deliver interpretation of compliance standards to ensure adherence to Merck policy

· Manage projects with minimal supervision, to analyze new security demands, develop production solutions and provide decision support

Manage responses to semi-annual Security Audit

Qualifications

Education Minimum Requirement: Bachelor's Degree or 5 years equivalent experience

Required Experience and Skills:

· Intermediate (1 or more years) knowledge of:

o DB2/Oracle Security

o PeopleSoft Security

o QMF/SQL Query

o Microsoft Access/Related Software with Macros

· Basic knowledge of:

o HR/Payroll/Benefits business function data

o Analytical Skills in Identifying System Structure Security Implications

Desired Experience and Skills:

· Problem Solving

· Understanding of Audit, Compliance and Segregation of Duties issues related to HR Security Access

Job
: Customer Service

Primary Location: IE-Leinster-Dublin
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-HR-Security-Associate-Analyst-Job/1754413/175441317544132012-06-15Merck/MSDCustomer Servicefull-timeUSDstarting0BSDublin, Leinster, IE
Description

1. Product Promotion:

- Drive opening of new business avenues for Critical care in own territory hospitals through promotion of BU products to respective Medical fraternity in order to generate the business of the CC product portfolio
- Use detail aids to support scientific selling and Liaison with the HOD's , Purchase committee and Drug Committee doctors at the institutions for inclusion of the CC Products in the pharmacopoeia

2. Territory Sales:

- To prepare a target list of customers as per therapy profile. Understand and implement marketing strategies to medical fraternity to generate prescriptions for the cc products.
- To maintain and balance right distribution of products to the Pharmacy.

3. Market Intelligence/ Sales Reporting

-Interact with paramedical staff in hospitals to seek inputs on competitor activities, patients moving on MSD products, new products in the hospital etc. to maintain intelligence on MSD and competitor activity in the hospital
- Provide field reports in terms of FIRM, Tracker and Sales statement etc. in order to update the sales MIS

4.Customer Relationship Management:

- Organizing and conducting CME's with the user department at the institution in coordination to create and build the market for MSD products
- Manage the relationship with KOL's. Build, maintain and grow new KBL's and support CRM-Scientific activities with KOL's

Qualifications

BSc/ B Pharma with 3+ years of total sales experience in the Pharmaceutical sector

Job
: Direct Sales Generic MAH

Primary Location: IN-MH-Mumbai
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Mumbai-Territory-Business-Manager-Mumbai-%28Oncology%29-Job-MH/1567420/156742015674202012-06-15Merck/MSDDirect Sales Generic MAHfull-timeUSDstarting0BSMumbai, MH, IN
Description

The establishment of the EMEA SBS Centre is part of MSD's strategy to create a multi-function, multi-lingual organization to support MSD at a regional level. The EMEA SBS Centre will support business transactions in the areas of Finance, Accounting and Managed Services such as travel and meetings.

We are now recruiting for key talent for our new SBS centre.

Description:

Reporting to the Service Team Manager or Supervisor, the Finance Analyst, is responsible for providing commercial services, in order to cash (OTC) areas such as billing, Accounts receivables (AR) and collections.

The primary activities that you will be performing include:

* Executing the transactions required and the services as defined in the OtC area.
* Supporting the launch of SAP across major markets in Europe.
* Partnering with key stakeholders (Finance, Sales Procurement, etc) to ensure that all transactional activity is properly recorded and compliant with country statutory and tax requirements.
* Seek out opportunities for streamlining and rendering service delivery more efficiently, and participates in special projects to support Shared Business Services objectives.
* Resolve related issues pertaining to OTC and an understanding of when, how and where to escalate cases as required to meet defined service levels.
* Additional responsibilities to support a new organization in Europe as required.

Qualifications

Education:

* Bachelors Degree required.

Preferred:

* A minimum of 2 years of demonstrated work experience within the General accounting and or PtP shared services area.
* Experience working in an organization providing services across multiple markets or geographies.
* A minimum of one year of experience working with SAP.
* High degree of integrity and personal ethics in implementing corporate policies and procedures
* Effective team player with collaborative focus
* Must be able to work in a fast-paced, dynamic environment, under pressure, and with a high degree of professionalism
* Must be comfortable in an environment of changing technologies and processes, and demonstrate flexibility in adjusting to new ways of working
* Experience working in a SOX404 environment.
* Strong oral and written communication skills.
* Flexible work arrangements will be considered based on business needs.

Job
: Financial Analysis

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 2

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Carlow-Order-to-Cash-Finance-Analyst-Job/1366986/136698613669862012-06-15Merck/MSDFinancial Analysisfull-timeUSDstarting0BSCarlow, Leinster, IE
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck Research Labs will be offering 2012 summer internships in the Global Structural Chemistry group (X-ray crystallography or Biomolecular NMR) at either its Kenilworth, NJ or West Point, PA sites. Internships will begin in early June 2012, and will run for 9-11 weeks.

A suitable candidate has a science background with interest in the use of X-ray crystallography and/or Biomolecular NMR in drug discovery. Not required, but a plus, would be experience in one or more of the areas of protein crystallization, X-ray theory, X-ray crystallography or Biomolecular NMR. Preference will be given to candidates having a strong math and/or physical science background with expertise in computers and computer programming. Candidates will gain firsthand experience in modern drug discovery, and will also make valuable contacts within the industry.

**Please note when applying for this position, the candidate MUST upload a cover letter or a personal statement letter and a copy of your unofficial transcript along with your resume.

Qualifications

Required:

* Currently pursuing a Ph.D. in Biomolecular NMR, X-ray crystallography, Computational Chemistry, Biophysics or a related field
* Applicants must be available for full-time employment for 9 - 11 weeks during the months of June - August 2012.

Preferred:

* Experience in one or more of the areas of protein crystallization, X-ray theory, X-ray crystallography or Biomolecular NMR
* Strong math and/or physical science background with expertise in computers and computer programming
* Science background with an interest in computers and drug discovery

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #CHE003379.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-NJ-Kenilworth
Other Locations: US-PA-West Point, US-MA-Boston, US-NJ-Rahway

Job Type
: Intern
Employee Status: Regular

Travel
: No
Number of Openings: 1

Relocation Provided
: Domestic (within country)]]>http://jobs.merck.com/job/Kenilworth-X-ray-CrystallographyBioNMR-Summer-Internship-2012-PhD-Job-NJ-07033/1729502/172950217295022012-06-15Merck/MSDInternfull-timeUSDstarting0BSKenilworth, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The successful candidate will be responsible for designing and implementing studies to support programs aimed at discovering and developing novel drugs to treat gram-negative bacterial infections.

In scope activities include (i) design and implementation of in vitro experiments using small molecules, recombinant proteins, disruptive nucleic acid technologies, and antibodies to identify potentially novel mechanisms or molecular targets impeding bacterial growth, (ii) evaluation of the efficacy and potential issues associated with the modulation of novel anti-bacterial targets (iii) characterization of on-target and off-target activities of small molecule leads, and (iv) identification of mechanisms of resistance to antibiotics in key pathogens

Qualifications

Education:

* Ph.D.

Required:

* Strong demonstrated technical skills in bacterial genetics of Gram negative bacteria, including gene knockouts and conditional expression, to validate antibiotic drug targets and adapt their utility for target-based whole cell screening and mechanism of action determination studies
* A strong publication record demonstrating intellectual leadership and contributions in his/her area of bacterial research
* Highly motivated, independent thinker who is able to assume project supervisory responsibilities
* Demonstrated ability to independently design and conduct experiments, analyze data and interpret results, and communicate findings and conclusions; develop novel methodologies or approaches as needed; thrive in a highly collaborative environment; and provide scientific mentorship to junior staff.

Preferred:

* A broad knowledge of basic cell physiology and biosynthesis pertaining to known antibiotic drug mechanisms (including cell wall, lipid polysaccharide, nucleic acid replication and protein synthesis) in Gram negative bacterial pathogens (key pathogens include Pseudomonas aeruginosa, Acinetobacter baumannii and Enterobacteriaceae spp.)
* A good understanding of available bacterial genomics (annotated genomes, transposon and/or disruption libraries, overexpression systems) and demonstrated use of such resources
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003601.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Biology-Discovery

Primary Location: US-NJ-Kenilworth
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: None]]>http://jobs.merck.com/job/Kenilworth-Biology-Team-Member-Antibacterials-Job-NJ-07033/1895222/189522218952222012-06-15Merck/MSDBiology-Discoveryfull-timeUSDstarting0BSKenilworth, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the direction of a Senior Director/Executive Director, the Associate Director has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs. This includes all phases of clinical development, study design, study placement, study monitoring and concern for the protection of human subjects who participate in the clinical trials.

* Reports to a Senior Director/Executive Director
* Supervises the activities of Clinical Associates and/or Medical Program Coordinators for specific research project to which assigned by the Senior Director/Executive Director.
* With the guidance of the Senior Director/Executive Director, the Associate Director is responsible for initiation of clinical Operational Plans for the development of new Merck drugs or for the completion of projects involving marketed drugs.
* With the guidance of the Senior Director/Executive Director, the Associate Director is responsible for planning and initiating clinical trials involving new Merck drugs or marketed products.
* Responsible for the development of approved protocols for clinical studies to which assigned and is responsible for the initiation, monitoring and completion of the clinical studies.
* Responsible for the analyzing and summarizing the clinical findings from studies for the purpose of decisions regarding safety and efficacy and to support investigational new drug submissions and new drug applications or clinical experience reports.
* Serves as a member of appropriate research project teams in regard to the development of new compounds in order to provide medical input and judgment.
* Works closely with the respective Marketing area and with Regulatory Affairs in the preparation of package circulars including review and revisions.
* Responsible for maintaining awareness of scientific developments within his/her area of expertise, both in terms of new methodology, new research activities and in terms of identification of competent, potential investigators.
* Required to establish communications with prominent clinical investigators in his/her particular field of interest, particularly those who will be willing and able to assist in the evaluation of Merck drugs.
* Expected to attend appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility.
* Assists the Senior Director/Executive Director in maintaining liaison with appropriate Corporate areas in order to keep them informed of the progress of the investigation of both Merck drugs and competitor drugs and in regard to expert opinion concerning scientific questions in his/her of responsibility.
* May travel on company business about (20%) of the time of order to visit clinical investigators in regard to potential or active clinical research projects

Qualifications

Education:

* M.D or M.D./Ph.D.

Required:

* Experience in industry or academia
* Willingness to work on programs in disease areas both within and outside of respiratory medicine

Preferred:

* Fellowship or equivalent training in one or more of the following areas (either adult or pediatric) strongly preferred: Pulmonary Medicine and/or Allergy.
* Significant research experience, either basic science or in clinical development, is strongly preferred.
* Board Certification or Eligibility

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CLI002464.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Clinical Research (M.D.)

Primary Location: US-NJ-Kenilworth
Other Locations: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Kenilworth-Associate-Director%2C-Clinical-Research-Respiratory-Job-NJ-07033/1401645/140164514016452012-06-15Merck/MSDClinical Research (M.D.)full-timeUSDstarting0BSKenilworth, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Infectious Disease is a key research area within the core franchises of drug discovery/development of Merck Research Laboratories (MRL). The antibacterial/antifungal department focuses on antimicrobial drug development. The intern position is within the antibacterial discovery group, dedicated to discovery and development of small molecules targeting key pathways in bacteria.

The successful candidate will be involved in supporting compound discovery of progressible lead molecules with potential therapeutic potential against Gram-negative bacterial pathogens including Escherichia coli, Pseudomonas aeruginosa and Acinetobacter baumannii. Participation in small molecule identification and progression and/or target validation projects using diverse genetic and biochemical strategies.

Intern will gain pharmaceutical research experience in early antibacterial drug discovery. Intern also provided opportunity to publish his/her work in collaboration with the team at the conclusion of the project. Experience will span day-to-day research within the antibacterial discovery group as well as the opportunity to attend internal seminars highlighting other drug discovery research within Merck.

Internship will run between 9-11 weeks beginning in June 2012. Housing is available for those candidates meeting the minimum distance requirement.

Qualifications

Required:

* Bachelor or Master's degree candidates with at least one year of education completed in Microbiology, Biochemistry or Molecular Biology
* Experience with sterile technique
* Must be able to complete a 9-11 week internship beginning June 2012 at Merck's facility in Kenilworth, NJ
* Must have at least 1 year of education remaining at the completion of the summer internship

Preferred:

* Basic microbiology and molecular biology skills and laboratory techniques
* Experience (academic or industry) with small molecules

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition BIO003441.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-NJ-Kenilworth

Job Type
: Intern
Employee Status: Regular

Travel
: No
Number of Openings: 1

Relocation Provided
: Domestic (within country)]]>http://jobs.merck.com/job/Kenilworth-Infectious-Disease-ResearchDiscovery-Internship-2012-BS-or-MS-Job-NJ-07033/1729508/172950817295082012-06-15Merck/MSDInternfull-timeUSDstarting0BSKenilworth, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Associate Director/Director reports to a Section Head in the Oncology Clinical Research Group. Under the guidance of their supervisor, the Associate Director/Director has primary responsibility for planning and directing clinical research activities including novel agents or marketed oncology products. Merck's Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Associate Director/Director will manage all phases of development through the entire life-cycle of clinical development, including but not limited to: study design, site identification, monitoring, safety assessment, analysis, regulatory reporting, and publication.

Specifically, the Associate Director/Director may be responsible for:

* Evaluating pre-clinical and translational work for the purpose of generating an early clinical development plan and Investigational New Drug applications
* Developing clinical strategies for investigational or marketed Oncology drugs
* Planning clinical trials (design, operational plans, settings) based on these clinical development strategies
* Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Oncology drugs
* Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication
* Participation in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds.

In executing these duties, the Associate Director/Director may:

* Supervise the activities of Clinical Scientists in the execution of clinical studies
* Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects
* assist the Section Head in ensuring that appropriate Corporate personnel are informed of the progress of studies of Merck's and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.

The Associate Director/Director is responsible for maintaining a strong scientific fund of knowledge by:

* Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies
* Identification of scientifically and operationally strong investigators who can assist in the development of Merck's investigational and marketed drugs
* Establishing communications with prominent clinical investigators in his/her particular field of interest, particularly those who will be willing and able to assist in the evaluation of Merck drugs
* Attending appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility.

To accomplish these goals, the Associate Director/Director may:

* Author detailed development documents, presentations, budgets, and position papers for internal and external audiences
* Facilitate collaborations with external researchers around the world
* Travel on company business about twenty (20) percent of the time to manage future or ongoing clinical research projects.

Position will be based out of Kenilworth, NJ facilities, however arrangements can be made for the Director to be based in Upper Gwynedd, PA if preferred. The managing Section Head will be based in Kenilworth.

Qualifications

Education:
* M.D. - Board Certified or Eligible in Oncology (and Hematology)

Requirements:

* Scientific expertise in clinical trials and drug development.
* Demonstrated record of scientific scholarship and achievement
* Proven track record in clinical medicine and background in biomedical research
* Strong interpersonal skills, as well as the ability to function in a team environment

Preferred:

* Prior specific experience in clinical research and prior publication
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CLI002514.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Clinical Research (M.D.)

Primary Location: US-NJ-Kenilworth
Other Locations: US-PA-Upper Gwynedd
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 2

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Kenilworth-Assoc_Dir_Director-Clinical-Research-Oncology-Job-NJ-07033/1511374/151137415113742012-06-15Merck/MSDClinical Research (M.D.)full-timeUSDstarting0BSKenilworth, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


We are looking for a motivated individual who will provide purification screening and process development support on our ongoing efforts in support of strain, process and pre-clinical development . The position offers an opportunity to gain experience in a wide range of protein purification, fermentation process development and analytical biochemistry techniques, with opportunities to make significant experimental and intellectual contributions to our ongoing efforts in characterization of the biological processes for glycoprotein production.

The responsibilities include but are not limited to:

* Purifying proteins employing various chromatographic techniques.
* Characterizing protein quality and stability using various biochemical/biophysical approaches.
* SDS-PAGE Gels, Western blot analysis, Protein concentration determination.
* Preparation of media, buffers and reagents from recipes.
* Prepare, set-up & clean lab- and pilot-scale bioreactors and chromatography systems using methods described in operating protocols.
* Execution of fermentation & purification experiments including collection of samples, entry of process data and harvest of broth by centrifugation.
* Proper handling, storage and disposal of biologic and chemical reagents and waste streams.
* Data gathering, entry and notebook keeping.
* Operation, maintenance and set-up of automated bioreactors, process chromatography systems and other instruments including HPLC, off-gas analyzers and automated reactor sampling systems.
* Preparation and testing of cryogenically stored cell banks.
* Working in multifunctional teams.
* Presenting experimental data at team meetings.

Qualifications

Minimum Education Required:

* A BS with 3 years of experience or MS degree in Biological Sciences/biochemistry or related field.

Minimum Skills or Experience Requried:

* Laboratory experience with execution of microbial fermentation and/or protein purification experiments; theoretical knowledge of microbiology, protein biochemistry, chemical kinetics & transport phenomena (fluid dynamics, heat & mass transfer) and practical training in aseptic techniques and GXP research environments
* Effective oral and written communication skills
* Working experience with AKTA Explorer.
* Capable of working independently in designing experiments and generating data.
* Demonstrated ability to work in a team environment and experience with purification /characterization of proteins.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MOL000280.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Molecular Discovery

Primary Location: US-NH-Lebanon
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Lebanon-Research-Biochemist-Job-NH-03756/1826383/182638318263832012-06-15Merck/MSDMolecular Discoveryfull-timeUSDstarting0BSLebanon, NH, US
Description

We are now recruiting for a dynamic, passionate and driven Brand & Customer Manager with a strong sales and marketing background (min 3 years experience) who will be critical to the ongoing success of the Anaesthesia business.

The successful applicant will have responsibility for developing and implementing marketing plans to ensure optimal business results within the therapy area whilst working towards organisational and Business Unit strategic objectives.

Within the context of the Regional Anaesthesia Business Unit, a component of the role (approx 20%) will be to develop, and lead, one of the European Marketing Centres of Excellence. The Italy CoE will be focused on engaging multiple stakeholders involved in improvement of preoperative care.

The Italy CoE lead will create local Italian programs, initiatives and projects with an eye towards how these could be adapted and executed in other markets and will serve as the regional "go to" point when markets are encountering issues and request support and advice.

Key responsibilities are:

Internal relationships

· Be the key point of contact for the sales force for all queries relating to products within your assigned therapy area, clearly communicating with passion their benefits whilst incorporating any feedback into the brand plan.

· Proactively lead core cross functional Brand Team to ensure efficient integration and collaboration across key functions contributing to the Brand.

· Brief sales force and other internal parties on brand and promotional strategy and associated materials.

· Ensure all projects are inline with over arching MSD franchise vision and support the goals of other products in the franchise where applicable.

Develop and implement promotional and non-promotional materials and programmes

Work with Sales and Marketing Leader to develop marketing strategy and plans for Italy.

Work with Brand Promotions and Multi Channel Communications to develop materials.

Commission / develop as appropriate promotional and non-promotional materials and programmes.

Customer relationships

Build and maintain relationships with KOLs, acting as an expert in the area.

Maintain thorough understanding of customer perspective and develop solutions which best meet customer needs and help improve patient outcomes, including HCP and patient education initiatives as appropriate.

Business operations

Proactively liaise and collaborate with various Italian functions, including Sales force, Customer Insight and Analytics, Business Services, Outcomes Research and Commercial Operations, External Affairs, Medical and Scientific Affairs, Finance, and Regulatory Affairs, to ensure optimal alignment and effective implementation of business plans.

Support regional business opportunities through appropriate marketing development

Day-to-day management of promotional budget to optimise effectiveness and efficiency in line with Merck compliance standards.

Conduct all business activities inline with Merck Sigma principles and a 'continuous improvement' mindset

Input to annual profit plan and long range operating plans

Conduct all activities in compliance with company policies and standards, and with the PMCPA Code of Practice and MHRA guidance.
Proactively liaise and collaborate with global colleagues.

Qualifications

Education and Skills Required

University degree

Minimum Experience Required

Marketing in the pharmaceutical industry

Field sales experience

Skills/Knowledge Required

Track record of success

Excellent project management and organisational skills, with evidence of delivery.

Ability to communicate at all levels with clarity and confidence evidence of effective cross functional teamwork and collaboration with the ability to work in a group and as an individual.

Experience in developing brand plans and have an understanding of the brand planning process.

Experience in sales force motivation and engagement.

Experience in developing customer relationships.

Ethics and integrity.

*LI-LS1

Job
: Brand Marketing

Primary Location: IT-62-Rome
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Groten-Brand-B&CM-Anesthesia-Job/1853556/185355618535562012-06-15Merck/MSDBrand Marketingfull-timeUSDstarting0BSRome, 62, IT
Description

Reporting to the SBS Regional Service Delivery Manager - Procure to Pay, the AP Service Lead is accountable within the EMEA Shared Service Centre for the management , execution and delivery of the accounts payable processes for all markets. The Service Lead is responsible for managing and directing day-to-day activities of AP Analysts supporting a group of Markets in the region as well as overseeing the activities of outsourced supplier partners.

The primary activities include, but are not limited to:

· Lead and manage the overall execution & delivery of the processes & services within the framework of compliance obligations, agreed service levels, specified metrics and targets.

· Provides feedback to the EMEA Service Delivery Director and leadership team on service performance, customer experience, and input on redesigning or updating services and processes in order to fulfill new standards of satisfaction.

· Understands the overall AP process and ensures compliance

· Maintains an understanding of all internal policies, procedures and procurement processes in order to effectively communicate requirements to business partners and suppliers. Ensures transactions comply with all corporate policies and auditing requirements.

· Implement new products/services as specified by the Shared Business Services Leadership and Source to Settle Process Councils/Process Owner to leverage existing operational processes and structure, produce opportunities for consolidation and capture economic savings.

· Keep abreast of external trends and benchmarks and provide revised service level commitments that are configured to regional concerns.

· Perform all required people management obligations including performance reviews, succession planning, talent assessments and workforce planning

Qualifications

* Bachelors Degree required, preferably in Accounting, Finance or Purchasing.
* A minimum of 5 years of demonstrated work experience within An Accounts Payable / Procurement Shared Services operations.
* Proven ERP implementation & operational delivery experience (SAP/Oracle…)
* Results driven, Target Oriented & competent with operational industry standard KPIs / Metrics
* A minimum of 3 years of demonstrated supervisory experience, leadership and people management abilities.
* Fluent in a second European language desirable.
* High degree of motivation, flexibility, strong time management and inter personal skills to manage high volumes effectively with minimal supervision
* Ability to make effective decisions while ensuring compliance with all corporate policies and procedures.
* Experience in customer relationship is necessary to deal effectively with internal and external customers and various levels of Merck management team.
* Strong computer skills required including the use of the MS suite of office products and web-based applications.
* Strong influencing and communication skills
* Experience in continuous improvement of processes and SOX Audit control

*LI-EM1

Job
: General Audit

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Carlow-PtP-Service-Lead-AP-Job/1862516/186251618625162012-06-15Merck/MSDGeneral Auditfull-timeUSDstarting0BSCarlow, Leinster, IE
Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


ESSENTIAL FUNCTION:

The Medical Affairs Manager will give scientific support to the Business units and assigned therapeutic areas. This position will be a key point of contact for health professional (Physicians, Pharmacists, Nurses) for Central America (Panama, Honduras, El Salvador, Costa Rica, Nicaragua, Guatemala), Dominican Republic and MSD. Will develop and implement Medical Affairs plans for assigned products. Observe and enforce corporate policies and local health regulations for each Central America and Republic Dominican (CARD) country, helping to achieve the objectives of the Medical Department and the Subsidiary.

MAIN RESPONSIBILITES:

* Scientific support to assigned Business units.
* Relationship with Scientific Leaders in CARD countries (Central America and Dominican Republic)
* Receive and process properly and on time (not more than 10 days) applications for scientific medical information to be processed from the Designated Point of Contact (DPOC)
* Promotional material review from the Centre of Excellence (CoE) or developed locally (on global certification) and revision of training materials and Market Access for approval of Medical / Legal time limits.
* Support Sales Force training
* Support Regional Medical Directors on assigned therapeutic areas.
* Support to Regulatory Affairs Department
* Interaction with Policy and Communications Departments.
* Contribute with scientific support to Market Access.

Qualifications

MD with postgraduate in internal or family medicine, pediatric, infectology, oncology, pharmacology or epidemiology

MBA or marketing postgraduate will be a plus.

Minimum 2 years experience in the pharma industry

Knowledge of medical affairs in Central America

Experience in clinical investigation

Advanced English

Communication and presentation skills

Strategic thinking and planning

Leadership experience and skills

Problem solving

Team work

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. MSD's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

*LI-KT1

Job
: Clinical Research Generic

Primary Location: PA-Panamá-Panamá
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/Panam%C3%A1-Medical-Affairs-Manager-Job/1762415/176241517624152012-06-15Merck/MSDClinical Research Genericfull-timeUSDstarting0BSPanamá, Panamá, PA
Description

To support our Human Health business and the related Global Support Functions.

The job would suit a highly motivated individual looking for an opportunity to grow their financial and business knowledge in a dynamic industry as the next step in their professional development.

Main tasks:

* Initially this role will be dedicated to activities (testing, training) related to the implementation of SAP business software solution for the MSD Switzerland as part of the worldwide rollout.

Then after go-live in October 2012:

· Engage in divisional planning processes - support sales & expense planning, forecasting and budget control activities for various divisions.

· Preparation and analysis of financial reports

· Monitor actual financial performance versus budget and review together with budget holders / Business clients

· Support Regional and Corporate Headquarter reporting requirements

· Initiate and lead process optimization projects, support Business Development projects

· Maintain, update and control financial IT systems and train end users

· Work closely with all local departments as a business partner

Qualifications

Education

· University degree in Finance, Economics or MBA

Required

· At least three years in a commercial environment; accounting knowledge a plus

· Strong analytical, very good organizational and communication skills

· Ability to work independently but also in a team.

· Flexible, versatile and confident person with high service-orientation and demonstrated business partnership skills

· Demonstrate a process improvement mindset

· Resilient and stays calm and focused during stressful situations

· Advanced computer skills (PC/ Microsoft Office, with advanced EXCEL /databases)

· Fluent (oral and written) in German and English essential; knowledge of French is an advantage.

· 6+ years relevant work experience (especially in pharmaceutical industry or training consulting)

· 3+ years experience in training development/ delivery

Desired

* SAP knowledge would be beneficial.
* Multi-lingual skills desired
* International/Global experience is a plus

Job
: Financial Analysis

Primary Location: CH-LU-Luzern
Employee Status: Regular

Travel
: No
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-Senior-Financial-Analyst-Job-LU/1804836/180483618048362012-06-15Merck/MSDFinancial Analysisfull-timeUSDstarting0BSLuzern, LU, CH
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Specialty Representative is a key member of the Neuropsychiatry Specialty Team and plays a critical role in supporting Merck's customer centric business model. He/she is responsible for working with the Neuropsychiatry Specialty Team to understand and identify Health Care Provider (HCP) customer needs, support pull-through activities relative to the customer strategy, and ensure that Merck is viewed as demonstrating value and better health outcomes to healthcare professionals and their patients.

The primary activities include:

* Communicates about product in a way that's meaningful and relevant to each individual customer; customizes discussions and client interactions based on understanding of customer's needs
* Engages in informed discussions about products with HCP customers - knowing when/how to seek and provide additional information
* Within select customer accounts acts as primary point of contact for customer, meet with key customers/personnel to understand practice structure, business model, key influencers Managed Care Organization (MCO), employers, state and local regulations)/network structure, customer needs and identifies business opportunities
* For select customer accounts/HCPs, coordinate with customer team to develop customer strategy - outlining strategy for interactions/ relationship, solutions and potential offerings for customer
* Partners with National Account Executives (NAEs) to maintain strong focus on Managed Care pull-through
* Shares learning and best-practices from one customer to help other customers meet their needs
* Demonstrates a focus on better health outcomes (beyond acquisition, considers the HCP and patient experience)
* Provides input into resource allocation decisions across customers
* Identifies and selects programs/services available in the library of Merck "resources" to address customer needs
* Works with solutions group (Headquarters - HQ) and/or Medical Account Executive (MAE) to develop and deliver relevant offerings that address desired customer needs
* Maintain current understanding of practice structure, business model, key influencers/ network structure and make information available to relevant stakeholders
* Collaborate and communicate effectively with extended "in-scope" customer team to ensure a consistent customer experience across Merck's divisions and functional areas; ensure integration with National Account Executive (NAE), Merck Vaccines (MV) personnel, Health Management Services (HMS) Manager, Solutions Consultant, Customer Strategies and Solutions (CSS), Regional Medical Director (RMD) and other key stakeholders to share key customer learning and support customer needs
* Outstanding in all competency areas (Account Management; External Market Focus; 1:1 Customer Interactions)
* Influences beyond their specific geography or product area

This territory covers New York North.

Requires no regular overnight travel.

Qualifications

Education:

* Required: BA/BS
* Preferred: MBA/MS

Required:

* Prior experience working in a scientific field or healthcare environment;

* Previous sales experience

* Prior experience developing new business opportunities with existing customers

* Experience establishing new customer relationships, understanding of Merck products and therapeutic areas

* Consistent performer in most competency areas

* Valid Driver's license

Preferred:

* Prior consulting or customer service experience
* Experience developing and executing a plan for engaging customers and meeting customer needs
* Understanding of Headquarter operations
* Ability to analyze metrics to assess progress against objectives
* Neuropsychiatry sales experience
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # DIR004389.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Channel Sales Generic

Primary Location: US-New York
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/New-York-City-Specialty-Representative-Neuropsychiatry-%28NY-North%29-Job-NY-10001/1895231/189523118952312012-06-15Merck/MSDChannel Sales Genericfull-timeUSDstarting0BSUS-New York
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


While working in a climate controlled warehouse, this position will perform a variety of warehouse activities including but not limited to:

* Picking and/or packing products to be shipped to our US customers.
* Storing, handling, preparing for shipment and documenting of hazardous materials/waste when necessary.
* Unloading, storing and loading materials in the warehouse using fork lifts, pallet jacks and dollies.
* Performs record keeping, ensuring the accuracy and condition of delivered materials.
* Adherence to company policies, procedures, and governmental regulations required.

*** This is a First Shift, Monday - Friday position. ***

Qualifications

Education Minimum Requirement:

* High School Diploma or equivalent

Required Experience and Skill:

* Minimum 2 years direct warehouse experience
* Ability to work in a team oriented environment

Desired Experience and Skills:

* Working knowledge of computer systems: SAP experience highly preferred, proficient in MS Office applications
* Ability to operate a forklift & other common warehouse equipment strongly preferred
* Ability to safely lift 50 lbs

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # WAR000169.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Warehousing

Primary Location: US-NE-Omaha
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/Omaha-Warehouse-Operator-Job-NE-68046/1889116/188911618891162012-06-15Merck/MSDWarehousingfull-timeUSDstarting0BSOmaha, NE, US
Description

The position of Clinical Trials Coordinator (CTC) has responsibility and accountability for supporting the conduct of SPRI clinical trials in his/her country. Under guidance from the Clinical Research Associates (CRAs) and the Area Medical Director, the CTC is responsible for administrative functions supporting the conduct of trials including tracking and updating subject enrollment, site payments, clinical supplies, and IRB/HA submission of essential clinical trial documents

MAJOR ACTIVITIES AND RESPONSABILITIES:

* Provides administrative support to Clinical Research Associates to implement, conduct and close out SPRI clinical trials in accordance with SPRI SOPs, ICH GCPs, and local regulatory requirements.
* Ensures timely delivery of clinical study documents to HQ Monitors, CLinDOc, local HA and IRBs. Follow up arrival and distribution of clinical and non-clinical supplies to site in the country.
* Assists CRAs in updating timetables in the clinical studies database (PROSIT)
* Performs documents reconciliation (checking documents on file against tracking lists), keeps tracking of safety alert reports, payments to sites, etc.
* Maintains controls of division records by ensuring documents are secured and readily available in an organized filling system
* Provides the Area Medical Director with information on the performance of clinical trials in his/her Area, getting reports from applications (Prosit, Opera, and others).

Qualifications

Education: Bachelor's degree. Preferred: Pharmacy, Medical, Nurse, Bioanalysis or related sciences.

Travel required (up to 4 days per week on site)

Languages: Spanish (mother tongue), English ( advanced)

Work Experience: Mininum two years in related functions. Four years would be a plus.

Skills:

Communication Skills: good oral and written communication skills in English. Must be able to convey information clearly and in timely manner, both in writing and verbally. Must be able to establish and maintain effective professional business relationship with clients. Has considerable impact on company image with outside callers.

Administrative Skills: highly organized, critical thinking, teamwork, proactive, detail and result oriented sense of urgency, ability to handle multiple tasks at the same time, highly creative.

Technical Skills: knowledge of MS Office (word, excel, powerpoint, outlook), telephone, fax, calculator, voice mail and projectors. Oriented to technology.

Interpersonal Skills: dependable, reliable, consistent, discreet, customer service oriented, flexible, assertive, tactful, trustworthy

Job
: Clinical Research Generic

Primary Location: VE-Caracas Capital District-Caracas
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Caracas-Clinical-Trials-Coordinator-%28CTC%29-Job/1855924/185592418559242012-06-15Merck/MSDClinical Research Genericfull-timeUSDstarting0BSCaracas, Caracas Capital District, VE
Descripción
Promueve los productos de la Franquicia de Anestesia con la clase médica. Prepara reportes de llamadas/visitas a clientes y reportes de

ventas/gastos. Se mantiene actualizado en cuanto al producto de la compañía y productos de la competencia mercado farmacéutico.

RESPONSABILIDADES Y FUNCIONES:

* Llegar a cumplir con los objetivos de ventas establecidos para la Franquicia de Anestesia.

* Participación activa en el análisis del potencial del negocio en Panamá para el lanzamiento de nuevos productos

* Promoción de productos de Anestesia en el territorio asignado

* Organizar eventos científicos locales

* Mantener un target de médicos actualizado

* Alcanzar su objetivo de visita (frecuencia & promedio) de acuerdo a los parámetros establecidos.

* Responsable de los asuntos inherentes al negocio (pedidos, cartera e inventarios)

* Realización y seguimiento de programas especiales

* Cumplir con las normas y procedimientos establecidos por la empresa en cada una de las actividades inherentes al negocio

* Chequear la segmentación médica, manteniendo y actualizando información de los clientes y completando los reportes de visitas.

* Proponer acciones de promoción para incrementar la inclusión y utilización de nuestros productos en hospitales.

* Proveer información clave y detallada a su objetivo médico que asegure un incremento en la prescripción de los productos a su cargo.

* Proveer y mantener actualizada la información de la competencia (Ej. Tácticas y actividades de marketing)

* Mantener y guardar una confidencialidad todo lo relacionado a productos, costos, precios, cuotas de ventas y cualquier otra información asignada, de acuerdo a las normas de compliance.

* Llevar un control estricto de los gastos de viaje, promoción, o especiales, y presentar a la Gerencia de División para su aprobación en el

* tiempo requerido y acordado.

* Mantener un desarrollo continuo y auto conocimiento de los productos de biotecnología de la Empresa.

* Participar activamente en los lanzamientos, promociones o juntas de ventas organizadas en el ámbito local o regional

- Participación activa en el análisis del potencial de los diferentes mercados para el lanzamiento de nuevos productos

Cualificaciones
Escolaridad:

Licenciatura en Farmacología o carreras relacionadas al área de la salud.

Competencias Técnicas:
Experto en ventas especializadas y administración de su territorio a nivel del mercado Hospitalario. Conocimientos sobre
análisis y planeación de negocios, pensamiento y planeación estratégica, financieros.

Idioma: Nivel intermedio de inglés (escrito, hablado)

Experiencia
Mínimo cuatro (4) a cinco (5) años como Visitador Médico de productos hospitalarios con un desempeño, de preferencia con
experiencia en el mercado de Anestesia.

Habilidades o Conocimientos adicionales: independiente, enfoque a resultados, relaciones interpersonales, perseverancia, comunicación

efectiva, experiencia en el área comercial, tanto en clientes privados como instituciones, trabajo en equipo y bajo presión,

Habilidades de Liderazgo, proactivo, disposición inmediata de atención al cliente.

Se requiere conocimiento de MS Office (Word, Excel y Power Point)

*LI-KT1

Puesto
: Ventas

Ubicación principal: PA-Panamá-Panamá
Tipo de acuerdo laboral: Fijo(a)
Viajes: No
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Panam%C3%A1-Representante-de-Ventas-Anestesia-Job/1855919/185591918559192012-06-15Merck/MSDVentasfull-timeUSDstarting0BSPanamá, Panamá, PA
Description

The Opportunity

We are seeking a Project Manager / Business Analyst to join our Managed Services team and support our Travel, Card, Meetings, and Creative Studios services. This role reports to the Director of Portfolio Management and would be located in EMEA.

The role requires both broad and deep business and technology knowledge with the ability to take a solution through the development lifecycle including: planning, design, specification, construction, debugging, configuration management, unit and system acceptance testing, knowledge transfer and solution support and documentation. The role requires a strong individual who is resourceful, confident under pressure, and has demonstrated skill in both Application Development and Business Development.

A successful candidate will have unique opportunity to bring analytic, process and technical skills to compliment a highly-qualified team, and work in a fast paced environment where their contribution will be highly valued.

Primary Responsibilities

* Project results responsibility - Manage key projects, responsible to deliver project and key agreed project deliverables. Working in a cross functional environment, drive execution and monthly program reporting.
* Leading Project Team(s) - Forming respective teams, leading team meetings, developing critical path schedules, developing metrics and process to evaluate progress, planning action steps, addressing and resolving issues and risks, publishing and reviewing status documents.
* Requirements Development - Ability to work with the business teams to document their requirements. Negotiate with the requestors to align their requests in support of the overall IT and SBS program objectives.
* Resource Management - Prioritize projects and activities in support of annual objectives. Ensure the team is committed and engaged for all phases of Project Realization Process (PRP). Ensure appropriate business resources are engaged and committed during the project life cycle.
* Strong communication skills - Clearly convey information and ideas through a variety of media to individuals or groups. (i.e.: Organizes communication; adjusts to audience; ensures understanding; comprehends communication from others.)
* Adaptability/Flexibility - Demonstrates the ability to maintain professionalism and a positive attitude when encountering changes in the workplace. (i.e.: Seeks to understand changes; maintains positive attitude when dealing with change; makes appropriate behavioral adjustments when needed.)
* Initiates Action - Takes prompt action to accomplish objectives; takes action to achieve goals beyond what is required; is proactive. (i.e.: Responds quickly; takes independent action; goes above and beyond)
* Value realization & sustainment - Define processes and toolsets for benefits realization; measure actual vs. anticipated benefits for projects
* Issue management - Develop and utilize processes and tools for rigorous integrated issue management with escalation points as necessary
* Risk management - Identify and map all risks based on severity and probability, developing mitigation plans and escalating as necessary; the development and management of standard risk identification and response capabilities to manage risk across the program.

Qualifications

* BA/BS in Computer Science, Management Information Systems, Project Management or related discipline
* Minimum of 3-5 years experience in Project or Program Management, history of successful project execution; proven experience leading larger and complex programs
* Critical thinking, analytical skills and business acumen needed to make decisions and solve problems
* A high level of motivation and a self starting attitude
* Six Sigma methodology experience (Green or Black Belt level)
* Excellent oral and written communication skills
* Strong analytical and creative problem solving skills
* Devotion to accuracy, detail, analytic consistency and data integrity
* Ability to multi-task in an environment with changing priorities
* A strong work ethic
* Knowledge of Shared Business Services model

*LI-EM1

Job
: Administrative Svcs Generic

Primary Location: IE-Leinster-Dublin
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Dublin-Project-Manager-Business-Analyst-Job/1874869/187486918748692012-06-15Merck/MSDAdministrative Svcs Genericfull-timeUSDstarting0BSDublin, Leinster, IE
Description

1. Product Promotion:

- Drive opening of new business avenues for Critical care in own territory hospitals through promotion of BU products to respective Medical fraternity in order to generate the business of the CC product portfolio
- Use detail aids to support scientific selling and Liaison with the HOD's , Purchase committee and Drug Committee doctors at the institutions for inclusion of the CC Products in the pharmacopoeia

2. Territory Sales:

- To prepare a target list of customers as per therapy profile. Understand and implement marketing strategies to medical fraternity to generate prescriptions for the cc products.
- To maintain and balance right distribution of products to the Pharmacy.

3. Market Intelligence/ Sales Reporting

-Interact with paramedical staff in hospitals to seek inputs on competitor activities, patients moving on MSD products, new products in the hospital etc. to maintain intelligence on MSD and competitor activity in the hospital
- Provide field reports in terms of FIRM, Tracker and Sales statement etc. in order to update the sales MIS

4.Customer Relationship Management:

- Organizing and conducting CME's with the user department at the institution in coordination to create and build the market for MSD products
- Manage the relationship with KOL's. Build, maintain and grow new KBL's and support CRM-Scientific activities with KOL's

Qualifications

BSc/ B Pharma with 3+ years of total sales experience in the Pharmaceutical sector

Job
: Direct Sales Generic MAH

Primary Location: IN-GJ-Ahmedabad
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Ahmedabad-Territory-Business-Manager-Ahmedabad-%28Critical-Care%29-Job-GJ/1885950/188595018859502012-06-15Merck/MSDDirect Sales Generic MAHfull-timeUSDstarting0BSAhmedabad, GJ, IN
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Informatics department develops, supports and enables the application of informatics across Merck, in partnership with quantitative organizations throughout the company. Our world-class team is currently seeking outstanding informatics professionals to join our global team of informaticists and engineers. Successful candidates will have the opportunity to collaborate with talented and dedicated colleagues to make a difference in patient healthcare.

The Software Engineering Lead for Modeling and Simulation is responsible for leading one or more concurrent software projects meeting the software and information technology needs of modelers and statisticians within Merck's Global Clinical Development research organization.

This position is within the Informatics Research Tools and Scientific Computing leadership team.

The key activities for this position include:

* Work with business and quality leads to manage project scope, roadmap, timeline and quality targets.
* Oversee all aspects of the Software Development Lifecycle; feature roadmap, project planning, functional requirements, system architecture and design, software development, system testing, user acceptance testing, installation, transition to support team.
* Identify, secure and manage the required human and financial project resources.
* Coordinate with numerous internal organizations to plan, provision and configure project resources and infrastructure (hardware, software, licenses, support).
* Engage and manage external partners and vendors for the development and/or delivery of software products and services to meet project needs.
* Establish SMART project objectives (Specific, Measurable, Achievable, Relevant and Timely), and report periodically on project status to the Informatics IT leadership team.
* Evaluate and select software solutions that support project needs, and are consistent with existing Merck standards.
* Contribute to the Informatics IT department culture including communication of best practices and lessons learned.

Qualifications

Education:

* Bachelor degree in appropriate technical, scientific, or engineering discipline (Masters or PhD preferred)

Required:

* Minimum of 6 years of professional software engineering experience.
* Minimum of 3 years professional experience leading teams (>5 people) either as direct reports or via outsource arrangement.
* Ability to organize and execute projects including defining and assigning tasks, budgeting and documentation; ability to prioritize, organize and multi-task in high-pressure situations.
* Ability to clearly communicate technical and non-technical information verbally and in writing.
* Ability to work with and manage a diverse group of professionals globally; experience hiring IT personnel.
* Ability to balance multiple competing constituencies and their needs.
* Demonstrated proficiency in at least one of the following programming languages: C++, Java, C# or Javascript.
* Proficiency in LINUX, UNIX and Windows operating systems.
* Proficiency in Agile, phased delivery and evolutionary prototyping software development processes.

Preferred:

* Experience developing or delivering Health Authority Regulated systems in the Pharmaceutical industry.
* Experience in developing scientific applications.
* PMP certification.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ENG002346.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-PD1

Job
: Engineering

Primary Location: US-MA-Boston
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Senior-Software-Engineer-%28Modeling-&-Simulation%29-Job-MA-02108/1792954/179295417929542012-06-15Merck/MSDEngineeringfull-timeUSDstarting0BSBoston, MA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The successful candidate will be responsible for coordinating in silico ADME efforts at their site and for collaborating with modelers and DMPK scientists globally to drive strategy in predictive ADME.

They will provide a strategic and tactical view within and between the groups responsible for ADME data generation and interpretation (Pharmacokinetics, Pharmacodynamics and Drug Metabolism, PPDM) and computational methods development and project support (Chemistry Modeling and Informatics, CM&I) focusing on the interplay between modeling ideas/needs and requirements for experimental data generation.

They will take a lead in educating PPDM in the use of in silico tools and to promote their uptake and increased use within PPDM, and similarly educate within CM&I on the experimental methods and their utility. Raising awareness within other disciplines will be another important responsibility of this in silico ADME scientist.

In doing this work they will collaborate closely with CM&I and PPDM staff to drive education and uptake of model usage within PPDM. Specifically this is aimed at increasing the use of calculated and measured physicochemical properties to understand DMPK data and to ensure state-of-the-art modelling techniques are applied to DMPK datasets.

They will work with the project assigned PPDM and CM&I staff to provide consultancy and direction in the use of data and techniques.

At a tactical level, they will work with PPDM and CM&I staff to define in silico model requirements and contribute to their establishment. Additionally assessing and refining in-house capabilities for across the R&D process.

It is expected that the candidate would maintain a portfolio of basic research into modeling techniques that could be applicable to DMPK and/or assay formats to generate the appropriate data.

Qualifications

Education Minimum Requirement:

* PhD or equivalent in chemistry, DMPK or computational sciences

Required Experience and Skills:

* Experienced DMPK scientist or computational/medicinal chemist with at least 7 years of experience working in a multidisciplinary environment, who has developed and formally pursued an interest in DMPK modeling
* Expertise in dealing with experimental DMPK and data generation appropriate for in silico ADME model building
* Knowledge of current state-of-the art in terms of modeling techniques and approaches
* Ability to communicate results and influence project leaders and senior scientists from other disciplines

Desired Experience and Skills:

* Track record of presentation/publication in the field of in silico ADME
* Ability to build and refine modern computational models

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CHE003449.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Chemistry

Primary Location: US-MA-Boston
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-In-Silico-ADME-Scientist-%28Boston%29-Job-MA-02108/1809488/180948818094882012-06-15Merck/MSDChemistryfull-timeUSDstarting0BSBoston, MA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Informatics department develops, supports and enables the application of informatics across Merck, in partnership with quantitative organizations throughout the company. Our world-class team is currently seeking outstanding informatics professionals to join to join our global team of medical, health, clinical, and translational informaticists. Successful candidates will have the opportunity to collaborate with talented and dedicated colleagues to make a difference to patient healthcare.

The Clinical Research Informatics Lead Analyst will be responsible for developing and executing informatics programs to enable Merck clinical and translational research objectives. Focus client areas will include clinical and preclinical modeling, simulation, and biostatistics within Merck Research Labs. This individual will work collaboratively with modeling and simulation scientists and/or other quantitative scientists across Merck Research Labs to understand their strategic objectives and business needs, and will translate external trends from the biological, medical and technology perspective into informatics strategy, partnering with business leaders in both Merck Research Labs and the Global Services organizations to identify and develop informatics capabilities to address these needs. The successful candidate will manage cross functional teams to implement informatics programs, effectively defining and communicating objectives, processes, milestones and deliverables, as well as supporting critical efforts in a "hands-on" manner as needed. The successful candidate will foster effective relationships with functional groups across the organization and establish and maintain a network of external relationships, including leading researchers in both academic and industry environment.

Responsibilities may include:

* Developing and applying methods, tools, and systems for analysis, modeling, and visualization, and/or automating information pipelines to address modeling and simulation business objectives, in line with a cohesive informatics/IT roadmap
* Working with existing technical and project management resources to deliver new IT capabilities, either through commercial solutions, internal development, external partner sourcing, or crowdsourcing.
* Providing hands on support for analysis objectives and translating these needs and objectives into enabling informatics capabilities
* Identifying opportunities for collaborative development of health informatics capabilities and/or application of real-world healthcare data to predictive modeling and simulation needs. Executing on partnerships and collaborations relevant to utilization of real-world data streams as part of Merck's Global Health IT strategy
* Helping to develop and to manage external modeling and simulation scientific partnerships to provide access to novel capabilities for Merck.
* Enhancing the scientific reputation of Merck and the Informatics organization through publishing and/or or presenting technical papers to internal and external audiences, and/or contributing to patent applications

Qualifications

Education Requirements

* Bachelors degree in an appropriate field of study, including bistatistics, bioinformatics, or bioengineering.
Advanced degree or equivalent experience strongly preferred

Required Experience and Skills:

* A minimum of seven years of relevant work experience in clinical research informatics, biomedical informatics, bioinformatics and/or drug discovery
* Demonstrated success at managing complex scientific partnerships and large multi-phase projects spanning multiple organizations
* Outstanding written and verbal communication and presentation skills with ability to effectively communicate with diverse groups including software engineers, bench scientists, data analysts, and upper management
* Experience with software design, user interface design and product management.
* Ability to manage complex and shifting requirements.
* Excellent team-building and interpersonal/management capabilities;
* Demonstrated history as a self-motivating, productive, innovative, interdisciplinary leader in translational, health or clinical research informatics as evidenced by a strong research and publication record,
* Ability to combine extensive knowledge of emerging technologies with broad organizational focus. Capability to quickly grasp new technological concepts and convey their value to clients and collaborators.
* Demonstrated ability to collaborate with external vendors and partner companies to develop innovative informatics and analytics solutions to meet emerging healthcare, pharma, and/or patient/consumer needs.
* Attention to detail is essential and excellent organizational skills are a must.
* Ability to conceive of and translate a strategic vision into tactical implementation that provides incremental value to clients while driving toward that vision.

Preferred Experience and Skills:

* The diversity of subject matter will require a creative mind, deploying imaginative strategies, and a dedication to solving complex and challenging problems
* Experience communicating at the senior executive (VP) level, skills in negotiation and relationship skills along with high personal integrity, credibility, and energy
* Demonstrated ability to collaborate with external vendors and partner companies to develop innovative informatics and analytics solutions to meet emerging industry needs.
* Program/ Project Management abilities as they relate to working across multiple business areas, divisions and with industry, public and private partnerships
* Proficiency in programming, statistical and database skills, including Perl, Linux/Unix , Matlab, R, SAS, and/or SQL.
* Familiarity with predictive modeling and simulation, particularly in the context of clinical research and development is highly desirable.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # QUA002815.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quantitative Sciences Generic

Primary Location: US-MA-Boston
Other Locations: US-CA-San Francisco
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Clinical-Research-Informatics%2C-Lead-Analyst-Job-MA-02108/1824634/182463418246342012-06-15Merck/MSDQuantitative Sciences Genericfull-timeUSDstarting0BSBoston, MA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The candidate's responsibilities include but are not limited to:

* Involvement in the design and synthesis of chemical libraries in support of small molecule drug discovery programs at MRL Boston.
* Active and detailed discussion with medicinal chemistry project teams to match chemical libraries with the current project issues and timelines.
* Collaborate with molecular modeling and informatics, procurement of building blocks and validation of the correct chemistry for each chemical library.
* The candidate will provide scientific leadership of their own parallel medicinal chemistry projects and may provide scientific supervision to other parallel chemistry group members.
* A significant proportion of this role is laboratory based.
* There may be the opportunity to take part in or lead matrix teams at both the site and global level depending on the candidates ability and expertise.

Qualifications

Education Required:

* MS BS in Chemistry

Education Desired:

* PhD in Organic Chemistry

Skills and Education:

* Minimum 5 years experience in parallel medicinal chemistry in a pharmaceutical research environment.

* Strong background of synthetic organic chemistry.

* Broad understanding of modern medicinal chemistry concepts.

* Successful application of advanced chemoinformatics SAR analysis and library design techniques.

* Track record of successful impact of parallel chemistry to drug discovery programs.

* Track record of publications, papers, conference talks and posters in the parallel medicinal chemistry area.

* Experience dealing with external collaborators on the execution of parallel chemistry projects.

* Broad experience with tools such as MS Office, Pipeline Pilot and Spotfire.

* Broad experience of parallel chemistry protocol development and optimization.

* Experience in parallel chemistry techniques such as solution phase parallel synthesis, solid phase synthesis and high throughput purification and analysis.

* Some experience in supervision or scientific mentoring is required.

* Effectively utilize CROs to drive projects.

* Effectively communicate research plans and progress.

* The candidate should be a strong collaborator and communicator with experience of success in matrix teams.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CHE003408.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-JI1

Job
: Chemistry

Primary Location: US-MA-Boston
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Automated-Synthesis-&-Purification-Chemistry-Team-Member-Job-MA-02108/1750655/175065517506552012-06-15Merck/MSDChemistryfull-timeUSDstarting0BSBoston, MA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


* Coordinate with Oncology Franchise Head to understand Research & Development (R&D) Strategies and prioritize detailed Knowledge Discovery/Knowledge Management (KD/KM) needs.
* Develop and execute a KD/KM strategy to deliver Scientific and Competitive Intelligence in support of strategic decision-making in franchises/areas of responsibility.
* Coordinate with the KD/KM Leadership Team, internal and external partners to design and deliver industry-leading Research Services capabilities in franchises/areas of responsibility.
* Provide information science leadership and subject matter expertise for strategic MRL Initiatives (e.g., Connectivity) and contribute to content evaluation processes for the One Merck Digital Library.

· Provide scientific and project leadership on multiple Knowledge Discovery/Knowledge Management (KD/KM) projects in support of research activities (e.g., target validation and prioritization; lead identification & optimization; preclinical development; and identification of potential external partnership opportunities).

· Leverage KD/KM tools, databases, systems and other knowledge resources to provide optimal support to R&D project teams, in areas of interest including Oncology and Biologics.

· Manage contractors/consultants, and ad hoc project teams to deliver high quality results to impact decision making in R&D.

Qualifications

Education

* A masters degree required, Ph.D. or other equivalent educational background in one of the Life Sciences areas

Required Experience and Skills

* Excellent oral and written communication skills, effective teamwork and partnership experience,
* Analytics skills (e.g., natural language processing, text mining, data visualization, etc.) are critical for this position.
* At least 5 years of experience in successfully conducting and managing drug research and development projects in the pharmaceutical industry.

Preferred Skills:

* Deep knowledge of at least one Life Sciences area, plus broad drug R&D knowledge.
* Demonstrated ability to take on new projects and successfully deliver results in fast-paced, dynamic and multifunctional environments.
* Demonstrated proficiencies in the application of information science resources to impact drug R&D (e.g., STN, Dialog, Linguamatics, Pathway Analysis and visualization tools, pipeline databases such as T-Pharma or Prous, and patent information resources).
* Proven record of innovative and critical thinking, and excellent problem-solving ability.
* Proven track record of high quality scientific publications in peer-reviewed journals.
* Proven skills in managing cross-functional project teams to deliver impactful results.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # COR000160.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Corp. Dev. & Licensing Generic

Primary Location: US-MA-Boston
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Oncology-Knowledge-Lead-Job-MA-02108/1868791/186879118687912012-06-15Merck/MSDCorp. Dev. & Licensing Genericfull-timeUSDstarting0BSBoston, MA, US
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

RESUMEN DE LA POSICION

Visitar un número determinado de Médicos para proveer información clave detallada y maximizar así, las ventas y el crecimiento sostenido de la participación de mercado de acuerdo a las estrategias de mercadeo.

Alcanzar los objetivos de venta y maximizar la participación de mercado de los productos asignados a su territorio.

PRINCIPALES RESPONSABILIDADES:

- Incrementar el Market Share de los productos en promoción de su líne
- Alcanzar el presupuesto anual de ventas para su linea
- Desarrollar el plan de negocios de su territorio para maximizar el número de visitas de su target médico.
- Asegurar una óptima calidad del panel médico a su cargo (Potencial según los parámetros definidos), mediante la revisión sistemática del mismo y actualización oportuna.
- Alcanzar su target de visita (frecuencia & promedio) de acuerdo a los objetivos establecidos.
- Chequear la segmentación médica, manteniendo y actualizando información de los clientes y completando los reportes de visitas.
- Proponer acciones de promoción para incrementar la participación en el mercado y el servicio al cliente.
- Proveer información clave y detallada a su target médico que asegure un incremento en la prescripción de los productos a su cargo.
- Proveer y mantener actualizada la información de la competencia (Ej. Tácticas y actividades de marketing)
- Coordinar ciclos de visita con colegas del distrito para maximizar la cobertura y el impacto médico.
- Visita a farmacias para saber la rotación y situación del mercado

Cualificaciones
Grado profesional, preferiblemente en ciencias de la salud.

Español (lengua madre). Ingles (Intermedio)

Deseable 1 año como visitador medico y/o vendedor de productos especializados, preferiblemente en Laboratorio Multinacional.

Conocimientos del Software de Microsoft office, manejo de Internet.

Comportamientos de líder (responsabilidad compartida, trabajo en equipo, integridad)

Nuestros empleados son la clave del éxito de nuestra empresa. Demostramos nuestro compromiso con nuestros empleados ofreciéndoles un programa de recompensas competitivo y valioso. Los beneficios en MSD están diseñados para apoyar la amplia gama de objetivos, necesidades y estilos de vida de nuestros empleados y de muchas de las personas que constituyen lo más importante en sus vidas.

*LI-KT1

Puesto
: Ventas

Ubicación principal: VE-Caracas Capital District-Caracas
Tipo de acuerdo laboral: Fijo(a)
Viajes: Sí, un 75% del tiempo
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Caracas-Representante-de-Ventas-Unidad-Cardiometabolica-Job/1848104/184810418481042012-06-15Merck/MSDVentasfull-timeUSDstarting0BSCaracas, Caracas Capital District, VE
Description

Merck Sharp & Dohme - where patients come first

Merck Sharp & Dohme Biologics (Ireland) Ltd. is a subsidiary of Merck & Co. Inc., New Jersey, USA, one of the leading healthcare companies in the world.

Located on the periphery of Carlow Town, Merck Sharp & Dohme Biologics (Ireland) Ltd. is our latest Irish facility, joining existing Merck Sharp & Dohme operations in Tipperary and Dublin. The vaccines, biologics and other products we will formulate in our new Carlow facility could ultimately be used by millions of people across the world.

We are now seeking applications from energetic, motivated and innovative people interested in becoming part of this exciting new phase in our global development. Working with likeminded individuals, you will join a growing dynamic team in a newly constructed, contemporary environment. Successful applicants in each of the positions outlined here will make an important contribution to our overall operations in Carlow, Ireland and worldwide.

This role is one of our exciting job opportunities right now:

Production Operator

The successful candidate will be part of the Operations team (Integrated Process Team-IPT) providing support to the filling processes at our Vaccines Formulation / Fill facility in MSD Carlow.

* The incumbent will be responsible for participating in C&Q and Validation activities to support start up by being and active member in our cross functional suite teams.
* Following Qualification and start up the role will include responsibility for the development of SOP's, routine operations and monitoring of production equipment using MES/DCS and PLC based systems.
* The Successful candidate will also be responsible for delivery of training, maintaining housekeeping, and 5S in all production areas while focusing on continuous process improvement using Lean Principles.

Qualifications

* Applicants will have a 3rd Level qualification in Science/Engineering related discipline, and 3-5 years experience in the biotech / pharmaceutical industry.
* Applicant should have previously demonstrated strong team skills, flexibility, motivation, ability to troubleshoot/problem solve, with a strong emphasis around safety and compliance practices.
* Applicants should actively support, participate and embrace an empowered team culture and have excellent communication skills
* Aseptic/Sterile Manufacturing experience required.

Job
: Production / Operator

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 4]]>http://jobs.merck.com/job/Carlow-Production-operator-Job/947331/9473319473312012-06-15Merck/MSDProduction / Operatorfull-timeUSDstarting0BSCarlow, Leinster, IE
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Future Talent Program features paid internships targeted to start in June 2012 for 10 - 12 weeks and will include one or more projects. Housing is available for those interns meeting the housing distance guideline. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals. The projects that you work in can be in one of the following areas:

PROCESS DEVELOPMENT, SCALE UP AND LAUNCH

* Work in teams to bring research discoveries to full production scale by applying engineering, biology, chemistry and pharmaceutics skills to bench-scale processes.
* Conceive, develop and implement new processing and manufacturing technologies
* Work with teams to develop processes for new products, using chemically- or biologically- derived products
* Support process development and product development with pilot plant scale up, drug supply preparation and technology transfer to operations groups

EQUIPMENT AND FACILITIES DESIGN

* Design and build advanced manufacturing plants, laboratory and office facilities
* Involvement with all phases of project management from the first engineering drawing to the last phase of project start up

MANUFACTURING

* Support line production and maintenance operations
* Maintain manufacturing processes at high levels of performance
* Engineer plant site improvements to enhance safety, quality and the environment
* Optimize existing processes to achieve improvements in process quality, yield and efficiency.

STATISTICS

* Researching possible statistical approaches
* Implementing the best approach in software and reporting on the results
* Work with staff members on on-going consulting projects

LOCATIONS: Rahway, NJ; West Point, PA; Summit, NJ;Whitehouse Station, NJ; Elkton, VA; Durham, NC

Specific internship openings in MMD are as follows:

* Analytical Chemistry in Development and Supply (West Point, PA, Rahway, NJ) performs analytical development and support for new chemical, biological and pharmaceutical processes;
* Center for Material Science & Engineering (West Point, PA; Rahway, NJ; Summit, NJ) performs analytical evaluation of raw materials, intermediates, and final products to aide in investigation and process improvement evaluations
* Center for Mathematical Science (West Point, PA) performs statistical analysis of current process and process improvements across Merck;
* Chemical Process Development & Commercialization (Rahway, NJ) and Pharmaceutical Commercialization Technology (West Point, PA, Summit, NJ) groups perform process development and demonstration for new chemical and pharmaceutical processes;
* Global Vaccines Technology and Engineering (West Point, PA, Elkton, VA, Durham, NC) is responsible for process implementation, validation and maintenance for biological processes;
* Biologics Manufacturing Science & Commercialization (Rahway, NJ, West Point, PA) is responsible for the development and implementation of vaccine and therapeutic protein processes;
* Global Technical Operations (West Point, PA, Elkton, VA) is responsible for continuous improvement of existing processes.
* Global Engineering Services (Cokesbury, NJ with projects at other sites) is responsible for designing and project management for capital projects;
Vaccine Operations (West Point, PA, Elkton, VA, Durham, NC) is responsible for oversight and continuous improvement for vaccine manufacturing

Qualifications

Qualifications:

Education:

* Working toward graduate degree in Chemistry, Biology, Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Statistics or related field

Requirements:

* Available for 10 week internship beginning June 2012
* Strong personal character and ethics
* Superior Communication and Interpersonal Skills
* Excellent Academic Achievement, Analytical Ability
* Good team player and ability to work independently
* U.S. citizen or lawful permanent resident of U.S.
*
Titers may be required for this position

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ADM004909.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-VA-Elkton
Other Locations: US-NC-Durham-RTP, US-NJ-Rahway, US-PA-West Point, US-NJ-Summit, US-NJ-Whitehouse Station

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1

Relocation Provided
: None]]>http://jobs.merck.com/job/Elkton-MMD-Graduate-Intern-2012-Job-VA-22827/1729513/172951317295132012-06-15Merck/MSDInternfull-timeUSDstarting0BSElkton, VA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Senior Manufacturing Supervisor will ensure that supervised personnel manufacture products Right the First Time per standard operating procedures and in compliance with cGMPs, safety, and environmental regulations. Due to the high impact nature of this role it is essential that the incumbent demonstrate integrity, credibility, and flexibility in their daily performance so as to motivate others to do the same.

The supervisor will manage the production of vaccine, adjuvant, and bulk biologics and the associated hourly workforce to ensure attainment of business results. The incumbent will effectively collaborate within a team environment with the responsibilities of production execution, effective administration of personnel performance policies and procedures, management of conflict and change, and the identification and implementation of continuous improvement initiatives.

The supervisor will work with technical staff in supporting equipment startup, process and area qualification, SOP and training development, process validation, and the training and development of the operating staff to support commercial demand in a biologics manufacturing facility. The supervisor will perform and participate in safety, environmental, and quality audits and investigations and be involved in implementation of related corrective actions.

Under the general direction of an Area Head/ IPT business lead, the supervisor will also be responsible for coaching and mentoring new supervisors.

This position will work various shifts during startup and process validation periods, and ultimately be on a 12 hour rotating shift.

Qualifications

Required:

* B.S. with in Science or Engineering

* Minimum of three (3) years working experience in cGMP mAB, biological, sterile, vaccine, or pharmaceutical environment.

Desired Experience/Skills:

* Leadership and interpersonal skills to motivate direct reports and peers to excel and "own" the process

* Flexibility to perform various tasks to support the business.

* Lean, Six Sigma problem solving skills coupled with a continuous improvement mindset

* Ability to prioritize, focus on and obtain business results

* Excellent communication and organizational skills

* Technical writing experience related to procedures and investigations

* Delta V and SAP experience

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAN001189.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Manuf./Operations Generic

Primary Location: US-VA-Elkton
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: Other (see Work Schedule)

Hazardous Materials
: None]]>http://jobs.merck.com/job/Elkton-Senior-Manufacturing-Supervisor-Job-VA-22827/1790668/179066817906682012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSElkton, VA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


At Merck & Co., Inc Manufacturing facility in Elkton, Virginia, we currently have multiple Senior Manufacturing Supervisor positions open at the Stonewall Plant; which is located in the Shenandoah Valley along the Shenandoah River and the Blue Ridge Mountains. The facility is just a short distance from major state universities: University of Virginia and James Madison University.

The Senior Manufacturing Supervisors will ensure that supervised personnel manufacture products Right the First Time per standard operating procedures and in compliance with cGMPs, safety, and environmental regulations. Due to the high impact nature of this role it is essential that the incumbent demonstrate integrity, credibility, and flexibility in their daily performance so as to motivate others to do the same.

The supervisors will manage the production of API's and/or Sterile Bulk API and the associated hourly workforce to ensure attainment of business results. The incumbent will effectively collaborate within a team environment with the responsibilities of production execution, effective administration of personnel performance policies and procedures, management of conflict and change, and the identification and implementation of continuous improvement initiatives.

The supervisors will work with technical staff in supporting equipment startup, process and area qualification, SOP and training development, process validation, and the training and development of the operating staff to support commercial demand in an API or Bulk Sterile API manufacturing facility. The supervisors will perform and participate in safety, environmental, and quality audits and investigations and be involved in implementation of related corrective actions.

Under the general direction of an Area Head/ IPT business lead, the supervisors will also be responsible for coaching and mentoring new supervisors.

These positions will work various shifts during startup and process validation periods, and ultimately be on a 12 hour rotating shift.

Qualifications

Required:

* High School Diploma or GED Equivalent
* Minimum of three (3) years working experience in cGMP API, biological, sterile, vaccine, pharmaceutical or food environment.

Desired Experience/Skills:

* Leadership and interpersonal skills to motivate direct reports and peers to excel and "own" the process
* Flexibility to perform various tasks to support the business.
* Lean, Six Sigma problem solving skills coupled with a continuous improvement mindset
* Ability to prioritize, focus on and obtain business results
* Excellent communication and organizational skills
* Technical writing experience related to procedures and investigations
* Delta V and SAP experience

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition MAN001677.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Manuf./Operations Generic

Primary Location: US-VA-Elkton
Employee Status: Regular
Number of Openings: 3

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/Elkton-Senior-Manufacturing-Supervisor-Job-VA-22827/1804832/180483218048322012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSElkton, VA, US
Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.




Under the supervision of the management, performs administrative duties related to the receipt and distribution of mail, maintenance of electronic filing systems for the Global Safety department.

In addition, collaborates with staff within the organization as well as cross-functionally.

Qualifications

Bachelors degree preferably in Language studies, Information & Documentation, Secretarial Tasks or Administrative areas.

Skills in computer systems

Strong sense of responsibility

Detail orientated and quality driven

Work effectively in a team.

Follow up and control

Fluent English Read, Written and oral

Stress tolerance

Time management skills

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. MSD's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

Job
: Clinical Data Management

Primary Location: CO-Distrito Capital de Bogotá-Bogotá
Employee Status: Temporary
Number of Openings: 2]]>http://jobs.merck.com/job/Bogot%C3%A1-Assistant-Data-Coordinator-Job/1711017/171101717110172012-06-15Merck/MSDClinical Data Managementfull-timeUSDstarting0BSBogotá, Distrito Capital de Bogotá, CO
Description

The Quality Manager is deputy of the Responsible Person (QRP), the registered contact to the Swiss Health Authorities for quality issues and maintains an open and transparent relationship with the Health Authority Swissmedic, the Regional Inspectorate and the Cantonal Health Authority.

The QM supports the implementation of directives issued by the QRP in GMP/GDP matters in the quality interests of MSD Merck Sharp & Dohme AG (distribution in Switzerland) as well as for Essex Chemie AG, Schering-Plough Central East AG, MSD International GmbH, and Merck Sharp & Dohme IDEA AG (trade with pharmaceuticals in foreign countries).

The QM supports the QRP in overseeing the quality systems and processes, in accordance with local and international regulations and internal MSD standards.

The QM together with the QRP is in contact with colleagues in Switzerland, colleagues in the quality organization of countries supplied by legal entities, and the regional office of EMEA Quality Operations to effect Quality requirements and to ensure GxP compliance within her jurisdiction.

The Quality Manager is supporting the QP in the following tasks:

1. General Management Responsibilities

* Responsible to Swissmedic and company management to assure GXP compliance for Lucerne operations.
* Awareness and implementation of applicable regulations and dissemination to relevant colleagues.
* Developing and maintaining an operational pharmaceutical quality assurance system.
* Developing and maintaining a local documentation system that encompasses working instructions, descriptions of procedures and protocols.
* Ensuring that all business is conducted in accordance with the Swiss law on Medicinal Products [HMG, 2. Kapitel: Arzneimittel , Abschnitt 3: Einfuhr, Ausfuhr und Handel im Ausland und AMBV, 2. Kapitel, Art. 10 Fachtechnisch verantwortliche Person (Bewilligung für die Einfuhr, den Grosshandel und die Ausfuhr), Art. 14 Fachtechnisch verantwortliche Person (Bewilligung für den Handel im Ausland)] as well as with company policies; in both of them the QP has the authority to issue directives
* Ensuring that all regulatory approvals and authorizations are obtained for the legal entity for import, wholesale, and export of pharmaceuticals or trade in foreign countries resp.
* Ensuring the traceability of purchases and sales of medicinal products and recording the necessary information concerning this.
* Ensuring a procedure for recalls.
* Direct Quality supervision of the local contractor for warehouse and distribution services / secondary packaging and obtain insight into the business processes relevant for Good Distribution Practice
* Contact person for Quality/Technical Agreements defining GXP responsibilities.
* Notification of critical trends and emerging quality deficiencies to Swissmedic.
* Decision making for all Quality issues.

2. Responsibilities for the Swiss Market (MSD Merck Sharp & Dohme AG)

* Release of commercial products for the market independent from commercial functions (primarily based on the release of the QP of the manufacturer).
* DPOC for PQCs: Processing complaints or defects in quality (forwarding to manufacturer, tracking, information to customers, periodical evaluations) and deciding on or possibly initiating measures necessary as a result, such as recalling a batch from the Swiss market.
* DPOC for suspected CDT cases (counterfeits/diversion/tampering)
* Processing quality defects and deciding on or possibly initiating measures necessary as a result, such as recalling a batch/product from the Swiss market in cooperation with manufacturing site, QA management and local HA
* Taking decisions concerning destruction of returns
* Forwarding requests for exceptional re-use of returns (request for waiver to redistribute) to Vice President Quality Operations Europe, Middle East, Africa
* Overall responsibilities for GXP activities in the relabeling of IMPs.
* Planning and monitoring of general GDP training of employees (initial training, GxP-awareness training).
* Quality oversight / auditing for external service providers (e.g. external warehouse).

3. Responsibilities for trade in foreign countries (ECAG, SPCE, MSD IG, MSD IDEA, Sinova)

* Interactions with relevant authorities and production sites
* Assuring quality systems and processes in accordance with Swiss law and MSD policies
* Developing and maintaining a documentation system for quality related activities (eg. supplier verification)
* Ensuring that all regulatory approvals and authorizations are obtained for the legal entities
* license for trading pharmaceuticals in foreign countries
* license for trading narcotics in foreign countries

* Supplier/customer certification controls
* Planning and monitoring GDP trainings of employees locally and support on request of at the country sites
* Planning and overseeing/performing internal and external audits
* Ensuring the traceability of purchases and sales of medicinal products and recording the necessary information concerning this.
* Narcotics: overall responsibility for processes undertaken by ECAG manufacturers/suppliers; annual stock taking - report to Swissmedic.

4. Critical Interactions

* Interaction with the Health Authorities Swissmedic, Regional Inspectorate, and the Cantonal Health Authority
* Meeting regularly with Swiss Logistic and Regulatory to assure alignment of activities
* Meeting regularly with Supply Chain Management and Supply Chain Operations
* Close cooperation with Pharmacovigilance Country Lead
* Participating in regular meetings with EMEA Regional Quality Operations

Qualifications

Required:

· Higher education (e.g. Masters degree) in pharmacy, medicine, biology or a comparable discipline with extensive experience) or some years of experience

· Need to fulfill the requirements to act as a QP (based on Swiss Law).

· Experience as a Qualified or Responsible Person, preferably in Switzerland.

· Familiar with local Swiss, European and international GXP regulations.

· Documented experience in GXP regulations.

· Excellent analytical and problem solving skills, based on science, data and understanding of regulatory requirements in a complex and evolving environment; ability to apply sound risk management.

· Fluency in English and German and preferably also French.

Job
: Medical Information Services

Primary Location: CH-LU-Luzern
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Luzern-Quality-Manager-MSD-Switzerland-Deputy-Qualified-Person-Job-LU/1862950/186295018629502012-06-15Merck/MSDMedical Information Servicesfull-timeUSDstarting0BSLuzern, LU, CH
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position is responsible for the research and investigation of all variances to the physical inventory. Position will handle/control the consigned warehouse 3PL distribution networks, inventory control at those locations and reconciliations of that inventory. The analyst will review current operational SOP's and recommend changes by validating and analyzing data. The analyst will be responsible to pull and research data and recommend new and improved processes. The position may support US distribution, logistics, transportation, International exports/imports. The position will perform assigned tasks and support various logistical departments.

Qualifications

Required:

* B.S. in inventory management/materials management/logistics or related field.

* 3+ years experience in inventory management/production systems/import/export/warehousing preferred.

* Must have prior experience in cycle counting, controls and analysis.

* Must have strong analytical skills.

* Proficiency in computer systems, SAP or equivalent.

* Must have a strong working knowledge of Excel, Access and Power Point.

* Able to work with data, validation and present results.

* Experience with process management, Green Belt preferred.

* Proven ability to prioritize workload and handle multiple projects at the same time.

* Position requires close working relationships with the other departments.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. merck.com/careers to create a profile and your resume for requisition # WAR000148.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-JE1

Job
: Warehousing

Primary Location: US-NE-Omaha
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Omaha-Distribution-Analyst-Job-NE-68046/1558419/155841915584192012-06-15Merck/MSDWarehousingfull-timeUSDstarting0BSOmaha, NE, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position, under the direction of the Customer Service Supervisor will be responsible for butn ot limited to:

* Inbound telephone calls
* Account Management
* Order processing
* Product related questions
* Account and order related questions

This position will interact with Merck Animal Health's customers, Sales Representatives, Marketing, and Management.

Work hours will be between 8 am - 5 pm Monday through Friday.

Qualifications

Education Minimum Requirement:

* High School Graduate or Equivalent, College Degree preferred

Required Experience and Skills:

* Minimum one year experience in Customer Service Environment.
* Proficient in MS Office applications.
* Excellent telephone skills.
* Ability to handle customers in difficult situations.
* Ability to work in a team oriented environment.

Desired Experience and Skills:

* Agricultural/Animal Science background.
* SAP Experience.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # XXXXXXXX.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Customer Service

Primary Location: US-NE-Omaha
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Omaha-Customer-Svcs-Rep-I-Animal-Health-Job-NE-68046/1862951/186295118629512012-06-15Merck/MSDCustomer Servicefull-timeUSDstarting0BSOmaha, NE, US
Beschreibung
Merck Sharp & Dohme-Chibret AG ist die Schweizer Niederlassung der Merck & Co., USA. Merck entwickelt, produziert und vertreibt weltweit innovative Medikamente und gehört international zu den führenden Pharmaunternehmen. Weltweit arbeiten ca. 100'000 Mitarbeiter für uns.

Die Schweizer Organisation beeinhaltet die Unternehmungen MSD International GmbH, Merck Sharp & Dohme-Chibret AG, Essex Chemie AG, Schering Plough Central East und Werthenstein BioPharma GmbH mit gesamthaft 700 Mitarbeitern.

Wir offerieren ein

2- Jahres Graduate Programm im Bereich Information Technology Services Group

Sie werden in diesem Programm als Business Analyst im Global Human Health IT Europe/Canada eingesetzt werden.

Aufgaben:

• Business Anforderungen anhand von Umfragen erstellen, Analyse von Dokumenten, Workshops durchführen, Umfragen organisieren, Business Analyse erstellen und Task & Workflow Analysen erstellen

• Sämtliche Informationen evaluieren, Informationen filtern und Prioritätenlisten erstellen

• Verstehen der Business needs und Herausforderungen

• Standardprozesse einführen und kommunizieren

• Businesslösungen erarbeiten und intern anbieten

• Schnittstelle zwischen dem Business und IT für sämtliche Anfragen bezüglich Verbesserungen, Koordination mit der IT Abteilung

• Unterstützung beim Testing und Vorbereitungen, Design von Test Szenarien und Test Scripts

Qualifikationen

• Erfolgreicher Hochschul oder Universitätsabschluss im 2012 (Richtung: Computer Sciences, Computer Engineering, Information Management, Mathematik, Telecommunications, Wirtschaftsinformatik)

• Fliessende Englischkenntnisse in Wort und Schrift, weitere Sprachen von Vorteil

• Problemlösungsfähig und Konfliktlösungsfähig

• Hohe analytische Fähigkeiten

• Technisches Verständnis mit entsprechender Ausbildung sind ein absolutes Plus

• Gute Kommunikationsfähigkeit, sollte sich gut intern mit dem Business verständigen können und entsprechende Präsentationsfähigkeiten haben

• Interesse oder Kenntnisse der Pharmaindustrie sind ein Plus

• Reisetätigkeit erwünscht

Job
: Unternehmensanalyse

Primärer Standort: CH-LU-Luzern
Mitarbeiterstatus: Permanent
Reisebereitschaft: Ja, 15 % der Zeit
Anzahl offener Stellen: 1
Externes Job Ausschreibungsportal: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-GRADUATE-PROGRAMM-Business-Analyst-im-Bereich-Information-Technology-Services-Job/1891871/189187118918712012-06-15Merck/MSDUnternehmensanalysefull-timeUSDstarting0BSLuzern, CH-LU
Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


SUMMARY OF THE POSITION

Represents the Company in all SPRI sponsored research clinical trials. Evaluates and recommends potential sites and investigators for the implementation of clinical studies. Monitors the development and quality of such trials, ensuring that they arte in compliance with SPRI Standard Operating Procedures and applicable regulations, and that patient rights are respected.

MAJOR ACTIVITIES AND RESPONSABILITIES:

* Selects potential sites and investigators
* Conducts site initiation, close - out and interim monitoring visits
* Verifies the accuracy of clinical supply accountability records
* Performs the reconciliation of clinical supplies
* Is responsible for collecting, recording and ting all the documentation related to the trial
* Reviews data supplied by investigators, follow up data discrepancies and keeps investigators informed about observations made during monitoring visits and corrective actions needed
* Ensures that all applicable regulatory requirements (e.g. ICH, GCP guidelines, FDA requirements and local regulations) are complied with

Qualifications

Education: MD or BS, MS, PhD in Biology, Molecular Biology, Microbiology, Chemistry, Pharmacology, Pharmacy or Nursing.

Languages: Spanish (mother tongue). English (Advanced).

Work Experience: 3 years of full time related clinical research experience.

Skills: Willingness to work with electronic tools.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. MSD's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

*LI-KT1

Job
: Clinical Research Monitor(CRA)

Primary Location: VE-Caracas Capital District-Caracas
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Caracas-Clinical-Research-Associate-%28CRA%29-Job/1889123/188912318891232012-06-15Merck/MSDClinical Research Monitor(CRA)full-timeUSDstarting0BSCaracas, Caracas Capital District, VE
Beschreibung
Die Position, Hospital Sales Representative Anesthesia, ermöglicht dem Mitarbeiter eine, verantwortungsvolle und gestaltungsreiche Aufgabe innerhalb der neuen MSD-BU-Struktur Anästhesie Europa einzunehmen.

Der Mitarbeiter arbeitet mit einer hohen Eigenverantwortlichkeit und einem effizienten Gebietsmanagement unter besonderer Berücksichtigung der Marketing-Strategie. Dabei wird die Möglichkeit geboten, Projekte zu übernehmen und den Marketing/Sales Manager bei der Umsetzung und Konzeption zu unterstützen.

Die Aufgabe des Mitarbeiters ist es, die vorgegebenen Bridion-Verkaufsziele durch gezielte, kundenorientierte Aktivitäten zu erreichen. Dabei sind die klinischen Vorteile für den Kunden (Arzt, med. Mitarbeiter, Patienten, etc.) hervorzuheben und die ethischen Grundsätze von MSD einzuhalten.

Haupttätigkeiten:

* Sales und Marktanteil: Der Mitarbeiter steuert dazu bei, die vorgegebenen Verkaufszahlen und Marktanteile auf seinem/ihrem Gebiet zu erreichen. Dies geschieht dadurch, dass die Leistungsvorgaben der unten angeführten Aktivitäten zu 100% erfüllt werden.

* Produktbesprechung: Der Mitarbeiter implementiert Marketingstrategien durch Kundengespräche, welche sich auf den Patienten bzw. Therapie/Einsatz-Gebiete konzentrieren. Er/sie präsentiert Fakten, Vorteile und Limitierungen die auf den individuellen Gesprächspartner bzw. Gesprächsgruppen abgestimmt sind und welche die vermehrte Verschreibung innerhalb einer Indikation unterstützen. Jedes Kundengespräch hat eine erfolgsorientierte Zielsetzung. Diese Zielsetzung ist bestimmt durch frühere Gespräche, reflektiert die Verkaufs/Marketing-Strategie, spezifiziert die derzeitige Perspektive des Kunden, ein erwünschtes Resultat und Aktivitäten welche der Mitarbeiter unternehmen kann, um das erwünschte Ziel zu erreichen. Das Gespräch ist auf Fakten bezogen, gibt eine ausgewogene Perspektive von Vorteilen und Limitierungen (Kontraindikationen, gebotener Vorsicht) welche auf das besprochene Produkt und Patientenprofil abgestimmt sind. Alle Fakten sind durch bewilligte Evidenz (Klinische Studien, Diskussion Aids) unterstützt.

* Netzwerkpflege:
Mit externen Kunden (wie Ärztezielgruppen, Pflegepersonal, Spitalapotheker, BUDs, Brand Manager, Market Access, Pharmakovigilanz, Einkauf, Medizin.
Kennen und Nutzen von Entscheidernetzwerken. Erheben von Abläufen der Therapieströme und Patientenbetreuung

* Scientific Leader-Betreuung und Unterstützung der Entscheidungsträger durch Information über Produkteigenschaften und wirtschaftlichen Vorteilen

* Gebietsmanagement: Der Mitarbeiter erstellt einen Gebietsplan aus, welcher in einer prioritisierten Liste von Kunden resultiert, die mit entsprechender Frequenz und Effektivität besucht werden. Der Plan legt fest, wen der Mitarbeiter besucht, was zu tun ist, und definiert eine Strategie, wie die gewünschten Resultate erzielt werden. Der Plan enthält weiters einen Besuchsplan für alle priorisierten Kunden und reflektiert die entsprechende Priorität. Der Plan achtet auch auf die Effektivität des Weges zwischen den einzelnen Kunden. Aufzeichnungen über die Gespräche mit Kunden werden später dazu benutzt, um den Inhalt des nächsten Gespräches zu planen.

* Erkennen und Lösen von systemischen Problemen.

* Reisetätigkeit zum Besuch der Ansprechpartner im entsprechenden Gebiet.

* Kenntnisse über Produkt und Krankheitsbild: Der Mitarbeiter kann während Produkttrainings inhaltlich richtige Information in mündlicher Diskussion und schriftlicher Form wider geben. Alle Aussagen über Produkt und das Krankheitsbild sind richtig und in Übereinstimmung mit dem Label.

* Veranstaltungen: Der Mitarbeiter plant, organisiert, und implementiert Veranstaltungen welche ihn/sie beim Gebietsmanagement und dem entsprechenden Plan unterstützen (i.e. Roundtable Diskussionen). Jede Veranstaltung ist in Übereinstimmung mit Verkaufs/Marketing-Strategien und den Plänen des Gebietsmanagement. Der Plan für jede Veranstaltung beinhaltet auch Folgeaktivitäten mit eingeladenen Kunden um deren Commitment zu stärken. Alle Veranstaltungen werden innerhalb des zugewiesenen Budgets abgewickelt.

* Berichte (Reports): Der Mitarbeiter liefert alle Berichte 100% genau und 100% termingerecht ab. Alle verfügbaren elektronischen Systeme sind zu benutzen, wie vom Management angewiesen. Anfragen vom Management für Informationen oder Aktivitäten sind richtig und innerhalb der erwarteten Zeitspanne zu erfüllen. Regelmäßige Reports und Besprechungen zur Strategischen und taktischen Abstimmung

* Persönliche Weiterentwicklung/Team Entwicklung: Der Mitarbeiter steuert zu seiner/ihrer eigenen beruflichen Weiterentwicklung bei. Der Mitarbeiter unterstützt die Teamentwicklung, indem er/sie sich aktiv an Cyclemeeting und anderen Teamdiskussionen beteiligt.

Qualifikationen

Fähigkeiten, Kompetenzen :

* Sehr gutes Produktwissen; Kenntnis der Erkrankungsbilder und Versorgungsorganisation
* Mindestens 4 Jahre erfolgreiche Erfahrung im Verkauf der Pharmaindustrie, davon mindestens 2 Jahre Erfahrung mit Spezialisten
* Bachelor Degree im Paramedizinischen Bereich oder ähnliche Ausbildung
* Lösungsgsoriente Vorgehensweise
Hohe Eigenverantwortlichkeit und Reisebereitschaft
Kaufmännisches Denken, und Verhandlungsgeschick

Job
: Channel-Vertrieb, allgemein

Primärer Standort: CH-LU-Luzern
Mitarbeiterstatus: Permanent
Reisebereitschaft: Ja, 75 % der Zeit
Anzahl offener Stellen: 1
Externes Job Ausschreibungsportal: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-Hospital-Sales-Representative-Anesthesia-Job/1858712/185871218587122012-06-15Merck/MSDChannel-Vertrieb, allgemeinfull-timeUSDstarting0BSLuzern, CH-LU
Description

Active Pharmaceutical Ingredients (API's) zijn de grondstoffen voor geneesmiddelen, die op (bio)chemische wijze geproduceerd worden. De faciliteiten van API Operations in Oss produceren in totaal ruim 100 verschillende actieve grondstoffen. Naast 'eigen' grondstoffen produceert API Operations ook producten voor externe partijen. Meer informatie daarover is te vinden op www.msdapi.com. Om productie van API's professioneel te ondersteunen, werkt MSD met Center of Excellence Global Technical Operations (CoE GTO API), die bestaat uit ongeveer 100 collega's.

Op dit moment zoeken wij een Lab Technician Chemie. Als Lab Technican zet je zelfstandig (series) van experimenten op en voert deze uit. Het werkgebied is procesoptimalisatie, trouble shooting en/of process developement volgens de geldende EHS (Environment, Health & Safety) en GMP richtlijnen. Zelfstandig analyseer en interpreteer je resultaten en doe je voorstellen voor vervolgexperimenten. Onderzoeksresultaten worden zowel mondeling als schriftelijk door je gerapporteerd (in Nederlands en/of Engels). Middels literatuur blijf je op de hoogte van vakinhoudelijke ontwikkelingen. Tot slot begeleid je soms een stagiair.

Qualifications

* Heeft een afgeronde HBO-opleiding Chemie, Chemische Technologie of aanverwant.

* We vragen minimaal drie jaar relevante ervaring binnen je vakgebied.

* Je dient ervaring te hebben met upscaling en downscaling van chemische productieprocessen en tevens aanpalende (analytische) vakgebieden.

* Je bent stressbestendig en flexibel ingesteld en functioneert zowel zelfstandig als in teamverband goed.

Voor meer informatie kun je contact opnemen met Ivo Eggen op ivo.eggen@merck.com of 0412 - 66 3220.

Job
: Lab Technician

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Lab-Technician-Chemistry-GTO-API-Job-NB/1895223/189522318952232012-06-15Merck/MSDLab Technicianfull-timeUSDstarting0BSOss, NB, NL
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position (Senior Business Analyst) will report to the Discovery & Preclinical Sciences (DPS-IT) Client Services Director aligned to the Boston Site.

The incumbent will be responsible for providing account management and client engagement capabilities, focused on the In Vitro Pharmacology, In Vivo Pharmacology, and Franchise Biology teams in Boston. The responsibilities include strategy alignment and portfolio governance, accountability for outcomes of program execution, as well as facilitating business continuity activities in partnership with DPS-IT Laboratory Operations and Automations

The incumbent will need to effectively partner across Merck Research Informational Technology subdivisions including Informatics IT, Project and Pipeline Management, and Business Planning and Operations. Establishment of strong partnerships, aligned and consistent communication and program alignment will be crucial for delivering business critical technologies and realization of business value.

Primary Activities:

Identify business demand and critical objectives to develop technology roadmaps, strategic plans, and portfolio management. Includes participating and leading business and IT process improvements leveraging Six Sigma.

Development of Business Proposals including key performance indicators, identification of business value and return on investments. Activity includes developing processes and system tools to automate the tracking and reporting of metrics for performance improvements.

Ensure effective and timely collaboration and communications with key partners across the business and Information Technology areas.

In collaboration with the Program Management Office, accountable for establishing plans, schedules, resource demands, and ensuring adherence for business adoption, project scope, resourcing and funding.

Ensure activities, projects and services are in alignment with corporate policies and departmental procedures including Merck's Software Development Lifecycle.

Engage partners across MRL IT and Global Services to ensure effective design, planning and delivery.

Actively participate in DPS and MRL activities to improve departmental processes and delivery, including "Innovation projects".

Qualifications

Education:

* A bachelor's degree in computer science or life sciences discipline is required. An advanced degree would enhance the candidate's qualifications, but is not required.

Required:

* Minimum of (10) years of demonstrated experience working in or supporting Pharmaceutical Research & Development. Focus in Biology is preferred.
* Minimum of (3-5) years experience operating in a supervisory or leadership role.
* Demonstrated experience as a credible thought leader in the pharmaceutical industry with strong leadership and interpersonal skills.
* Demonstrated ability to analyze complex business processes, define opportunities and collaborate on delivering solutions.
* Exceptional strategic and tactical planning competencies.
* Mastery of relationship management, partnering, and well-developed interpersonal skills; including engagement with senior and executive management.
* Ability to develop, articulate and build support for long-term visions and supporting technology road-maps.
* Exceptional management skills to enable effective collaboration in a matrixed organization.
* Ability to effectively delivery solutions and value in cross-functional teams.
* Ability to develop and maintain expertise in business functions, processes, requirements and partner on development of technology solutions.
* Ability to quickly adapt to changing technologies and business environments.
* Influencing skills with the ability to educate, inform, and influence business partners on business value, expectations, solution enablement and emerging technologies.
* Strong presentation, verbal and written communication skills.
* Experience in delivering solutions in accordance to Software Development Lifecycle.

Preferred:

* Six Sigma Certification would enhance candidate's qualification, but is not required.
* Experience with Laboratory Information Management Systems and Electronic Notebooks

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BUS000502.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Business Analysis

Primary Location: US-MA-Boston
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Senior-Business-Analyst-Job-MA-02108/1889120/188912018891202012-06-15Merck/MSDBusiness Analysisfull-timeUSDstarting0BSBoston, MA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck's Clinical Pharmacology group seeks an individual to provide leadership and experience in translational medicine in Neuroscience, Cardiovascular Disease, or Infectious Diseases. Qualified individuals with a focus in other therapeutic areas of medicine should also apply.

Clinical Pharmacology moves therapeutic compounds swiftly from the preclinical arena into human studies. While driving pharmaceuticals toward human proof of concept, Clinical Pharmacology studies contribute key data that support safety, tolerability, efficacy, and the pharmacokinetic and pharmacodynamic profiles for each compound throughout its development. The ultimate goal of our work is to provide an early assessment of efficacy or safety, thus ensuring that we bring forward into late clinical development those new compounds that have the highest likelihood of becoming new and valuable medicines. For compounds reaching late clinical development, Clinical Pharmacology develops dosage recommendations in different populations or in conjunction with other medicines.

At Merck a team approach is used to drug development. This position will interact with experts in discovery sciences, preclinical safety, phamacokinetics and drug metabolism, medicinal chemistry, pharmaceutical sciences, late stage clinical development, product development, regulatory sciences and program management with the intent to coherently and efficiently develop new drugs. Clinical Pharmacology interacts with other experts in translational medicine including Modeling and Simulation, Experimental Medicine, Clinical Imaging and Merck's Clinical Development Laboratory, bringing cutting-edge science to program decisions.

Responsibilities include and are not limited to the following:

* Development and execution of the Clinical Pharmacology strategy for a given program from preclinical candidate approval through the worldwide marketing application.
* Key member of the early development team, providing a leadership role on the team with regard to design and execution of early clinical development strategy.
* Clinical Pharmacology activities for a given program.
* Authors initial program clinical plans, the early development plan, Clinical Pharmacology Phase I studies through Phase Ib.
* Timely and safe execution of CP program studies.
* Ensure appropriate technical transfer of experimental medicine qualified platforms.
* Interact closely with internal and external clinical study support staff and scientists (including discovery research, biostatistics, drug metabolism, regulatory affairs, and global clinical trials operations).
* Provide Clinical Pharmacology support for programs through the worldwide marketing application filing including supportive registration documents and presentations.
* Clear, timely communication and interpretation of Clinical Pharmacology results to Franchise, Function, and governance committees.

Qualifications

Education Required:

* M.D. or M.D./Ph.D.

Skills or Experience Required:

* Demonstrated record of scientific scholarship and achievement.
* Proven track record in clinical medicine and background in biomedical research is essential.
* Strong interpersonal skills, as well as the ability to function in a team environment are essential.
* Excellent written and verbal communication skills.

Skills or Experience Preferred:

* Prior specific experience in clinical research and prior publication is desirable but not necessary.
* Board Certification or Eligibility

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CLI002638.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Clinical Research (M.D.)

Primary Location: US-MA-Boston
Other Locations: US-NJ-Kenilworth, US-PA-Upper Gwynedd, US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Associate-DirectorDirector-Clinical-Research-Job-MA-02108/1740533/174053317405332012-06-15Merck/MSDClinical Research (M.D.)full-timeUSDstarting0BSBoston, MA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Chemistry Modeling and Informatics group of the Global Structural Chemistry Department within Merck Research Laboratories is seeking PhD interns for their summer internship program. The intern will be embedded in the Modeling and Informatics group and will conduct research on a project relevant to drug discovery. The intern will also attend the group meetings to gain a wider perspective of the role of computational chemistry within the discovery process in the pharmaceutical industry.

A suitable candidate has a science background with an interest in computers and drug discovery. Not required but a plus would be experience in one or more areas of computational chemistry like molecular dynamics, ligand based and/or structure based drug design methods like molecular docking, quantitative structure activity relationships, chemoinformatics, or quantum mechanical calculations. We are seeking candidates with strong academic performance, communication skills, teamwork, and the ability to work in a multi-functional environment.

This internship is offered at our research facilities in Rahway, NJ, Kenilworth, NJ, West Point, PA, or Boston, MA. It is a paid 9-11 week internship targeted to start in June 2012. A weekly stipend will be provided. Housing and transportation to and from work are available for those interns meeting the housing distance guideline.

**Please note when applying for this position, the candidate MUST upload a cover letter or a personal statement letter and a copy of your unofficial transcript along with your resume.

Qualifications

Required:

* Currently pursuing a Ph.D degree in Computational Chemistry or related field.
* Science background with an interest in computers and drug discovery
* Must be available for full-time employment for 9 - 11 weeks during the months of June - August 2012.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #CHE003378.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-MA-Boston
Other Locations: US-NJ-Kenilworth, US-PA-West Point, US-NJ-Rahway

Job Type
: Intern
Employee Status: Regular

Travel
: No
Number of Openings: 1

Relocation Provided
: Domestic (within country)]]>http://jobs.merck.com/job/Boston-Modeling-&-Informatics-Drug-Discovery-Summer-Intern-2012-PhD-Job-MA-02108/1729503/172950317295032012-06-15Merck/MSDInternfull-timeUSDstarting0BSBoston, MA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


With appropriate direction and in compliance with departmental Standard Operating Procedures (SOPs), MRL study requirements, and all applicable local, state and federal regulations and guidelines, performs animal care functions and technical services for the various animal species. Provides input to supervisory staff on best practices, including writing and revising SOPs. Under direction of the research veterinarian, performs technical services including rodent surgery, animal restraint, dosing, and sample collection.

* Provides animal care as directed and in accordance with existing SOPs.
* Performs tasks associated with research project support including surgical procedures, drug dosing, sample collection, restraint, and other experimental procedures. Contributes to comples research projects by carrying out assigned work which includes recording of experimental data for inclusion in project reports.
* Assembles, sets up, and operates any necessary experimental equipment or apparatus, including automated blood sampling devices.
* Participates in recommended educational and training opportunities to further develop technical competence in his/her area of assigned responsibility.
* Receives, counts, handles properly, distributes and signs for shipments of animals or supplies. May perform inspections of animals, separating sexes, health monitoring, etc. Informs supervisor and/or veterinary staff of results.
* Maintains vivarium support areas, biological monitoring and the sentinel program.
* Documents the feeding, watering, environmental enrichment, and exercise of animals.
* Participates in educational opportunities to improve technical skills and knowledge of laboratory animal science.
* Is included in rotational weekend and holiday duty, including surgical animal care and treatments.
* Performs other animal care-related department duties, as appropriate.

Qualifications

Education Minimum Requirement:

* Bachelor's degree

Required Experience and Skills:

* At least 2 years experience dosing rodents (oral, IV, IP) in a research setting.
* Performs with minimal direct supervision.

Desired Experience and Skills:

* AALAS Laboratory Animal Technologist certification.
* Appropriate advanced education may be considered in lieu of AALAS LATg certification
* Experience with rodents and laboratory canines in a pharmaceutical research setting.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # LAB000199.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Laboratory Animal Services

Primary Location: US-MA-Boston
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Research-Animal-Specialist-II-Job-MA-02108/1812614/181261418126142012-06-15Merck/MSDLaboratory Animal Servicesfull-timeUSDstarting0BSBoston, MA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


As a member of the Oncology project teams, the individual will conduct in vitro experiments using a variety of tools to assess novel targets and/or novel pharmacological agents. The researcher will develop and utilize cell-based assays to define mechanism of action and target engagement for different targets and pharmacological agents.

The primary responsibilities of the Oncology Team Member include

* Conducts in vitro cellular assays to support validation of novel targets.
* Conducts in vitro cellular assays to characterize the mechanism of action of novel pharmacological agents.
* Designs research protocols and conducts experiments using standard and innovative scientific approaches.
* Executes the assigned research projects with some scientific direction.
* Collaborates with team members and other discovery groups within the organization.
* Analyzes data, troubleshoots problem, and interpret experimental results.
* Presents findings and conclusions.

Qualifications

Minimum Education Requirement:

* B.Sc. degree in biological sciences with minimum 2 years industry or equivalent academic laboratory experience.

Preferred Education Requirement:

* M.Sc. degree in biological sciences with 0-2 years industry or equivalent academic laboratory experience

Preferred Skills and Experience:

* Demonstrated skills and track record of conducting research in vitro, including cell culture
* Skilled in studying the function of target genes in a cellular environment using a variety of analytical approaches (biochemistry, molecular and cellular biology)
* Skilled in developing cell-based assays
* Demonstrated relevant subject matter expertise in the area of Oncology and cell signaling
* Demonstrated ability to accurately record data/experiments and to communicate in written and oral forms
* Demonstrated ability to thrive in a team environment
* Flexibility in changing project needs which are driven by results
* Demonstrated ability to communicate clearly and candidly

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MOL000281.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Molecular Discovery

Primary Location: US-MA-Boston
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Biology-Program-Team-Member-Oncology-Job-MA-02108/1868784/186878418687842012-06-15Merck/MSDMolecular Discoveryfull-timeUSDstarting0BSBoston, MA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Reporting directly to the Biologics CMC Site Head, the Senior Regulatory Scientist is responsible for providing CMC regulatory strategy and developing regulatory documentation to

support worldwide registration of new molecular biologic entities, line extensions of approved products, as well as maintenance/regulatory compliance of approved products.

As the CMC representative on multiple teams within Merck Manufacturing Division (MMD) and Merck Research Laboratories (MRL), the senior manager is expected to

manage products during the entire product lifecycle for dossiers in the US, EU, and rest of world (RoW). Prior CMC regulatory experience in biologics is essential for this

position, and knowledge of biosimilar regulatory environment is highly desirable.

Major Responsibilities and Activities

* In consultation with the CMC Site Head, supports project teams by providing strategic input into product development, supply plans and agency meetings.
* Serves as the regulatory CMC member of Integrated Development and Supply Teams and Global Regulatory Teams.

* Serves as CMC regulatory lead at all health authority meetings, and is responsible for driving timely completion of high-quality responses to health authority inquiries

* Works independently to compile data in support of new and in-line biotechnology product licenses/registrations worldwide. Responsibilities include authoring of
* CMC documentation to be included in regulatory submissions.

* Reviews proposed changes in the manufacturing, testing or packaging of a biologic substance/product and provides recommendations regarding the potential regulatory impact on product registration.

* Manages product lifecycle by preparing documentation to assure compliance with existing registrations.

Other activities may include:

* Develops familiarity with regulations and regulatory guidelines and strategy.

* Identifies pertinent regulatory requirements addressed in CMC documents

* Gains general understanding of technical, clinical and commercial manufacturing developments that may impact regulatory submissions and approvals

* Develops working knowledge of regulatory standards, practices, corporate policies, practices and departmental SOPs/work practices.

* Assists with the review of critical documents and compliance-related documents in accordance with department processes.

* Where appropriate and with prior direction and guidance, may represent CMCBiologics at project and professional meetings.

Please note this position is in Kenilworth, NJ.

Qualifications

Required Education:

* Minimum BS in biological science or related engineering field (e.g. molecular biology, biochemistry, biochemical engineering, chemical engineering, mechanical engineering, microbiology) is required. Other fields of degrees may be considered.

Experience or skills Required:

* Minimum 4 years of experience in CMC regulatory affairs composing regulatorystrategies and submissions that address phase-specific biological research and manufacturing requirements for the licensure of biological products is required for this position.

* CMC regulatory experience with biotechnology products is required

* Demonstrated sound understanding of related fields (e.g., manufacturing, analytical, quality assurance) and the ability to be creative and imaginative in the approach to new and diverse problem solving. Demonstrated ability to generate innovative solutions to complex regulatory problems and effectively work with and communicate to key stakeholders.

* Working understanding of the domestic and international regulations that govern the licensure of biotechnology products.

* Meticulous attention to detail.

* Strong oral communication and technical writing skills.

* Demonstrated superior communication skills in multicultural settings and ability to communicate complex issues in a succinct and logical manner. Strong listening skills.

* Proven experience in critically reviewing detailed scientific information and assessing whether technical arguments are presented clearly and conclusions are adequately supported by data.

* Proven experience in directing multiple, simultaneous projects and managing projects to aggressive timelines.

* Proven experience in assessing project risks and, where appropriate, recommending contingency plans and strategies to mitigate risk.

* Sets clear priorities in support of departmental objectives. Demonstrates flexibility in responding to changing priorities or dealing with unexpected events.

* Strong working knowledge of business systems and compliance requirements related to the manufacture of biologics.

Preferred Experience:

* MS or PhD preferred
* Regulatory CMC experience with monoclonal antibodies, biosimilars, or therapeutic proteins is highly preferred.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #REG000894.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Regulatory Affairs Liaison

Primary Location: US-NJ-Kenilworth
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Kenilworth-Regulatory-CMC-Senior-Manager-Job-NJ-07033/1708742/170874217087422012-06-15Merck/MSDRegulatory Affairs Liaisonfull-timeUSDstarting0BSKenilworth, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The successful candidate will be responsible for coordinating in silico ADME efforts at their site and for collaborating with modelers and DMPK scientists globally to drive strategy in predictive ADME.

They will provide a strategic and tactical view within and between the groups responsible for ADME data generation and interpretation (Pharmacokinetics, Pharmacodynamics and Drug Metabolism, PPDM) and computational methods development and project support (Chemistry Modeling and Informatics, CM&I) focusing on the interplay between modeling ideas/needs and requirements for experimental data generation.

They will take a lead in educating PPDM in the use of in silico tools and to promote their uptake and increased use within PPDM, and similarly educate within CM&I on the experimental methods and their utility. Raising awareness within other disciplines will be another important responsibility of this in silico ADME scientist.

In doing this work they will collaborate closely with CM&I and PPDM staff to drive education and uptake of model usage within PPDM. Specifically this is aimed at increasing the use of calculated and measured physicochemical properties to understand DMPK data and to ensure state-of-the-art modelling techniques are applied to DMPK datasets.

They will work with the project assigned PPDM and CM&I staff to provide consultancy and direction in the use of data and techniques.

At a tactical level, they will work with PPDM and CM&I staff to define in silico model requirements and contribute to their establishment. Additionally assessing and refining in-house capabilities for across the R&D process.

It is expected that the candidate would maintain a portfolio of basic research into modeling techniques that could be applicable to DMPK and/or assay formats to generate the appropriate data.

Qualifications

Education Minimum Requirement:

* PhD or equivalent in chemistry, DMPK or computational sciences

Required Experience and Skills:

* Experienced DMPK scientist or computational/medicinal chemist with at least 7 years of experience working in a multidisciplinary environment, who has developed and formally pursued an interest in DMPK modeling
* Expertise in dealing with experimental DMPK and data generation appropriate for in silico ADME model building
* Knowledge of current state-of-the art in terms of modeling techniques and approaches
* Ability to communicate results and influence project leaders and senior scientists from other disciplines

Desired Experience and Skills:

* Track record of presentation/publication in the field of in silico ADME
* Ability to build and refine modern computational models

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CHE003450.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Chemistry

Primary Location: US-NJ-Kenilworth
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Kenilworth-In-Silico-ADME-Scientist-%28Kenilworth%2C-NJ%29-Job-NJ-07033/1809489/180948918094892012-06-15Merck/MSDChemistryfull-timeUSDstarting0BSKenilworth, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Category and Shopper Insights Manager leads an innovative, insights-driven, customer-facing team to influence and impact decision-making, resource allocation, and plans of action resulting in increased sales growth and volume. The CSIM is a source of expertise regarding actionable category and shopper insights based on marketplace knowledge and data-driven research. The incumbent builds strong customer relationships and influences sales teams through relevant category data and shopper insights knowledge with an innovative approach. The CSIM recruits, develops, and coaches team members to maximize the impact of data analysis and insights while fostering team collaboration and sharing of best practices.

Key responsibilities may include, and are not limited to the following:

* Partners with account teams to identify, develop and influence short/long term category strategies
* Translates category and shopper insights into strategic customer-centric solutions for retain partners
* Leads, motivates, trains and develops Customer Category team members
* Coaches team members on utilization of data analysis and related tools and resources to maximize impact for sales growth
* Coaches team members to increase understanding and application of category and shopper insights which result in actionable solutions
* Recruits and on-boards for vacant roles to ensure development of departmental talent
* Partners with customer to cultivate rapport and ensures two-way communication, data sharing, alignment, and customer understanding of MCC brands
* Leverages marketplace knowledge, trends, and customer needs to provide guidance to direct reports resulting in insights-driven solutions for account teams
* Partners with account teams to apply qualitative and quantitative shopper insights during the development of marketing programs
* Reviews syndicated research to synthesize customized and actionable recommendations, such as category merchandising based on shopper behavior and trends
* Develops and delivers insights-driven presentations to internal and external retail partners to articulate strategies and action plans
* Creates and presents insights-based merchandising recommendations that drive both category growth and MCC sales growth
* Negotiates foe and allocates optimal data spend across teams
* Communicates with customer and account teams in order to identify issues and research needs
* Maximizes use of resources to derive shopper insights that lead to the development of related action plans
* Fosters collaborative teamwork with, and presents insights-driven solutions to internal-cross-functional teams in order to determine best practices, research, and strategies
* Travel of 25% - 30% is required for this position

Qualifications

Education:

* Required: Bachelor's degree
* Preferred: Master's degree (MBA)

Required:

* Minimum 7 years of work experience
* Experience with CPG industry or analytical experience
* Expertise with analytical tools and resources
* Category management knowledge and expertise
* Strong data analysis and interpretation skills
* Strong interpersonal skills
* Understand and leverage category and shopper insights internally and externally
* Plan strategically toward goal achievement
* Lead and develop a team
* Strong written and verbal communication skills
* Strong computer proficiency with Microsoft Office and database information sources
* Travel of 25% - 30% is required for this position

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # DIR004116.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-JN1

Job
: Direct Sales - Nondurable Goods

Primary Location: US-OH-Cincinnati
Other Locations: United States
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Cincinnati-Category-and-Shopper-Insights-Manager-Job-OH-45201/1764630/176463017646302012-06-15Merck/MSDDirect Sales - Nondurable Goodsfull-timeUSDstarting0BSCincinnati, OH, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The internship will be within the Pathology Department at the Palo Alto site of Merck Research Laboratories (MRL). The central mission of the Palo Alto site of MRL is Biologics Discovery. The site has extensive and long-standing expertise in development of monoclonal antibodies and other engineered proteins for therapeutic purposes. Work conducted at the Palo Alto site is currently focused on addressing unmet medical needs in oncology, respiratory disease, immune-mediated disease, and diabetes.

The intern project will involve work with the Duolink Proximity Ligation Assay (PLA). PLA is a technique by which protein-protein interactions in cells and tissues can be identified and quantitated. In this technique, antibodies against two proteins of interest are applied to a sample, as in standard immunhistochemistry. The primary antibodies are then detected by a pair of secondary antibodies each of which has an oligomer tag. If the antibodies are within sufficiently close proximity, the oligomers bound to the secondary antibodies will hybridize and can be amplified in a rolling circle amplification process in which the amplification products are fluorescently labeled. In this method, each detected interaction yields a discrete fluorescent spot, allowing quantitation of the interactions across samples. Our lab is in the process of optimizing this method on formalin-fixed paraffin-embedded tissues, and is looking to a) improve our ability to quantitate protein-protein interactions with this technique by enhancing signal brightness to allow full-slide scanning across a large dynamic range of signal for subsequent digital image analysis, and to b) enhance the technique's flexibility by developing techniques for multiplexing it with other labeling methodologies, including variations on standard immunohistochemistry/immunofluorescence and in situ hybridization. In addition to methods development work with this assay, several applications of the technique to evaluate protein-protein interactions between antigen pairs involved in recognition of particular proteins involved in the immune response in inflammatory disease and cancer are pending and could form part of the intern project.

The Palo Alto site of MRL provides a vibrant and exciting research environment where the selected intern will get the opportunity to learn cutting-edge techniques with broad application while experiencing from the inside what it is like to work in pharmaceutical discovery.

Qualifications

Required:
* Experience working in a laboratory environment and a high level of comfort with basic laboratory techniques and procedures

* Bachelor level or Master level candidate with at least 1 year remaining before graduation at time of internship

* Degree field must be in Biological Sciences or a major that falls under that category

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #PAT000106.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-CA-Palo Alto

Job Type
: Intern
Employee Status: Regular

Travel
: No
Number of Openings: 1

Relocation Provided
: Domestic (within country)]]>http://jobs.merck.com/job/Palo-Alto-Biologics-Discovery-Pathology-Summer-Intern-2012-BS-or-MS-Job-CA-94301/1729543/172954317295432012-06-15Merck/MSDInternfull-timeUSDstarting0BSPalo Alto, CA, US
Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Process Specialist position will be created based in SBS commitment to maintain the accuracy and top quality of the services delivered to our clients.
This position will be mainly responsible to review and maintain the proper documentation and compliance for End to End processes and procedures within the RtR area. Also, the incumbent will be the liaison between clients (markets), Accountants and contractors to ensure our SLA indicators are met and that our processes are procedures are properly followed.
Based on the feedback received from Clients, peers, managers and Metric analysis, this position should analyze processes in order to develop, coordinate and implement process improvements.
Also, should be an operative and permanent support for the daily operation and monthly / annual closes. This assignment includes the processes and P&P training to the new hires in the area.
Finally, This position should coordinate with the SBS internal control area the implementation of the self assessment plan and develop the mitigation plans for any opportunity identified.

MAIN DUTIES/RESPONSIBILITES/ACTIVITIES:

* Support the daily operation and perform non routine activities, including Legal Entity Integration and Interim Solution projects
* Develop and implement process improvements.
* Coordinate the self assessment implementation and mitigation plan.
* Stay abreast, communicate and ensure for any Corporate policies and procedure changes in order to give the correspond training and to the RtR and markets.
* Maintain the policies and procedures updated.
* Organize training and induction to the area.
* Establish a fluid communication with the Manager, Accountants and the Customer Service Specialist in order to identify improvements areas.
* Analyze the monthly metric and develop new ones as needed.

Qualifications

Bachelor Degree (Accounting, Taxes, Audit, Finance or any other Finance related degrees)

Master Degree degree will be a plus: (Process and Methods)

8-12 years experience working in Finance and accounting areas. In addition, strong leadership, delivery of results to middle and upper management.

Language Skills: Fluent in Spanish and Intermediate to advanced in English. (Portuguese will be a plus).

Technical Skills:
Advanced knowledge in EXCEL (Macros, Pivot Tables), Power Point (presentations) and JDEdwards are required. Visual Basic, MS Project, MS Visio, Cognos, ClickView, or SAP Experience are desired.

Soft skills:
Lead by influence
Customer focus mentality. Strong communication and collaboration skills are required to work with the Multicultural team.
Self Motivated, Proactive, Open Minded and able to manage pressure.
Multi tasking profile, teamwork oriented. Eager to learn and share knowledge with team.
Special attention to details.
High Analytical and problem solving Skills are required.
Sigma experience is required and Green/black Belt Sigma is highly desirable.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. MSD's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

Job
: Project Management Generic

Primary Location: CL-Santiago Metropolitan Region-Santiago
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Santiago-Process-Specialist-SBS-Job/1840118/184011818401182012-06-15Merck/MSDProject Management Genericfull-timeUSDstarting0BSSantiago, CL
Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


:

* Manage site pre-selection and validation process. Support local investigator meetings, ensure contracts and applicable regulatory documentation is obtained prior to study start. Facilitation of all aspects of IRB/ERC and Regulatory Agency submissions (including local IC). PPOC for all logistical and operational issues and facilitate general communication.
* Ensure clinical trials are effectively executed and completed within budget, timelines and meeting enrollment commitments as well as routine updating of CTMS and other clinical systems. Pro-active trial management to identify challenges, develop effective mitigation plans and to appropriately escalate and inform all relevant parties.
* Ensure management of clinical trials are done in compliance with ICH-GCP, Merck global standards, local laws and regulations. To maintain quality standards, the CPM is involved in additional protocol specific training and might be supporting co-monitoring with a CRA. Providing country specific guidance and oversight to CRO's where needed.
* Oversee drug and clinical supplies management to ensure sites have timely availability of required materials to avoid disruption of protocol deliverables and to oversee appropriate final disposition of IMP.

Qualifications

* Education: Bachelor's Degree or equivalent in relevant Life Science or Health Care area.
* Language: Fluent English skills
* A minimum of 6 years of relevant experience in clinical research

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. MSD's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

Job
: Clinical Research

Primary Location: GT-Guatemala-Guatemala
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Guatemala-Clinical-Project-Manager-Job/1694175/169417516941752012-06-15Merck/MSDClinical Researchfull-timeUSDstarting0BSGuatemala, Guatemala, GT
Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Responsible Pharmacist will be responsible for managing quality and compliance activities at the VENCO OFC in agreement with MSD Farmaceutica C.A quality policies and local regulatory requirements. Performs release to local market after country-specific requirements are met.

PRIMARY ACTIVITIES: Include but is not limited to other duties assigned.

* Be in compliance with local Ministry of Health requirements for OFC and all specifics operation for VENCO.
* Manage regulatory agencies inspections and corporate audits. Serves as the main escort in these inspections. In coordination with MMD Quality Venezuela´s Lead, assures a comprehensive response is assembled for any observation obtained, and that these are thoroughly closed by Site personnel on agreed due date.
* Conduct local release of product, as defined by local regulatory agencies, following satisfactory completion of all required activities.
* Administrate local SOP system in compliance to Merck standards
* Actively coordinate with central MMD Quality (QO, QA, and Complaint unit), Regulatory Affairs, Central Safety and other groups as needed to perform job duties.
* Coordinate / investigate atypicals deviations detected during the receiving of the product and prior to distribution, in conjunction with the OFC Quality Operation Manager of CDG as well as, deviations detected after the product was distributed. Report these events to local Management for appropriate closure.

* Coordinate the investigation of complaints (internal & external) with product source of supply. Review completed investigation and prepare response letter to customer, as applicable. In conjunction with the OFC Quality Operation Manager of CDG.

* Assure final disposition decision is made at appropriate Quality level for returned goods.

* Participate / manage fact finding activities, as required. Coordinate local recall activities, as required.

* Actively participate in the OFC local meetings and other site / regional / divisional initiatives, as required.

* Administers QMS for VENCO Site as needed.

Qualifications

* Knowledge of GMP regulations and expectations, Safety requirements.
* Excellent managerial and problem solving skills.
* Strong leadership and interpersonal skills.
* Self-starter and able to handle multiple priorities.
* Able to work under pressure.
* Ability to provide direction and control in Quality topics

EDUCATION AND/OR Experience:

- Bachelor Degree in Pharmacy.

- At least Five (5) years of experience in quality control and / or production in the pharmaceutical industry.

COMMUNICATION SKILLS: Includes basic/minimum requirements needed.

- Good oral and written communication skills, both in English and Spanish.

- Ability to read and interpret technical documents, such as agency regulations, corporate / divisional guidelines.

SPECIFIC SKILLS

- Problems solving abilities.

- Knowledge of computer software: Excel, Word, PowerPoint

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. MSD's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

*LI-KT1

Job
: Qual Assurance & Ops Generic

Primary Location: VE-Caracas Capital District-Caracas
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Caracas-Responsible-Pharmacist-Job/1855921/185592118559212012-06-15Merck/MSDQual Assurance & Ops Genericfull-timeUSDstarting0BSCaracas, Caracas Capital District, VE
Description

Afdeling

Facilities Management (FM) levert en draagt zorg voor een uitgebreid pakket van huisvesting en lokatiediensten, zodat onze klanten zich kunnen concentreren op hun kerntaken. Wij doen dit effectief en efficiënt, op een veilige manier en conform wet- en regelgeving.

De Functie

Hoofdtaken van de Manager Reliability Engineering zijn:

* Leiding geven aan het verbeteren van de prestatie van de
* productiemiddelen van de productie-sites en Facilities Management conform de Merck-standaarden.Verantwoordelijk voor het handboek Reliablity Engineering.
* Leiding geven cq deelnemen aan verbeterprojecten op gebied van reliability engineering en gerelateerde IT-ondersteuning.
* Sturing geven aan het toepassen van methodologieën op gebied van reliability engineering en zonodig hierbij faciliteren.

Je bent verantwoordelijk voor:

* Is als proceseigenaar verantwoordelijk voor het functioneel- en uniform gebruik van het Computerized maintenance management system (CMMS) en de optimalisatie-activiteiten.
* Is als proces eigenaar verantwoordelijk voor het tactisch beheer van de Miantenance Repair Operations (MRO) voorraden, het anayliseren op functionaliteit en het optimaliseren van de voorraden.
* Is als Installatieverantwoordelijke van FM eindverandwoordelijk voor een veilige bedrijfsvoeringvan elektrische installaties van FM. De operationele uitvoering is gedelegeerd aan derden.

Qualifications

Wij vragen

* Technisch geschoold op academisch niveau
* Master Maintenance & Asset Management is een pré.
* Six Sigma green belt, black belt is een pré
* Technische kennis op alle vakgebieden
* Min. 5 jaar ervaring in de techniek
* Min. 5 jaar ervaring met reliability engineering en een CMMS
* Min. 5 jaar ervaring met reliability analysis tools
* Beheersen van Nederlands en Engels in woord en geschrift
* Beheersen van groepsgericht leiderschap en adviesvaardigheid

We bieden

Houd je ervan te worden uitgedaagd, steeds weer, dan is MSD een goede keuze als werkgever. We hebben uitstekende arbeidsvoorwaarden en je krijgt er alle mogelijkheden om je verder te ontwikkelen en door te groeien. MSD geeft je veel ruimte voor eigen initiatief en je krijgt veel verantwoordelijkheid.

Contact

Voor meer informatie over de functie kun je contact opnemen met Willy Gommers, Lead Contract Management FM; 0412 662172

Job
: Facilities Management

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Manager-Reliability-Engineering-Job-NB/1862514/186251418625142012-06-15Merck/MSDFacilities Managementfull-timeUSDstarting0BSOss, NB, NL
Description

MSD in Lucerne/Switzerland is a Swiss subsidiary of the successful global pharma-ceutical company Merck & Co. Inc. with its headquarters in USA. Approx. 100'000 employees are currently working for us globally and we are showing strong growth.

Our Swiss operations include MSD International GmbH, Merck Sharp & Dohme-Chibret AG, Essex Chemie AG, Schering Plough Central East AG and Werthenstein BioPharma GmbH with currently 700 employees.

We are currently offering a

2 year GRADUATE PROGRAM within our Information Technology Services Group

The Global Human Health IT Europe/Canada intern will work under supervision of Regional Commercial Operations Lead and will support in:

* Gather requirements using interviews, document analysis, requirements workshops, surveys, site visits, business process descriptions, scenarios, business analysis and task & workflow analysis

* Evaluate information gathered from multiple sources, reconcile conflicts, decompose high-level information into details, abstract up from low-level information to a general understanding and distinguish user requests from the underlying true needs.

* Quickly understands the business issues and data challenges

* Communicates and applies process standards

* Communicates effectively with clients to identify needs and evaluate alternative business solutions

* Identifies client processes strengths and weaknesses and suggests areas of improvement

* Liaison between the business partners and the technology teams. Serves as the link between the customer community and the software development team through which requirements flow.

* Assists in the testing effort and preparations; design and execute the core test scenarios and test scripts

Qualifications

* Recent graduate (not before 2011)- University degree ( Computer Sciences, Computer Engineering, Information Management, Mathematics, Telecommunications, Business Administration with emphasis Information Technology ) from accredited university
* Able to communicate clearly and fluently in English. Both written and verbal communication at all levels of the organization is required. Other languages are considered an advantage but are not required.
* Excellent verbal and written communication skills and the ability to interact professionally with a diverse group, peers, managers and subject matter experts.
* Pharmaceutical industry knowledge is a plus
* Must be able to perform impact analysis scenarios, fit/gap analysis activities and testing.
* Strong analytical skills required, including a thorough understanding of how to interpret customer business needs and translate them into operational requirements.
* You are a good relationship builder, able to manage client expectations, capable in conflict resolution and problem solving
* Having a strong technical background is an absolute plus.
* Willing to travel

Primary Location: CH-LU-Luzern

Job Type
: Full Time
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1

Relocation Provided
: None]]>http://jobs.merck.com/job/Luzern-Business-Analyst-for-Commercial-Operations-Job-LU/1799259/179925917992592012-06-15Merck/MSDFull Timefull-timeUSDstarting0BSLuzern, LU, CH
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

El Representante de Ventas es responsable de promover y vender los distintos productos asignados, a través de visitas y contactos directos con Médicos, Profesionales de Salud, Especialistas, Farmacias, Hospitales, Instituciones, y / o cualquier otro medio reconocido y recomendado por la empresa, con el objetivo de sobrepasar las expectativas de los clientes y alcanzar las metas trazadas por la División.

PRINCIPALES RESPONSABILIDADES/FUNCIONES:

- Incrementar el Market Share de los productos en promoción de su línea
- Alcanzar el presupuesto anual de ventas para su línea.
- Desarrollar el plan de negocios de su territorio para maximizar el número de visitas de su target médico.
- Asegurar una óptima calidad del panel médico a su cargo (Potencial según los parámetros definidos), mediante la revisión sistemática del mismo y actualización oportuna.
- Alcanzar su target de visita (frecuencia & promedio) de acuerdo a los objetivos establecidos.
- Chequear la segmentación médica, manteniendo y actualizando información de los clientes y completando los reportes de visitas.
- Proponer acciones de promoción para incrementar la participación en el mercado y el servicio al cliente.
- Proveer información clave y detallada a su target médico que asegure un incremento en la prescripción de los productos a su cargo.
- Proveer y mantener actualizada la información de la competencia (Ej. Tácticas y y actividades de marketing)
- Coordinar ciclos de visita con colegas del distrito para maximizar la cobertura y el impacto médico.
- Visita a farmacias para saber la rotación y situación del mercado.
- Mantener y guardar una confidencialidad todo lo relacionado a productos, costos, precios, cuotas de ventas y cualquier otra información asignada, de acuerdo a las normas de compliance.
- Llevar un control estricto de los gastos de viaje, promoción, o especiales, y presentar a la Gerencia de Distrito para su aprobación en el tiempo requerido y acordado.
- Mantener un desarrollo continuo y auto conocimiento de los productos de la empresa y técnicas de promoción, y asegurar un nivel alto de maestría de los mismos.
- Participar activamente en los lanzamientos, promociones o juntas de ventas organizadas en el ámbito local o regional.

Cualificaciones
- Escolaridad: Licenciatura en Farmacología o carrera relacionada.
- Competencias técnicas: Alto conocimiento del cargo, manejo del territorio, proceso de ventas técnicas, manejo de gente.
- Idiomas: Nivel intermedio de inglés (escrito, hablado)
- Experiencia: Mínimo 2 a 4 años de experiencia como Visitador Médico o vendedor de productos éticos de empresas multinacionales.
- Habilidades o Conocimientos adicionales: Atención a clientes, comunicación efectiva, pro-activo, sentido de urgencia, trabajo en equipo y bajo presión. Se requiere conocimiento de MS Office (Word, Excel y Power Point)

Nuestros empleados son la clave del éxito de nuestra empresa. Demostramos nuestro compromiso con nuestros empleados ofreciéndoles un programa de recompensas competitivo y valioso. Los beneficios en MSD están diseñados para apoyar la amplia gama de objetivos, necesidades y estilos de vida de nuestros empleados y de muchas de las personas que constituyen lo más importante en sus vidas.

*LI-KT1

Puesto
: Ventas general

Ubicación principal: NI-Managua-Managua
Tipo de acuerdo laboral: Fijo(a)
Viajes: No
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Managua-Representante-de-Ventas-Job/1824609/182460918246092012-06-15Merck/MSDVentas generalfull-timeUSDstarting0BSManagua, Managua, NI
Description

Biostatistics and Research Decision Sciences (BARDS) biedt wereldwijd ondersteuning aan alle divisies van Merck. De BARDS afdeling omvat diverse functies zoals statistiek, statistisch programmeren, epidemiologie en health economics. BARDS-Oss maakt deel uit van de Europese zone binnen het wereldwijde BARDS netwerk. Je gaat werken met state of the art technologieën, houdt je bezig met nieuwe medicijnontwikkeling binnen een wereldwijde multidisciplinaire setting. Dit biedt uitgelezen kansen voor starters die kwantitatieve kennis willen opbouwen als Junior Statisch Ontwikkelaar/Programmeur binnen het multidisciplinaire team in Oss.

De vacature

* Bijdragen aan high-quality statistische programma's voor de ondersteuning bij klinische onderzoeken, indieningprogramma's en ad hoc vragen. Je gebruikt hierbij voornamelijk SAS als programmeertaal.
* Ontwikkelen en valideren van SAS programma's, datasets analyseren en output rapporteren (tabellen, lijsten en statistische analyses).
* Het uitvoeren van import en export routines voor interne en externe data.

Qualifications

* Afgeronde academische opleiding met een significante statistisch/kwantitatieve component (bijvoorbeeld chemie, wiskunde/statistiek of fysica).
* Enige ervaring met programmeren (bij voorkeur in SAS of SPSS).
* Interesse in data analyse en statistische dataverwerking..
* Uitstekende communicatievaardigheden en zin om in een internationaal team met diverse nationaliteiten te werken.
* Drive for results gecombineerd met een hoog niveau van accuratesse.
* Goede Engelse communicatievaardigheden.

Job
: Statistical Programming

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Junior-Statistisch-OntwikkelaarProgrammeur-Job-NB/1895230/189523018952302012-06-15Merck/MSDStatistical Programmingfull-timeUSDstarting0BSOss, NB, NL
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Senior Software Engineer - Database Development is responsible for delivering software and process solutions in the translational biology and bioinformatics realms. We specifically work in emerging scientific areas that require exploration and innovation. The Senior Software Engineer provides technical and engineering leadership for one or more concurrent software development projects. This position is within the Informatics Research Tools and Scientific Computing team within Informatics IT.

The key activities for this position include:

* Work with program leads to define project requirements and manage project scope, roadmap, timeline and quality targets, from a database/backend perspective
* Perform and/or oversee all aspects of the project Software Development Lifecycle, including design, implementation, installation, acceptance, and transition to support and operations teams.
* Provide technical leadership and mentoring to project staff; solve key software development problems that arise during project execution
* Identify and manage the required human and financial project resources
* Coordinate with other internal organizations to plan, provision and configure project resources and infrastructure (hardware, software, licenses, support)
* Engage and manage external partners and vendors for the development and/or delivery of software products and services to meet project needs
* Establish SMART project objectives (specific, measurable, achievable, relevant and timely), and report periodically on project status to the Informatics IT leadership team
* Evaluate and select software solutions that support project needs, and are consistent with existing Merck standards
* Contribute to the Informatics IT department culture including communication of best practices and lessons learned.

Qualifications

Education:

* Bachelor's degree in appropriate technical, scientific, or engineering discipline.

Required:

* Minimum of 6 years of professional software engineering experience developing database centric applications using Microsoft SQL Server and/or Oracle technologies.
* Minimum of 3 years professional experience leading teams (>5 people) either as direct reports or via outsource arrangement.
* Demonstrated ability to organize and execute projects including defining and assigning tasks, budgeting and documentation; ability to prioritize, organize and multi-task in high-pressure situations.
* Demonstrated ability to clearly communicate technical and non-technical information verbally and in writing.
* Demonstrated ability to work with and manage a diverse group of professionals globally.
* Demonstrated ability to balance multiple competing constituencies and their needs.
* Demonstrated proficiency in the following programming languages: Transact SQL, PL/SQL, C#/.NET 4.0.
* Proficiency in SQL Server and Oracle environments: triggers, stored procedures, DDL, jobs, ETL, etc.
* Proficiency in LINUX, UNIX and Windows operating systems.
* Proficiency in Agile, phased delivery and evolutionary prototyping software development processes.

Preferred:

* Knowledge of the drug discovery process.
* Experience in developing scientific applications, specifically in bioinformatics or genomics.
* SQL Server related certifications.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ENG002363.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Engineering

Primary Location: US-MA-Boston
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Senior-Software-Engineer-Database-Development-Job-MA-02108/1871142/187114218711422012-06-15Merck/MSDEngineeringfull-timeUSDstarting0BSBoston, MA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Senior Software Engineer - Cloud Applications is responsible for delivering software and process solutions that take advantage of Cloud based architectures. The Senior Software Engineer provides technical and engineering leadership for one or more concurrent software development projects. This position is within the Informatics Research Tools and Scientific Computing team within Informatics IT.

The key activities for this position include:

* Work with program leads to define project requirements and manage project scope, roadmap, timeline and quality targets.
* Perform and/or oversee all aspects of the project Software Development Lifecycle, including design, implementation, installation, acceptance, and transition to support and operations teams.
* Provide technical leadership and mentoring to project staff; solve key software development problems that arise during project execution.
* Identify and manage the required human and financial project resources.
* Coordinate with other internal organizations to plan, provision and configure project resources and infrastructure (hardware, software, licenses, support).
* Engage and manage external partners and vendors for the development and/or delivery of software products and services to meet project needs, including Cloud based products or services.
* Etablish SMART project objectives (specific, measurable, achievable, relevant and timely), and report periodically on project status to the Informatics IT leadership team.
* Evaluate and select software solutions that support project needs, and are consistent with existing Merck standards.
* Contribute to the Informatics IT department culture including communication of best practices and lessons learned.

Qualifications

Education:

* Bachelor's degree in appropriate technical, scientific, or engineering discipline.

Required:

* Minimum of 6 years of professional software engineering experience developing enterprise grade applications.
* Minimum of 3 years of professional software engineering experience architecting and developing cloud based solutions.
* Minimum of 3 years professional experience leading teams (>5 people) either as direct reports or via outsource arrangement
* Demonstrated ability to organize and execute projects including defining and assigning tasks, budgeting and documentation; ability to prioritize, organize and multi-task in high-pressure situations
* Demonstrated ability to clearly communicate technical and non-technical information verbally and in writing
* Demonstrated ability to work with and manage a diverse group of professionals globally
* Demonstrated ability to balance multiple competing constituencies and their needs

Technical Skills:

* Demonstrated proficiency in implementing software solutions that leverage cloud services - like Amazon Web Services.
* Proficiency in modern technologies related to Big Data processing (Hadoop, HIVE, Cassandra, etc.).
* Proficiency in LINUX, UNIX and Windows operating systems.
* Proficiency in Agile, phased delivery and evolutionary prototyping software development processes.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ENG002357.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-PD1

Job
: Engineering

Primary Location: US-MA-Boston
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Senior-Software-Engineer-Cloud-Applications-Job-MA-02108/1868781/186878118687812012-06-15Merck/MSDEngineeringfull-timeUSDstarting0BSBoston, MA, US
Description

The Process Support Specialist will be responsible for generating and expediting review and approval process for Production Equipment Standard Operating Procedures and Standard Work Instructions.

The Process Support Specialist will support Production Start-up Activities through Documentation Generation, Equipment and Process Investigations following from qualification or Process Quality Issues, Job Safety Assessments and expediting our New Chemical Introduction process.

The successful candidate will achieve results through collaboration with other IPT members and members from other departments (Quality, Technical Operations, Environmental Health and Safety).

Key Responsabilities:

1. Writing Standard Operating Procedure's (SOP's) and Standard Work Instructions (SWI's) for Equipment and Process Systems.

2. Generating Material Specifications and expediting the approval process for non/in-direct materials.

3. Generating training documents.

4. Documentum System experts for documents review/approval and documentum system work flow expedition Participate in manufacturing, packaging and customer complaint investigations across all IPT's.

5. Formatting SOP's and assisting Technicians with movement of SOP's though Review/Approval process.

6. Expediting and assisting in completion of JSA's for SOP's/SWI's, Calibrations & PM's

7. Change Controls generation and close out.

8. Raising CAPA's and conducting investigations.

9. AIR expedition - invtestigations and action items closeout.

10. New Chemical Introduction - process completion and closure of action items.

Qualifications

· Science/Engineering Qualification is desirable but not essential.

· 2-3 Years manufacturing experience in a GMP production environment is required.

· Strong Technical Writing Skills are required.

· Experience with Automated production and ERP systems (SAP & Documentum equivalent) desirable but not essential.

· Strong communication skills both verbally as well as written.

· Strong planning and organising skills.

Job
: Manuf./Operations Generic

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Carlow-Process-Support-Specialist-Job-L/1531832/153183215318322012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSCarlow, Leinster, IE
Description

The establishment of this EMEA SBS Centre is part of MSD's strategy to create a multi-function, multi-lingual organization to support MSD at a regional level. The EMEA SBS Centre will initially support business transactions in the areas of Finance, Accounting and Managed Services such as travel and meetings.

We are now recruiting for key talent for our new SBS centre.

Description:

Reporting to the Service Team Manager or Supervisor, the Finance Analyst, is responsible for providing commercial services in cash applications.

The primary activities that you will be performing include:

* Executing the transactions required and the services as defined in the OtC area.
* Supporting the launch of SAP across major markets in Europe.
* Partnering with key stakeholders (Finance, Sales Procurement, etc) to ensure that all transactional activity is properly recorded and compliant with country statutory and tax requirements.
* Seek out opportunities for streamlining and rendering service delivery more efficiently, and participates in special projects to support Shared Business Services objectives.
* Resolve related issues pertaining to OTC and an understanding of when, how and where to escalate cases as required to meet defined service levels.
* Additional responsibilities to support a new organization in Europe as required.

Qualifications

Qualifications:

Education:

* Bachelors Degree required.
* Business Level fluency (oral and written) in French required.

Preferred:

* A minimum of 2 years of demonstrated work experience within the General accounting and or PtP shared services area.
* Experience working in an organization providing services across multiple markets or geographies.
* A minimum of one year of experience working with SAP.
* High degree of integrity and personal ethics in implementing corporate policies and procedures
* Effective team player with collaborative focus
* Must be able to work in a fast-paced, dynamic environment, under pressure, and with a high degree of professionalism
* Must be comfortable in an environment of changing technologies and processes, and demonstrate flexibility in adjusting to new ways of working
* Experience working in a SOX404 environment.
* Strong oral and written communication skills.
* Flexible work arrangements will be considered based on business needs.

Job
: Financial Analysis

Primary Location: IE-Leinster-Dublin
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Dutch-or-French-Collections-Analyst-Job-L/855119/8551198551192012-06-15Merck/MSDFinancial Analysisfull-timeUSDstarting0BSDublin, Leinster, IE
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

El Representante de Fuerza Especial Anestesiología es responsable de lograr la cobertura de su cuota de ventas asignada para su territorio, así mismo es responsable de llevar a ejecución los 4 comportamientos descritos en el modelo de Competencias del Representante de Fuerza de Ventas, así como modelar las conductas de liderazgo y valores corporativos de MSD, ser ejemplo de comportamiento apegado a la comercialización ética corporativa.

PRINCIPALES RESPONSABILIDADES

Visitar instituciones de Gobierno, Instituciones Descentralizadas y Hospitales Privados, en áreas de Quirófano, Transfer y de Descanso en donde se contacte a los Anestesiólogos que son nuestros clientes primarios con el Objetivo de Informar y Promover los productos asignados, con el objeto de Impactar sobre el hábito prescriptivo de nuestros clientes, y con ello lograr que todos los pacientes tengan seguridad en los procesos quirúrgicos y mantener e incrementar la calidad de vida, base fundamental y razón de ser de nuestra Empresa.

Cumplir con las obligaciones descritas en la Descripción de Trabajo del Representante de Fuerza Especial de Anestesiología.

Ejecutar los Comportamientos del Modelo de Ventas, descrito en el Modelo de Competencias del Representante de Ventas MSD.

Identificar Oportunidades de Negocio a nivel institucional (Público) y Privado, así como demostrar sensibilidad en los procesos de negociación estratégica para éstas mismas instituciones hospitalarias

Cualificaciones
Carrera profesional terminada

Experiencia laboral anterior: Mínimo 2 años como representante de ventas en industria farmaceutica y/o areas de consumo

Residencia en D.F. con disponibilidad para viajar a Pachuca (40% del tiempo)

Conocimientos técnicos

Conocimientos médicos o de biología (deseable)

Experiencia como ejecutivo de cuenta o en negociación (deseable)

Diseño y redacción de propuestas de negocio

Estar dispuesto a viajar

Analítico y habilidades financieras (de preferencia)

Idioma:

Deseable Inglés

Competencias y Habilidades

Alta capacidad de negociación

Extraordinario nivel de persuasión

Capacidad de toma de decisiones

Comunicación eficaz verbal y escrita

Orientación a resultados y alto empuje

Excelente manejo de relaciones interpersonales para generar vínculos comerciales

Visión estratégica para generación de negocio

Alta capacidad de análisis

Facilidad de aprendizaje

Capacidad de trabajar bajo presión

Trabajo en equipo

Creatividad, dinamismo, alto sentido de responsabilidad y compromiso

Disponibilidad de cambio de residencia.

Nuestros empleados son la clave del éxito de nuestra empresa. Demostramos nuestro compromiso con nuestros empleados ofreciéndoles un programa de recompensas competitivo y valioso. Los beneficios en MSD están diseñados para apoyar la amplia gama de objetivos, necesidades y estilos de vida de nuestros empleados y de muchas de las personas que constituyen lo más importante en sus vidas.

Puesto
: Ventas general

Ubicación principal: MX-Distrito Federal-Benito Juárez
Tipo de acuerdo laboral: Fijo(a)
Viajes: Sí, un 50% del tiempo
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Benito-Ju%C3%A1rez-Representante-de-Ventas-Anestesia-Job/1871145/187114518711452012-06-15Merck/MSDVentas generalfull-timeUSDstarting0BSMexico City, Distrito Federal, MX
Description

The Global Supply Chain Planning Lead for Process Improvement Supply Planning will lead a project team of ca. 5-8 people. Key focus is the identification and implementation of improvements in the processes surrounding Supply Planning and S&OP, their link to the Manufacturing Sites and to support the (SAP ECC) implementation within the E2E Planning Hub working closely together with the Supply Planning and MMD Site Planning teams.

Key to the role is the transition of the existing organization to the new processes and tools that will be delivered with the SAP implementation and the job holder is expecting to achieve this through coaching and mentoring the Supply Planning team in close collaboration with the GSCP Supply Chain Hub Planning Manager and his/her direct reports.

The primary activities include but are not limited to supervising and leading the following activities:

SAP ECC Implementation

* Evaluating SAP ECC Template (SAP ECC) vs. current AS-IS capability and requirements and identifying gaps.
* Developing a roadmap and delivering solutions to resolve those gaps
* Responsibility for the successful delivery of the SAP ECC SNP sub-stream within agreed time and budget
* Implementing agreed service, safety stock and planning parameters within the SNP tool set as defined by the Inventory Management Centre of Excellence (IM CoE).

Process Improvement in Supply Planning

* Responsible for the rapid, continuous improvement of Supply Planning and S&OP processes, including the continued migration of these processes onto the SAP ECC APO Supply Planning modules and supporting systems.
* Responsible in close collaboration with the GSCP Supply Chain Hub Planning Manager for giving direction to manufacturing sites to ensure that planned production and inventory levels are met (including allocation plans); and then to monitor, track, and report actual production and inventory performance against these forecasted results.
* Contributes to and leads efforts to improve other processes that enable improved production and inventory planning and tracking. This includes improving S&OP, KPI tracking, SAP APO system functionality, and reporting through BI.
* Responsible for coordination, evaluation, and continuous improvement of the planning team and creating a positive climate where people want to do their best.

Qualifications

Education:

* Bachelor's degree in mathematics, engineering, business or related Supply Chain field
* APICS CPIM or CSCMP certification is desirable
* Six Sigma / Lean (Master) Black Belt desirable
* Fluent in SCOR methodology

Skills Required:

* 5-10 years of management and finished product and raw materials planning experience in a related production or operations role preferable within different industries
* Project Management
* Demonstrated track record of improving and optimizing S&OP and Supply Planning processes and systems
* Detailed knowledge of SAP APO is a pre-requisite preferably as a super user or subject matter expert
* Ability to perform detailed analyses to diagnose and identify opportunities to improve supply planning systems
* Strong analytical capacity including advanced knowledge of Excel and demonstrated competence with data structures/SQL
* Critical thinking and problem solving skills, including familiarity with operations tools and concepts such as DMAIC, Lean 5S, SCOR
* Ability to present complex analysis in understandable forms to business stakeholders

Competencies required for the role

* Strong People Leader who has led sizeable teams of direct reports and demonstrated influencing skills to lead cross-functional project teams
* Strong Team-player
* E2E Understanding of Supply Chain with great experience in Demand Planning, Supply Planning, S&OP, Inventory Management
* Strong communicator at all levels of the organization
* Strong holistic thinking when analyzing and improving supply chain processes
* Willingness to be flexible and to work in a rapidly changing environment. Must be able to push forward on efforts, even when all of the requirements have not been defined

*LI-DR1

Job
: Supply Chain Mgmnt Generic

Primary Location: CH-LU-Luzern
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-Global-Supply-Chain-Planning-Lead-Process-Improvement-Supply-Planning-Job-LU/1889118/188911818891182012-06-15Merck/MSDSupply Chain Mgmnt Genericfull-timeUSDstarting0BSLuzern, LU, CH
Description

External Manufacturing Relationship Manager (ExMRM), in partnership with the respective functional representatives, is responsible for ensuring reliable supply of quality Merck product at a competitive cost from the applicable contract manufacturer(s) and appropriate integration in Merck's supply chain. The ExMRM is the owner and primary point of contact for all dealings between Merck Manufacturing division and the external party and establishes boundaries and ground rules of engagement. The contract manufacturers that each ExMRM is accountable for will depend upon factors such as: product type, size and/or complexity of supply agreement, geography, etc.

* The External Manufacturing Relationship Manager (ExMRM) is the primary owner of MMD (Merck Manufacturing Division's) relationship with the contract manufacturer and point of contact for all dealings between the two parties. The EMRM serves as the air traffic controller of all information between MMD and the contract manufacturer and establishes boundaries and ground rules of engagement.
* The ExMRM is responsible for all operational related activities and be the focal point for:

1. Dispute resolution (w/ appropriate escalation)
2. Production Planning
3. Materials Management (MRP entries, Logistics)
4. Quality issues (Deviation Management, Product Release, Change Control)
5. Technology issues
6. Oversight of shop floor production (determining when an ExM functional rep should be deployed to the External Party's (EP) facility)
7. OpEx and Continuous Improvement activities

* The ExMRM partners with ExM Procurement, ExM Quality, and ExM Technology on commercial aspects of relationship, including Identify, Select, Negotiate and Re-negotiate/terminate, as required. ExMRM may not involved in all transactional interactions if they can be managed/delegated to a functional area but will be kept apprised of status/resolutions, etc.
* The ExMRM participates on the cross-functional team that Product Source Management assembles following a Supply Chain Committee (SCC) approved siting/source change to an external party and assume primary ownership of the new source.
* The ExMRM facilitates the collection of EP capacity information (e.g. stated capacity, firm capacity, future capacity plans, time horizon / lead times required, comments/concerns, etc.) in preparation for future Assumption Based Reviews (ABRs) and ensures template completion.
* The ExMRM is responsible for maintaining the integrity of the Joint Service Procedure (JSP), ensuring alignment with the Supply and Quality agreements and appropriate document revision and distribution control.
* The ExMRM is responsible for inventory control. Depending on the location of goods (at External Party or at Merck), ExMRM ensures adequate documentation of material disposition. In some markets, ExM Operations may need to witness the destruction of goods (to prevent counterfeiting) or have the External Party certify the destruction, per destruction procedures described in the JSP.
* The ExMRM is responsible for ensuring contract terms agreed upon by MMD and the External Party are executed including purchase orders, forecasts, deliveries, and approving invoice payments.
* The ExMRM partners with the ExM OpEx expert and ExMOrg Representatives (e.g. technical, quality, procurement, etc.) to identify External Party OpEx / continuous improvement opportunities and supports implementation once approved. The ExMRM may commit resources provided Merck and the EP would share in the costs and benefits of such operational improvements.
* The ExMRM facilitates and participates in periodic Business and Relationship Review Meetings. The ExMRM also prepares an annual "state of the union" presentation for the relationships s/he manages which includes successes and failures in order to leverage across ExMOrg.

Qualifications

Education/Experience:

* Bachelors degree preferably in the Engineering, Science or Business and a minimum 5 years experience in commercial /business and manufacturing (operations, quality, technology, planning) function required (or equivalent combination of education/experience).

Skills:

* Excellent interpersonal, communication, collaboration, negotiation, analytical, and project management skills required.
* Has demonstrated leadership, problem solving, and team building abilities and sensitivity to diverse cultures.
* Must posses the ability to work independently with coaching as needed.
* Must be able to gather appropriate information to inform decisions in an ambiguous environment and know when to seek guidance.
* Able to be the one face of MMD to the external party.

*LI-DR1

Job
: Qual Assurce - 3rd Party Manuf

Primary Location: CH-LU-Luzern
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Quality-External-Manufacturing-Relationship-Manager-Job-GA/1840106/184010618401062012-06-15Merck/MSDQual Assurce - 3rd Party Manuffull-timeUSDstarting0BSLuzern, LU, CH
Description

1. Product Promotion:

- Drive opening of new business avenues for Critical care in own territory hospitals through promotion of BU products to respective Medical fraternity in order to generate the business of the CC product portfolio
- Use detail aids to support scientific selling and Liaison with the HOD's , Purchase committee and Drug Committee doctors at the institutions for inclusion of the CC Products in the pharmacopoeia

2. Territory Sales:

- To prepare a target list of customers as per therapy profile. Understand and implement marketing strategies to medical fraternity to generate prescriptions for the cc products.
- To maintain and balance right distribution of products to the Pharmacy.

3. Market Intelligence/ Sales Reporting

-Interact with paramedical staff in hospitals to seek inputs on competitor activities, patients moving on MSD products, new products in the hospital etc. to maintain intelligence on MSD and competitor activity in the hospital
- Provide field reports in terms of FIRM, Tracker and Sales statement etc. in order to update the sales MIS

4.Customer Relationship Management:

- Organizing and conducting CME's with the user department at the institution in coordination to create and build the market for MSD products
- Manage the relationship with KOL's. Build, maintain and grow new KBL's and support CRM-Scientific activities with KOL's

Qualifications

BSc/ B Pharma with 3+ years of total sales experience in the Pharmaceutical sector

Job
: Direct Sales Generic MAH

Primary Location: IN-TN-Coimbatore
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Coimbatore-Territory-Business-Manager-Coimbatore-%28HIV%29-Job-TN/1853559/185355918535592012-06-15Merck/MSDDirect Sales Generic MAHfull-timeUSDstarting0BSCoimbatore, TN, IN
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Technical Lead, Clinical Informatics

The Informatics IT (IIT) department within Merck is a multidisciplinary department composed of scientists, computational biologists, software developers and IT professionals who work closely with researchers throughout the drug development pipeline to provide cutting edge, innovative solutions to complex problems. IIT's portfolio includes Merck's global high-performance compute strategy, internal and external sequencing/analysis capabilities and global health informatics strategy development and realization.

The clinical informatics technical lead position will oversee the creation and management of a nimble software engineering presence in the bay area to support Merck's increasing efforts in Health Informatics. In this management role she/he will directly contribute to the architecture, development and implementation of key technologies and platforms to support and drive Merck's relationships with health IT and point-of-care organizations. As a technical lead in health informatics, she/he will also work with members of the Discovery, Global Clinical Development, Regulatory Affairs, and IT organizations to help implement a cohesive, global platform strategy to support partnering around real world healthcare data and capabilities to benefit Merck's R&D pipeline and patients with unmet medical needs.

Responsibilities:

* Lead the creation and management of a nimble software development team of 2+ engineers
* Provide technical and managerial oversight of the development and release of new IT/Informatics capabilities, through a combination of internal development and external partner sourcing.
* Be active in product design, technical design, architecture and quality engineering
* Help develop and manage partnerships throughout the organization to understand their strategic objectives
* Proactively monitor external trends to identify innovative solutions and partnering opportunities
* Provide technical expertise in the review of potential external collaborators and investment opportunities
* Approximately 25-50% hands-on development

Qualifications

Education Reqirments:

* Bachelor's or Master's Degree in Computer Science or related field

Required Experience:

* 4+ years of hands-on software web and database experience
* Strong skills in Java programming, Java design patterns and server side Java.
* Working knowledge of key Java technologies ideally including Spring, Hibernate and jQuery.
* Experience with J2EE Application servers like Tomcat
* Strong SQL skills: Oracle, SQL Server or MySQL
* Strong current Unix/Linux skills
* Experience managing relationships with external partners and contracted workers
* Experience implementing development, quality assurance and release management processes
* Solid communication skills, creative problem solving skills and attention to detail
* Strong time-management and independent-judgment skills required
* Motivated to make a difference in human health

Desired Experience:

* Software development experience within a HIPAA compliant research or clinical setting
* Experience negotiating statements of work and task orders
* Experience contributing to the development, architecture, and/or business analysis of open-source development efforts
* Experience with and knowledge of pharmaceutical drug development
* Hands-on experience with cloud computing technologies

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003548.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Bioinformatics

Primary Location: US-CA-San Francisco
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/San-Francisco-Technical-Lead%2C-Clinical-Informatics-Job-CA-94101/1780438/178043817804382012-06-15Merck/MSDBioinformaticsfull-timeUSDstarting0BSSan Francisco, CA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Informatics department develops supports and enables the application of informatics across Merck, in partnership with quantitative organizations throughout the company. Our world-class team is currently seeking outstanding candidates to join to join our global team of diverse informatics professionals, spanning engineering, modeling and simulation, knowledge management, biomedical and health informatics, computational biology and translational informatics. Successful candidates will have the opportunity to collaborate with talented and dedicated colleagues to make a difference to patient healthcare.

The Health Informatics Data Scientist will be responsible for developing, prototyping and enabling new capabilities to utilize real world health data in combination with Merck proprietary information to enable discovery, development and commercialization objectives. The successful candidate will operate at the interface of translational, clinical and health informatics programs and collaborate with other quantitative scientists

to develop and apply real world health data and novel informatics capabilities to benefit Merck's R&D pipeline and patients with unmet medical needs.

Responsibilities may include:

* Acquiring, evaluating and meaningfully melding rich clinically and commercially-relevant healthcare data sources, including formulating validation strategies and methods to ensure accurate and reliable data.
* Developing innovative approaches to clinical data classification, analysis and modeling to unlock new trends and to conceptualize new approaches to address business challenges.
* Developing and applying methods, tools, and systems for analysis, modeling, and visualization, and/or automating information pipelines
* Prototyping and defining rich tooling that enables others to effectively explore and visualize datasets and analyses.
* Developing hypotheses, analyzing data, and providing direct analytical support to multiple business areas, and/or automatics information pipelines.
* Executing on and evaluating project outcomes in collaboration with functional area and therapeutic area teams.

Qualifications

Education:

* Minimum Masters Degree in computer science, statistics, biophysics, computational biology, or other relevant field
* Advanced degree (PhD) in computer science, statistics, biophysics, computational biology, or other relevant field preferred

Required:

* A minimum of three years of relevant experience
* Demonstrated history as a self-motivating, productive, innovative, interdisciplinary data scientist as evidenced by a strong research and/or publication record.
* Experience in analyzing and visualizing large volumes of data and utilizing advanced computational methods.
* Experience in developing computational tools and/or data products to solve questions, ideally relevant to healthcare.
* Ability to work creatively and flexibly, both independently and as part of a team.
* Strong organizational, interpersonal, and problem solving skills.
* Attention to fine details and work processes.
* Desire and ability to learn new skills, systems and processes.
* Ability to analyze user requests, define requirements, develop project plans and report conclusions.
* Excellent written and oral communications skills.
* Working knowledge and experience in SQL and relational database systems and statistical modeling tools such as SAS or R.
* Thorough knowledge of research methodology and statistical methods.
* Desire to make a difference to patients and improve healthcare.

Preferred:

* Significant experience with real world outcomes in an academic, industry or healthcare setting.
* Experience with SPARQL, linked open data, semantic technologies, ontologies, knowledge engineering.
* Experience with mobile technologies, consumer health platforms and/or gaming approaches is desirable.
* Working knowledge of health information systems.
* Working knowledge of standard clinical terminologies, coding systems, and data standards.
* Working knowledge of pattern recognition and data classification algorithms.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003550.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-PD1

Job
: Bioinformatics

Primary Location: US-CA-San Francisco
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/San-Francisco-Health-Informatics-Data-Scientist-Job-CA-94101/1816965/181696518169652012-06-15Merck/MSDBioinformaticsfull-timeUSDstarting0BSSan Francisco, CA, US
Description

Under the guidance of the Senior Director, Intelligence, incumbent manages the collection, analysis and dissemination of timely, relevant and predictive threat intelligence to Merck decision makers' worldwide. Incumbent will also monitor and assess product security risks, as well as, support ongoing investigations to identify trends, parties involved and other information deemed appropriate. Additionally, incumbent will have a lead role in managing the relationships with contract providers of related programs, systems and information that facilitate their responsibilities. Incumbent delivers independently, and upon request, high level analytics that fully support the Global Security Group's mission and vision.

Superior Intelligence Analysis professional with a minimum of five years collecting, analyzing and disseminating strategic and tactical intelligence experience. Minimum of a Bachelors of Arts, in Intelligence; Political Science; History; or related discipline.

Demonstrate a proven ability to identify security threats, report pertinent information.

Excellent research and writing skills under extremely tight deadlines and competing demands.

Able to perform under pressure and respond rapidly to breaking situations. Also, work in varying situations, from committee work in which a "team player" approach is essential to situations in which considerable independence and self-motivation is required.

Must demonstrate a high degree of performance in all Merck leadership skills, most notable the ability to think and act strategically.

Qualifications

10 years experience

Bachelors' Degree. Masters preferred

Job
: Global Security

Primary Location: IE-Leinster-Dublin
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Regional-Intelligence-Manager%2C-EMEA-Job-L/1689825/168982516898252012-06-15Merck/MSDGlobal Securityfull-timeUSDstarting0BSDublin, Leinster, IE
Description

Responsible and accountable for supporting all Automation and IT components of the process. On-floor support of manufacturing activities.

Active participation in the Tier process and proactively resolving technical issues before they impact the business priorities.

Ensure supply of high quality product through ensuring equipment and system availability; maximize performance through continuous process improvement initiatives and other relevant project support.

Ensure compliance with, implementation and maintenance updates of local Carlow specific SOP's and technical documentation eg. Change Management, Problem Incident Management.

Ensure's adherence with Merck IT standards. Following business processes in the execution and support of A&IT systems in Carlow.

Required to comply with Merck Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.

Participate effectively in writing/revising/ rolling out accurate operational procedures, training documents and maintenance procedures for various IPT systems; ensure all work is carried out in line with same.

Responsible for supporting a culture of Continuous Improvement by deploying Merck Six Sigma tools within MMDIT on projects such as: problem solving, standardization, reducing cycle time, Lean principles within the process.

Work collaboratively to drive a safe and compliant culture in Carlow.

o Extensive technical and operational expertise in one of more of the following disciplines:

o Computer Systems Validation

o MIS Systems

o Business Systems

o Manufacturing Execution Systems

o Instrumentation/Automation & Control

o BMS / SCADA / DCS Systems

o Control System/Shopfloor Integration

o Financial Systems / Inventory Management Systems / SAP

o Proficiency in Microsoft Office and job related computer applications required

o Understanding of mechanical/electrical/pneumatic processes

o Equipment and process validation

o Pharmaceutical and Biotechnology manufacturing processes

o Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices

o Report, standards, policy writing skills required

o Knowledge, and ideally application, of industry standard training documentation systems/methods

o Lean Six Sigma Methodology experience desired

Qualifications

o Bachelors Degree or higher preferred; ideally in a Computer Science, Business Information Systems, Software Engineering or Automation/Process Control discipline

Job
: Engineering

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Carlow-Systems-Engineer-Job-L/1703536/170353617035362012-06-15Merck/MSDEngineeringfull-timeUSDstarting0BSCarlow, Leinster, IE
Description

MSD in Lucerne/Switzerland is a Swiss subsidiary of the successful global pharmaceutical company Merck & Co. Inc. with its headquarters in USA. Approx. 100'000 employees are currently working for us globally and we are showing strong growth.

Our Swiss operations include MSD International GmbH, Merck Sharp & Dohme-Chibret AG, Essex Chemie AG, Schering Plough Central East AG and Werthenstein BioPharma GmbH with currently 700 employees.

Within our EEMEA organization we are currently recruiting a role as

Compliance and Operations Regulatory Affairs Associate Lead, EEMEA (Eastern Europe, Middle East & Africa)

Under the supervision of the EEMEA Regional Regulatory Affairs Lead, the incumbent provides support to the EEMEA Regional Regulatory Affairs Lead in directing the regulatory function, in order to ensure timely products registrations in compliance with related regulatory areas. The scope of roles and responsibilities of the job covers all countries in the EEMEA region, including Turkey and Russia.

Primary Activities:

· Support the EEMEA Regional Regulatory Affairs Lead by providing operational and compliance oversight of all regulatory activities in the EEMEA countries and assist in the development of EEMEA regional regulatory strategies for achieving fast registrations while securing compliance.

· Support submissions and approvals as per targets assigned by EM for EEMEA

· Support execution on the agreed regulatory action plan for submissions and approvals within the Region.

· Support countries to ensure compliance at the local level with global, regional and local policies and procedures.

· Secure that the internal systems/tools are populated in line with the Merck policies and procedures.

· Join the Regional Medical Councils on an ad hoc basis ensuring value adding input from countries. Repairing agenda items and minutes in a timely manner by tracking progress and follow up on agreements.

· Support marketed product labeling and quality compliance, in line with internal and local regulatory policies, as well as securing timely product re-registrations.

· Quality function

· Participate in the review and development of EM/RA practices and policies, and provide training accordingly to the countries in scope.

· Secure compliance of local regulatory practices with the relevant SOPs through a quality audit system.

· Ensure processes efficiency, optimization and technical alignment across countries in scope.

· Support the EEMEA Regional Regulatory Affairs Lead in the management of the country Regulatory Affairs Leads within EEMEA

· Coordinate training activities to ensure skill development in countries keeps pace with the need for competitive regulatory strategy and company procedures, including new regulatory professionals.

· Create a seamless relationship and teamwork between assigned countries and RA EEMEA in order to establish best practices sharing and where possible, resources sharing.

· Develop close and seamless working relations with each assigned country, contributing to achieving local and regional objectives through building partnerships at the local level.

· Cooperate with MMD regarding the implementation of specific programs and tools, and ensure that manufacturing/quality related issues are managed in a consistent way, through robust processes in line with the MSD standards.

· Set up KPIs for ensuring that performance can be measured going forward.

· Responsible for Team site administration

· Participate in business development initiatives involving the countries in scope by providing input from/to countries.

· May represent RA EEMEA in professional association and working groups, e.g., PhRMA, in specific situations.

· It is recognized that this role will require considerable regulatory and leadership experience, track record, and clear leader behaviors focused at collaboration & shared accountability.

Qualifications

· Advanced degree in Science preferred with 5+ years relevant regulatory experience or

· B.A. or B.S. degree with emphasis in Science, Health Care or related fields with 10+ years related experience including 8 years relevant regulatory experience (generally 5-10 years of experience)

· Excellent written, verbal communication skills including presentation skills

· Demonstrate Leader Behaviors:

· Ability to work in cross-functional team environment

· Demonstrate an ability to Learn and Listen

· Ability to lead, coach and develop coach others and to build effective teams

· Cross-functional Teamwork and Collaboration

· Shared Accountability and Transparency

· Business Integrity

· Strong interpersonal skills with ability to demonstrate strategic and analytic thinking

· Demonstrate an ability to negotiate and influence others effectively; adept at conflict management.

· Incumbent should have supervisory skills or potential to manage a small group of regulatory professionals.

· Ability to manage and lead multiple, complex projects and timelines in a matrix team environment

Job
: Regulatory Affairs/Compliance

Primary Location: CH-Lucerne
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Compliance-and-Operations-Regulatory-Affairs-Associate-Lead%2C-EEMEA-Job/1792963/179296317929632012-06-15Merck/MSDRegulatory Affairs/Compliancefull-timeUSDstarting0BSCH-Lucerne
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Inventory Production Specialist will be responsible for the organization's (IPT) ordering of components and materials for processing and/or packaging. Sets ordering schedules based on scheduled orders, component, materials supply, and volume required to meet order demand and to ensure maximum production quantity and quality on shift. Responsible for programs to establish and maintain quality standards of existing components, materials, etc., as well as developing mechanisms allowing production employees to focus on, safety, quality, production and continuous improvement. Support the development of policies procedures and methods to check product, material, components and/or operational quality and improve same.

Plans and prepares manufacturing production schedules and departmental workflows to establish sequence and lead time of each production operation to meet shipping dates according to sales forecasts or customer orders. Expedites the review of MPR's that could result in the shipping delays and alters schedules to meet unforeseen conditions. Analyzes batch production requisitions data to drive the ordering processes. Prepares production reports and reviews documents, such as production schedules, staffing matrix, and specifications, to harvest all necessary information such as materials, and any other priorities.

Takes responsibility for administration of the organization's warehouse ordering, including processing, and making sure all components and supplies packaging record specific, and general use materials are expedited to the manufacturing floor. The review of all source documents, MPR's prior to production release and after batch completion. All documents must be error free before and after the previously referenced condition. Accounts for all components', materials and supplies in the manufacturing facility. Oversees receipt, proper staging, and return of finished goods, components, materials, and related reporting in accordance with established procedures. Prepares and coordinates schedules for shipping to control the flow of finished goods and regulate manufacturing hallway space to make sure it is well organized. Ensures effectiveness of operating procedures, relative to components and all components and materials' brought in from the warehouse finished goods, left over components and materials returned to the warehouse as well as hallway space utilization.

Qualifications

Education:

High School Diploma or equivalent.

Required:

* Minimum 5 years relevant work experience in Production, Manufacturing support or related Operational support areas.
* Must have strong demonstrated PC skills using Microsoft Office Suite. Proficiency using Word, Excel preferred.

Desired:

* 2 year Associate' Degree preferred
* An understanding of information systems, such as MRP II systems (SAP, MRP Repository etc.), and Supply Chain Views.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PRO009316.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Production / Operator

Primary Location: US-TN-Cleveland
Employee Status: Regular
Number of Openings: 4]]>http://jobs.merck.com/job/Cleveland-Inventory-Production-Specialist-Job-TN-37311/1714920/171492017149202012-06-15Merck/MSDProduction / Operatorfull-timeUSDstarting0BSCleveland, TN, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Forklift operator will be responsible for the operation of the counter balance forklieft, narrow aisle lift and the electric jack. Other responsibilities include, but are not limited to......

* Continuous use of RDT computer terminal using WMS/SAP materials management system.
* Service manufacturing by delivering materials and picking up returns to stock with strict control over inventories.
* Load and unload trailers as required.

Qualifications

Education:

High School Diploma or equivalent

Required:

Prior experience operating a fork lift

Must be able to pass physical examination per corporate requirements for powered industrial operators

Must be able to pass OSHA required powered industrial truck evaluation after in-class and on-the-job training

Must be able to lift up to 25 pounds without assistance, and assist in maneuvering materials weighing up to 1000 pounds.

Desired:

Prior work experience in the pharmaceutical industry

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # WAR000161.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Warehouse Operator

Primary Location: US-TN-Cleveland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Cleveland-Forklift-Operator-Job-TN-37311/1772850/177285017728502012-06-15Merck/MSDWarehouse Operatorfull-timeUSDstarting0BSCleveland, TN, US
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

El Coordinador de Labeling será la persona encargada y responsable de todos los asuntos relacionados con la planificación, desarrollo, aprobación y rechazo de materiales de embalaje y obras de arte, para todos los productos de la empresa según las políticas y procedimientos de MSD y los requisitos de GMP y la legislación local. Requiere un alto grado de conectividad con otras áreas en la empresa, tanto local como internacional.

PRINCIPALES RESPONSABILIDADES:

- Coordinación y Planificación: Coordinar y anticiparse a los cambios que serán aplicables al etiquetado, especialmente pero no se limita a las renovaciones, actualizaciones de seguridad, las variaciones químicas y técnicas, los cambios legales, cambios de lugares de fabricación, nuevos productos y presentaciones de lanzamiento.
- AMS Blue Leader: Es la herramienta electrónica para la gestión de obras de arte para los sitios de MSD. Sin embargo deberá tener en cuenta que para otros sitios, deberá estar a cargo también de otras herramientas. Mantener los indicadores de productividad y el rendimiento según las puntuaciones recomendadas para la región.
- Materiales en aprobación : Mantener un repositorio local de las materias aprobadas con el fin de cumplir tanto con la legislación local y los procedimientos de MSD.
- Auditorías: Realizar auditorías periódicas y auto verificación del cumplimiento

Cualificaciones
Profesional Universitario: Ingeniero Químico, Químico Farmacéutico o ciencias relacionadas.

Experiencia mínima de 2 años en el área regulatoria.

Experiencia en el desarrollo / revisión / aprobación del etiquetado y artwoks de compañías farmacéuticas multinacionales.

Habilidad para investigar, excelente comunicación escrita y habilidad para sintetizar información a ser presentada tanto internamente como a las agencias regulatorias. Habilidad para trabajar en múltiples proyectos.

Conocimiento del marco legal regulatorio.

Nuestros empleados son la clave del éxito de nuestra empresa. Demostramos nuestro compromiso con nuestros empleados ofreciéndoles un programa de recompensas competitivo y valioso. Los beneficios en MSD están diseñados para apoyar la amplia gama de objetivos, necesidades y estilos de vida de nuestros empleados y de muchas de las personas que constituyen lo más importante en sus vidas.

*LI-KT1

Puesto
: Especificaciones de etiquetado

Ubicación principal: CL-Santiago Metropolitan Region-Santiago
Tipo de acuerdo laboral: Fijo(a)
Viajes: No
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Santiago-Coordinador-de-Labeling-Job/1799251/179925117992512012-06-15Merck/MSDEspecificaciones de etiquetadofull-timeUSDstarting0BSSantiago, CL
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

El Representante de Ventas es responsable de lograr los objetivos de negocio del territorio asignado, a través de la promoción de productos de alta especialidad (Anticonceptivos, Antiinflamatorios, Corticoides), servicios a los médicos y otros profesionales de la salud, asegurando la efectiva implementación de la estrategia de marketing y alineado a la cultura ética, compliance, políticas y procedimientos de MSD, así como apegado a las regulaciones del gobierno de Chile.

PRINCIPALES RESPONSABILIDADES:

Es responsable de lograr la cobertura de venta a través de visita y asesoria a médicos, clientes / cuentas clave en consultas, hospitales y clínicas de gobierno y privada: médicos, residentes, matronas, influencias técnicas y administrativas.

a) Alineado a las estrategias de marketing de cada uno de sus productos de alta especialidad.
b) Desarrollando, implementando y dando seguimiento a su plan de ventas.
c) Procurando uso de nuestros productos y el abastecimiento conforme a los marcos existentes.

d) Asesorando a los clientes acerca del manejo y ventajas de los tratamientos de MSD para los pacientes mediante la búsqueda y entrega de información clínica de diversas fuentes así como ofreciendo servicios y soluciones diferenciados.
e) Analizando y evaluando el potencial de negocio para identificar oportunidades de nuevas oportunidades.
f) Desarrollando negocios a través del continuo diseño de nuevos modelos para clientes clave.
g) Planeando, organizando, ejecutando y dando seguimiento a sus eventos de Educación Médica Continua (EMC).
h) Consolidando las relaciones con clientes clave a largo plazo.
i) Participando e integrando actividades para el desarrollo de eventos médicos, tales como convenciones, reuniones clínicas, congresos, etc. Así como en la licitación e inclusión de productos a las instituciones bajo su responsabilidad.

Cualificaciones
* Título Universitario del área de salud.(Preferencia).

* Dos años de experiencia como Representante de Ventas en la Industria Farmacéutica .

* Residencia en Antofagasta, con disponiblidad para viajar al Norte (Arica, Iquique) aproximadamente el 50% del tiempo.

* Capacidad para trabajar en equipo.

* Alta orientación al cliente

* Capacidad de detectar oportunidades de negocio e innovar

* Adaptabilidad

* Proactividad

* Muy buen nivel para relaciones interpersonales.

* Iniciativa.

* Capacidad de organización y planificación.

* Habilidad para analizar y resolver problemas.

* Conocimiento de las zonas de trabajo

* Negociación.

* Comunicación de alto impacto.

* Presentaciones efectivas.

Nuestros empleados son la clave del éxito de nuestra empresa. Demostramos nuestro compromiso con nuestros empleados ofreciéndoles un programa de recompensas competitivo y valioso. Los beneficios en MSD están diseñados para apoyar la amplia gama de objetivos, necesidades y estilos de vida de nuestros empleados y de muchas de las personas que constituyen lo más importante en sus vidas.

Puesto
: Ventas general

Ubicación principal: CL-Antofagasta-Antofagasta
Tipo de acuerdo laboral: Fijo(a)
Viajes: Sí, un 50% del tiempo
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Antofagasta-Representante-de-Ventas-Job/1812619/181261918126192012-06-15Merck/MSDVentas generalfull-timeUSDstarting0BSAntofagasta, Antofagasta, CL
Description

Doel van de functie

Het initiëren, ontwikkelen, optimaliseren en implementeren van patiëntenprogramma's en activiteiten die de toediening van onze geneesmiddelen (REMICADE en SIMPONI) op het gebied van Immunologie verbeteren en vergemakkelijken met oog voor behoeften van de voorschrijvers, specialistisch verpleegkundigen en de patiënt. De programma's worden ontwikkeld in nauwe samenwerking met marketing, sales, medical, PR en Market Access team met als doel de vastgestelde commerciële doelstellingen te realiseren.

* Verantwoordelijk voor initiëren en ontwikkelen van patiënten programma's en activiteiten in lijn met de strategie van de Product plannen Immunology in samenwerking met de verschillende Brand Teams, PR en het Market Access team.
* Optimaliseren van bestaande patiënten programma's en activiteiten in samenwerking met de verschillende Brand Teams, PR en het Market Access team.
* Implementeren van de patiënten programma's en activiteiten in samenwerking met verschillende interne en externe partijen.
* Opstellen en implementeren van project plannen.
* Zorgdragen voor up-to-date kennis over de omgeving, producten, marktontwikkelingen in relatie tot zorg, ziektekosten en ziektebeeld.
* Kwalificeren als gelijkwaardig gesprekspartner op het gebied van patiëntenzorg en -programma's.
* Opbouwen, onderhouden en verdiepen van de relatie met de diverse stakeholders alsmede het signaleren van potentiële kansen, in lijn met gemaakte plannen, teneinde implementatie en ontwikkeling van patiënten programma's en activiteiten te verhogen.
* Genereren van kwalitatief hoogwaardige interactie met de diverse stakeholders binnen ziekenhuizen, (specialisten (in opleiding), specialistisch verpleegkundigen en ziekenhuisapothekers, ziekenhuis management) en andere belanghebbenden die betrokken zijn bij het initiëren, ontwikkelen, optimaliseren en implementeren van patiëntenprogramma's en activiteiten

Qualifications

Functie-eisen

* HBO-opleiding.
* Minimaal 3 jaar ervaring als Product Specialist en/of Account Manager of vergelijkbare functies binnen de farmaceutische industrie.
* Kennis van project management is een pré.

Vereiste competenties

Samenwerken
Handelt vanuit het groepsbelang en levert samen met anderen een bijdrage aan het gemeenschappelijke resultaat.

Plannen en organiseren
Organiseert middelen en werkzaamheden zodanig dat de gestelde doelstellingen worden behaald.

Resultaatgerichtheid
Maakt SMART-resultaatafspraken en toetst of gestelde doelstellingen worden gerealiseerd.

Overtuigingskracht
Is in staat door overredingskracht invloed uit te oefenen op de ideeën en standpunten van anderen.

Initiatief
Reageert proactief door zaken te initiëren en in gang te zetten.

Omgevingsbewustzijn
Is extern georiënteerd en alert op ontwikkelingen in de gezondheidszorg die van invloed zijn op MSD.

*LI-LVG1

Job
: Product Dev Proj/Prog Mgmnt

Primary Location: NL-NH-Haarlem
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Haarlem-Patient-Support-Program-Manager-Immunologie-Job-NH/1858713/185871318587132012-06-15Merck/MSDProduct Dev Proj/Prog Mgmntfull-timeUSDstarting0BSHaarlem, NH, NL
Description

The RtR Project Manager will lead the movement of activities from regional business units to a global shared services operating model. The RtR Project Manager will be responsible for providing Project Management support and structure and will work closely with service leads to coordinate, plan, transition and execute the deployment of activities. Also, the Project Manager will be responsible for overseeing the stabilization effort (Hypercare) after go-live.

Primary
DUTIES:

Project Management - Plan

* Work with Transition Manager to estimate project staffing and in defining project team roles and responsibilities
* Develop and/or review estimates and estimating assumptions for the project's schedule, effort, and cost using established estimating models, leading practices, and past experience

Project Management - Delivery

* Execute and maintain project plan working with other leads, including reporting on project status and issue/risk management
* Manage relationships and coordinate work between different teams at different locations
* Ensure that the project team follows all quality assurance processes, including periodic reviews
* Ensure that all requirements, project plans, and change in scope are communicated to all affected team members
* Collaborate with training lead to ensure SBS staff are fully trained and are ready for the transitioned work
* Coordinate a mock service delivery to prepare for go-live and identify any gaps in the transition

Project Management - Stabilization

* Provide necessary support for transitioned processes after go-live
* Monitor service level and adjust processes as needed

Qualifications

Required:

* Qualified Accountant with a minimum of 5 years relevant work experience including a minimum of 3 years direct experience in managing/leading a project team.
* Experience in the finance/accounting shared services department of a multinational company
* Effective people manager with focus on teamwork and collaboration
* Experience with SAP/ERP systems
* Must be able to work in a fast-paced, dynamic environment, under pressure, and with a high degree of professionalism
* Must be comfortable in an environment of changing technologies and processes and demonstrate flexibility in adjusting to new ways of working
* Excellent problem/resolution skills and an understanding of when, how, and where to escalate cases as required to meet defined service levels
* High degree of integrity and personal ethics in implementing corporate policies and procedures
* Strong project management skill with the ability to manage all aspects, including providing overall guidance and direction to the project and overseeing financial management activities.
* Demonstrated leadership in achieving objectives in a matrix organization, coordinating projects and services across boundaries.
* Must have excellent communication, negotiation and influencing skills along with high personal integrity, credibility, and energy.
* Knowledge of Finance processes is required.
* Experience of working with finance & accounting teams & processes

Education Requirements:

Bachelors Degree in Finance or Accounting and Accounting qualification

Desired: PMI / PRINCE 2certification & previous experience with SAP is desirable.

Job
: Project Management Generic

Primary Location: IE-Leinster-Dublin
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Accounting-Project-Manager-Job-L/1510514/151051415105142012-06-15Merck/MSDProject Management Genericfull-timeUSDstarting0BSDublin, Leinster, IE
Description

External Manufacturing Relationship Manager (ExMRM), in partnership with the respective functional representatives, is responsible for ensuring reliable supply of quality Merck product at a competitive cost from the applicable contract manufacturer(s) and appropriate integration in Merck's supply chain. The ExMRM is the owner and primary point of contact for all dealings between Merck Manufacturing division and the external party and establishes boundaries and ground rules of engagement. The contract manufacturers that each ExMRM is accountable for will depend upon factors such as: product type, size and/or complexity of supply agreement, geography, etc.

* The External Manufacturing Relationship Manager (ExMRM) is the primary owner of MMD (Merck Manufacturing Division's) relationship with the contract manufacturer and point of contact for all dealings between the two parties. The EMRM serves as the air traffic controller of all information between MMD and the contract manufacturer and establishes boundaries and ground rules of engagement.
* The ExMRM is responsible for all operational related activities and be the focal point for:

1. Dispute resolution (w/ appropriate escalation)
2. Production Planning
3. Materials Management (MRP entries, Logistics)
4. Quality issues (Deviation Management, Product Release, Change Control)
5. Technology issues
6. Oversight of shop floor production (determining when an ExM functional rep should be deployed to the External Party's (EP) facility)
7. OpEx and Continuous Improvement activities

* The ExMRM partners with ExM Procurement, ExM Quality, and ExM Technology on commercial aspects of relationship, including Identify, Select, Negotiate and Re-negotiate/terminate, as required. ExMRM may not involved in all transactional interactions if they can be managed/delegated to a functional area but will be kept apprised of status/resolutions, etc.
* The ExMRM participates on the cross-functional team that Product Source Management assembles following a Supply Chain Committee (SCC) approved siting/source change to an external party and assume primary ownership of the new source.
* The ExMRM facilitates the collection of EP capacity information (e.g. stated capacity, firm capacity, future capacity plans, time horizon / lead times required, comments/concerns, etc.) in preparation for future Assumption Based Reviews (ABRs) and ensures template completion.
* The ExMRM is responsible for maintaining the integrity of the Joint Service Procedure (JSP), ensuring alignment with the Supply and Quality agreements and appropriate document revision and distribution control.
* The ExMRM is responsible for inventory control. Depending on the location of goods (at External Party or at Merck), ExMRM ensures adequate documentation of material disposition. In some markets, ExM Operations may need to witness the destruction of goods (to prevent counterfeiting) or have the External Party certify the destruction, per destruction procedures described in the JSP.
* The ExMRM is responsible for ensuring contract terms agreed upon by MMD and the External Party are executed including purchase orders, forecasts, deliveries, and approving invoice payments.
* The ExMRM partners with the ExM OpEx expert and ExMOrg Representatives (e.g. technical, quality, procurement, etc.) to identify External Party OpEx / continuous improvement opportunities and supports implementation once approved. The ExMRM may commit resources provided Merck and the EP would share in the costs and benefits of such operational improvements.
* The ExMRM facilitates and participates in periodic Business and Relationship Review Meetings. The ExMRM also prepares an annual "state of the union" presentation for the relationships s/he manages which includes successes and failures in order to leverage across ExMOrg.

Qualifications

Education

* Bachelor's degree preferably in Engineering, Science or Business.

Experience

* 5+ years relevant work experience in commercial /business and manufacturing (operations, quality, technology, planning) function required (or equivalent combination of education/experience).

Skills/Capabilities

* Excellent interpersonal, communication, collaboration and negotiation skills.
* Excellent analytical and project management skills.
* Demonstrated leadership, problem solving, and team building abilities and sensitivity to diverse cultures.
* Ability to work independently with coaching as needed. Must be able to gather appropriate information to inform decisions in an ambiguous environment and know when to seek guidance.
Ability to be the one face of MMD to the external party.

Job
: Manufacturing & Quality

Primary Location: CH-LU-Luzern
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-External-Manufacturing-Relationship-Manager-Job-LU/1832076/183207618320762012-06-15Merck/MSDManufacturing & Qualityfull-timeUSDstarting0BSLuzern, LU, CH
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

El Gerente de Franquicia - Respiratorio es responsable de realizar los análisis entendiendo al mercado, la competencia y el entorno, así como, es encargado de planificar, adaptar e implementar efectivamente las estrategias de mercadeo, y de generar diferentes planes, programas y actividades apropiadas para cada producto, con el propósito de lograr los objetivos de ventas establecidos.

Debe conocer a través del contacto permanente con los médicos claves, la fuerza de venta y los eventos médicos, para entender a nuestros clientes, el entorno y sus necesidades.

Es encargado de la transmisión de las comunicaciones estratégicas a la Fuerza de ventas por medio de las reuniones periódicas y de los entrenamientos, así como los procesos internos de planificación del negocio relacionados con el producto asignado.

PRINCIPALES ACTIVIDADES:

Análisis y planeación:

- Implementar efectivamente estrategias de mercadeo a través del análisis del mercado local.
- Consolidar y completar la información del plan de mercadeo global, adaptándolo al mercado local.
- Liderar los procesos de planeación del negocio (LROP, SPOC, PP).
- Elaborar el proceso de las proyecciones de venta y mercadeo del producto asignado.
- Diseñar el presupuesto anual del producto.
- Control y seguimiento del presupuesto promocional asignado a cada producto.
- Planificar los entrenamientos de las estrategias de mercado y de productos para la fuerza de ventas.
- Realizar la adaptación del plan de acción regional a las necesidades locales identificando los mensajes claves, las estrategias de muestreo y manteniendo los lineamientos de targeting.
- Planificar y coordinar los programas de alto impacto corporativo.

Contacto permanente con el negocio:

- Entender al cliente y sus necesidades a través del contacto permanente.
- Validar estrategias que están siendo utilizadas en el campo por los representantes.
- Validar los mensajes que están siendo utilizados a través de reuniones periódicas y/o entrenamientos.
- Evaluar e Identificar las acciones de la competencia para tomar las acciones necesarias.

Fase de comunicación:

- Aprobación y elaboración del material promocional, seleccionado por el gerente regional.
- Iniciar el proceso de aprobación médico-legal de los materiales promociónales y programas relacionados a cada producto.
- Control y seguimiento del material promocional y de las muestras de los productos.
- Realizar la distribución del material promocional de vuelta y eventos

Planeación de los diferentes eventos y congresos:

- Planificar y participar aquellos congresos o eventos que se consideren estratégicos para la franquicia.

Cualificaciones
Profesional Universitario de preferencia con estudios de cuarto nivel en Marketing.

Dos o más años de experiencia en gerencia de productos, mercadeo, y afines. De preferencia experiencia en manejo de productos respiratorios éticos.

Nivel intermedio-avanzado del idioma inglés

Capacidad de análisis, comunicación, planificación y seguimiento, relaciones interpersonales, orientación al logro y al cliente, compromiso, flexibilidad, liderazgo y creatividad e innovación.

Nuestros empleados son la clave del éxito de nuestra empresa. Demostramos nuestro compromiso con nuestros empleados ofreciéndoles un programa de recompensas competitivo y valioso. Los beneficios en MSD están diseñados para apoyar la amplia gama de objetivos, necesidades y estilos de vida de nuestros empleados y de muchas de las personas que constituyen lo más importante en sus vidas.

*LI-KT1

Puesto
: Gestion de productos

Ubicación principal: VE-Caracas Capital District-Caracas
Tipo de acuerdo laboral: Fijo(a)
Viajes: Sí, un 25% del tiempo
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Caracas-Gerente-de-Franquicia-Respiratorio-Job/1835820/183582018358202012-06-15Merck/MSDGestion de productosfull-timeUSDstarting0BSCaracas, Caracas Capital District, VE
Description

Description

The Solution Verification & Test - Service Lead role for EMEA is responsible for supporting the regional SV&T protfolio by assisting business partners; IS Client Services and Solutions Delivery organizations with defining scope, strategy, schedules, and required funding for testing. Develops and maintains the SV&T Demand Management and Master Plan aligned with the various PMO's, SV&T and Solution Delivery initiatives. Prioritize workloads to project IT regulatory commitments and scheduled timelines. Provides technical expertise during validations, design reviews, acceptance testing and training and when applicable, ensure adherence to CFR Part 11, GxP, Computer Validation Procedures and SDLC concepts in accordance with company policy.

This position reports to the Regional Director, Application Management Services and is matrixed to the Director SV&T to ensure consistency in testing services as well as to utilized the SV&T Managed Service.

The nature of the position requires excellent oral and written communication skills and proven leadership in complex team situations. The incumbent will ensure that all SLC concepts are applied in accordance with company policy.

The position will interact with several levels in the organization and will be critical in establishing good relationships with numerous regional Client Services and Solutions Delivery areas and with other global functions.

Primary activities include, but are not limited to:

ý Partner with functional leaders and peers to develop SV&T strategic plans; manage the SV&T portfolio of applications to ensure alignment and proper support within agree upon SLAs/OLAs. Manage the appropriate intent, people, and solution delivery risk while providing leadership and guidance in developing robust mitigation plans.

ý Develop and drive the strategy and vision of the demand planning function to keep pace with business structure and priorities; including external benchmarking, continuous improvement of process, systems and defining resource levels, roles, and responsibilities

ý Identify and recommend ways to optimize resource allocation and functional alignment across the SV&T organization.

ý Lead efforts to identify opportunities and create solutions to optimize the SV&T organization by using Lean Six Sigma tools and executing continuous process improvement projects.

ý Establish strategies, coach and mentor all levels of the organization to promote the utilization of the methodologies and tools to fully realize the benefits of Delivery Services and divisional objectives.

ý Develop systems and methodologies to create, capture, share and leverage knowledge across SV&T group and with our internal and external partners.

ý Communicate objectives and priorities to all team members; identify and coach associates with management potential; promote teamwork at peer and all other levels; effectively utilize each team member to his/her full potential. He/she is responsible for the SV&T resources based on his/her geography. Responsible for the interaction of Solution Delivery with the rest of Global functions ( HR, Finance, GS, etc).

Qualifications

· Bachelor's degree required in Computer Science, Engineering or equivalent.

· Minimum 10 years applied work experience in pharmaceutical experience with emphasis on leadership, software development, business analysis and testing.

· Prior experience using and/or overseeing IS QA and Validation testing teams and methodologies.

· Ability to build, work and manage global and diverse teams and vendors.

· Prior hands on experience developing the full SDLC deliverable set and leading the validation of systems that meet user needs and comply with company and regulatory standards.

· Proven Project Management/Portfolio Management-resource planning

· Certified Lean Six Sigma Green Belt or equivalent preferred.

· Skilled in the enabling integrated methodologies and tools including: Change Management, Knowledge Management, Portfolio Management, Lean Six Sigma, Behavior Coaching and Consequence Management and Inclusion Behaviors

· Excellent skills using IT applications to organize and analyze data

· Embraces, practices, and exemplifies the principles and capabilities outlined in the Merck Leadership Behaviors

· Excellent facilitation, consultation ,and Influence skills including experience with outsourced service providers

· Demonstrated ability to interact and communicate with all levels of business leadership and operational teams.

· Demonstrated ability to lead multiple diverse resources and establish training and development plans.

Demonstrated ability to think strategically

*LI-EMI

Job
: Business Consulting

Primary Location: IE-Leinster-Dublin
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-AMS-Solution%2C-Verification-&-Test-Service-Lead-EMEA-Job/1851264/185126418512642012-06-15Merck/MSDBusiness Consultingfull-timeUSDstarting0BSDublin, Leinster, IE
Description

Afdeling

Process Development and Commercialization (PDC). De afdeling is verantwoordelijke voor de late fase van de ontwikkeling van het manufacturing process (kweek en zuivering) van biological drug substances (o.a. process karakterisatie en kwalificatie, productie van grondstof voor fase 3 kliniek). Daarnaast is PDC verantwoordelijk voor de introductie van het process in de commerciële fase (o.a opschaling, schrijven van registratie documentatie, beantwoorden van vragen health authorities).

De Functie

Hoofdtaken van de Biotechnologisch Lab.assistent zijn:

• In-transferreren en opschalen van ontwikkelde celkweekprocessen gevolgd door een overdracht naar large scale manufacturing manufacturing en technical operations.

• Betrokken zijn bij Process Performance Qualification op grote schaal.

• Karakterisatie van celkweekprocessen door middle van Design of Experiments als onderdeel van procesvalidatie (Quality by Design)

• Participeren in het opzetten van analytiek voor in-process analysis relevant voor celkweekprocessen

Je bent verantwoordelijk voor:

• Opstellen werkplan middels productieplanning en rapportage van resultaten (Report)

• Zefstandig uitvoeren van celkweekprocessen, verwerken en interpreteren van resultaten

• Opzetten analytiek (in overleg met andere afdelingen)

• Uitvoeren van werkzaamheden volgens GMP en EHS-richtlijnen

Qualifications

Wij vragen

• HBO met voor voor celkweek relevante opleidingen en ervaring

• Goede communicatieve eigenschappen voor samenwerking in multi-disciplinaire teams

• Zelfstandig kunnen werken.

• "Out of the box" denkvermogen

• Goede kennis van Engelse taal in woord en geschrift

• Kennis van statistiek is gewenst

• Kennis van Quality by Design principles is gewenst

• Deelname aan weekend- en semafoondienst

• Percentage in dienst 100

We bieden

Houd je ervan te worden uitgedaagd, steeds weer, dan is MSD een goede keuze als werkgever. We hebben uitstekende arbeidsvoorwaarden en je krijgt er alle mogelijkheden om je verder te ontwikkelen en door te groeien. MSD geeft je veel ruimte voor eigen initiatief en je krijgt veel verantwoordelijkheid.

Contact

Voor meer informatie over de functie kun je contact opnemen met Wout van Grunsven, Section Head PDC; 0412 66 1251

Job
: Lab Technician

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-1ste-Biotechnologisch-Laboratorium-Assistent-Job-NB/1853554/185355418535542012-06-15Merck/MSDLab Technicianfull-timeUSDstarting0BSOss, NB, NL
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Quality Manager will provide leadership for the following Site Quality Unit functions:

Incoming Quality, In-Process Quality, Supplier Quality, CAPA/DV. This role will also manage approx. 4 direct reports and 13 indirect reports, and will itself report up to the Site Quality Director. Other major functions will include, but are not limited to......

Manage Quality Systems designed to achieve compliance with FDA Regulations (21 CFR Parts 210/211 Drug, 21 CFR Part 820 Medical Device) as well as ISO 13485 for Medical Device, other applicable international regulations, and the Merck Quality Manual.

Serve as Management Representative for Medical Devices per 820.20(b)(3) and ISO 13485. Participate in Design Control, ISO 14971 Risk Assessment, and CE Mark as medical device SQU.

Incoming Quality tasks: (approximately 20%)

NOE, SOP, disposition forms, TI, protocol, technician issues, CDR, QCR, quality assessments

In-Process Quality tasks: (approximately 30%)

NOE, SOP, remediation protocols, qualification & PKV protocols, TI, disposition forms, MPR, SWO, technician issues, QCR, scrap forms, complaint investigations, conditional use forms, quality assessments, IPT support as Quality Center of Excellence

CAPA tasks: (approximately 30%)

review investigations, verify CAPA, interim reports, monthly metrics

General SQU tasks: (approximately 20%)

Medical device management representative, equipment & instrument forms, site layout, training forms, PMP & Development, expense reports, company store orders, system access forms, , behavior coaching consequence management, MRB, SQU Support as backup for LIR / APR / Validations, review monthly IPQO audits

Qualifications

Education:

Bachelor's degree in science, engineering, or related areas of study.

Required:

At least 3 years of prior experience managing Quality related manufacturing functions.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition QUA002914.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Qual Assurance & Ops Generic

Primary Location: US-TN-Cleveland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Cleveland-Mgr-Qual-Operns-Job-TN-37311/1853562/185356218535622012-06-15Merck/MSDQual Assurance & Ops Genericfull-timeUSDstarting0BSCleveland, TN, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Chemist I is a position within Analytical Services, Quality Operations responsible for providing laboratory testing of samples for quality disposition in support of manufacturing operations, product supply chain, and post-market stability.

The Chemist I, based on assignment, may also be responsible for instrument operation, logging of samples and data review. Additional responsibilities include; performing calibrations & preventive maintenance of lab equipment, training others as needed, participating in laboratory investigations, writing / revising SOPs and test procedures.

Administration: (approximate time spent - 25%)

Documents all work in accordance with site procedures and reviews documentation of others to provide test article disposition. Writes / revises lab SOPs. Provides SOP training.

Laboratory Operations / Testing: (approximate time spent - 75% )

Operates analytical instrumentation as needed to support testing. Prepares laboratory samples for instrumental analysis. Assists in laboratory investigations.

Qualifications

Education:

Bachelor's degree in science, engineering, or related areas of study.

Required:

At least 3 years of work experience in a Quality Control Laboratory setting.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition QUA002898.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality Operations

Primary Location: US-TN-Cleveland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Cleveland-Chemist-I-Job-TN-37311/1853563/185356318535632012-06-15Merck/MSDQuality Operationsfull-timeUSDstarting0BSCleveland, TN, US
Description

Department

Analytical Development and Validation (ADV) is a scientific Center of Excellence responsible for advanced analytical characterization of protein products. Over 60 highly trained professionals support development of commercial manufacturing processes, develop and validate quality control assays and perform complex analytical characterization and trouble-shooting. The in-depth expertise on analyses of proteins is crucial to the MSD network and is truly unique in the Netherlands.



You will implement develop and execute highly advanced characterization techniques for proteins products, including light scattering methods and analytical ultracentrifugation. You will use these techniques to support development of commercial manufacturing processes and to prove validity of QC assays. You will act as a technical lead in protein characterization, deliver technical reports for regulatory purposes and provide (trouble-shooting) support worldwide.

Qualifications

Desired Skills & Experience

You are a PhD in pharmaceutical, biochemical or biophysical sciences with expert knowledge in characterization of proteins. Demonstrated ability to independently plan and execute tasks. Strong results orientation, can-do mentality, excellent interpersonal/communication skills and fluent in English.

Information

For more information on the position please contact John den Engelsman, Section Head ADV; 0412 66 9881

Job
: Lab Technician

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Analytical-Scientist-%28non-GMP%29-Job-NB/1855912/185591218559122012-06-15Merck/MSDLab Technicianfull-timeUSDstarting0BSOss, NB, NL
Description

Overview

The core mission of this role is to anticipate, manage, and respond on key business issues as they are impacted by government policies and industry trends. As such, the successful candidate will be the face of MSD Mexico with relevant industry and government agencies.

The candidate's main responsibility is to ensure alignment with corporate guidelines and procedures, and to provide direction, coordinating and overseeing planning and execution of public and external affairs strategies and programs by the subsidiary, helping create a favorable environment in which the policy agenda can be carried out, marketing objectives can be achieved, company reputation can be enhanced, and risks are anticipated and adequately mitigated. This will be achieved through interaction with relevant industry associations, government officials and policy makers, and other external groups in the country

Essential Function

1. Represent and advocate on behalf of MSD Mexico with local institutions on key policy issues areas impacting the business in the country, as well as its reputation. Manage crises and politically-sensitive issues.

2. Manage and coordinate the external affairs activities of the Mexican subsidiary, including its participation in relevant industry associations, its philanthropic and corporate-responsibility initiatives, and efforts to strengthen or preserve the company's reputation amongst key stakeholders and the general public.

3. Along with other corporate fuctions, establish and execute market access plans for new and existing products in their policy-sensitive and regulatory aspects.

4. Assess political and policy-related risks and opportunities in the country and propose strategies to deal adequately with such matters.

5. Work with the local Executive Committee to develop long-term, evidence-based strategic external affairs plans for each policy product that will enable MSD Mexico to communicate the right messages to the right audiences and influence outside constituencies in a way that will move forward the subsidiary's policy agenda and help shape the external environment.

Qualifications

*Bachelors Political Science, Economics, Health Sciences, Business Administration, Marketing, Finance Required

*Masters Desired

Skills/Knowledge

* Strong analytical skills, especially on policy and political analysis

* Strong focus on execution and a proven record of working efficiently as part of complex teams

* Sophisticated understanding of the Mexican political landscape

* Excellent communication and writing skills, ability to craft sensitive advocacy messages

* Good experience in complex negotiations, negotiating with hostile stakeholders under pressure

* Basic project management skills and understanding of financial concepts

* Well-developed interpersonal skills with experience in interacting with colleagues and external stakeholders at various levels are required

Minimum Experience Required/Preferred

A minimum of 7 years of relevant experience in government affairs, policy analysis, political or business-government negotiations, crisis management.

Some experience with corporate reponsability initiatives and philanthropy
Should have experience interacting with wide range of external stakeholders, as well as demonstrable good access to key governmental authorities and institutions. Familiarity with NGOs and opinion leaders would be desirable.

*LI-KL1

Job
: Global Policy/Communications Generic

Primary Location: MX-Distrito Federal-Álvaro Obregón
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/%C3%81lvaro-Obreg%C3%B3n-External-Affairs-Manager-Job/1868782/186878218687822012-06-15Merck/MSDGlobal Policy/Communications Genericfull-timeUSDstarting0BSÁlvaro Obregón, Distrito Federal, MX
Description

The Emerging Markets Operations Director reports to the Senior Director, Emerging Markets Planning and Execution, who in turn reports to the President of the Emerging Markets Region. The Emerging Markets Region accounts for approximately 18% of overall Merck Pharmaceutical and Vaccine sales, and is comprised of over 100 countries spanning Latin America, Asia Pacific, Eastern Europe, the Middle East, and Africa.

Responsibilities include, but are not limited to:

· Supports Regional President with development of business update presentations, working closely with regional leaders and key functions, i.e. communications, finance, HR and Country Leadership;

· Coordinates review of overall operational performance through the management and tracking of key performance indicators (scorecard, budget, 5 year plan);

· Serves as the primary point of contact for the planning and management of the regional calendar;

· Coordinates country visits / business reviews, senior management visits and key internal meetings such as Emerging Markets Leadership Team (EMLT) meetings;

· Establishes the structure, governance, oversight and control necessary to manage key regional initiatives in an integrated way.

· Identifies opportunities to simplify processes and activties.

· As needed, directly leads or supports key initiatives by shaping project charters, gathering and analyzing data, and implementing solutions.

· Maintains and continuously improves the Emerging Markets Teamsite, ensuring that relevant and up to date information is readily accessible to all relevant parties.

Qualifications

Qualifications

· Experience in marketing / sales or finance.

Education

· Master's Degree.

Personal Characteristics

· Motivation/drive for result

· Excellent communication skills

· Ability to operate in matrix environment

· Customer-centric thinking

· Entrepreneurship - willing to take reasonable risks (to improve business)

· Interpersonal skills - excellent collaborator and easy to get along with

· Willing to travel

· Optimistic and Passionate

· Open to feedback & learning

Desired

· Experience in multiple geographies

· Knowledge of 1 Emerging Markets Language beyond English

· Deep understanding of cultures in the Emerging Markets

· Experience with project management / continuous improvement / scorecard methodologies.

Expertise in power point and in building clear and impactful business presentations.

*LI-DR1

Job
: Strategic Planning

Primary Location: CH-LU-Luzern
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Luzern-Operations-Director%2C-Emerging-Markets-Job-LU/1871156/187115618711562012-06-15Merck/MSDStrategic Planningfull-timeUSDstarting0BSLuzern, LU, CH
Description

Establishes and maintains the planning systems and methodologies using SAP and other planning tools

Manages daily to monthly finite supply planning and execution schedule for IPT team activities.

Completes "what-if" scenarios in support of unplanned adjustments to schedules or changes in demand, to facilitate early impact assessment of planned and unplanned changes.

Updates the visual factory board based on demand changes and complete work order assignment against the forecasts, to identify special requirements prior to release and/or manufacturing.

Participates as a member of the IPT group.

Supports continuous improvements initiatives to eliminate waste in supply, production and planning processes using continuous improvement methodologies such as Lean Six Sigma.

Continuously uses best practice methodologies and lean production principles.

Creates and maintains batch work orders in SAP to support the generation of production schedules for the Plant.

Qualifications

Relevant third level qualification required (science, engineering or other technical field preferred) OR minimum, with 5-10 years related technical industry experience required.

* Five years experience in the biotech / pharmaceutical GMP industry.
* Experience in high speed manufacturing environment an advantage.
* Experience with HVAC, Autoclaves, SIP/CIP, Formulation an advantage.
* Experience of six sigma and lean methology.
* Applicant should have previously demonstrated strong team and communication skills, flexibility, motivation, ability to project.
* Applicants should actively support, participate and embrace an empowered team culture and have excellent communication skills

Job
: Production Planning & Control

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Carlow-Production-Finite-Scheduler-Job-L/1705735/170573517057352012-06-15Merck/MSDProduction Planning & Controlfull-timeUSDstarting0BSCarlow, Leinster, IE
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

PROPOSITO GENERAL DE LA POSICION:

Este Puesto es responsable en el inicio, desarrollo, implementación, diseño y control de planes de mercadeo, material promocional de distribución, y desarrollo de campañas publicitarias, con el fin de promover y distribuir con éxito sus productos o franquicias en la Región, siguiendo los lineamientos y programas de la Casa Matriz, y aprobación del Gerente de Franquicia de la Unidad de Especialidades respectivo.

La función también implica dar soporte y asesoría al Gerente de Franquicia en todas sus funciones relacionadas con el mercadeo y distribución de los productos de su portafolio, lo cual implica involucrarse en temas relacionados con ventas, coordinación y difusión de las estrategias de los productos o franquicias a su cargo, ejercer liderazgo con el equipo de ventas y participar en las decisiones claves de la Unidad.

RESPONSABILIDADES Y FUNCIONES:

- Capaz de coordinar la ejecución de los Planes Estratégicos y Tácticos de la Unidad de Especialidades a través de la fuerza de venta en la región CARD.
- Persona a cargo de la confección de los Planes de Mercadeo de los Core Product de la Unidad de Especialidades
- A cargo de coordinar las reuniones con el Centro de Excelencia para seleccionar y someter los materiales promocionales de acuerdo a las SOP para el sometimiento y aprobación de materiales promocionales.
- A cargo del desarrollo y ejecución de Programas Estratégicos para garantizar los resultados de los Core Poducts.
- Manejo de datos de IMS (Market Share, Índice de Evolución, Market Dynamics e indicadores de Epidemiológicos), para utilizarlos en el análisis y herramientas de toma de decisiones
- Manejo organizado del Forecast de productos de la Unidad de Especialidades en conjunto con el departamento de Demanding Planning.
- Amplio conocimiento y manejo del negocio hospitalario/Institucional (Licitaciones, Análisis de Pliego, Estrategias de Precio, competidores, departamento de compras, inclusiones de productos en los comités de Farmacoterapia etc.)
- Manejo y coordinación en el Lanzamientos de Productos al Mercado de Gubernamental/ Institucional
- Capacidad de Tabular e interpretar datos epidemiológicos de la Enfermedad para establecer planes de acciones específicos con los Core Products
- Manejo y optimización del presupuesto de la Unidad de Especialidades ( P&L, Materiales promocionales, Actividades, Congresos, Patrocinios)
- Manejo de paquete de Office ( Power Point, Excell, Word, y opcional conocimiento de programas diseño de artes)
- Coordinación efectiva con los departamentos de soporte (Regulatorio, Medical, Finanzas, Demand Planning, Market Access etc.)
- Dar soporte efectivo a la fuerza de ventas (Coaching, entrenamiento, políticas etc)
- Participar en programas regionales de entrenamiento ( Marketing, Train the Trainer, Summit y Simposios)
- Establecer un enlace efectivo de comunicación con el Líder de Mercadeo Regional para alinear la estrategia regional y adaptarla la estrategia local.
- Participar en reuniones periódicas con el Gerente de Unidad de Negocio/Franquicia para brindar informes del desempeño de la línea de producto a su cargo.

Cualificaciones
REQUERIMIENTOS ACADEMICOS / EXPERIENCIA:

Escolaridad: Profesional de las Ciencias de la Salud ( Farmacéutico, Médico)

Especialidad: Grado académico demostrable y preferible Estudios de Mercadeo.

Lenguajes: Ingles - español (bilingüe)

Experiencia: Experiencia amplia en el manejo de Productos de Especialidades o Productos Hospitalarios entre 2 a 5 años.

Habilidades o Conocimientos adicionales:

- Conocimiento profundo de la línea de Productos de Especialidades para trasmitir los conocimientos a la fuerza de ventas
- Capacidad demostrada de Negociación con los Comités de Farmacoterapia, Lideres de Opinión, Comités de Compra, ONG y Programas Nacionales de HIV.
- Capacidad demostrada para la Creación y Ejecución de las Estrategias de la Unidad de Especialidades orientadas a médicos especialistas
- Persona orientada al cumplimiento de los objetivos y mostrar un alto desempeño
- Pro-activo, dinámico, orientado a brindar coaching y Capacidad de Liderazgo

*LI-KT1

Puesto
: Gestion de productos

Ubicación principal: PA-Panamá-Panamá
Tipo de acuerdo laboral: Fijo(a)
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Panam%C3%A1-Gerente-de-Producto-de-Especialidades-Job/1784419/178441917844192012-06-15Merck/MSDGestion de productosfull-timeUSDstarting0BSPanamá, Panamá, PA
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Cleveland site is located on 60 acres in the foothills of the Smokey Mountains. The site's mission is to be the primary plant for the support of the Consumer Healthcare business. Cleveland manufactures high-volume liquids, ointments, creams, aerosols, bag-on-valve products, cosmetics and medical devices. It also manufactures tablet blister packages.

The Sr. Technician II is a position within Analytical Services, Quality Operations responsible for providing laboratory testing of samples for quality disposition in support of manufacturing operations, product supply chain, and post-market stability. The Sr. Technician II, based on assignment, may also be responsible for logging of samples, performing calibrations & preventive maintenance of lab equipment, training others as needed, participating in laboratory investigations, writing / revising SOPs.

Administration: (approximate time spent - 25%)

Documents all work in accordance with site procedures and reviews documentation of others to provide test article disposition. Writes / revises lab SOPs. Provides SOP training.

Laboratory Operations / Testing: (approximate time spent - 75% )
Performs organoleptics and physical testing of laboratory samples. Prepares laboratory samples for instrumental analysis. Prepares laboratory standards and solutions. Assists in laboratory investigations.

Qualifications

Education Minimum Requirement: Bachelor's degree in related area preferred, two years college in related area.

Required Experience and Skills - 3 years relevant QC laboratory experience. effective communication & writing skills. Applies knowledge of cGMP regulations and audit practices and standards as pertaining to laboratory controls. Strong multi-tasking skills are required.

Preferred Experience and Skills - Experience in the calibration and maintenance of laboratory equipment.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # QUA002564.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality Operations

Primary Location: US-TN-Cleveland
Employee Status: Regular
Number of Openings: 3

Hazardous Materials
: Laboratory reagents]]>http://jobs.merck.com/job/Cleveland-Sr_-Technician-II-Job-TN-37311/1356401/135640113564012012-06-15Merck/MSDQuality Operationsfull-timeUSDstarting0BSCleveland, TN, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Stability Technician will ensure stability samples are properly collected and entered into the Post-Market Stability program. Additionally, this position is responsible for the daily monitoring of stability chambers and pulling of samples for stability interval testing. Major functions of this role include, but are not limited to.....

* monitors production to ensure open stability requests are filled,
* manages receipt and staging of stability samples,
* performs routine monitoring of stability chambers,
* pulls stability samples for interval testing per approved protocols,
* participates in stability study initiation,
* executes annual retain review,
* participates in stability chamber inventory audits and maintenance following established procedures in a FDA regulated QC analytical chemistry laboratory.

The Stability Technician is responsible for completion of all required training and maintaining training requirements. Additionally, the Stability Technician is responsible for adherence to site documentation practices and timely completion of laboratory assignments.

Qualifications

Required:

At least two years of post-secondary education in science, engineering, or related field of study.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # QUA002913.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Qual Assurance & Ops Generic

Primary Location: US-TN-Cleveland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Cleveland-Stability-Technician-Job-TN-37311/1862521/186252118625212012-06-15Merck/MSDQual Assurance & Ops Genericfull-timeUSDstarting0BSCleveland, TN, US
Description

This position will report to the RtR Manager of the EMEA Shared Business Services Centre. Responsibilities will include:

* The provision of accounting services to the EMEA region including transaction processing, general accounting and reporting
* Monthly and quarterly close in accordance with strict reporting deadlines
* Establishing and standardizing policies and procedures to drive efficiency and improved business productivity
* Implementing policies, operational controls and procedures to ensure efficient and accurate services to customers in EMEA
* Assistance with recruitment & development of a high performance team
* Working with internal and external auditors to complete statutory & internal control audits
* Maintenance of KPI's & metrics
* Transition of accounting processes to the SBS Centre and to SAP
* Budgeting & forecasting
* Ad hoc projects

Qualifications

Qualifications:

Required:

* Qualified Accountant with a minimum of 6 years relevant work experience
* Experience in the finance/accounting shared services department of a multinational company
* Effective people manager with focus on teamwork and collaboration
* Experience with SAP/ERP systems
* Experience in dealing with internal and external auditors (in a SOX environment)
* Change/project management experience
* Must be able to work in a fast-paced, dynamic environment, under pressure, and with a high degree of professionalism
* Must be comfortable in an environment of changing technologies and processes and demonstrate flexibility in adjusting to new ways of working
* Excellent problem/resolution skills and an understanding of when, how, and where to escalate cases as required to meet defined service levels
* High degree of integrity and personal ethics in implementing corporate policies and procedures

Education Requirements: Bachelors Degree in Finance or Accounting and Accounting qualification

Job
: Treasury Operations

Primary Location: IE-Leinster-Dublin
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Accounting-Manager-Job-L/1510510/151051015105102012-06-15Merck/MSDTreasury Operationsfull-timeUSDstarting0BSDublin, Leinster, IE
Description

The Improvement Engineer will be responsible for supporting process and equipment investigations and troubleshooting issues.

Will complete Improvement projects for the IPT and participate in Site Kaizen activities on behalf of IPT.

The Improvement Engineer will also collaborate with other IPT members and members from other departments (Quality, Technical Operations, Environmental Health and Safety) in completion of the tasks above.

Key Responsabilities:

1. Change Controls Generation & Closeout

2. Completing Process Safety Risk Assessments and Action Item Closeout

3. Completing Process and Equipment FMEA and Action Item Closeout

4. Troubleshooting and investigation of Process related issues using Lean Six Sigma Tools

5. Lead Kaizen activities for IPT on Processes and Systems

6. Participate in Kaizen activities (EHS, Quality etc.) across the site on behalf of IPT

7. Work under the guidance of site LSS Engineers and Operations coach to apply lean tools to process data in order to complete process improvements (e.g. SPC, SMED and standardised work etc.)

8. Work with validation, maintenance and production operators in investigation of equipment performance issues.

9. Assist with 5S, and TPS implementation in the IPT.

10. Participate in HAZOP's on behalf of IPT and develop to lead HAZOP's if required.

11. Complete review and approval of technical documentation incl. Automation Change Controls, Automation Detailed design documents, Validation Protocols and Site Standard Operating Procedures as required.

12. Lead Root Cause investigations for Equipment and Process issues and incidents.

Qualifications

* Primary Degree in Engineering or Science disciplines preferred.
* 2-3 yrs experience in GMP production environment (Operations/Engineering) is required.
* Experience in Buffer Prep, Component Prep, Formulation/Fill equipment, PLC /DCS systems or Isolator technology considered an advantage.
* Lean qualification and experience desirable but not essential.
* Strong technical skills are required.
* Strong teamwork and communication skills essential.
* Ability to support a portfolio of initiatives and serve multiple internal customers is required.

Job
: Manuf./Operations Generic

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Carlow-Improvement-Engineer-Job-L/1538425/153842515384252012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSCarlow, Leinster, IE
Description

The Medical Science Liaison is part of the country Medical Department. Key interactions are with the Brand and Customer Managers, Commercial Managers, the Specialist Sales Forces and Key Account Managers.

Overall

• Serve as the country scientific expert for the assigned franchise(s) under the guidance of a Medical Advisor

• Visit on a regular base defined customers and convey information about the latest development in the assigned indication (e.g. most actual publications, etc.)

• (Develop and) execute Medical Affairs Plan

Scientific Leadership

• Interact with Scientific Leaders (SL's)/specialists and provide extra support to sales force for assigned products

• Develop and maintain strong scientific network

• Develop projects with SL and other stakeholders to facilitate adoption of best medical practices for physicians, health care institutions and patients

• Organize and participate on local advisory boards

• Hold balanced and scientific presentations about the disease area, therapies and latest developments in context with assigned products and competitors

• Collect customer needs from SLs and provide to Customer & Disease Understanding Manager locally

• Participate at national and international scientific meetings to apply newest knowledge and feed-back to relevant stakeholders

• Support the SL in development and execution of IISPs

• Support local clinical research operations (suggestions for investigators, objectives, design, sites, studies)

• Support the development of protocols for local and non-interventional studies

• Reinforce the scientific and evidence-based medicine oriented image of the company

Internal Support

• Provide scientific support to achieve marketing/strategic objectives

• Facilitate the inclusion of Merck products in hospital formularies and in local Therapeutic Guidelines

• Participate in strategic defence of Merck products with key decisions makers

Medical Information Requests

• Respond to medical inquiries from local customers not covered by the medical information group/ developed by global or regional

Medical Review

• Limited review of regionally developed materials to ensure compliance with local legal regulations, to customized local materials and to locally developed customer materials

Sales Training Support

• Provide sales reps with information on new studies, competitors, issues

Train reps in all medical aspects of the franchise

Qualifications

Skills

· Excellent communication and people skills

· Ability to work in a very scientific context and to communicate in a very clear and simple way if needed

· Solid knowledge of disease area and therapies, preferably immunologyAbility to work in a matrix organization

· Fluency in English and French or German

· PC (MS office, Internet search engines)

Education & Experience

University degree from accredited university in medical, pharmaceutical or biological science

*LI-DR1

Job
: Marketing

Primary Location: CH-LU-Luzern
Employee Status: Regular

Travel
: Yes, 75% of the time
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-Medical-Science-Liaison-Job-LU/1842909/184290918429092012-06-15Merck/MSDMarketingfull-timeUSDstarting0BSLuzern, LU, CH
Description

Biostatistics and Research Decision Sciences (BARDS) scientists provide global support across all divisions of Merck spanning product discovery through manufacturing and marketing. The BARDS organization is comprised of various functional areas such as statistics, statistical programming, epidemiology and health economics. BARDS-Oss is part of the European region within the global BARDS network and add valuable expertise and experience that will support the regional vision of BARDS. Working with state of the art technologies, exciting new drugs and in a global multidisciplinary setting, you will enjoy the challenges of applying your quantitative expertise as a member of a multidisciplinary team in Oss.

Your tasks:

* Develop and manage epidemiological studies to support products in development and marketed products as needed
* Provide epidemiological support in company discussions about development and safety issues of company products
* Screen scientific literature, evaluate and write reports or publications on (pharmaco)-epidemiological information relevant to the safety of the product or general disease epidemiology of the therapeutic area supported
* Statistical and/or epidemiological evaluation of data from epidemiological databases
* Critically evaluate the adequacy of clinical trial endpoint validation, especially patient-reported outcomes or novel endpoints intended to support labeling, and develop strategic plan for validation of endpoints as needed to support clinical development.

Qualifications

* Medical Degree (MD) or University Degree (WO) in Paramedic and minimum of two years of relevant (pharmaco)epidemiological experience
* Education in Epidemiology (preferably PhD/Epidemiologist level B)
* Broad understanding of global regulatory requirements for epidemiology
* Understanding of fundamental principles of biostatistics, epidemiology, human biology, and basic medical sciences
* Knowledge of health care delivery systems and health care databases
* Ability to innovate
* Sense of urgency, ability to multitask and work under pressure
* Demonstrated team player and able to collaborate with experts and maintain network with peers
* Excellent written and oral communication in English, interpersonal & influencing skills

More information: Egbert Biesheuvel +31 412 663922, egbert.biesheuvel@merck.com or Julie Chandler +1 267 305 7574 julie.chandler@merck.com

Job
: Automation and Maintenance

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 3]]>http://jobs.merck.com/job/Oss-Epidemiologist-Job-NB/1881757/188175718817572012-06-15Merck/MSDAutomation and Maintenancefull-timeUSDstarting0BSOss, NB, NL
Descripción
El Gerente Asociado del Centro de Procesamiento de Datos de Farmacovigiláncia es responsable por garantizar el oportuno cumplimiento de los procesos del Centro de Procesamiento de datos dentro de lo tiempos estipulados y con la calidad esperada y por orientar al equipo a cargo en el proceso de revisión, análisis y procesamiento de información clínica relacionada con el reporte de eventos adversos. Adicionalmente es responsable por la orientación, desarrollo y supervisión del grupo de Coordinación de Datos de Farmacovigilancia a su cargo y participa en el desarrollo de nuevos proyectos: Interacción entre grupos funcionales del GTM.

RESPONSABILIDADES PRINCIPALES:

- Responsable por asegurar el cumplimiento de tiempos indicados por la Agencia Regulatoria en el reporte de eventos adversos. Ejecución de reportes para su envío a la casa Matriz y Agencia Regulatoria. Esto incluye revisión de documentos antes de someterlo. Esta persona es responsable por asegurar los procesos previos a las inspecciones regulatorias. Conocimiento del proceso de auditoria, seguimiento de documentos requeridos.
- Revisión de datos clínicos antes del procesamiento de los casos. Brindar soporte en entrenamiento técnico al grupo en caso de requerirlo. Participación en actividades tanto locales como regionales. Interacción constante con Gerentes de otros- Data Management Center y grupos de casa Matriz, que forman parte del proyecto de Fármaco Vigilancia. Trabajo conjunto en la optimización de procesos e identificación de necesidades de entrenamiento.
- Manejo de Indicadores de Gestión. Análisis de resultados de Gestión. Administración de la carga de trabajo del personal que le reporta para lograr el cumplimiento de los tiempos deseados con la calidad esperada.
- En concordancia con las guías de manejo de datos y las buenas prácticas clínicas (GCP, ICH), realiza la supervisión del proceso de manejo de datos.Atención y soporte a los clientes externos a través de la retroalimentación de los resultados.
- Desarrollo de personal: seguimiento y manejo de procesos como Evaluacíón de Desempeño, Plan de Desarrollo Personal. Supervisión y acompañamiento en el proceso de desarrollo del grupo a su cargo.

Cualificaciones
- Profesional en Medicina .
- Experiencia mínima de 1 año en cargos afines o investigación clínica preferiblemente .
- Liderazgo en manejo de proyectos y equipos.
- Excelente manejo de relaciones interpersonales de todo nivel.
- Comunicación de alto impacto.
- Avanzado desarrollo en Planeación, Organización y Análisis.
- Alto nivel de ingles.
- Habilidades para trabajar en equipo y orientación a la calidad

Puesto
: Administración de datos clínicos

Ubicación principal: CO-Distrito Capital de Bogotá-Bogotá
Tipo de acuerdo laboral: Fijo(a)
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Bogot%C3%A1-Gerente-Asociado-del-Centro-de-Datos-de-Farmacovigilancia-Job/1783345/178334517833452012-06-15Merck/MSDAdministración de datos clínicosfull-timeUSDstarting0BSBogotá, Distrito Capital de Bogotá, CO
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview:

The incumbent will provide feedback on bills of material, labor routings, and demonstrated capacity issues to Manufacturing Management to collaborate as owners of accountability for achieving, maintaining, and continuous improvement of labor routing 95 - 100% metric performance and bill of material 98-100% metric performance.

Additional responsibilities are as follows:

* Read work order and job specifications to determine prescribed setup and equipment operation.
* Print forms from shared drive.
* Operate/manage production line machinery (depending on complexity).
* Pull and deliver samples to lab per SOP.
* Obtain written approval for test specimen from lab.
* Schedule line rotations.
* Printing/verifying case labels.
* Perform and document attribute checks for product quality during product inspection.
* Determine and document line efficiencies.
* Demonstrate efficiency in use of time keeping system.
* Demonstrate efficiency in use of statistical software.
* Control charting (SPC) - data collection.

Please note: Position could be either 1st, 2nd or 3rd shift. Also, willingness/ability to work off-shift is preferred.

Qualifications

Educational requirements:

* High School Diploma or Equivalent.

Required skills and Experience:

* Prior manufacturing experience, fluency in computer usage.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PRO008965.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Production / Operator

Primary Location: US-TN-Cleveland
Employee Status: Regular

Travel
: No
Number of Openings: 10

Shift (if applicable)
: 2nd

Hazardous Materials
: Aerosol and Alcohol-based products]]>http://jobs.merck.com/job/Cleveland-Operator-I-Job-TN-37311/1473786/147378614737862012-06-15Merck/MSDProduction / Operatorfull-timeUSDstarting0BSCleveland, TN, US
Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.




The Associate Data Coordinator (Pharmacovigilance) applies data management expertise and computer skills in support of the Pharmacovigilance operation in Data Management Center.

The incumbent is responsible for the following: analyzing, triaging, processing and ting to HQ, according to standard operating procedures and product guidelines, all adverse experience information received from investigational and marketed products for the further reporting to the FDA and/or other regulatory agencies by WPS.

He is responsible of performing all PV reporting activities appropriately including; tracking, reviewing, coding, and computer entry in order to accomplish the established targets of compliance, quality and productivity.

In addition, interacts effectively and works closely with people across functional areas within the organization and global customers.

Essencial Functions:

* Perform data entry of all adverse experience information received and release to HQ through internal data base within the timeframe. Make sure data quality and data consistency between source data and data entered in the database.
* By daily triaging, determines, on the basis of standard operating procedures and US FDA regulations, the prompt or periodic classification of each adverse experience contained in the reports received for Merck marketed and investigational products. Provides training/mentoring for new employees and serves as a resource for less experienced GDMS-PV.
* Participate on training activities for Pharmacovigilance GDMS as needed. Work on Certification process for all the different types of reports in the establish timeframe.
* Actively participate and ensure effective communications with involved WPS mentors to maintain consistency and an appropriate learning process.
* Communicate need for process re-evaluation and provide improvement suggestions to Data Management Center Pharmacovigilance management.

Qualifications

* Bachellor Degree - Medicine
* Experience in a hospital, data management or clinical research is preferred.
* Self motivated, excellent in work planning and time management.
* Excellent oral and written English skills (100%).
* Good computer skills.
* Good sense and awareness of regulations and policies.
* Able to work under the pressure, strong sense of responsibility and accountability.
* Adequate oral and written skills.
* Appropriate management of time and tasks organization.
* Team work abilities.
* Quality orientation
* Desirable experience in project management and good clinical practices regulations GCP and ICH.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. MSD's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

Job
: Clinical Data Management

Primary Location: CO-Distrito Capital de Bogotá-Bogotá
Employee Status: Temporary
Number of Openings: 1]]>http://jobs.merck.com/job/Bogot%C3%A1-Associate-Data-Coordinator-Pharmacovigilance-Job/1691724/169172416917242012-06-15Merck/MSDClinical Data Managementfull-timeUSDstarting0BSBogotá, Distrito Capital de Bogotá, CO
Description

Responsible for the development and implementation of real estate strategies and transactions on a global basis from conceptual scope of development through project execution and turnover. In the role of "business strategist", the incumbent will be involved in the acquisition, disposition and leasing of real estate assets for the Company, its divisions, subsidiaries and joint ventures. In addition, the position functions as a project manager providing critical leadership to multidisciplinary, internal alliance teams. Project assignments often involve complex, high profile, multimillion dollar facility and property requirements. The Portfolio Manager reports to the Director, Transactions & Portfolio Management, GRES. Achieve financial, strategic, and occupancy targets established by the Director of GRES in conjunctions with the business unit.

Participate annually with Merck Governance in the development of the Annual Strategic Plan for the portfolio.

Duties, Responsibilities, Activities:

* The focus of this position is portfolio management and client relationship management. The Portfolio Manager must provide the direction and leadership for all aspects of managing the regional portfolio for each assigned region, including Merck's "internal" team members and any outside consultants participating in supporting portfolio objectives. Develop regional Occupancy Plans and consolidate into a Business Plan each year with continuous updating
* The incumbent is expected to provide corporate real estate leadership and advisory on existing and new business development initiatives involving property acquisitions, dispositions, leasing and strategic planning. He/She ensures that all real estate issues are addressed to meet the customer's business goals, as well as compliance with company and department policies, standards and practices.
* Develop, in conjunction with FM leads an annual strategic financial plan including initiatives for cost savings.
* Prepare a budget and expenditure / income forecast on a cash basis by property, region portfolio.
* Prepare property, regional capital expenditure budgets annually.
* Develop innovative concepts for short and long term cost reductions & service improvements.
* Provide strategic advice including variance reports & benchmark data.
* The Portfolio Manager will have a high degree of interdependency in how they operate with other cross functional teams on a daily basis. They are responsible for establishing the broad parameters for how the business will operate within specific contractual boundaries.
* The position will be required to exercise judgment which will have organizational wide impacts. The position will be responsible for interacting directly with senior staff and operation personnel within Merck
* Demonstrated ability to lead, manage and influence business relationships in a positive direction including negotiation and successful conflict resolution.
* Proven capacity to successfully manage a business contact including ability to understand, interpret and respond to management, operational and financial information and trends.
* Experience in developing portfolio strategic plans and strategic occupancy plans.
* Demonstrated ability to manage budgets and provide timely and reliable management reports.
* The incumbent must understand the customer's business plan, identify key success factors, determine real estate requirements, conduct market studies, obtain proposals, prepare financial analyses of alternatives, establish the appropriate real estate strategy, execute the strategy, and negotiate the commercial contract or lease agreement. In addition, the incumbent must coordinate, as appropriate, the participation in each project of other stakeholder's technology. The incumbent will also interview, qualify and retain, as necessary, real estate consultants, agents and appraisers and supervise the contracting and reimbursement of their services.
* The incumbent is a seasoned business and real estate professional with extensive transactional experience and is the primary customer relationship manager for their assigned region. He/she is expected to establish and maintain "key" contacts and interfaces with internal stakeholders and external resources. The results achieved through the management of complex processes and a variety of internal and external resources are the key factors as opposed to the size of a directly supervised staff.
* Demonstrated ability to prioritize work with tight deadlines.
* Demonstrated capacity to deal with ambiguity and address complex problems within a changing work environment
* The incumbent is expected to access real estate industry trends, market information and the real estate organizations within "best practice" companies and leverage the information to continuously improve GRES strategies, responsiveness and deliverables.

Qualifications

Bachelor's degree required

A minimum of twelve (12) years experience within a variety of professional real estate organizations; a BA/BS Degree with formal training in planning, commercial or industrial real estate development, business or architecture; significant exposure to domestic and international real estate markets, and a proven record of success in both domestic and international real estate projects. In addition, the incumbent must possess excellent leadership/organizational skills and the ability to elicit confidence from senior management and other key stakeholders through the incumbent's knowledge and judgment. Excellent communication and negotiations skills are a prerequisite.

The position plays a key role in the procurement of cost effective facility resources on a global basis to support success of the business.

Decision Making: Describe the degree of empowerment or autonomy the position has to take action & make decisions

On a daily basis, the incumbent has a high degree of autonomy to make decisions and advance assignments within his/her sphere of responsibility.

Problem Solving: Describe the skills & knowledge required to identify, delineate & resolve problems

The incumbent must have the ability to analyze and interpret various business, real estate, finance and market data in support of facility and real estate projects.

Influence/Liaison: Describe the degree of influence/interaction this position has internally & externally

The position has a high degree of contact and interaction with both internal and external stakeholders and the potential to be highly influencial as the situation warrants.

THIS POSITION CAN BE BASED ANYWHERE IN EMEA.

Job
: Real Estate & Facil Generic

Primary Location: IE-Leinster-Dublin
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Dublin-Real-Estate-Regional-Portfolio-Manager-Job-L/1354335/135433513543352012-06-15Merck/MSDReal Estate & Facil Genericfull-timeUSDstarting0BSDublin, Leinster, IE
Descripción
Bajo la direccion del Director/Gerente de Farmacovigilancia, el Gerente de DMC es responsable por liderar parte de la operación del Centro de Dtos de Farmacovigilancia. Promueve y brinda soporte al desarrollo integral del staff bajo su supervisión a través de la revisión y evaluación de su plan de desempeño y principios de liderazgo. Así mismo, el o ella debe estimular la interacción dentro de MRL para alcanzar los objetivos en común.

Actividade principales:
1. Desarrollar el plan carrera para 2-15 reportes directos, asignar funciones, conducir la evaluación periodica de habilidades así como la valoración anual de desempeño, entrenamiento para el desempeño, proveer retroalimentación del actual desempeño, proveer premios y reconocimiento y estalecer prioridades.
2. Proveer oportunidades de desarrollo para los empleados, incluyendo asignaciones que impliquen reto de crecimiento. Desarrollar estrategias de promoción y sugerir promociones. Asegurar que los empleados reciban el entrenamiento y acompañamiento apropiado para ser exitosos en sus asignaciones.
3. Maximizar la efectividad del staff a través del trabajo con los empleados para asegurar un volumen de trabajo real que soporte valor agregado y balance vida-trabajo, calcular la duración y dificultad de las tareas y proyectos, anticipando y ajustando por obstaulos y retrazos y elevando la complejidad del asunto con el nivel gerencial apropiado.
4. Incrementar la efectividad funcional a través del soporte que brinda a los resultados del departamento, simplificando y estandarizando procedimientos, compartir buenas prácticas y liderar esfuerzos para mejorar continuamente.

Cualificaciones
Profesional graduado en Medicina, Enfermeria y/o carreras del área de la salud.
Experiencia mínima de 5 años en gerenciamiento de datos y supervisión de grupos de trabajo en CROs o dentro de la Industria Farmaceutica en estudios clinicos.
Excelente communicación oral y escrita en ingles.

Puesto
: Administración de datos clínicos

Ubicación principal: CO-Distrito Capital de Bogotá-Bogotá
Tipo de acuerdo laboral: Fijo(a)
Viajes: No
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Bogot%C3%A1-Gerente-del-Centro-de-Datos-Job/1855911/185591118559112012-06-15Merck/MSDAdministración de datos clínicosfull-timeUSDstarting0BSBogotá, Distrito Capital de Bogotá, CO
Description

The successful candidate will be part of the Operations team (Integrated Process Team-IPT) providing support to the filling processes at our Vaccines Formulation / Fill facility in MSD Carlow.

Key Responsibilities

* Responsible for detailed maintenance, calibrations, PMs and troubleshooting of manufacturing equipment.
* Initial activities will include developing standard operating procedures (SOPs), preventative maintenance (PMs) plans and calibration procedures as required to support start up of our facility.
* Routine Operations will include Troubleshooting and maintaining process instrumentation and equipment, perform root cause analysis on system failures and substandard equipment performance, using standard tools and methods, to resolve machine and system issues e.g. FMEA, Fishbone diagrams, 5 why's etc, all under aseptic/clean room conditions.
* In addition the successful candidate will operate the process equipment to support Operations activities.
* Responsible for delivery of training, maintaining housekeeping, and 5S in all areas while focusing on continuous process improvement using Lean Principles.

Key Experience

* Five years experience in the biotech / pharmaceutical GMP industry.
* Experience in high speed manufacturing environment an advantage.
* Experience with HVAC, Autoclaves, SIP/CIP, Formulation an advantage.
* Applicant should have previously demonstrated strong team skills, flexibility, motivation, ability to troubleshoot/problem solve, with a strong emphasis around safety and compliance practices.
* Applicants should actively support, participate and embrace an empowered team culture and have excellent communication skills

Qualifications

Education

* Time served apprenticeship in one of the following Mechanical, E&I or equivalent, diploma in Engineering or related discipline.

Job
: Production / Maintenance

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Bellmore-Maintenance-Facility-Maintenance-Technician-Job-NY/1703556/170355617035562012-06-15Merck/MSDProduction / Maintenancefull-timeUSDstarting0BSCarlow, Leinster, IE
Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


:

To be responsible for maintaining the General ledger, analysis of expense accounts as well as balance sheet accounts recommending accruals and adjustments as needed for two market operations. Review input of accounts payable and receivable. Manage intercompany, bank reconciliations and Fixed Asset operation. Review financial results with RtR Manager to ensure their understanding of the reported financial results.

MAIN RESPONSIBILITES:

* Perform Business accounting functions including preparation and analysis of monthly financial and management reports.
* Review for accuracy, completeness and input general ledger records weekly and monthly.
* Perform Ad Hoc financial analysis as assigned by Manager.
* Perform monthly expense and balance sheet account reconciliation and analysis for Market review.
* Identify, follow up and resolve accounts reconciliation with overdue/aged items.
* Work with the preparation of the monthly and quarterly financial reporting package and assist in audit requests as needed.
* Preparing work papers for audit and self assessments reviews.
* Coordinating and/or working on special projects as assigned by the Manager.
* Performing back-up functions for positions in the accounting department

Qualifications

Bachelor's Degree: (Accounting, Taxes, Audit, Finance or any other Finance related degrees). Master degree will be a plus.

6-10 years experience working as a accounting leader in Finance and accounting positions, supervising staff and delivering monthly/quarterly financial statements.

Language Skills: Fluent in Spanish and Intermediate to advanced in English. (Portuguese will be a plus).

Technical Skills:
Advanced knowledge in EXCEL (Macros, Pivot Tables), JDEdwards Experience.

Soft skills:
Customer focus mentality. Strong communication and collaboration skills are required to work with the Multicultural team.
Self Motivated, Proactive, Open Minded and able to manage pressure. Self Organization, Learning and Analysis capacity, Negotiation, Achievements orientation and Innovation
Multi tasking profile, teamwork oriented. Eager to learn and share knowledge with team.
Experience in leading a team.
Special attention to details.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. MSD's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

Job
: General Accounting

Primary Location: CL-Santiago Metropolitan Region-Santiago
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Santiago-Senior-Accountant-SBS-Job/1840110/184011018401102012-06-15Merck/MSDGeneral Accountingfull-timeUSDstarting0BSSantiago, CL
Description

Department

Process Development and Commercialization (PDC). The department is responsible for late stage development manufacturing process (cell culture en purification) van biological drug substances (process characterization and qualification, production of material for phase 3 clinical). Furthermore PDC is responsible for the introduction of the process in the commercial phase (amongst other things up-scaling, writing of registration documentation, answering of questions by health authorities).



Leads a team of associates on the transfer in, scale-up, and characterization of purification processes for therapeutic proteins, specifically monoclonal antibodies for late stage clinical supply, qualification and commercialization. Interfaces with early development, technical operations and manufacturing groups to facilitate a smooth knowledge transfer and utilizes advanced skills in QbD, DoE, PAT and data analysis, to drive characterization studies and CMC enabling documentation resulting in successful licensure across multiple regulatory agencies.

Participates and is the purification Subject Matter Expert in regulatory inspections and is experienced with the required GMP and regulatory guidelines. Initiates and manages 3rd party development activities, inclusive of Scopes of Work, and reviews and approves applicable protocols and reports. Identifies new technologies and works to implement these as new platforms with cross-functional early and late development teams

Qualifications

Desired Skills & Experience

PhD in biological sciences, Biochemistry, Biochemical Engineering, or equivalent with a minimum of 3-5 years relevant industry experience in developing protein purification processes for late-stage and commercial manufacturing

* Must have experience with tech transfer and characterization of late stage processes
* Proven leadership with a minimum of 1-2 years of supervisory experience
* Detailed knowledge of relevant regulatory and quality guidelines and GMP requirements, and experience with BLA/MAA submissions
* Clear and concise communication skills, both written and spoken
* Manages resources to accommodate multiple milestones in late clinical development and commercial characterization
* Demonstrates flexibility to accommodate change in directions or timelines
* Fosters collaborations across multiple groups for efficient utilization of resources in solving technically challenging problems
* Must have strong and effective organizational, people management and interpersonal skills
* Excellent analytical and technical skills are required along with demonstrated initiative and innovative thinking within a team environment
* Percentage in service 100

Contact

For more information on the position please contact Wout van Grunsven, Section Head PDC; 0412 66 1251

Job
: Project Management

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Project-Manager-Scientist-DSP-Development-Job-NB/1851271/185127118512712012-06-15Merck/MSDProject Managementfull-timeUSDstarting0BSOss, NB, NL
Description

MSD in Lucerne/Switzerland is a Swiss subsidiary of the successful global pharmaceutical company Merck & Co. Inc. with its headquarters in USA. Approx. 100'000 employees are currently working for us globally and we are showing strong growth.

Our Swiss operations include MSD International GmbH, Merck Sharp & Dohme-Chibret AG, Essex Chemie AG, Schering Plough Central East AG and Werthenstein BioPharma GmbH with currently 700 employees.

For our Shared Business Service Center in Lucerne we are currently looking to fill the position for a

Legal Director Middle East Region

In this role you will be based in Lucerne/Kriens, Switzerland, you will report to the Managing Counsel for EEMEA in Switzerland, and will be responsible for handling all legal matters in the Middle East and North/West Africa.

Key Responsibilities:

* Support of the Regional Managing Director for the Middle East (in Dubai, U.A.E) and his management teams in the region as well as the local teams in North/West Africa.
* Protect the legal interests of the company and its personnel. In particular you will ensure the company complies with all legislative requirements such as anti-corruption/ anti-bribery (including the U.S. Foreign Corrupt Practices Act), fair competition and antitrust legislations, local regulatory requirements, labor issues, privacy, etc., including any local business standards and industry regulations or codes.
* Risk management: The Legal Director will provide advice to the Compliance Officers and others supporting their role in routine monitoring of compliance across the company and will actively monitor potential legal issues.

Qualifications

We are looking for a qualified lawyer with at least 8 years PQE in-house experience in a multinational organization and/or with a private practice background in a top tier law firm as well as with experience from the territories in question.

The following skills and attributes are essential for the role:

· Ability to identify key issues and consistently apply a high standard of integrity, professionalism, legal knowledge, expertise and business ethics,

· Ability to provide commercially focused and value-added legal advice,

· Strong drafting and negotiation skills,

· Ability to design, implement and administer compliance programs and procedures.

· Very strong communication skills, both verbal and written,

· English, French (both written and spoken) and preferably Arabic,

· Ability to work autonomously as well as within a team environment,

· Ability to influence cross-functional teams and senior management in the business,

· Balance a practical "can do" attitude with appropriate management of risk and compliance with Legal and Company Policy requirements.

Candidates with a background in pharmaceuticals -in an in-house capacity or in private practice - - will be at an advantage, though candidates from other relevant sectors will be considered.

*LI-DR1

Job
: Legal Management & Operations

Primary Location: CH-LU-Luzern
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-Legal-Director-Job-LU/1889122/188912218891222012-06-15Merck/MSDLegal Management & Operationsfull-timeUSDstarting0BSLuzern, LU, CH
Beschreibung

Die Position, Hospital Sales Representative Anesthesia, ermöglicht dem Mitarbeiter eine, verantwortungsvolle und gestaltungsreiche Aufgabe innerhalb der neuen MSD-BU-Struktur Anästhesie Europa einzunehmen.

Der Mitarbeiter arbeitet mit einer hohen Eigenverantwortlichkeit und einem effizienten Gebietsmanagement unter besonderer Berücksichtigung der Marketing-Strategie. Dabei wird die Möglichkeit geboten, Projekte zu übernehmen und den Marketing/Sales Manager bei der Umsetzung und Konzeption zu unterstützen.

Die Aufgabe des Mitarbeiters ist es, die vorgegebenen Bridion-Verkaufsziele durch gezielte, kundenorientierte Aktivitäten zu erreichen. Dabei sind die klinischen Vorteile für den Kunden (Arzt, med. Mitarbeiter, Patienten, etc.) hervorzuheben und die ethischen Grundsätze von MSD einzuhalten.

Haupttätigkeiten:

* Sales und Marktanteil: Der Mitarbeiter steuert dazu bei, die vorgegebenen Verkaufszahlen und Marktanteile auf seinem/ihrem Gebiet zu erreichen. Dies geschieht dadurch, dass die Leistungsvorgaben der unten angeführten Aktivitäten zu 100% erfüllt werden.

* Produktbesprechung: Der Mitarbeiter implementiert Marketingstrategien durch Kundengespräche, welche sich auf den Patienten bzw. Therapie/Einsatz-Gebiete konzentrieren. Er/sie präsentiert Fakten, Vorteile und Limitierungen die auf den individuellen Gesprächspartner bzw. Gesprächsgruppen abgestimmt sind und welche die vermehrte Verschreibung innerhalb einer Indikation unterstützen. Jedes Kundengespräch hat eine erfolgsorientierte Zielsetzung. Diese Zielsetzung ist bestimmt durch frühere Gespräche, reflektiert die Verkaufs/Marketing-Strategie, spezifiziert die derzeitige Perspektive des Kunden, ein erwünschtes Resultat und Aktivitäten welche der Mitarbeiter unternehmen kann, um das erwünschte Ziel zu erreichen. Das Gespräch ist auf Fakten bezogen, gibt eine ausgewogene Perspektive von Vorteilen und Limitierungen (Kontraindikationen, gebotener Vorsicht) welche auf das besprochene Produkt und Patientenprofil abgestimmt sind. Alle Fakten sind durch bewilligte Evidenz (Klinische Studien, Diskussion Aids) unterstützt.

* Netzwerkpflege:
Mit externen Kunden (wie Ärztezielgruppen, Pflegepersonal, Spitalapotheker, BUDs, Brand Manager, Market Access, Pharmakovigilanz, Einkauf, Medizin.
Kennen und Nutzen von Entscheidernetzwerken. Erheben von Abläufen der Therapieströme und Patientenbetreuung

* Scientific Leader-Betreuung und Unterstützung der Entscheidungsträger durch Information über Produkteigenschaften und wirtschaftlichen Vorteilen

* Gebietsmanagement: Der Mitarbeiter erstellt einen Gebietsplan aus, welcher in einer prioritisierten Liste von Kunden resultiert, die mit entsprechender Frequenz und Effektivität besucht werden. Der Plan legt fest, wen der Mitarbeiter besucht, was zu tun ist, und definiert eine Strategie, wie die gewünschten Resultate erzielt werden. Der Plan enthält weiters einen Besuchsplan für alle priorisierten Kunden und reflektiert die entsprechende Priorität. Der Plan achtet auch auf die Effektivität des Weges zwischen den einzelnen Kunden. Aufzeichnungen über die Gespräche mit Kunden werden später dazu benutzt, um den Inhalt des nächsten Gespräches zu planen.

* Erkennen und Lösen von systemischen Problemen.

* Reisetätigkeit zum Besuch der Ansprechpartner im entsprechenden Gebiet.

* Kenntnisse über Produkt und Krankheitsbild: Der Mitarbeiter kann während Produkttrainings inhaltlich richtige Information in mündlicher Diskussion und schriftlicher Form wider geben. Alle Aussagen über Produkt und das Krankheitsbild sind richtig und in Übereinstimmung mit dem Label.

* Veranstaltungen: Der Mitarbeiter plant, organisiert, und implementiert Veranstaltungen welche ihn/sie beim Gebietsmanagement und dem entsprechenden Plan unterstützen (i.e. Roundtable Diskussionen). Jede Veranstaltung ist in Übereinstimmung mit Verkaufs/Marketing-Strategien und den Plänen des Gebietsmanagement. Der Plan für jede Veranstaltung beinhaltet auch Folgeaktivitäten mit eingeladenen Kunden um deren Commitment zu stärken. Alle Veranstaltungen werden innerhalb des zugewiesenen Budgets abgewickelt.

* Berichte (Reports): Der Mitarbeiter liefert alle Berichte 100% genau und 100% termingerecht ab. Alle verfügbaren elektronischen Systeme sind zu benutzen, wie vom Management angewiesen. Anfragen vom Management für Informationen oder Aktivitäten sind richtig und innerhalb der erwarteten Zeitspanne zu erfüllen. Regelmäßige Reports und Besprechungen zur Strategischen und taktischen Abstimmung

* Persönliche Weiterentwicklung/Team Entwicklung: Der Mitarbeiter steuert zu seiner/ihrer eigenen beruflichen Weiterentwicklung bei. Der Mitarbeiter unterstützt die Teamentwicklung, indem er/sie sich aktiv an Cyclemeeting und anderen Teamdiskussionen beteiligt.

Qualifikationen

Fähigkeiten, Kompetenzen :

* Sehr gutes Produktwissen; Kenntnis der Erkrankungsbilder und Versorgungsorganisation
* Mindestens 4 Jahre erfolgreiche Erfahrung im Verkauf der Pharmaindustrie, davon mindestens 2 Jahre Erfahrung mit Spezialisten
* Bachelor Degree im Paramedizinischen Bereich oder ähnliche Ausbildung
* Lösungsgsoriente Vorgehensweise
Hohe Eigenverantwortlichkeit und Reisebereitschaft
Kaufmännisches Denken, und Verhandlungsgeschick

Job
: Channel-Vertrieb, allgemein

Primärer Standort: CH-LU-Luzern

Mitarbeiterstatus: Permanent

Reisebereitschaft:: Ja, 75 % der Zeit

Anzahl offener Stellen: 1

Externes Job Ausschreibungsportal
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-Hospital-Sales-Representative-Anesthesia-Job-LU/1858709/185870918587092012-06-15Merck/MSDChannel-Vertrieb, allgemeinfull-timeUSDstarting0BSLU, CH
Description

With the initiation of the new Modeling & Simulation (M&S) organization in 2010, MSD has taken a next step in the application of M&S to enhance decision making in its R&D projects. Structured around a central M&S department, the new organization integrates and leverages existing and evolving quantitative skills across the R&D organization, aiming to optimally support R&D project teams. A key partner function in this M&S organization is the Clinical PK-PD group within PPDM (Pharmacokinetics, Pharmacodynamics & Drug Metabolism) located in Oss, The Netherlands.

As an Experienced Pharmacometricians you will participate in an unique, multidisciplinary M&S environment, focused on enhancing decisions through integrated, innovative M&S approaches in a collaborative teamwork setting. We provide you with the opportunity to have significant impact on critical decisions in a dynamic R&D environment. There is much room further development both scientifically and personally in a diverse, science driven organization, by participating in and leading multidisciplinary teams, as well as by coaching and mentoring of colleagues. Our group consists of junior and experienced scientist with a collegial atmosphere, both locally as well as globally.

Qualifications

* Background/training on the interface of pharmacological/pharmaceutical and quantitative sciences. PhD or equivalent experience in e.g. Pharmaceutical Sciences, Biomedical Sciences, Chemical/Biomedical engineering, Biostatistics.
* At least five years of in depth, post academic modeling & simulation experience in the context of pharmaceutical R&D, including areas such as PK-PD modeling, disease modeling, competitor modeling and trial simulations, preferably demonstrated by a track record of peer-reviewed publications.
* Prior experience in pharmaceutical industry, in multidisciplinary team setting.
* Proficient in the use of NONMEM, S-Plus/R, Perl, SAS and/or other pharmacometric software tools.
* Excellent verbal and written communication skills.

Information

For more information about the vacancy please contact Rik de Greef, tel. +31 (0)412 662321.

Job
: Pharmacokinetics/Drug Metab

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 3]]>http://jobs.merck.com/job/Oss-Experienced-PharmacometricianPK-PD-Scientist-%282x%29-Job-NB/1881756/188175618817562012-06-15Merck/MSDPharmacokinetics/Drug Metabfull-timeUSDstarting0BSOss, NB, NL
Beschreibung
Summary:

Durchführung von Fermentation mit tierischen Zellkulturen im Massstab von 100L -2000L mit allen dazu gehörenden Vorbereitungsarbeiten. Verantwortlich die Qualifizierung und den Unterhalt der Anlagen. Alle Arbeiten unterliegen den cGMP Richtlinien und müssen auch dementsprechend dokumenteiert werden.

Job Description and Responsibilities

The primary activities include but are not limited to:

* Vorbereitung, Durchführung und Nachbereitung von Fermentationen
* Führt die zur Prozesskontrolle nötigen Analysen selbständig nach gegebenen Verfahren durch
* Unterhalt der zur Fermentation und Analyse verwendeten Anlagen und Apparaturen
* Kennt und befolgt die Richtlinien für cGMP von WAG und SP in seinem Aufgabenbereich
* Erarbeitet, wenn nötig mit dem Engineer Controls & Compliance Biotech und dem Vorgesetzten, GMP relevante Dokumente (z.B. Batch Sheet's, SOP's, Solution Sheets, Qualifizierungs Unterlagen).
* Führt Qualifizierung nach Anweisungen des Vorgesetzten oder des Engineers Controls & Compliance selbständig durch
* Bestellt wenn notwendig Chemikalien und Verbrauchsmaterialien nach Bedarf

Qualifikationen

Education:

Chemie oder Biologie Laborant, Chemikant

Skills Required:

cGMP Erfahrung, Englisch,

Competencies required for the role (max. 5)

Exaktes und verlässliches Arbeiten, Bereitschaft für unregelmässige Arbeitszeit incl. Wochenendarbeit, Teamarbeit, flexibel, bereit für Neues

Job
: Biologie/Entdeckung

Primärer Standort: CH-LU-Luzern
Mitarbeiterstatus: Permanent
Anzahl offener Stellen: 1
Externes Job Ausschreibungsportal: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-Laborant-Fermentation-Job/1848111/184811118481112012-06-15Merck/MSDBiologie/Entdeckungfull-timeUSDstarting0BSLuzern, CH-LU
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande

El Representante de Ventas-Anestesia es responsable de lograr los objetivos de negocio , a través de la promoción de productos de alta especialidad, asegurando la efectiva implementación de la estrategia de marketing y alineado a la cultura ética, compliance, políticas y procedimientos de MSD, así como apegado a las regulaciones del gobierno de Chile.

Es responsable de lograr la cobertura de venta a través de visita y asesoría a médicos, clientes / cuentas clave, hospitales y clínicas de gobierno y privada: médicos, residentes, enfermeras, influencias técnicas y administrativas.

- Alineado a las estrategias de marketing de cada uno de sus productos de alta especialidad.
- Desarrollando, implementando y dando seguimiento a su plan de ventas.
- Procurando uso de nuestros productos y el abastecimiento conforme a los marcos existentes.
- Asesorando a los clientes acerca del manejo y ventajas de los tratamientos de MSD para los pacientes mediante la búsqueda y entrega de información clínica de diversas fuentes así como ofreciendo servicios y soluciones diferenciados.
- Analizando y evaluando el potencial de negocio para identificar oportunidades de nuevas oportunidades.
- Desarrollando negocios a través del continuo diseño de nuevos modelos para clientes clave.
- Planeando, organizando, ejecutando y dando seguimiento a sus eventos de Educación Médica Continua (EMC).
- Consolidando las relaciones con clientes clave a largo plazo.
- Participando e integrando actividades para el desarrollo de eventos médicos, tales como convenciones, reuniones clínicas, congresos, etc. Así como en la licitación e inclusión de productos a las instituciones bajo su responsabilidad.

Cualificaciones
* Título Universitario.

* Conocimientos del Area Hospitalaria.

* Mínimo tres años de experiencia como representante en la Línea de Especialidades de la Industria Farmacéutica.

* Manejo del idioma inglés y manejo de PC a nivel usuario.

* Capacidad para trabajar en equipo

* Alta orientación al cliente.

* Capacidad de detectar oportunidades de negocio e innovar.

* Adaptabilidad.

* Proactividad.

* Muy buen nivel para relaciones interpersonale

* Iniciatia

* Capacidad de organización y planificación.

* Habilidad para analizar y resolver problemas.

Nuestros empleados son la clave del éxito de nuestra empresa. Demostramos nuestro compromiso con nuestros empleados ofreciéndoles un programa de recompensas competitivo y valioso. Los beneficios en MSD están diseñados para apoyar la amplia gama de objetivos, necesidades y estilos de vida de nuestros empleados y de muchas de las personas que constituyen lo más importante en sus vidas

*LI-KT1

Puesto
: Ventas general

Ubicación principal: CL-Santiago Metropolitan Region-Santiago
Tipo de acuerdo laboral: Fijo(a)
Viajes: No
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Santiago-Representante-de-Ventas-Anestesia-Job/1855918/185591818559182012-06-15Merck/MSDVentas generalfull-timeUSDstarting0BSSantiago, CL
Description

Today's Merck is a global healthcare leader working to help the world be well. Through our medicines, vaccines, biologic therapies, and consumer and animal products, we work with customers and operate in more than 140 countries to deliver innovative health solutions.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. As part of our team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Reporting to the Director, Regulatory,
Primary Responsibilities Include:

* The preparation, filing and follow-up of federal regulatory submissions;
* The review and evaluation of clinical, manufacturing and marketing oriented documentation;
* Providing Regulatory support in a timely and professional manner to internal customers (Marketing, Operations, Legal, Medical,) and external customers (Health Canada).

Qualifications

* B.Sc. or M.Sc. in a health-related science field;
* Minimum 3 years experience in pharmaceutical industry;
* Knowledge of the Food and Drugs Act and Regulations, as well as an understanding of the drug development process;
* Be highly organized;
* Be professional;
* Be capable of managing several projects simultaneously under tight deadlines;
* Have good business acumen;
* Think and act strategically;
* Demonstrate good judgment and initiative;
* Possess good negotiation skills, diplomacy and tact;
* Have the ability to work effectively in a team environment;
* Have excellent oral and written communication skills in French and English;
* Language: Bilingual (French and English).

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

Merck is an equal opportunity employer, proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes ted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-MT1

Job
: Regulatory Affairs Generic

Primary Location: CA-QC-Montreal (Kirkland)
Employee Status: Temporary
Number of Openings: 1]]>http://jobs.merck.com/job/Montreal-%28Kirkland%29-TMP-Project-Manager%2C-Regulatory-Affairs-Merck-Consumer-Care-%28temp_-mandate-15-month-Job-QC/1883041/188304118830412012-06-15Merck/MSDRegulatory Affairs Genericfull-timeUSDstarting0BSMontreal (Kirkland), QC, CA
Description

Responsible for the development of Rt Reports to support batch release in the Manufacturing Execution System (MES). As part of a plant team he/she will provide direct support for the design, development and release of Rt Report in the Rt Reporting system. He/she will ensure that objectives are effectively achieved, consistent with Merck's requirements to ensure compliance, safety and reliable supply to our customers.
Responsible for the Data Retrieval and Rt Report design development and release to support activities such as engineering studies, process development studies and process simulation studies. Define the content of Rt Reports with knowledge of vaccine and biologics products and critical process parameters (CPPs). Completes Design Review and liaises with MMD-IT to enable the development of the reports in line with schedule. Ensure that the reports are streamlined and in line with all site procedures and standards. Delivery of the Rt Reports Delivery of End User training based on Audience analysis

Qualifications

* Bachelors Degree or higher preferred; ideally in a Science, Engineering or other Technical discipline
* Rt Reporting and MES knowledge and experience required
* Proficiency in Microsoft Office and job related computer applications required
* Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices
* Report, standards, policy writing skills required
* Equipment and process validation experience
* Sterile filling processes and equipment
* Lean Six Sigma Methodology experience desired
* Effective communication and interpersonal skills to interface effectively with all levels of colleagues in a team environment, and with external customers
* Understand the specific responsibilities of all Carlow departments as they relate to ones own department, understanding the business processes ones department supports
* Customer service
* Self motivated
* Flexible approach

Job
: Engineering Generic

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Carlow-Report-Process-Steward-Job/1703533/170353317035332012-06-15Merck/MSDEngineering Genericfull-timeUSDstarting0BSCarlow, Leinster, IE
Descripción
Objetivo General

Asesorar al negocio en los proyectos de inversión y en su operación, siendo proveedor de análisis financiero de los riesgos y oportunidades, a fin de maximizar la utilidad y retorno de la compañía

Responsabilidades

1. Realizar planes a largo plazo (Long Range Operating Plan=LROP) de ventas y gastos para la unidad de negocios asignada.
2.- Realizar presupuesto de ventas y gastos para la unidad de negocios asignada.
3.- Crear plan de gastos operativo de todas las áreas de soporte (Global Support Functions=GSF).
4.- Llevar seguimiento del presupuesto, el Forecast, restatements y actuales cada mes para realizar trimestralmente el envío de información a la Región.
5.- Enviar P&L´s (venta, costo, gasto promocional, gasto fuerza de ventas y gastos administrativos) de las unidades de negocio con los respectivos comentarios de las desviaciones más significativas. Información por GSF, Unidad de Negocios, Franquicia y Producto.
6.- Dar seguimiento al presupuesto y realizar actualizaciones estimadas (Forecast) tanto para ventas como para gastos de todas las áreas de soporte y unidad de negocio asignadas.
7.- Apoyar en la elaboración de presentaciones para el comité ejecutivo o para la región de acuerdo de las necesidades.
8.- Apoyo a la Gerencia de Planeación Financiera a la elaboración y envío de reportes varios.
9.- Dar soporte financiero a la unidad de negocio y áreas de soporte asignadas.
10.- Analizar precios de venta actuales vs. precios de listas de todos los productos de la Unidad de Negocios asignada.
11.- Backup en liberación de pedidos de gobierno.
12.- Apoyar con los requerimientos de Auditoria Interna y Externa.
13.- Conocer y manejar todos los sistemas necesarios para el área de Planeación Financiera.
14.- Desarrollar, implementar y administrar herramientas o nuevos sistemas en casos de requerirse para mejorar procesos de área.
15.- Verificar que la estructura contable de la Unidad de Negocio y áreas de soporte sea correcta y de ser necesario solicitar la creación

Cualificaciones
Experiencia mínima de 5 años en planeación financiera, área contable y/o Finanzas

Evaluación de proyectos, manejo presupuestal y análisis financiero

Manejo Avanzado de Excel

Inglés Avanzado

Puesto
: Análisis financiero

Ubicación principal: MX-Distrito Federal-Álvaro Obregón
Tipo de acuerdo laboral: Fijo(a)
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/%C3%81lvaro-Obreg%C3%B3n-Analista-de-Planeacion-Financiera-Sr-Job/1877977/187797718779772012-06-15Merck/MSDAnálisis financierofull-timeUSDstarting0BSÁlvaro Obregón, Distrito Federal, MX
Description

Under the direction of the Regional Lead, HR Shared Services, the incumbent is responsible for providing high quality, timely customer support to Managers and Employees in his/her country / region. As the primary representative of the HR Shared Services organization at the local / regional level, the SBS HR Country / Region Specialist is a critical member of the Regional team and plays an integral role in the successful realization of the COMET Hire-to-Retire initiative and the HR Transformation. The SBS HR Country / Region Specialist EEMEA handles complex issues which cannot be resolved at the first point of contact by the HR Contact Center team. He/she interfaces directly with members of the Conatct Center, the HR Centers of Excellences, Legal, IT, and 3rd party benefit providers to resolve Manager and Employee inquiries and requests.

Primary Activites:

- Provides outstanding customer support in helping to accurately resolve cases in a timely manner

- Establishes strong working relationship and high degree of credibility and respect with local client base

- Maintains a thorough awareness and understanding of the global and local Merck and HR SBS processes, policies, products and services

- Serves as overflow and backfill for other SBS HR Case Managers as necessary

- Assists in identify and creating solutions for recurring/significant issues to support the Direct Access channel

- Provides guidance on the creation and on-going maintenance of job-aids to support the Direct Access channel

- Educates employees and managers on policies, processes and the use of the HR Portal for Direct Access

- Works with the Centers of Expertise, managers and employees to interpret policies and determine exceptions/variations

- Contributes ideas and actions towards the continuous improvement of processes and policies both globally and locally within area of influence

- Plans and organizes work within a defined set of duties

- Maintains professional relationships with internal contacts (My support Center, Transaction Processors, Business Partners, Centers of Expertise) and external vendors

- Partners with the HR COEs to ensure that policies, processes, and guidelines are implemented consistently across the corporation by serving as the customer facing link to Managers and Employees

- Participates in special projects to support the HR Shared Services Portfolio and other Company initiatives as needed; utilizes skills and perspectives in a broader context

Qualifications

Required skills:

- Bachelors Degree with a minimum of 3 years of relevant work experience, including a demonstrated record of customer focused service

- Deep understanding and knowledge of local / regional country HR business processes

- Excellent problem/resolution skills and an understanding of when, how, and where to escalate cases as required to meet defined Service levels

- Ability to utilize ticket management system

- High degree of integrity in handling personal and confidential data/information

- Strong oral and written communication in both preferably Eastern European or Middle East Language and English

- Teamwork and collaborative focus

- Must be able to work in a fast-paced dynamic environment, under pressure, and with a high degree of professionalism

- Must be comfortable in an environment of changing technologies and processes and demonstrate flexibility in adjusting to new ways of working.

- Demonstrated track record of primary goal achievement and high level of motivation.

Additional Desired skills:

- Familiarity with Six Sigma concepts and willingness/interest in obtaining Six Sigma certification

- Experience with SAP for HR.

Job
: HR Call Center

Primary Location: IE-Leinster-Dublin
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-SBS-HR-Country-Region-Specialist-EEMEA-Job/1768637/176863717686372012-06-15Merck/MSDHR Call Centerfull-timeUSDstarting0BSDublin, Leinster, IE
Description

We have an opportunity available for a Lead Supplier Management to join our Enterprise Technical & Application Services (ETAS) Application Management Services (AMS) team in EMEA and AP regions . The role is responsible for the development, planning, tracking and analysis of the monthly, annual and long-range finances for Application Management Services.

The incumbent will collaborate across service functions within AMS to assemble monthly financial forecasts across the business unit. The incumbent will be responsible for developing and ting monthly accruals and quarterly forecasts to ETAS Business Management. The incumbent will provide budget and resource capacity information to support project and resource managers and maintain compliance with all SOX404 accounting requirements by assuring monthly financial close for capital and expense budgets occur without error. The incumbent will manage cost allocations and chargeback, investigate and resolve variances in forecasted expenses, manage organizational restatements and ensure timely and accurate payment of invoices. The incumbent will ensure any identification of performance credits in the Managed Services contracts and maintain financial aspects of the value assurance program.

The incumbent will collaborate with all levels of international and domestic AMS Staff. This position also requires the incumbent to be highly flexible and demonstrate a high level of intensity in working at a precise level of detail. The incumbent must display business awareness of the AMS Portfolio while maintaining accountability of his/her specific areas of responsibility. Additionally, this role will provide leadership to team members in the financial forecasting processes

Areas of accountability:

- Work as a financial analyst in adding and/or changing AMS scopes of work to contracted Suppliers.

- Develop and maintain relationships with different EMEA region country level finance departments.

- Discuss financial consequences of potential AMS scopes of work with stakeholders (both Merck as well as Suppliers) and seek and track savings opportunities.

- Facilitate and prepare financial part of (Governance) approval and support eventual contracting of AMS scopes of work with Supplier and eventually ensure proper requisition for approved AMS scopes of work (projects and major/minor changes).

- Manage AMS budget development.

- Evaluate, analyze, report and review AMS financial performance with stakeholders (both Merck as well as Supplier) and make recommendations to addressed issues.

Qualifications

Education:

BA/BS in business administration of finance or related field.

Required:

The candidate must have a minimum Bachelors Degree with an MBA preferred and have at least 5 years of relevant work experience. The ability to apply data analysis and reporting techniques to complex financial data is required. Excellent attention to detail and a passion for continuous improvement. Flexibility is required to interact globally across time zones. Ability to work well in a team environment and develop working relationships with AMS functional areas in achieving cost controls, expense reductions, and optimization of financial resources. Must demonstrate the ability to manage multiple priorities. Must also possess high motivation and strong client focus

Preferred:

Proven record of financial experience and/or proficiency.

Proficiency with Merck's SAP Financial Systems.

Proficiency in Microsoft Office suite of products: Word, Excel, and PowerPoint.

Capacity to analyze information and report the results to management.

Produce monthly financial scorecard metrics.

Conduct monthly analysis of financial results as compared to plan, targets and the forecast.

Evaluate process and systems to identify areas of better integration, automation or simplification chargeback.

Facilitate ongoing tracking, reporting and management of the financial & business processes including quality assurance and adoption.

Manage the analysis and reporting of project financial aspects of initiatives within and related to the AMS Portfolio.

Monitors the financial transactions to ensure they remain within budget.

Work in partnership with ETAS CoE's, IT Procurement, Suppliers, and Clients to deliver on financial management objectives.

Understanding of Merck's finances (capital and expense), along with knowledge of Merck's financial systems.

*LI-EM1

Job
: Financial Analysis

Primary Location: IE-Leinster-Dublin
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1

Shift (if applicable)
: N/A

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Financial-Analyst-Job/1851261/185126118512612012-06-15Merck/MSDFinancial Analysisfull-timeUSDstarting0BSDublin, Leinster, IE
Description

De functie

* Eenvoudige productiewerkzaamheden uitvoeren (handmatig en/of machinaal) conform de geldende regels t.a.v. GMP en EHS
* Verrichten van lijnombouwen
* Ontdekken en melden van defecten en verstoringen en oplossen van eenvoudige verstoringen
* Verricht ondersteunende IPT-specifieke werkzaamheden (bv. aangaande schoonmaak, aanvullen hulpmaterialen, monstername, etc.)
* Is aantoonbaar op de hoogte van de voor hem/haar geldende procedures en richtlijnen
* Bewakenprocesvoortgang en signaleren van productieapparatuur
* Bedienen, controleren en onderhouden van productieapparatuur
* Bijhouden productiegegevens (werklijsten/procesdocumenten)
* Bijdragen aan continu verbeteren (TIER, 5S en Kaizen)

Qualifications

Wij vragen

* VMBO
* 3 jaar werkervaring in een productieomgeving
* Continu aandacht op compliance, kwaliteit en veiligheid
* Klantgericht
* Goede communicatieve vaardigheden
* Teamplayer

Contact

Informatie over de functie bij Paul Mies, 0412 66 8332

Job
: Production / Operator

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Operator-Level-II-Job-NB/1895233/189523318952332012-06-15Merck/MSDProduction / Operatorfull-timeUSDstarting0BSOss, NB, NL
Description

Department

The Center of Excellence Biotech Technical Operations gives technical support, process support - troubleshooting and continuous improvement - to the local Biotech upstream and downstream Integrated Process Teams (manufacturing), is involved by process fit / introduction of new processes in the production facilities and cooperates with other technical groups in the global network.

Function

The Process Lead will lead a team that is dedicated to a downstream Integrated Process Team within Biotech for 2nd line trouble shooting and process improvement projects for commercial processes. You are a member of a local multidisciplinary product team. Resposible with the team for continous process surveillance, deviation handling, process performance and data trending. Assesses improvement proposals on process impact. Delivers input and updates into high level project plan and budget for the product team lead.

Major tasks

· Responsible with team for 2nd line trouble shooting per process area

· Responsible with team for continuous process surveillance, deviation handling, process performance and data trending

· Performs with team process quality impact investigations and root cause analysis in case of deviations

· Responsible for continuous validation strategy and Tech Ops technical reports

· Identify opportunities for improvement (quality, cost, speed, waste reduction etc.) and assesses improvement proposals on process impact

· Initiates and coordinates all process related improvements based on manufacturing strategy including lab activities and change control management

· Responsible for writing change protocols and validation reports

· Writes/approves Master Production Document and reviews with team Master Batch records, recipes and process related documentation

· Writes /reviews regulatory files (CMC modules) and technical documents.

· Pro-actively applies change management and Lean Six Sigma tools as enablers for success

· Contributes to the recruitment and retaining of employees, the execution of training programs and the execution of all performance management activities

· 40% leadership activities, 60% scientific tasks

· Direct reports 3-5 Bsc/Msc/PhD level

· Indirect reports 4-8 laboratory technicians

Qualifications

· Academic degree/PhD in life sciences (Biotechnology or related) or comparable level through experience (must)

· A minimum of 5 years experience in biologics manufacturing and/or managing biotechnological development projects (must)

· Proven strong scientific, project & people management skills (must)

· Strong communicator and ability to build bridges between groups and organizations. Ability to create a team spirit (must)

· Knowledge of GMP guidelines (must)

· Willingness to certify for or possessing Green Belt or Black belt degree (must)

· Passion for Lean and Continuous Improvement (must)

· Customer focused, process oriented and data driven

· Good command of writing and speaking in (basic) Dutch and (fluent) English (must)

· Percentage in service at least 90%

Job
: Tech Specialty/Skilled Trade

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Processlead-DSP-Job-NB/1862518/186251818625182012-06-15Merck/MSDTech Specialty/Skilled Tradefull-timeUSDstarting0BSOss, NB, NL
Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the general supervision of the Medical Director / Medical Manager (MM), the MM / Medical Advisor (MA)/ manages the medical activities for one or more therapy area(s) for Argentina, partners with: Global Clinical Trial Operations (GCTO) regarding clinical trials, Regulatory Affairs regarding interaction with Regulatory Agency, Pharmacovigilance regarding adverse events, and partners with marketing and market access regarding all relevant activities related to the therapy area(s). In compliance with all applicable country regulation and Merck policies and procedures, the MM, MA is responsible for:

* Contributing to short and long-term objectives by optimizing medical and clinical excellence throughout the product lifecycle within the therapeutic area
* Developing Medical Affairs strategy via Medical Affairs Plan (MAP) for incumbent's therapy area(s) in the country, and take appropriate action to ensure proper implementation
* Establishing, managing and owning high level scientific and clinical interactions with customers: Scientific leaders, speakers, investigators, scientific societies, Medical/Scientific Academies, or the like
* A major part of the MM/MA role is to have a high level of scientific interaction with customers, hence at least 50% of the job should be spend on customer interactions in the form of emails, telephone calls, face-to-face meetings whether pre-scheduled or un-scheduled (run-ins at congresses, symposia, or the like)
* Being recognized by customers and colleagues as the MSD expert in therapeutic area
* Providing medical and scientific advise and input to business units, market access and others as required as well as input into health economics
* High level scientific and medical/clinical interactions with regulatory and reimbursement authorities

Strategic Activities

Overseeing all local Medical Affairs activities within the therapy area(s). Enhancing company reputation and profile by representing the company's Scientific Leadership in relevant external and internal cross-functional, regional task forces or boards (e.g. externally: Pharmaceutical Branch Association (Lif); internally: Regional Medical Affairs Team (RMAT)) where relevant and feasible.

Developing MAP including relevant strategies related to:

Brand imperatives, key medical activities, outline specifics for the country (e.g. different standard of care, reimbursement timeline different than others, etc.). Prioritize and define unmet scientific- and medical needs, and clinical care gaps. Identify scientific leaders and discussions needed as well as developing tactics including, but not limited to:

* Promote, planning, initiation and implementation of Merck Investigatorinitiated Studies Program (MISP) including prepare/review protocols as needed, participate in MISP committee meetings, writing the contracts and securing final clinical study report / manuscript. MM/MA secures that the administrative MISP activities are handed over to CTO for execution
* The planning, initiation and implementation of local Clinical Evaluations (market experience programs/patient programs or other study types initiated locally) including preparation/review of protocols as needed in alignment with product franchise strategy, securing Sr. Management Approval. Execution of such programs lies with local MRL clinical operations or externally via CRO. MM/MA must secure final clinical study report / manuscript
* Secure input to Merck HQ-sponsored study allocation as well as national MSD site selection and investigators. Maintain and update information for local study feasibility on continuous basis and provide timely reply to HQ Request for Information for local study feasibility (RFI1) in coordination with GCTO
* Provide timely reply to HQ study tender (RFI2). Provide input to site selection in coordination with GCTO
* Implementing publication policy for the therapy areas, eg. securing production of review articles or the like
* In co-operation with Country Lead Clinical Operations provide input to publication for HQ-sponsored trials within the therapy area
* Identify meeting, symposia, congresses, Continuous Medical Education (CME), research grants/fellowships within the therapy area
* Active participation in strategic business activities aligned with the subsidiary objectives and Scorecard.
* Development of the scientific platform for the CME.
* Generate and distribute high quality medical information.
* Active participation in the local Medical Council
* Active participation in the new product launches.
* Development of the scientific perspective of the "Speakers" forums.

External Scientific and Medical/Clinical Interaction

These activities include:

* Securing MSD achieving scientific leadership by identifying Scientific Leaders and developing and managing a frequent and sustained dialogue with scientific leaders, investigators, and speakers.
* Plan and execute national and regional advisory boards and Expert Input Forums.
* Contribute to MSD sponsored meetings and CME events, including engaging Scientific Leaders as speakers, development of slide kits and giving own lecture as relevant active participation in symposia and congresses.
* Contribute to formulary and clinical guideline development.
* Provide medical and scientific training and support/advise to customers.
* Responsible for DPOC medical information requires and possible back up of DPOC administrator.
* Give Scientific and Strategic support to marketing on Patients Programs.
* Relationship with NGOs to explore common areas of interest with the business.
* Support to emerging markets initiatives.

Internal Scientific and Medical/Clinical Interaction

These activities include:

* Providing medical and scientific training, internal medical expertise, support/advise within the therapeutic area to colleagues regardless of business unit and business function.
* Act as extended support for the Medical Services Manager function (if applicable to the contry) when needed.
* Providing scientific support for CMEs.
* Provide input to Market Access for access plans and programs including pricing, reimbursement and public affairs.
* Participate in national, regional and company cross functional teams.
* Be aware of local licensing opportunities (Business opportunities) and direct these to the Business Development lead at the country or MSD Licensing and External Research Division.
* Close interaction with RDMAs, MRL, Regulatory, Market Access, Pharmacovigilance and Compliance
* Promote and ensure alignment with corporate policies, procedures and quality standards.
* Collaborates with the FCPA process
* Maintenance of internal database
* Promotional Materials, labels and Press Release approval
* Support sales force training program

Qualifications

Education:.

* The position requires a Medical Degree
* Relevant prior experience can replace the above mentioned preferred degree requirements.
* Previous management experience is preferred
* MBA and/or previous experience in marketing, medical affairs, Research or as an MSL would be an asset

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. MSD's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

*LI-KT1

Job
: Regulatory Affairs/Compliance

Primary Location: AR-Buenos Aires-Vicente López
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Vicente-L%C3%B3pez-Medical-Affairs-Manager-Job/1883040/188304018830402012-06-15Merck/MSDRegulatory Affairs/Compliancefull-timeUSDstarting0BSVicente López, Buenos Aires, AR
Beschreibung

Merck Sharp & Dohme-Chibret AG ist die Schweizer Niederlassung der Merck & Co., USA. Merck entwickelt, produziert und vertreibt weltweit innovative Medikamente und gehört international zu den führenden Pharmaunternehmen. Weltweit arbeiten ca. 100'000 Mitarbeiter für uns.

Die Schweizer Organisation beeinhaltet die Unternehmungen MSD International GmbH, Merck Sharp & Dohme-Chibret AG, Essex Chemie AG, Schering Plough Central East und Werthenstein BioPharma GmbH mit gesamthaft 700 Mitarbeitern.

Wir offerieren ein

2- Jahres Graduate Programm im Bereich Information Technology Services Group

Sie werden in diesem Programm als Business Analyst im Global Human Health IT Europe/Canada eingesetzt werden.

Aufgaben:

• Business Anforderungen anhand von Umfragen erstellen, Analyse von Dokumenten, Workshops durchführen, Umfragen organisieren, Business Analyse erstellen und Task & Workflow Analysen erstellen

• Sämtliche Informationen evaluieren, Informationen filtern und Prioritätenlisten erstellen

• Verstehen der Business needs und Herausforderungen

• Standardprozesse einführen und kommunizieren

• Businesslösungen erarbeiten und intern anbieten

• Schnittstelle zwischen dem Business und IT für sämtliche Anfragen bezüglich Verbesserungen, Koordination mit der IT Abteilung

• Unterstützung beim Testing und Vorbereitungen, Design von Test Szenarien und Test Scripts

Qualifikationen

• Erfolgreicher Hochschul oder Universitätsabschluss im 2012 (Richtung: Computer Sciences, Computer Engineering, Information Management, Mathematik, Telecommunications, Wirtschaftsinformatik)

• Fliessende Englischkenntnisse in Wort und Schrift, weitere Sprachen von Vorteil

• Problemlösungsfähig und Konfliktlösungsfähig

• Hohe analytische Fähigkeiten

• Technisches Verständnis mit entsprechender Ausbildung sind ein absolutes Plus

• Gute Kommunikationsfähigkeit, sollte sich gut intern mit dem Business verständigen können und entsprechende Präsentationsfähigkeiten haben

• Interesse oder Kenntnisse der Pharmaindustrie sind ein Plus

• Reisetätigkeit erwünscht

Job
: Unternehmensanalyse

Primärer Standort: CH-LU-Luzern

Mitarbeiterstatus: Permanent

Reisebereitschaft:: Ja, 15 % der Zeit

Anzahl offener Stellen: 1

Externes Job Ausschreibungsportal
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-GRADUATE-PROGRAMM-Business-Analyst-im-Bereich-Information-Technology-Services-Job-LU/1891865/189186518918652012-06-15Merck/MSDUnternehmensanalysefull-timeUSDstarting0BSLU, CH
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

DESCRIPCION DE LA POSICION

Brindar la informacion y analisis necesario para la toma de decisiones relacionada con el calculo de incentivos asegurando asi la posicion competitiva de la empresa en el mercado y rentabilidad; asimismo responsable de los procesos de Segmentacion, Targeting y CRM.

PRINCIPALES RESPONSABILIDADES

- Apoyar la toma de decisiones de uso de recursos, con evidencia que ayude a mejorar su impacto y rentabilidad.
- Asegurar el diseño y la implementación de instrumentos CRM que fomenten la toma de decisiones centrada en los médicos así como la asignación de recursos en los médicos más importantes para la corporación
- Diseñar y supervisar la implementación de mecanismos que favorezcan la identificación de oportunidades de mayor efectividad en nuestros recursos humanos y de promoción.
- Asegurar las mecánicas necesarias en la administración del plan de incentivos a fin de que dicho plan: Opera acorde al diseño establecido, con los procedimientos de aseguramiento de calidad y tecnologías de soporte necesarios para asegurar confiabilidad al 100%, con el diseño de mecanismos de entrenamiento, comunicación y la documentación de modificaciones al plan durante el ciclo anual de su vigencia, asegurando la operación acorde a los procedimientos formalmente establecidos para ello
- Coordinar la evaluación y estudio de las implicaciones del plan, a fin de presentar las propuestas necesarias para asegurar cumplimiento a presupuesto y/o rectificación de parámetros
- Anualmente liderar el proceso de rediseño al plan de incentivos, estableciendo un vínculo de entendimiento entre las necesidades de clientes y negocio
que aseguren instrumentos de pago financieramente responsables y altamente motivadores para nuestros empleados

- Desarrollo de personal - La posicion tiene a su cargo dos analistas de nivel medio a Senior.
- Organizar a los equipos de trabajo para que se logren potencializar nuestras entregas con la interpretación de resultados
- Propiciar un clima de confianza, respeto, aprendizaje y colaboración donde auténticamente existan oportunidades de crecimiento y desarrollo
- Propiciar la visibilidad adecuada para que el trabajo y aportaciones de cada uno de los elementos del grupo sea así percibido por el resto de la organización
- Crear un ambiente donde se favorezca la innovación y la pasión

Cualificaciones
Titulado de las carreras de:
Ingeniería Industrial o de Sistemas, Actuaría, Economía

Manejo de paquetería avanzada de Office:
Excel, Word, Power Point

Manejo numérico superior a promedio
Habilidades sólidas de análisis - síntesis
Experiencia en manejo de datos de ventas y administración de plan de incentivos mínimo 3 años en la industria farmaceutica.
Capacidad para traducir esquemas complejos en términos prácticos y simples
Cómodo para dirigirse a audiencias diversas interactuando como parte fundamental de su puesto en atención a fuerza de ventas con excelente actitud de servicio
Tolerancia a la frustración
Inglés: 80%

Por la naturaleza de la función todos los requisitos mencionados en el apartado anterior son indispensables, principalmente la experiencia en el area dentro de la misma industria.

Nuestros empleados son la clave del éxito de nuestra empresa. Demostramos nuestro compromiso con nuestros empleados ofreciéndoles un programa de recompensas competitivo y valioso. Los beneficios en MSD están diseñados para apoyar la amplia gama de objetivos, necesidades y estilos de vida de nuestros empleados y de muchas de las personas que constituyen lo más importante en sus vidas.

Puesto
: Atención al cliente

Ubicación principal: MX-Distrito Federal-Benito Juárez
Tipo de acuerdo laboral: Fijo(a)
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Mexico-City-Supervisor-de-Productividad-Job/1895226/189522618952262012-06-15Merck/MSDAtención al clientefull-timeUSDstarting0BSMexico City, Distrito Federal, MX
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

DESCRIPCION DE LA POSICION

Alimentación, comparación y análisis de datos de mercado a diferentes niveles de agregación- desagregación (e.g.ruta-terriotrio-distrito-area-nacional) para orientar y contribuir a la mejor toma de decisiones en cuando a estrategias/tácticas de ventas y mercadotecnia

PRINCIPALES RESPONSABILIDADES/ACTIVIDADES:

Asegurar la entrega de información competitiva en tiempo y forma. Diseñar y ejecutar procesos de aseguramiento de la calidad para la información entregada.

Desarrollar métodos de análisis que permitan profundizar hallazgos y conclusiones así como la detección áreas de oportunidad que permitan la mejora de nuestro negocio.

Análisis e intercambio de ideas con los gerentes de producto, de área y distrito acerca de los hallazgos observados
Aplicar y ampliar fuentes de información de ventas y mercadotecnia. Revisión y monitoreo de actividades de la competencia para detectar y anticipar cambios significativos en el entorno.
El responsable participará en el proceso de automatización de rutinas actualmente manuales para nuestros reportes lo que llama a un profesional altamente capaz de interactuar con clientes, así como generar vistas simples de relaciones complejas.

- "Protrack" coordinador:
Proceso de solicitud de material promocional en Protrack. Seguimiento de la aprobación y la comunicación de solicitud de cambio
Proceso de la ATF en coordinación con los Servicios Médicos
- Análisis de ventas interna
B2B y el análisis de las prescripciones
Preparar informes y presentaciones para los Gerentes de Distrito, Gerentes de Unidades de Negocio y fuerza de ventas con respecto a los resultados del mercado. Bila tablero de apoyo
Proporcionar los datos y el índice de rendimiento clave para el socio de la región para hacer algunos informes: Bila DDD; Bila PM.
de calidad y control.
- Apoyar el proceso de incentivos.

Cualificaciones
Titulado con carrera que haya facilitado manejo numérico y habilidades de análisis, preferentemente: Ingeniería, Economía
Administración, Mercadotecnia (Promedio sup. 90)
Cómodo para trabajar con números y facilidad para interpretación de cifras en su relación con múltiples variables
Manejo avanzado de paquetería Office
Experiencia en trabajos previos de análisis multidimensional de información
Experiencia en uso de bases de información secundaria en la industria farmacéutica IMS, Close-up, Knobloch:

Habilidades numéricas así como capacidad de análisis y síntesis de información superior a promedio
Iniciativa y orientación a resultados
Alta capacidad de concentración y capacidad para trabajar bajo presión
Comunicación eficaz verbal y escrita
Organización y control, para dar seguimiento a múltiples requerimientos simultáneos
Orientado a resultados y facilitador del cambio
Colaboración y trabajo en equipo
Actitud de servicio

*LI-KT1

Puesto
: Inteligencia/investigación de mercado

Ubicación principal: CL-Santiago Metropolitan Region-Santiago
Tipo de acuerdo laboral: Fijo(a)
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Santiago-Analista-Inteligencia-de-Mercado-Job/1804837/180483718048372012-06-15Merck/MSDInteligencia/investigación de mercadofull-timeUSDstarting0BSSantiago, CL
Description

Tasks:

* Initiate, lead and coach strategic, tactical and operational improvement programs of varying nature on site and (inter departmental level
* Develop and transfer knowledge of lean six sigma (LSS) and change execution management (CEM) within and across site(s)
* Collaborate with peers in the Merck Network via best practice sharing or via coaching and participation during improvements initiatives of other sites.
* Coordinate the deployment of lean six sigma (Merck Production System (MPS)) within the organisation

Qualifications

* Bachelor or Master degree in (Bio)Chemistry / Process Technology, Chemical Engineering or equivalent qualifications (must).
* A minimum of 5 years work experience from which 3 years experience in a manufacturing related role (must).
* Proven Analytical and Problem Solving skills (must).
* Strong project management skills & proven ability to manage complex projects (must).
* Hands on experience with application of most of the following Lean and Six Sigma tools and techniques: standardized work, scientific problem solving (PDCA), value stream mapping, SMED, mistake proofing, 5S, Visual factory, DMAIC (must).
* Passion for Lean / Continuous Improvement and willing to make personal change (must).
* Strong coaching, influencing and listening skills (must).
* Customer focused, process oriented and data driven (must).
* Ability to influence and communicate with all levels of the organisation from shop floor to senior management (must).
* Good command of writing and speaking in Dutch and English (must).
* Willingness to certify for or possessing Black Belt degree or MBB degree (advantage)
* 32 - 40 hours available (must)

*LI-WVG1

Job
: Product Dev Proj/Prog Mgmnt

Primary Location: NL-NB-Oss
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Lean-Six-Sigma-Projectmanager-Biotech-Job-NB/1862511/186251118625112012-06-15Merck/MSDProduct Dev Proj/Prog Mgmntfull-timeUSDstarting0BSOss, NB, NL
Description

MSD in Lucerne, Switzerland is a Swiss subsidiary of the global pharmaceutical company Merck & Co. Inc. with its headquarters in the USA. Approx. 90,000 employees are working for MSD globally, 650 of which are based here in Switzerland. Our Swiss operations include MSD International GmbH, Merck Sharp & Dohme-Chibret AG, Essex Chemie AG, Schering Plough Central East AG and Werthenstein BioPharma GmbH.

For our Swiss HR Organization we are currently looking for an:

HR Generalist

The Switzerland Human Resources Team supports multiple and highly diverse client groups across Switzerland, most of which are located at our four major sites across the Canton of Lucerne. Our clients include international HQ organizations as well as organizations supporting local Switzerland operations. Our HR team specializes in focusing specific organizations, however, work together as a team to provide consistent high-level services to all client groups.

The initial focus for the successful candidate will be to support our Werthenstein BioPharma GmBH site which is a research and manufacturing site of nearly 180 employees. The position will be responsible for supporting the Site Management Team, employee relations, organizational design, tracking HR Metrics, supporting budgeting process, coaching Managers on employee development, and supporting efforts to build a strong site culture. As a member of the Switzerland HR team, additional diverse projects may be assigned. The position will also handle all required HR Administration as needed.

Core Responsibilities:

· Provide client support to our employees in collaboration with the HR Managers

· Advise managers on use of our HR programs, processes and systems

· Pro-actively identify areas for process improvement

· Handling all administrative aspects of the employee life cycle from entry to departure

· Supporting new employee on-boarding

· Data analysis and reporting

Qualifications

· BA or BS degree or equivalent level of education specialization in HR preferred

· Experience working in an international environment

· Strong written and oral German and English

· Strong teamwork and collaboration focus

· High level of flexibility, positive attitude towards change

· Knowledge of Swiss labor law

· Strong analytical skills (strong command of Excel and preferably some HRIS experience)

This is an outstanding opportunity for someone looking to develop their career in an international organization. If you are interested in this career opportunity and want to become part of the development of our company please apply online

Job
: HR Generic/Consultant Generic

Primary Location: CH-LU-Luzern
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-HR-Generalist-Job-LU/1809486/180948618094862012-06-15Merck/MSDHR Generic/Consultant Genericfull-timeUSDstarting0BSLuzern, LU, CH
Description

To lead, implement and report on process/cleaning validation projects. To lead equipment/ Controlled Temperature Units (CTU's) qualification studies. To provide support to all other validation activities. Assert a high level of technical expertise across a range of different equipment/processes/products qualification/validation

TECHNICAL APPLICATION

· Validation documentation - drafting, reviewing and approving validation documentation.

· To lead the execution of equipment/CTU qualification, Container Closure Integrity (CCI) and Filter validation programs

· To lead cleaning validation and process validation programs

· Accountable for scheduling, tracking, reporting and achieving project deadlines

· To lead cycle development of equipment sterilization/ depyrogenation/ cleaning cycles.

· Input into the core aspects of Manufacturing and Cleaning SOP's.

· Participation in the development of continuous improvement programs

· Actively contribute to project teams.

· Lead and co-ordinate the execution of the re-qualification program.

· Mentoring junior validation engineers.

· Conducting and participating in Risk assessments

Information Gathering and Data Analysis

· Performing data analysis and determining conclusions reached.

· Make informed decisions / recommendations around conclusions reached from data analysis.

Signing off and approving protocols, reports, change controls and process deviations.

Compliance:

Understanding and applying industry specific compliance standards/regulations to all Qualification/Validation activities.

Qualifications

B.Sc. /B.A. degree required (science, engineering or other technical field preferred)

· Experience in IMB/FDA environment advantageous.

· Strong technical writing and communication skills

· Ability to close items to completion.

· Ability to pay high level of detail and QA data to very high standard

· Demonstrated leadership, interpersonal, technical aptitude, and problem solving skills.

· Strong team skills, including ability to co-ordinate various departments to support validation programs.

· Project Management skills.

· Must be goal-oriented and able to prioritize and manage risks.

· Must have experience in sterile/vaccine operations.

Job
: Engineering

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Carlow-Validation-Engineer-Job/1835817/183581718358172012-06-15Merck/MSDEngineeringfull-timeUSDstarting0BSCarlow, Leinster, IE
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

El cargo de Gerente de Trade Marketing reporta al Director de Unidad de Negocios y tiene como principal objetivo el liderar y dar el soporte estratégico y táctico a Mercadeo y Ventas para que la organización pueda crecer rentablemente mientras que consistentemente logra los objetivos financieros y estratégicos planteados en el corto y largo plazo.

Principales funciones:

- Definir e implementar el plan promocional de Trade Marketing en los principales clientes
- Coordinar con los Gerentes Regionales de Ventas la implementación de los planes y promociones definidas en el plan promocional anual
- Gestionar el presupuesto anual de Trade Marketing
- Analizar en profundidad la rentabilidad de las promociones
- Definir, hacer seguimiento y tomar correctivos en función a los indicadores claves de ventas
- Definir, elaborar y optimizar la ubicación/exhibición de los productos en el punto de venta
- Implementar en clientes claves junto con la fuerza de ventas, revisiones de negocio
- Colaborar en el cumplimiento de los objetivos de venta y rentabilidad de la Unidad de Negocio
- Liderar la implementación en el país de iniciativas globales de ventas y trade marketing

Cualificaciones
- Profesional universitario, con estudios de postgrado (deseable).
- Experiencia de más de 5 años en diversos roles de venta y/o trade marketing (deseable en compañías de consumo)
- Debido al nivel de exposición internacional, se requiere nivel avanzado del idioma inglés.
- Demostrados logros en su área de gestión/negocios.

Competencias:

- Comprobada capacidad de análisis, planeación estratégica, comunicación, ejecución, seguimiento y orientación a resultados.
- Impacto e influencia, habilidades de negociación y buen manejo relaciones interpersonales.
- Capacidad de Innovación.
- Demostrada capacidad en toma de decisiones gerenciales a tiempo
- Capacidad de manejo de múltiples prioridades

*LI-KT1

Puesto
: Marketing

Ubicación principal: VE-Caracas Capital District-Caracas
Tipo de acuerdo laboral: Fijo(a)
Viajes: Sí, un 25% del tiempo
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Caracas-Gerente-de-Trade-Marketing-Job/1855916/185591618559162012-06-15Merck/MSDMarketingfull-timeUSDstarting0BSCaracas, Caracas Capital District, VE
Description

We have an opportunity available for a Lead Supplier Management to join our Enterprise Technical & Application Services (ETAS) Application Management Services (AMS) team in the EMEA region. The role is responsible to manage supplier relationships, invoices and contracts in the EMEA and AP regions, while supporting global AMS goals. The incumbent must be able to work with Partners, AMS tower leads, Service Management and Governance (SM&G) and other related areas to ensure the AMS Managed Services contracts are fulfilled and properly executed. The incumbent must have a clear understanding of the application landscape's technology and contracted service level agreements with the different service delivery suppliers. Understanding of the AMS Managed Services contract framework, stakeholders (both Merck as well as Suppliers), sourcing and procurement processes and policies is required.

Areas of accountability:

* Work as a service lead in adding and/or changing AMS statements of work to contracted Suppliers.
* Develop and maintain supplier relationships
* Discuss potential AMS statements of work with stakeholders (both Merck as well as Suppliers) and seek and track savings opportunities. Share opportunities with the Global Supplier Management lead to ensure alignment with global strategy.
* Prepare, facilitate (Governance) approval and eventual contract AMS statements of work with Supplier and ensure proper requisition for approved AMS statements of work
* Understand AMS budget development based on Supplier pricing for AMS statements of work (projects and major/minor changes).
* Provide education and guidance to regional stakeholders (both Merck as well as Suppliers) regarding value of adopting and complying with the AMS Managed Services contract framework (process, procedures, policies, technology, tools etc.).
* Measure the quality and timeliness of regional contract deliverables which may impact contract compliance and/or future contract decisions.
* Understand core operations management variables and calculations essential to ensuring the supplier is effectively delivering services for regional deliverables.
* Contract Management - Ensure Managed Services contract compliance for regional deliverables.
* Execute standardized Contract Change Control and implement contract change orders.
* Develop Managed Services Contract expertise and provide contract understanding assistance to regional AMS stakeholders.
* Understand, and measure the performance credits and earnbacks.
* Identify opportunities for additional value creation
* Provide continuous feedback to the suppliers on their performance.
* Ensure the supplier invoices are reviewed and validated with the regional AMS Service Delivery Leads.
* Liaise and stay in alignment with the Global Supplier Management Lead and the Supplier Management & Governance (SM&G) organization
* Escalate unresolved financial contract compliance issues to the Global Supplier Management Lead and the SM&G organization
* Understand and review the demand portfolio with the suppliers and regional AMS Service Delivery Leads to add or change AMS Statements of work

Qualifications

Education:

* BSc. in technology and preferably in computer science or related field.

Required:

* A minimum of 8-10 years of relevant work experience, with demonstrated expertise in IT Service Delivery Management and Sourcing Management function, including the ability to understand the end to end process across the various components of Merck's IT Operating Model function spanning IT Client Services and IT Solutions Delivery, Shared Services, MS&O, and Infrastructure Services.
* Solid understanding of IT Service Delivery Management (ITIL) and Project Management (preferably PMP).
* Proficient in Systems Development Lifecycle Methodologies.
* Excellent communication and interpersonal skills, including collaboration, facilitation, and decision making.

Preferred:

* Prior experience with sourcing AMS statements of work with application management service suppliers.
* Prior experience in working in a matrix environment with collaboration across multiple organizations (both Merck as well as Suppliers).
* Solid understanding of the Managed Services Operating Model and Governance
* Prior experience in Maintenance, Support, and Operations function as well as Project Management function.

*LI-EM1

Job
: IT Generic

Primary Location: IE-Leinster-Dublin
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Regional-Supplier-Management-Lead-Job/1840119/184011918401192012-06-15Merck/MSDIT Genericfull-timeUSDstarting0BSDublin, Leinster, IE
Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Supplier Development & Performance Management (SD&PM) Field Generalist:

This positions can be located in Xochimilco (Mexico) or Campinas (Brazil)

Responsible for serving as the primary point of contact with Suppliers for MMD sites within the region. Responds to requests from SD&PM-Core and other MMD representatives outside of the region to manage Suppliers within the region.

Responsible for implementing procedures and best practices supporting Merck's Supplier Development & Performance Management program, under the direction of the SD&PM Relationship Manager. The incumbent will exercise leadership in monitoring and maintaining Supplier compliance with worldwide regulatory requirements, current Good Manufacturing Practices (cGMPs), MMD Quality Manual, and pertinent legal and / or business contract requirements. Key responsibilities include leading Supplier Deviation investigations, evaluation and execution of Supplier Change Management, upskilling Suppliers, and interfacing with MMD sites associated with Supplier issues within the region. The incumbent will assist the SD&PM Relationship Manager in calibrated Quality oversight and interfacing with Procurement and Technology colleagues.

The incumbent will possess Analytical, Scientific, Technical, Manufacturing, and / or Quality experiences in order to effectively administer and control Quality and Technical programs and projects needed to manage Suppliers, under the direction of the SD&PM Relationship Manager.

Primary Roles include, but are not limited to:

* Travels up to 50% of the time, to and from Supplier sites and MMD sites within the region.
* Serves as the primary point of contact to Suppliers in the region.
* Responsible for coordination, oversight and communication on matters related to the cGMP status with the Suppliers. Must understand worldwide regulatory requirements and current Good Manufacturing Practices associated with materials supply.
* Acts as a liaison between Suppliers and internal Merck site personnel.
* Travels to and from Suppliers' locations to resolve Manufacturing, Quality, Technical and supply issues as well as facilitating overall Quality improvements to proactively prevent Supplier issues.
* Provides support to the Suppliers to facilitate, qualify, and / or validate materials for new product introductions.
* Provides compliance input and support for implementation of analytical methodology and process development initiatives.
* Coordinates and evaluates Supplier-initiated or Merck-initiated Change Control associated with materials supply.
* Coordinates, communicates and oversees general technical matters pertaining to Suppliers, including understanding and optimizing component / material usage and upskilling Suppliers to provide improved materials and services.
* Partners with SD&PM Quality, Procurement and Technology colleagues to provide efficient and effective solutions and Corrective Actions / Preventative Actions (CAPAs) to Supplier and / or site issue resolution, including Deviation Management, response to Supplier audit issues and customer complaints.
* Provides technical consultation, review and execution of Quality Agreements, Change Control Agreements and Supply Agreements.
* Tracks and monitors Supplier operational and quality performance. Escalates issues to the SD&PM Relationship Manager, SD&PM Technology Managers, and to site personnel.
* Assists in development and delivery of Supplier metrics and scorecards.
* Participates in periodic Business and Relationship review meetings with Suppliers

Qualifications

Education / Experience / Skills:

* BS/BA degree in Engineering, Science or Business is required
* Minimum 5 years experience in Quality, Technical, Manufacturing Operations, or related Business Operations working with products or processes is required.

Preferred Experience and Skills

* Demonstrated Quality, Technical and / or Manufacturing experience in the areas of chemical, pharmaceutical and / or vaccine manufacturing or packaging
* Six Sigma Black Belt, Green Belt of Yellow Belt certification
* Experience conducting technical investigations
* Knowledge and application of the Merck Leadership Behaviors
* Ability to develop and / or improve commercial relationships
* Ability to work within a matrix organization and leverage expertise from other Merck functions and departments
* Proven self-starter
* Knowledge of cGMPs, technical writing, data management collection and analysis
* Possesses excellent interpersonal, inclusion, and communication skills
* Appreciates and respects diversity, cultures, and norms
* Facilitates business negotiations in a professional mannerorks independently with all levels of the organization, and has demonstrated the following skills:
* Rapid / Disciplined decisions
* Acts with courage and candor
* Drives results
* Escalation of issues / concerns to management, as appropriate
* Ability to Prioritize, Align and Simplify

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. MSD's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

Job
: Qual Assurance & Ops Generic

Primary Location: MX-Distrito Federal-Xochimilco
Other Locations: BRZ-SP-Campinas
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 2

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Xochimilco-Supplier-Development-&-Performance-Management-%28SD&PM%29-Field-Generalist-Job/1868792/186879218687922012-06-15Merck/MSDQual Assurance & Ops Genericfull-timeUSDstarting0BSXochimilco, Distrito Federal, MX
Description

The Sourcing Manager is responsible for global category management and sourcing leadership of Multi Channel Marketing directly or indirectly through collaboration with regional and/or local sourcing professionals.

Sourcing Manager leads the Global team to support development and implementation of sourcing strategies in the area of Multi Channel and content for unbranded portals. Responsible to establish and lead cross-functional teams through the Sourcing Management Process and to provide strategy oversight for Global, Regional and Local components of the category. Responsible for identifying and managing savings targets and other key metrics to established targets. Responsible for sourcing, contracting, data gathering & analysis, compliance as well as process set up, management & continuous improvement.

* Category Scope: Sourcing Manager is responsible for commercial support of Marketing Services procurement categories, specifically Multi Channel Marketing content for unbranded portals. In collaboration with stakeholders and regional/local procurement
* professionals, creates and implements 3-5 year sourcing strategies
* Global Category Management: Leads and participates on global/regional teams to develop and implement global category roadmaps and ensures alignment on key initiatives and priorities for Multi Channel Marketing procurement categories
* Sourcing Management: Applies and leads the Sourcing Management Process to manage assurance of supply, quality, service, cost, innovation regulatory compliance with Marketing Services procurement categories resulting in strategies which optimize value and ensure appropriate risk management. Understands the Sourcing Management Process and how to apply required tools in the creation and implementation of source plans
* Proactive Cost Management: Achieves cost control, cost reduction, and cost containment targets and adds value to area of expenditure through a strong TCO orientation and process management
* Market Knowledge and Insight: Uses thorough market knowledge and data analysis to gain critical insights that drive the selection of Sourcing Strategies and continuous improvement activities. Actively participates in relevant industry conferences and events as appropriate. Ongoing self education through stakeholder engagement and publications
* Supplier Management: Responsible for building relationships with Global, International and Enterprise suppliers and managing key supplier performance against business requirements using proven processes (e.g. SRM); ensures adequate inclusion of diversity suppliers in selection process and contracts as applicable. Leads major Regional supplier relationships
* Stakeholder Management and Business Sponsorship: Proactively

Qualifications

Education: BS in Business, Procurement, Marketing, Finance or related field strongly preferred. MBA or advanced degree and/or relevant certification is desirable.

Experience: 7 to 10 years experience in strategic sourcing and global category management, Marketing or related role. Experience in international business desirable, including fluency in English (other languages advantageous).

Skills: Knowledge of Multi Channel Marketing, Medical Publishers and/or Indirect Procurement. Good interpersonal & communication skills. Cultural awareness & sensitivity required. Innovative, business & result oriented individual. Demonstrates solid leadership capabilities at the Manager level, with particular strength in collaboration, written and verbal communication, and cross-functional team work. Process oriented & analytical talented individual with solid IT application skills in Excel, SAP & overall MS Office applications. Eager to learn & to support an international team.

*LI-DR1

Job
: Services Purchasing

Primary Location: CH-LU-Luzern
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-Procurement-Multi-Channel-Marketing-Job-LU/1889119/188911918891192012-06-15Merck/MSDServices Purchasingfull-timeUSDstarting0BSLuzern, LU, CH
Description

De functie wordt uitgeoefend binnen de EHS organisatie van MSD Oss, die ongeveer 20 medewerkers telt. Je werkt ten behoeve van de productie van actieve pharmaceutisch ingrediënten en ondersteunt daarbinnen vooral de productie, technische en laboratorium organisatie. Je implementeert en vertaalt het corporate Process Safety Management programma in praktische procedures. Je speelt een belangrijke faciliterende rol bij uitvoering van veiligheidsstudies en reviews (FMEA, FMECA, HAZOP, What-if, PSSR). Je formuleert en bewaakt prestatie indicatoren ten aanzien van procesveiligheid, verricht PSM beoordelingen, inclusief beoordelingen van wijzigingen (Management of Change), en stelt verbeterplannen op. Je functioneert als Program Manager van een aantal van de corporate EHS programma's en levert een pro-actieve bijdrage aan global Community of Practise Process Safety Management. Tot slot ben je aanspreekpunt voor inspecties en audits door overheden en interne partijen.

Qualifications

Wij vragen

* Een technische HBO of WO opleiding en een afgeronde opleiding Hogere Veiligheidskunde
* Tenminste vier jaar ervaring binnen een complex industriële omgeving (farma of chemie);
* Communicatief in Nederlands en Engels (in woord en geschrift);
* Teamspeler, in staat tot motiveren en enthousiasmeren en bereid tot samenwerken;
* Diplomatiek met gevoel voor interne en externe belangenverhoudingen;
* Gezaghebbend en informeel sturend en beïnvloedend op alle organisatieniveaus;
* Stressbestendig en in staat om onder tijdsdruk juiste prioriteiten te stellen;
* Zelfstandig, autonoom handelend en verantwoordelijk.

Houd je ervan te worden uitgedaagd, steeds weer, dan is MSD een goede keuze als werkgever. We hebben uitstekende arbeidsvoorwaarden en je krijgt er alle mogelijkheden om je verder te ontwikkelen en door te groeien. MSD geeft je veel ruimte voor eigen initiatief en je krijgt veel verantwoordelijkheid. We hebben een speciaal netwerk voor onze jonge professionals die regelmatig workshops en bijeenkomsten organiseren waaronder ook sociale evenementen, die je de gelegenheid geven je collega's en het bedrijf te leren kennen.

Voor meer informatie kun je contact opnemen met Ralf Slangen, EHS Manager op ralf.slangen@merck.com of 0412 - 66 1699. Referentie nummer: 11860IK.

Job
: Env, Health & Safety Generic

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-EHS-Expert-Process-Safety-Management-Job-NB/1881754/188175418817542012-06-15Merck/MSDEnv, Health & Safety Genericfull-timeUSDstarting0BSOss, NB, NL
Description

Afdeling:

De afdeling Quality Control Biotech bestaat uit twee laboratoria die enerzijds verantwoordelijk zijn voor de analyse van monsters uit de Biotech productieprocessen, en anderzijds voor de analyse van vrijgifte- en stabiliteitsmonsters van Biotech producten. De afdeling Quality Control heeft 18 medewerkers en maakt deel uit van het Biotech Quality Centre of Excellence. De afdeling werkt nauw samen met o.a. de productiefabrieken en met de analytische ontwikkelingsafdeling.

Functie

* Uitvoeren van analyses t.b.v. vrijgifte en stabiliteit van Biotechnologische produkten
* Rapporteren, verifieren, valideren en evalueren van analytische resultaten
* Identificeren van wetenschappelijke en kwaliteitsissues, het ontwikkelen van oplossingen met de belanghebbenden en het implementeren van de verbeteringen
* Optreden als analytische expert voor directe collega's en andere afdelingen
* Deelnemen en initiëren van verbeter projecten
* Deelnemen en initiëren van trouble shooting activiteiten

Qualifications

* HLO Analytische (Bio) Chemie of soortgelijke opleiding
* Minimaal 4 jaar relevante ervaring
* Ervaring met het analyseren van eiwit moleculen is vereist
* Ervaring met GMP is vereist
* Ervaring met analyse techniek HPLC is vereist
* Ervaring met Electroforese is vereist
* Ervaring met Elisa is een pré
* Ervaring met ION Exchange is een pré
* Sterk in de nederlandse taal en goed in de engelse taal is vereist
* Goede communicatieve vaardigheden
* Resultaatgericht en een echte doe mentaliteit
* Min. 32 uur per week beschikbaar

Job
: Quality Lab Related

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Scientist-Quality-Job-NB/1866484/186648418664842012-06-15Merck/MSDQuality Lab Relatedfull-timeUSDstarting0BSOss, NB, NL
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

DESCRIPCION DE LA POSICION:

La posición reporta al Gerente de Investigación Clínica de GCTO (Organización de Operaciones de Ensayos Clínicos Globales) y está a cargo de las siguientes labores principales:

1.
Bajo la supervisión del Gerente de Investigación Clínica o Director de Investigación Clínica, deberá evaluar riesgos y beneficios para tomar decisiones.

2.
Operaciones Clínicas

1. Asegurar que los estudios clínicos son realizados en adherencia a ICH / GCP, estándares globales de la compañía, leyes y regulaciones locales
2. Asegurar que los proyectos bajo su responsabilidad son ejecutados y completados a tiempo, dentro del presupuesto establecido, cumpliendo el compromiso de ingreso de pacientes, identificando proactivamente retos y desarrollando planes efectivos de mitigación; escalando apropiadamente y, en tiempo adecuado, a las personas apropiadas cuando ocurran desviaciones al plan
3. Entrenar a los Monitores Clínicos (CRAs) participantes en el proyecto, en las características del protocolo, anticipando los retos de su implementación
4. Proporcionar información específica del país y supervisión de las actividades de los Centros de Investigación (CROs), para los proyectos asignados.
5. Gerenciar los procesos de pre-slección y validación
6. Responsable de la organización de Reunión Local de Investigadores para sus proyectos.
7. Supervisa las actividades de cierre de los centros al finalizar es estudio

3. Colaborar proactivamente en la generación de un ambiente laboral que estimule la creatividad, speak up y trabajo en equipo, buscando nuevas maneras de realizar el trabajo, mediante la ejecución de procesos fluidos con mínimos desperdicios.
4. Trabaja internamente con otros roles de investigación clínica: Gerentes de Investigación Clinica, Gerentes de Proyectos Clínicos, Monitores Clínicos, Gerente de Administración Clínica, Gerente de Calidad, Coordinadores de Estudios Clínicos asignando recursos de las deferentes áreas de GCTO Perú para obtener la exitosa ejecución de sus proyectos.
5. Trabaja con investigadores, proveedores y contratistas para segurar consistencia a través de la organización.

Cualificaciones
Profesional Universitario de Ciencias de Salud (Medicina, Biología, Nutrición o Farmacia y Bioquímica)

Experiencia previa como Monitor Clínico.

Competencias de liderazgo principalmente foco en el cliente, colaboración, comunicación rápida y disciplinada, implementación de acciones, honestidad y valentía.

Conocimiento de los procedimientos y regulaciones relacionados a la conducción de estudios clínicos.

Habilidad para liderar exitosamente equipos de trabajo inter funcionales.

Habilidad para coordinar y negociar con clientes internos y externos.

Disponibilidad para viajar aproximadamente un 50% porcentaje del tiempo (nacional e internacional).

Fluidez en el idioma inglés.

Nuestros empleados son la clave del éxito de nuestra empresa. Demostramos nuestro compromiso con nuestros empleados ofreciéndoles un programa de recompensas competitivo y valioso. Los beneficios en MSD están diseñados para apoyar la amplia gama de objetivos, necesidades y estilos de vida de nuestros empleados y de muchas de las personas que constituyen lo más importante en sus vidas.

Puesto
: Investigación clínica genérica

Ubicación principal: PE-Lima-Lima
Tipo de acuerdo laboral: Fijo(a)
Viajes: Sí, un 50% del tiempo
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Lima-Gerente-de-Proyectos-Cl%C3%ADnicos-Job-Lima/1781702/178170217817022012-06-15Merck/MSDInvestigación clínica genéricafull-timeUSDstarting0BSLima, Lima, PE
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

DESCRIPCION DE LA POSICION

Obtener de las autoridades venezolanas el registro sanitario necesario para la comercialización de los productos elaborados o importados por la Organización, así como garantizar el cumplimiento de los requerimientos sanitarios locales y las políticas de la Compañía para la comercialización de los productos de MSD Farmacéutica

PRINCIPALES RESPONSABILIDADES:

- Preparar las solicitudes de registro de nuevos productos, nuevas indicaciones y posologías de manera que cumplan con todas las regulaciones sanitarias locales, seleccionando, evaluando y organizando la documentación técnico-científica que se obtiene de Casa Matriz.
- Mantener actualizados los productos comercializados por la Empresa de acuerdo a las regulaciones sanitarias venezolanas y las políticas de registro de la Compañía.
- Obtener de las autoridades sanitarias la aprobación para realizar en Venezuela cada estudio de investigación clínica que se decida llevar a cabo con los productos, sometiendo la documentación y estudios requeridos.
- Hacer seguimiento al registro en Venezuela de las marcas de fábrica de la Compañía, necesarias para la comercialización de sus productos en el país y mantener actualizados los listados de las marcas disponibles.
- Revisar y aprobar conjuntamente con el Director Médico el arte final de todo el material promocional de los productos, de acuerdo a la política de mercadeo de la Compañía y a las condiciones del registro sanitario local.
- Supervisar y controlar al personal a su cargo asegurando que cumplan con las políticas y normas de la compañía.
- Participar en las reuniones de trabajo de las diferentes asociaciones relacionadas con la Industria Farmacéutica

Cualificaciones
Educación:

Profesional Farmacéutico.

Registrado en el Ministerio de Salud.

Miembro del Colegio de Farmacéuticos de Venezuela.

Registrado en el Instituto de Previsión Farmacéutica.

Idiomas:

Inglés (Nivel intermedio-avanzado).

Competencias:

Organización y planificación. Orientación al trabajo en equipo. Orientación a resultados. Toma de decisiones rápidas y disciplinadas, Candor y Coraje, impacto e influencia.

Experiencia:

4 años o más de experiencia laboral en el area regulatoria.

Nuestros empleados son la clave del éxito de nuestra empresa. Demostramos nuestro compromiso con nuestros empleados ofreciéndoles un programa de recompensas competitivo y valioso. Los beneficios en MSD están diseñados para apoyar la amplia gama de objetivos, necesidades y estilos de vida de nuestros empleados y de muchas de las personas que constituyen lo más importante en sus vidas.

*LI-KT1

Puesto
: Asuntos regulatorios genéricos

Ubicación principal: VE-Caracas Capital District-Caracas
Tipo de acuerdo laboral: Fijo(a)
Viajes: Sí, un 15% del tiempo
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Caracas-Gerente-de-Asuntos-Regulatorios-Job/1799257/179925717992572012-06-15Merck/MSDAsuntos regulatorios genéricosfull-timeUSDstarting0BSCaracas, Caracas Capital District, VE
Description

To lead, implement and report on process/cleaning validation projects. To lead equipment/ Controlled Temperature Units (CTU's) qualification studies. To provide support to all other validation activities. Assert a high level of technical expertise across a range of different equipment/processes/products qualification/validation

TECHNICAL APPLICATION

· Validation documentation - drafting, reviewing and approving validation documentation.

· To lead the execution of equipment/CTU qualification, Container Closure Integrity (CCI) and Filter validation programs

· To lead cleaning validation and process validation programs

· Accountable for scheduling, tracking, reporting and achieving project deadlines

· To lead cycle development of equipment sterilization/ depyrogenation/ cleaning cycles.

· Input into the core aspects of Manufacturing and Cleaning SOP's.

· Participation in the development of continuous improvement programs

· Actively contribute to project teams.

· Lead and co-ordinate the execution of the re-qualification program.

· Mentoring junior validation engineers.

· Conducting and participating in Risk assessments

Information Gathering and Data Analysis

· Performing data analysis and determining conclusions reached.

· Make informed decisions / recommendations around conclusions reached from data analysis.

Signing off and approving protocols, reports, change controls and process deviations.

Compliance:

Understanding and applying industry specific compliance standards/regulations to all Qualification/Validation activities.

Participates in internal and external audits and inspections.

Qualifications

B.Sc. /B.A. degree required (science, engineering or other technical field preferred)

· Experience in IMB/FDA environment advantageous.

· Strong technical writing and communication skills

· Ability to close items to completion.

· Ability to pay high level of detail and QA data to very high standard

· Demonstrated leadership, interpersonal, technical aptitude, and problem solving skills.

· Strong team skills, including ability to co-ordinate various departments to support validation programs.

· Project Management skills.

· Must be goal-oriented and able to prioritize and manage risks.

· Must have experience in sterile/vaccine operations.

*LI-SC1

Job
: Engineering

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Carlow-Validation-Engineer-Job/1835818/183581818358182012-06-15Merck/MSDEngineeringfull-timeUSDstarting0BSCarlow, Leinster, IE
Description

Incumbent will provide Security Administration for all users of Human Resource data. This includes transaction systems such as PeopleSoft, Time & Labor, LDS Reporting, myLEARNING, Training Information System, Severance Reporting tool, myPMP, Medgate, Cognos etc…as well as mainframe access in TSO and DB2, The responsibilities include but are not limited to the following:

· Provide Human Resource (HR) Data Security support of all HR Systems in test and production environments for global locations

· Provide security support for rollout of all new HR applications

· Develop and maintain associated documentation for supported systems and execute security schemes

· Provide support to the maintenance of the HR Security Web site content

· Audit and monitor use of systems, identifying problem areas as well as opportunities. Follow-up on questionable security violations and inform Manager of circumstances

· Manage records of security requests and associated additions/deletions/corrections daily to meet Merck compliancy requirements

· Manage tickets according to service targets

· Manage responses to semi-annual Security Audit

· Analyze and deliver interpretation of compliance standards to ensure adherence to Merck policy

· Manage projects with minimal supervision, to analyze new security demands, develop production solutions and provide decision support

· Develop and programs that extract data from SQL to report, clarify and/or resolve security issues as needed

Qualifications

Education Minimum Requirement: Bachelor's Degree or 7 years equivalent experience

Required Experience and Skills:

* Advanced (3 or more years) knowledge of:
* DB2/Oracle Security
* PeopleSoft Security
* QMF/SQL Query
* Microsoft Access/Related Software with Macro

Extensive knowledge of:

* HR/Payroll/Benefits business function data
* Analytical skills in identifying system structure Security Implications

Desired Experience and Skills:

* Problem Solving
* Understanding of Audit, Compliance and Segregation of Duties issues related to HR Security Access

Job
: Customer Service

Primary Location: IE-Leinster-Dublin
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-HR-Security-Senior-Analyst-Job/1764629/176462917646292012-06-15Merck/MSDCustomer Servicefull-timeUSDstarting0BSDublin, Leinster, IE
Description

Department

Process Development and Commercialization (PDC). The department is responsible for late stage development manufacturing process (cell culture en purification) van biological drug substances (process characterization and qualification, production of material for phase 3 clinical). Furthermore PDC is responsible for the introduction of the process in the commercial phase (amongst other things up-scaling, writing of registration documentation, answering of questions by health authorities).



Leads a team of associates on the transfer in, scale-up, and characterization of purification processes for therapeutic proteins, specifically monoclonal antibodies for late stage clinical supply, qualification and commercialization. Interfaces with early development, technical operations and manufacturing groups to facilitate a smooth knowledge transfer and utilizes advanced skills in QbD, DoE, PAT and data analysis, to drive characterization studies and CMC enabling documentation resulting in successful licensure across multiple regulatory agencies.

Participates and is the purification Subject Matter Expert in regulatory inspections and is experienced with the required GMP and regulatory guidelines. Initiates and manages 3rd party development activities, inclusive of Scopes of Work, and reviews and approves applicable protocols and reports. Identifies new technologies and works to implement these as new platforms with cross-functional early and late development teams

Qualifications

Desired Skills & Experience

PhD in biological sciences, Biochemistry, Biochemical Engineering, or equivalent with a minimum of 3-5 years relevant industry experience in developing protein purification processes for late-stage and commercial manufacturing

* Must have experience with tech transfer and characterization of late stage processes
* Proven leadership with a minimum of 1-2 years of supervisory experience
* Detailed knowledge of relevant regulatory and quality guidelines and GMP requirements, and experience with BLA/MAA submissions
* Clear and concise communication skills, both written and spoken
* Manages resources to accommodate multiple milestones in late clinical development and commercial characterization
* Demonstrates flexibility to accommodate change in directions or timelines
* Fosters collaborations across multiple groups for efficient utilization of resources in solving technically challenging problems
* Must have strong and effective organizational, people management and interpersonal skills
* Excellent analytical and technical skills are required along with demonstrated initiative and innovative thinking within a team environment
* Percentage in service 100

Contact

For more information on the position please contact Wout van Grunsven, Section Head PDC; 0412 66 1251

Job
: Project Management

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Project-Manager-Scientist-DSP-Development-Job-NB/1851270/185127018512702012-06-15Merck/MSDProject Managementfull-timeUSDstarting0BSOss, NB, NL
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position will have primary responsibility for addressing the global public policy implications of health technology assessments applied by governments in determining the reimbursement of medicines, in support of Merck business units and senior management. The incumbent will assist the Vice President, Global Public Policy (GPP) in identifying and developing policy responses to cross-cutting Health Technology Assessment (HTA) and related developments that could impact Merck's business, working in close consultation with GPP/Corporate Responsibility regional policy leads as well as the Global Market Access division. The Director will participate in Merck's Health Technology Assessment Coordinating Committee - the Committee responsible for developing and implementing Merck's global strategy for addressing HTA.

Primary Activities:

* Serve as an internal expert on international (i.e., ex-US) HTA and related issues affecting public policy development.
* Represent GPP/CR on HTA advocacy working group, including the development of objectives and priorities, implementation of work program, and outreach to relevant divisions within Merck and external HTA experts. This role will require close working relationship with Global Market Access and Merck Research Laboratories divisions and coordination with a wide array of internal stakeholders.
* Draft public policy positions and discussion papers on cross-cutting HTA and related international reimbursement issues.
* Interface with GPP/CR's regional policy staff, Merck's Global Market Access team and regional business experts on HTA issues to identify broad, public policy topics and ensure successful resolution.
* Help present Merck's views on HTA and other reimbursement issues to other areas of Merck and external audiences.
* Participate in trade association taskforces and working groups to address HTA topics affecting the pharmaceutical industry.
* Engage with external expert groups formed to guide HTA policy development globally, such as Health Technology Assessment international (HTAi) and International Society of Pharmacoeconimcs and Outcomes Research (ISPOR).
* Assist senior public policy and business leaders in advocating before government authorities and other external stakeholders Merck's positions on HTA and other reimbursement topics.
* Work with Vice President, Global Public policy to organize teams of professionals who gather information from different units within Merck to help formulate policy on increasingly complex HTA and related subject matters. These teams will initiate policy development, examine the interactions of public policy and business strategy, and be principally responsible for the finalization of policy positions and recommendations on issues transcending divisional boundaries.
* Help create forums and opportunities to share information among the policy and business leaders within the company to share best practices, spot emerging issues, and ensure appropriate harmony of approaches.
* Draft high level speeches and other presentations as part of industry roundtables or key opinion leader conferences.

Qualifications

Education Requirements:

* Bachelors Degree minimum

Required Experience / Skills:

* 10 or more years of experience in public policy.
* Knowledge of Health Technology Assessment systems and associated public policy issues.
* Experience with international pricing and reimbursement systems and advancing advocacy efforts to address public policy aspects of such systems.
* Ability to work with cross divisional and multi-functional teams within the Company to achieve consensus on policy positions.
* Superior written and oral communications skills in order to communicate complex policy issues within the Company, transmit information back to policy makers from affected Company units, and prepare senior management for policy forums.
* Experience participating in multi-functional teams in a large corporate setting.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # POL000119.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-PD1

Job
: Policy/Government Relations

Primary Location: US-DC-Washington
Other Locations: Ireland, IE-Leinster-Dublin, Switzerland, US-NJ-Rahway, US-PA-Upper Gwynedd, US-PA-West Point, NL-NH-Haarlem, US-NJ-Whitehouse Station, NL-NB-Oss, Italy, US-NJ-Kenilworth, Netherlands
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Washington-Director-Global-Public-Policy-Job-DC-20001/1848107/184810718481072012-06-15Merck/MSDPolicy/Government Relationsfull-timeUSDstarting0BSWashington, DC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Marketing Coordinator Job Responsibilities:

* Implements marketing and advertising campaigns.
* Tracks product sales by analyzing and entering sales data.
* Prepares marketing reports by collecting, analyzing, and summarizing sales data.
* Keeps promotional materials ready; inventorying stock; placing orders; verifying receipt.
* Plans meetings and trade shows by identifying, assembling, and coordinating requirements; establishing contacts; developing schedules and assignments.
* Maintain databases such as CRM systems.
* Monitors budgets by comparing and analyzing actual results with plans and forecasts.
* Updates job knowledge by participating in educational opportunities; reading trade publications and business books.

Qualifications

Education Minimum Requirement:

* Associate degree (required), B.S. or B.A. (desired) in marketing, business, agriculture communications, agriculture marketing

Required Experience and Skills:

* Computer proficiency with Microsoft Office. Excellent Word, Excel, PowerPoint (customized), and email (Outlook) skills
* Good communications skills
* Be able to operate under pressure and meet deadlines
* Good project management skills
* Sound understanding of the principles of marketing
* Ability to manage a campaign budget
* Good attention to detail
* Team player - works to ensure team goals are met or exceeded

Desired Experience and Skills -

* Minimum 2 years in marketing or sales administration experience

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAR004172.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Marketing Generic

Primary Location: US-KS-DeSoto
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/DeSoto-Marketing-Coordinator-Job-KS-66018/1809477/180947718094772012-06-15Merck/MSDMarketing Genericfull-timeUSDstarting0BSDeSoto, KS, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Responsibilities include but are not limited to:

* Help prepare USDA submissions for new veterinary biological products
* Review of Research Study Reports and Protocols
* Help ensure that all in-house USDA files are maintained appropriately
* Meet with R&D and Quality to obtain documents for submission
* Assists with obtaining documents for International registration of vaccines and for Certificates for Export of product
* Assists in preparation and submission of documentation relative to the acquisition of import, export and transit permits for biological products, research materials and controlled materials organisms, and monitors compliance with issued permits

Qualifications

Education Minimum Requirement:

* Bachelor of Science

Required Experience and Skills:

* Minimum 4 year science degree
* Computer skills (Microsoft)

Desired Experience and Skills:

* At least one year in a microbiology laboratory or other experience in pharmaceutical/vaccine/veterinary field.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # REG000950.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Regulatory Affairs Generic

Primary Location: US-KS-DeSoto
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/DeSoto-Regulatory-Affairs-Associate-Job-KS-66018/1868789/186878918687892012-06-15Merck/MSDRegulatory Affairs Genericfull-timeUSDstarting0BSDeSoto, KS, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck Sharp & Dohme Corp. currently has a Computer Validation Engineer position opening at its Wilson, North Carolina facility. The Wilson facility, located at the intersection of I-95 and US 264 Alternate, is a 500,000 square foot facility on 225 acres. As a Packaging Center of Excellence for Merck, the facility packages a variety of finished goods types for both domestic and international supply. The Wilson facility also includes one of Merck's Global Stability Centers of Excellence, which completes stability testing for active pharmaceutical ingredients and finished goods which are manufactured and supplied around the world. The facility has been in operation since 1983, and is located in Wilson, NC. Wilson, NC is conveniently located approximately 2 hours from NC beaches and 45 minutes from the state capitol, Raleigh, NC. Wilson is home to Vollis Simpson's Windmill Farm, the only North Carolina Baseball Museum and the Wilson Botanical Gardens.

The primary responsibilities of the Computer Validation Engineer include a variety of activities supporting our solid oral dosage packaging facility (packaging operations also includes secondary packaging of vial, syringe, and inhaler configurations). Main responsibilities include ensuring computer control systems and/or critical business systems comply with Merck's validation and regulatory requirements. This would include a technical understanding of information systems which include database & network applications, spreadsheets, data archive systems, MRP & inventory control systems, computerized maintenance management systems, etc. and automation systems which would include automated equipment & instruments, distributed control & SCADA systems, PLC applications, calibration & maintenance requirements, etc.

Specific areas of responsibility include, but are not limited to the following:

* Coordinating and performing activities to ensure the successful completion of computer validation projects.
* Actively participating in project teams and change control meetings to support site customers.
* Managing computer validation activities for given business areas among the Wilson site
* Providing guidance on computer validation and reviews computer validation. documentation to ensure consistency with site SOPs, divisional guidelines, policies, and regulatory requirements.
* Developing site SOPs relating to computer validation.

Qualifications

Qualifications

Required Education and Skills:

* Bachelors required
* Minimum of 4 years experience in a Quality function that supports compliance activities within pharmaceutical manufacturing facility.
* Expert knowledge of regulatory requirements/cGMPs especially as they pertain to computer validation activities.
* In depth knowledge of information systems and automation systems.
* Excellent written and oral communication skills (including technical writing).
* Experience in the development and management of metric/trend information.
* Excellent leadership skills, including collaboration and ability to identify and drive continuous improvement
* The candidate must also possess a high degree of problem solving ability (performance of root cause analysis) and have demonstrated ability to manage multiple priority projects/workload, ensuring timely completion.
* Strong knowledge of cGMPs and domestic and international regulatory requirements.

Preferred Skills:

* Masters degree
* Degree field in science, technical operations or engineering preferred.
* In-depth knowledge of domestic and international regulatory requirements.
* Experience designing and implementing lean business processes.
* SAP system experience.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition MAN001718.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Manuf./Operations Generic

Primary Location: US-NC-Wilson
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Wilson-Computer-Validation-Engineer-Job-NC-27893/1848101/184810118481012012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSWilson, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Wilson facility, located at the intersection of I-95 and US 264 Alternate, is a 500,000 square foot solid dosage / packaging site on 225 acres. The facility packages over 95% of physician samples in the U.S. market, including SINGULAIR, FOSOMAX, and MAXALT, among many others. The facility has been in operation since 1983, and was recently selected as Merck's Packaging and Stability Centers of Excellence for North America. Wilson, NC is conveniently located approximately 2 hours from NC beaches and 45 minutes from the state capitol, Raleigh, NC. Wilson is home to Vollis Simpson's Windmill Farm, the only North Carolina Baseball Museum and the Wilson Botanical Gardens.

The Analytical Chemist performs quality sampling, testing, and data review for bulk raw materials, active pharmaceutical ingredients, water, microbiological limits, primary packaging components, annual compendia component testing and finished pharmaceutical products.

* Tests, documents, reports, and provides second chemist review for stability samples.
* Interprets compendia and internal monographs, NDAs and Merck Quality Standards. Leads and documents investigations according to established procedures and recommends corrective actions.
* Basic knowledge in cGMP, CFR and other regulations in order to assure laboratory compliance.

Evaluate laboratory SOPs and recommend improvement opportunities to maintain compliance with corporate and regulatory guidelines. Develops or revises laboratory SOPs as required.

Qualifications

Required:

* B.S. degree in a science field required, preferably Chemistry
* Minimum of 1 year experience in a pharmaceutical laboratory
* Basic knowledge of analytical instrumentation with strong technical and interpersonal skills (ability to work in a team environment)
* Must have good technical writing skills and high attention to detail.
* Strong collaboration skills

Preferred:

* Lean Laboratory knowledge and experience
* Root cause analysis methodology

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # QUA002807.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality Lab Related

Primary Location: US-NC-Wilson
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Wilson-Analytical-Chemist-Job-NC-27893/1731304/173130417313042012-06-15Merck/MSDQuality Lab Relatedfull-timeUSDstarting0BSWilson, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck Sharp & Dohme Corp. currently has a Senior Level Quality Assurance Manager position opening at its Wilson, North Carolina facility. The Wilson facility, located at the intersection of I-95 and US 264 Alternate, is a 500,000 square foot facility on 225 acres. As a Packaging Center of Excellence for Merck, the facility packages a variety of finished goods types for both domestic and international supply. The Wilson facility also includes one of Merck's Global Stability Centers of Excellence, which completes stability testing for active pharmaceutical ingredients and finished goods which are manufactured and supplied around the world. The facility has been in operation since 1983, and is located in Wilson, NC. Wilson, NC is conveniently located approximately 2 hours from NC beaches and 45 minutes from the state capitol, Raleigh, NC. Wilson is home to Vollis Simpson's Windmill Farm, the only North Carolina Baseball Museum and the Wilson Botanical Gardens.

The Quality Assurance Manager reports directly to the site Quality Operations Director and leads a team of approximately 15 employees who are responsible for a variety of activities supporting our solid oral dosage manufacturing and packaging facility (packaging operations also includes secondary packaging of vial, syringe, and inhaler configurations). These activities include release of finished product to both domestic and international markets, product complaint management, deviation investigation and approval, computer validation, change control and management of internal and external audits and inspections (CDER and CBER). The Quality Assurance Manager is a recognized expert in both domestic and international regulatory requirements.

Primary areas of responsibility include:

* Responsible for quality assurance functions for plant wide systems/processes to include direct line support to production areas, finished product sampling and release, batch sheet reviews, complaint management, internal and external audits.
* Ensures that Quality Operations responsibilities for audits, investigations, regulatory document reviews, SOPs, change control documentation (including validation and qualification), computer validation, and other Quality Assurance related systems are properly implemented, conducted and documented.
* Responsible for the control and ultimate disposition of in-process materials and for the final release of finished goods from the site. Provides final approval of atypical investigations, emergency complaint investigations and validations.
* Establishes compliance direction for the site by ensuring adherence to divisional policies and guidelines as well as regulatory requirements. Proactively evaluates site compliance against emerging regulatory trends. Independently identifies and facilitates major compliance initiatives to improve compliance status and overall operational efficiency of the site. Actively participates in Plant/Quality committees and works with other site functional groups, such as the QO Laboratory, Production, Utilities, Site Services, and Maintenance to set direction for plant wide GMP initiatives.
* Manages the Quality Assurance area in accordance with company policy and applicable government regulations. Makes provisions to ensure job responsibilities of the Quality Assurance area are conducted in a timely and reliable manner.
* Performs the duties and responsibilities of the Director of Quality Operations in his/her absence. Acts as a key regulatory compliance liaison to interface with both domestic and international regulatory agencies during inspections (CDER and CBER). Primary departmental responsibility for assuring regulatory commitments are satisfactorily addressed. Serves as team leader and independently conduct audits of the Wilson facility.
* Ensures that Quality Assurance maintains the necessary human and capital resources to meet present and future needs of Operations and manages those resources to meet annual profit plan.
* Interviews and hires personnel. Ensures proper training of personnel is completed.

Qualifications

Required Skills:

* Bachelors or Masters degree
* Minimum of 8 years experience in pharmaceutical operations, technical operations and/or quality operations.
* Minimum of 4 years managerial experience in a Quality function that supports compliance and release activities within a GMP manufacturing facility.
* The candidate must possess highly developed communication, leadership and teamwork skills.
* The candidate must also possess a high degree of problem solving ability and have demonstrated ability to independently manage multiple high level priority projects/workload, ensuring timely completion.
* Has in-depth knowledge of cGMPs and domestic and international regulatory requirements.
* Must be able to provide technical direction and training to include Good Manufacturing Practice, safety practices, and documentation practices as they relate to the quality assurance of the product.

Preferred Skills:

* Degree field in science, technical operations or engineering preferred.
* At least 6 years experience in a Quality function desired
* Experience facilitating regulatory inspections/audits (CDER and CBER).
* In-depth knowledge of domestic and international regulatory requirements.
* Experience designing and implementing lean business processes.
* SAP system experience.
* Experience completing profit plan and budget activities.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # REG000859

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-BR1

Job
: Regulatory Compliance

Primary Location: US-NC-Wilson
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Wilson-Quality-Assurance-Manager-Job-NC-27893/1538422/153842215384222012-06-15Merck/MSDRegulatory Compliancefull-timeUSDstarting0BSWilson, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Wilson facility, located at the intersection of I-95 and US 264 Alternate, is a 500,000 square foot solid dosage / packaging site on 225 acres. The facility packages over 95% of physician samples in the U.S. market, including SINGULAIR, FOSOMAX, and MAXALT, among many others. The facility has been in operation since 1983, and was recently selected as Merck's Packaging and Stability Centers of Excellence for North America. Wilson, NC is conveniently located approximately 2 hours from NC beaches and 45 minutes from the state capitol, Raleigh, NC. Wilson is home to Vollis Simpson's Windmill Farm, the only North Carolina Baseball Museum and the Wilson Botanical Gardens.

The Analytical Chemist performs quality sampling, testing, and data review for bulk raw materials, active pharmaceutical ingredients, water, microbiological limits, primary packaging components, annual compendia component testing and finished pharmaceutical products.

* Tests, documents, reports, and provides second chemist review for stability samples.
* Interprets compendia and internal monographs, NDAs and Merck Quality Standards. Leads and documents investigations according to established procedures and recommends corrective actions.
* Advanced knowledge in cGMP, CFR and other regulations in order to assure laboratory compliance.
* Evaluate laboratory SOPs and recommend improvement opportunities to maintain compliance with corporate and regulatory guidelines. Develops or revises laboratory SOPs as required.

Please note this position is 2nd shift

Qualifications

Qualifications

Required:

* B.S. degree in a science field required, preferably Chemistry
* Minimum of 2 years experience in a pharmaceutical laboratory
* Advanced knowledge of analytical instrumentation with strong technical and interpersonal skills (ability to work in a team environment)
* Able to implement laboratory improvements and able to implement laboratory improvements and develop expertise in laboratory testing procedures.
* Must have good technical writing skills and high attention to detail.
* Strong collaboration skills

Preferred:

Lean Laboratory knowledge and experience

Root cause analysis methodology

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition QUA002888.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality Lab Related

Primary Location: US-NC-Wilson
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 2nd]]>http://jobs.merck.com/job/Wilson-Analytical-Chemist-Job-NC-27893/1826385/182638518263852012-06-15Merck/MSDQuality Lab Relatedfull-timeUSDstarting0BSWilson, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck, Sharp, & Dohme, Inc. currently has a Quality Assurance Analyst position opening at our Wilson, NC facility. The Wilson facility, located at the intersection of I-95 and US 264 Alternate, is a 500,000 square foot facility on 225 acres. As a Packaging Center of Excellence for Merck, the facility packages a variety of finished goods types for both domestic and international supply. The Wilson facility also includes one of Merck's Global Stability Centers of Excellence, which completes stability testing for active pharmaceutical ingredients and finished goods which are manufactured and supplied around the world. The facility has been in operation since 1983, and is located in Wilson, NC. Wilson, NC is conveniently located approximately 2 hours from NC beaches and 45 minutes from the state capitol, Raleigh, NC. Wilson is home to Vollis Simpson's Windmill Farm, the only North Carolina Baseball Museum and the Wilson Botanical Gardens.

The Quality Assurance Analyst for our solid oral dosage manufacturing and packaging facility reports to the Quality Assurance Coach to complete control of material, defect resolution, finished product release, batch sheet review, data compilation/support for internal/external audits and regulatory inspections, complaint investigations, product investigations, annual product reviews, regulatory document reviews, process change request activity, assessment of stability requirements, validation, data management, SOP development and review and other Quality Assurance related functions. The Quality Assurance Analyst is the primary source of advice, guidance and input regarding quality issues for production personnel and Merck divisional and intersite customers.

Specific areas of responsibility include, but are not limited to the following:

* Batch record review and bulk/finished product release activities
* Use of statistical methods in defect resolution
* Complaint and production investigations and writing technical reports
* Internal/external GMP audits and regulatory inspections
* Policy/procedure development and interpretation
* Review and approval of all GMP-related SOPs
* Improve compliance status of Wilson operations
* Equipment/process validation/qualification activities
* Review and approval of change control documents
* Regulatory document review
Track and trend compliance performance

Qualifications

Required Skills:

* Bachelors or Masters degree in science
* Minimum of 4 years experience in a Quality function that supports compliance and release activities within a pharmaceutical manufacturing facility
* Expert knowledge of regulatory requirements/GMP's
* Excellent written and oral communication skills (including technical writing), leadership and teamwork skills

* High degree of problem solving ability and demonstrated ability to independently manage multiple high level priority projects/workload, ensuring timely completion
* Identifies and reacts to changing trends
* Demonstrated expertise in multiple functional areas within Quality Assurance
* Strong collaboration skills
* Experience performing root cause analysis

Preferred Skills:

* Experience designing and implementing lean business processes
* SAP experience
* Experience in a production or operations role
* Strong ability to build and develop talent

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # QUA002801.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Qual Assurance & Ops Generic

Primary Location: US-NC-Wilson
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Wilson-Quality-Assurance-Analyst-Job-NC-27893/1729537/172953717295372012-06-15Merck/MSDQual Assurance & Ops Genericfull-timeUSDstarting0BSWilson, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Wilson facility, located at the intersection of I-95 and US 264 Alternate, is a 500,000 square foot solid dosage / packaging site on 225 acres. The facility packages over 95% of physician samples in the U.S. market, including SINGULAIR, FOSOMAX, and MAXALT, among many others. The facility has been in operation since 1983, and was recently selected as Merck's Packaging and Stability Centers of Excellence for North America. Wilson, NC is conveniently located approximately 2 hours from NC beaches and 45 minutes from the state capitol, Raleigh, NC. Wilson is home to Vollis Simpson's Windmill Farm, the only North Carolina Baseball Museum and the Wilson Botanical Gardens.

The Analytical Chemist performs quality sampling, testing, and data review for bulk raw materials, active pharmaceutical ingredients, water, microbiological limits, primary packaging components, annual compendia component testing and finished pharmaceutical products.

* Tests, documents, reports, and provides second chemist review for stability samples.
* Interprets compendia and internal monographs, NDAs and Merck Quality Standards. Leads and documents investigations according to established procedures and recommends corrective actions.
* Advanced knowledge in cGMP, CFR and other regulations in order to assure laboratory compliance.
* Evaluate laboratory SOPs and recommend improvement opportunities to maintain compliance with corporate and regulatory guidelines. Develops or revises laboratory SOPs as required.

Qualifications

Qualifications

Required:

* B.S. degree in a science field required, preferably Chemistry
* Minimum of 2 years experience in a pharmaceutical laboratory
* Advanced knowledge of analytical instrumentation with strong technical and interpersonal skills (ability to work in a team environment)
* Able to implement laboratory improvements and able to implement laboratory improvements and develop expertise in laboratory testing procedures.
* Must have good technical writing skills and high attention to detail.
* Strong collaboration skills

Preferred:

Lean Laboratory knowledge and experience

Root cause analysis methodology

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition QUA002884.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality Lab Related

Primary Location: US-NC-Wilson
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Wilson-Analytical-Chemist-Job-NC-27893/1826386/182638618263862012-06-15Merck/MSDQuality Lab Relatedfull-timeUSDstarting0BSWilson, NC, US
Description

This position is a pipeline position posting which is used for resume collection. We are currently collecting resumes for future opportunities at MSD across the Latin America region and will contact you if an opportunity arises.

Main Responsibilities:

* Fulfilling sales objectives

* Market knowledge and of competitors

* Organizing activities for training of positions

* Development and Implementation of action plans directed at customers

Qualifications

Qualifications:

* Minimum of two years experience in a similar position

* Ability to utilize computer technology

* Knowledge of the pharmaceutical sales process

* Client Oriented

* Results Oriented

* Direct and Transparent communication

* Initiative and driven

* Team Work

* Self-driven

Job
: Sales

Primary Location: PE-Lima-Lima
Other Locations: Brazil, Guatemala, Nicaragua, Costa Rica, Panama, Honduras, Mexico, Chile, Ecuador, Venezuela, Dominican Republic, El Salvador, Argentina, Colombia
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Lima-Sales-Representative-Job/1679789/167978916797892012-06-15Merck/MSDSalesfull-timeUSDstarting0BSLima, Lima, PE
Descripción
El programa de becas Erasmus busca estudiantes o recién licenciados que hayan realizado una beca Erasmus dentro de los últimos cuatro años para incoporarlos durante un periodo de 12 meses en alguno de nuestros depeartamentos: marketing, ventas, apoyo al negocio, médico, ensayos clínicos, finanzas, legal, etc. Durante esos 12 meses tendrá la oportunidad de aprender de los mejores profesionales y conocer el ambiente laboral de una compañía realmente global, siendo participe de importantes proyectos donde verá reflejado su trabajo en el día a día. Así mismo, dispondrá de un plan individualizado de desarrollo, con un tutor que velará por su aprendizaje real.

Cualificaciones
Requisitos mínimos:

- Licenciatura con título que la acredite
- Beca Erasmus en los últimos cuatro años
- Nivel alto de inglés
- Manejo a nivel avanzado del paquete Office
- Nivel alto de comunicación oral y escrita
- Orientación al cliente, capacidad de análisis y orientación a resultados
- Dinamismo e iniciativa para implementar nuevos proyectos y tomar decisiones rápidas

Requisitos deseables:

- Máster, preferiblemente MBA
- Experiencia laboral de 1-2 años
- Movilidad geográfica nacional e internacional

Puesto
: Servicios de RR. HH. /consultoría genéricos

Ubicación principal: ES-M-Madrid
Tipo de acuerdo laboral: Fijo(a)
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Madrid-Becas-2012-Internship-Talent-Program-Job-M/1781708/178170817817082012-06-15Merck/MSDServicios de RR. HH. /consultoría genéricosfull-timeUSDstarting0BSMadrid, M, ES
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Director, Merck Animal Health Communications has the following responsibilities:

Develops and implements communications strategies and programs in support of the business objectives of the U.S. region of Merck Animal Health; serves on the leadership team for the region and other key cross-functional teams, providing advice on strategic communications and business issues; serves as the liaison to external stakeholders, including third party groups, and shapes communications strategies for the news media; oversees the selection of, and ongoing interactions with, multiple PR agencies and related product budgets to implement comprehensive communications plans; directs internal and external communications activities in the region related to Merck Animal Heatlh-wide or company wide initiatives; provides executive communications support to region leader, and ensures proper alignment between product brands, corporate identity and media relations strategy.

1. Communications Strategy Development and Execution

* Creates, develops and implements annual communications plan and effective, innovative communications about products to support the U.S. Animal Health business.
* Serves on leadership team and advises senior management on communications about business issues.
* Develops and executes communications strategies and programs on major developments and issues for products or the business, including highly sensitive and volatile issues.
* Direct the activities of outside consultants and PR agencies as needed to ensure projects are up to Merck's quality and brand standards and are completed on time and within budget.

2. External Product Communications and Media Relations

* Develops and maintains clear, consistent and compelling messaging about the U.S. business and products for use in product communications, executive communications, internal communications, investor forums, public speeches and other communications venues.
* Manages the preparation, clearance, and dissemination of news releases and other written and electronic communications materials consistent with U.S. and international regulations and policies.
* Works closely with Global Communications, MAH and other Merck business colleagues to provide public relations direction and support for communications about MAH and its products, to help position the MAH business and Merck as global industry leaders.
* Acts quickly and decisively to anticipate and seize communications opportunities; recommends strategies to management, including risk assessments.
* In collaboration with the Corporate Media COE, develops media relations strategies to generate positive and/or balanced coverage in U.S. print and electronic news media about MAH business and its products.

3. Internal and Executive Communications

* Develops and delivers strategic internal communication plans to inform employees about the business and its strategies, and to heighten employee morale and engagement.
* Provides communications counsel and executive communications support to region head.
* Monitors progress against goals and modifies strategies and priorities in response to an extremely challenging and competitive business environment.
* Ensures consistent communications processes and procedures, coordinates communications activities, and shares best practices.

4. External Issues Management and Third Party Communications

* Where appropriate, develops and manages education programs and product communications programs; adapts programs and strategy throughout the year based on environment.
* Identifies and builds relationships with key external groups, when appropriate, and represents MAH to these organizations.

Qualifications

Education Requirements:

* Bachelor's degree in Business, Communications or Journalism or related field of study

Required Experience / Skills:

* 8 to 10 years' relevant animal health/pharmaceutical communications, marketing or public relations experience.
* Excellent judgment and problem solving skills, as well as core functional skills, such as writing and editing.

* Excellent strategic communications counseling, media relations, corporate social responsibility, issues management, executive speech writing and marketing communications experience and skills.

* Ability to develop and execute impactful internal and external communications strategies and programs, including understanding and navigating complex scientific and policy/regulatory issues, and ability to manage outside agencies and vendors.

* Superior executive/management skills such as relationship building and collaboration, problem solving, decision making, and motivating and leading teams.

* Ability to travel domestically and internationally.

Preferred Experience / Skills:

* Master's degree

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # GLO000182.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Global Policy/Communications Generic

Primary Location: US-KS-DeSoto
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/DeSoto-Director-Regional-Communications%2C-Merck-Animal-Health-Job-KS-66018/1877976/187797618779762012-06-15Merck/MSDGlobal Policy/Communications Genericfull-timeUSDstarting0BSDeSoto, KS, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck Animal Health is a leading manufacturer of vaccines for swine health. We are offering a summer internship opportunity at our R&D facilities as a member of a research team developing new solutions for protection of swine species against infectious disease pathogens. In this role, you will gain first hand experience in what it takes to bring a vaccine to the commercial market. Opportunities are available for candidates enrolled in undergraduate, graduate or doctoral degree programs. Candidates should have an interest in laboratory and clinical research, solving scientific problems; enjoy working in a highly-collaborative team environment, and should have excellent oral and written communication skills. Applicants should have a science background and a working knowledge of basic laboratory techniques. The successful candidate is expected to be open to learn throughout the internship and to be thorough and methodical about planned experiments. The intern should be committed to making an active contribution to team goals. General computer skills are essential, as are good communication skills and the ability to keep accurate records.

Summer Internship appointments are generally 9-11 weeks in duration and are normally 38.75 hrs/wk. Summer interns will receive an industry competitive stipend. This position does not provide housing or relocation assistance.

Qualifications

Required:

* Candidates must have a minimum junior standing in a four year bachelor program in a life science discipline.
* Must be available for a period of 9-11 weeks, beginning June 2012.

Preferred:

* Demonstrated career interest in swine science or swine veterinary medicine.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #RES001296.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-KS-DeSoto

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/DeSoto-Research-Intern-Animal-Health-Job-KS-66018/1792956/179295617929562012-06-15Merck/MSDInternfull-timeUSDstarting0BSDeSoto, KS, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under general supervision of Manager or Director, Epidemiology-BARDS (Biostatistics & Research Decision Sciences), responsible for the planning, execution, coordination of administrative functions, progress reporting, control analysis, and presentation of results from epidemiologic research studies conducted within Merck Research Laboratories (MRL), independently handling assigned duties and trouble shooting to ensure that objectives of the epidemiologic research program are met in a timely manner. Works closely with Clinical Research, Regulatory, Biostatistics, Human Health Division and investigators/study coordinators at external investigator sites to coordinate activities for epidemiologic research programs.

* Coordinates all aspects of epidemiologic research programs, including the preparation of the study protocol, and design of studies, ordering and shipping of all equipment and supplies, directing design and preparation of data collection forms, tabulating data and preparing data summaries for regulatory submissions, publications and technical reports, with delegation of certain tasks where possible. Effectively describes complex procedures for epidemiologic studies to outside investigators and their staff, and assists in study coordination, correspondence, progress reporting, documentation and training of outside staff conducting epidemiologic studies funded by MRL. Maintains up-to-date reference documents or database identifying status, documents and other pertinent correspondence.
* Directs activities such as data entry and transfer, file checking, and data audit of epidemiologic data to ensure high quality data. Writes basic to complex programs to process, retrieve, and summarize epidemiologic data, performing statistical calculations in consult with MRL Biostatisticians where necessary. Describes more complex programming needs to professional programmers and more complex statistical analyses to statisticians in other MRL areas. Requires basic knowledge of statistics, diverse computer systems, data retrieval processes, programming and database designs, including those within MRL and national public domain databases. Determines own approach to task and independently applies basic and more complex techniques.
* Independently performs data queries and summarizes epidemiologic information tabularly and graphically using data from national, internal or external sources in response to questions posed by more senior members of Epidemiology or by other departments within Merck, documenting research results in formal reports or manuscripts. Requires firm grasp of the appropriate literature and familiarity with data resources within and outside the department.
* Prepares oral presentations and written reports to effectively communicate results of epidemiologic studies to more senior staff members, and to Merck project teams, management, and individual investigators. Prepares abstracts and manuscripts for persentation at professional scientific meetings and submission to peer-reviewed journals. Supports senior epidemiology staff members in writing and summarizing results of research studies. Makes seminar presentations. Participates in training of new members of Epidemiology.
* Identifies technical problems arising in the conduct and analysis of epidemiologic studies, independently pursuing solutions. Participates in discussions with technical personnel at regulatory agencies and with clinical investigators, taking initiative in developing resolution or substudy protocols to address technical problems. Organizes own efforts to achieve goals. Maintains technical skills by reading journals and attending professional society meetings. Communicates with professionals outside Merck about technical problems.

Qualifications

Education:

* Master's degree in Epidemiology, or a closely related discipline, with equivalent experience and ability to conduct independent research in Epidemiology, or a closely related discipline, together with at least four years experience
* Doctoral degree in Epidemiology, or closely related discipline

Required:

* Exposure to statistics, basic sciences and/or medical research.
* Must have strong communication, interaction and organizational skills
* Academic or practical experience in experimental design and a basic knowledge of epidemiologic research, including statistics commonly used in epidemiologic studies.
* Familiar with software package(s) used to process epidemiologic data.

Preferred:

* Good communication skills (written and oral)
* Experience as a leader of teams, collaborative research experience, analytic knowledge, industry experience is desirable
* Experience in designing, implementing, analyzing and interpreting epidemiology studies and/or outcomes research studies
* Experience in drug and/or vaccine safety desirable.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # EPI000198.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-EK1

Job
: Epidemiology

Primary Location: US-PA-Upper Gwynedd
Other Locations: US-NJ-Springfield, US-NJ-Kenilworth, US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: N/A

Hazardous Materials
: None]]>http://jobs.merck.com/job/Upper-Gwynedd-Epidemiologist-Job-PA-19436/1816968/181696818169682012-06-15Merck/MSDEpidemiologyfull-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

Under the direction of a Senior Director or Director, the Associate Director has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs. This includes all phases of clinical development, study design, study placement, study monitoring and concern for the protection of human subjects who participate in the clinical trials.

* May supervise the activities of Associate Directors, Clinical Associates and/or Medical Program Coordinators for specific research project to which assigned by the Senior Director.
* With the guidance of the Senior Director, the Associate Director is responsible for initiation of clinical Operational Plans for the development of new Merck drugs or for the completion of projects involving marketed drugs.
* With the guidance of the Senior Director, the Director is responsible for planning and initiating clinical trials involving new Merck drugs or marketed products.
* Responsible for the development of approved protocols for clinical studies to which assigned and is responsible for the initiation, monitoring and completion of the clinical studies.
* Responsible for the analyzing and summarizing the clinical findings from studies for the purpose of decisions regarding safety and efficacy and to support investigational new drug submissions and new drug applications or clinical experience reports.
* Serves as a member of appropriate research project teams in regard to the development of new compounds in order to provide medical input and judgment.
* Works closely with the respective Marketing area and with Regulatory Affairs in the preparation of package circulars including review and revisions.
* Responsible for maintaining awareness of scientific developments within his/her area of expertise, both in terms of new methodology, new research activities and in terms of identification of competent, potential investigators.
* Required to establish communications with prominent clinical investigators in his/her particular field of interest, particularly those who will be willing and able to assist in the evaluation of Merck drugs.
* Expected to attend appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility.
* Assists the Senior Director in maintaining liaison with appropriate Corporate areas in order to keep them informed of the progress of the investigation of both Merck drugs and competitor drugs and in regard to expert opinion concerning scientific questions in his/her of responsibility.
* May travel on company business about twenty percent of the time of order to visit clinical investigators in regard to potential or active clinical research projects.

Qualifications

Education Minimum Requirement:

* M.D. Required

Required:

* Board Certification or Eligibility is preferred.
* Must have experience in industry or academia.
* Vaccine or Infectious Disease experience
* Demonstrated record of scientific scholarship and achievement.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CLI002596.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Clinical Research (Non-M.D.)

Primary Location: US-PA-Upper Gwynedd
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Upper-Gwynedd-Director-Clinical-Research-Job-PA-19436/1660008/166000816600082012-06-15Merck/MSDClinical Research (Non-M.D.)full-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Enterprise Learning Co-Op will assist in building a Social Learning program to support the Summer Intern Class of 2012. Utilizing Lean Sigma processes and internal and external social media tools, the Co-Op will provide HR with insight to the target audience and help create, execute and report on the program. Decisions during the planning phase will be made with the guidance of the project leaders; however this position has ultimate power when creating content to be consumed by the social group. By its nature, Social Learning is an organic, ground-up process that will be nurtured by the candidate

Primary Opportunities and Responsibilities of this position are as follows:

* By having a good technical understanding and ability to pick up new tools quickly, the candidate will be able to spot issues as they arise.
* By leveraging technology and having the ability to think quickly and act decisively, problems will be resolved on the fly.
* The candidate will have a unique opportunity to be a champion of social technology and the future path for training the next generation of employees at Merck.
* The candidate will also be stewards of a company's social media policy and tools and must demonstrate personal integrity and professionalism worthy of such responsibility. The candidate's work will be reflected on media properties both inside and outside the company.
* This job, and the pilot which the candidate will create, will provide the foundation for Social Learning within the enterprise. It will engage stakeholders and leaders within HR that Social Learning is a viable, valuable and worthwhile endeavor

Primary Activities include but are not limited to:

* Project Planning:
* Create VOC (Voice of the Customer)
* Write project charter
* Develop SIPOC
* Develop PIB (Project in a Box)
* Create project plan
* Identify mentor and former intern network

Project Execution:

* Blog to Intern community
* Interact with mentors and other program leaders
* Manage presence in social networking sites including Sync Community, Facebook, Twitter, and other similar community sites, posting on relevant blogs, engaging in dialogues and answering questions where appropriate
* Monitor dialogue across designated social media channels

Qualifications

Education:

* Relevant coursework towards a Bachelors degree is acceptable
* Education or experience in journalism, communications, marketing or public relations is preferred

Required:

* A minimum of 1 years of course work with direct relevant social media management experience required

* Proficiency Level in MS Office required

* Strong project management and organizational skills; ability to multi-task

* Self-starter who is solutions-oriented, thrives under pressure, enjoys fast-paced work and is dedicated to quality

* Extremely motivated and in search of a challenging, enriching opportunity

* Ability to effectively communicate information and ideas in written and verbal format, and build and maintain relationships

* Must be able to work in team environment, requiring participatory decision-making/cooperative interactions among employees

* Accuracy and attention to detail

* Excellent interpersonal skills and service-oriented attitude

Preferred:

* Interactive media experience
* Possesses a functional knowledge of HTML
* Develop creative videos as well as blog posts and threaded discussion responses
* Mastery of Social Media Tools: Must be proficient in the tactical use of core platforms (Facebook, Twitter, blogs, YouTube, etc.)
* Course work in Instructional Design
* Experience or coursework in marketing and/or web technology
* Course work in learning theories
* Experience with Social Learning technologies in a business setting

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # HR 000272.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-PA-Upper Gwynedd

Job Type
: Intern
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/Upper-Gwynedd-Enterprise-Learning-Co-Op-Job-PA-19436/1729541/172954117295412012-06-15Merck/MSDInternfull-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview:

Merck BioVentures, is responsible for assisting in developing commercialization strategies and execution of these strategies for Biosimilar drug candidates in late stage clinical development.

The Device Regulatory Lead in Merck BioVentures is responsible for developing the global device regulatory strategy for the entire portfolio of biologic products in order to ensure timely approval for the use of delivery devices associated with biologics products. The position would include developing device filing requirements by region including Device Risk assessments for various filing scenarios.

In this position your responsibilities include but are not limited to:

* Device regulatory development and approval strategy for entire portfolio of biologic products.
* Device approval requirements by region including Device Risk assessments for different filing scenarios.
* Key contact with external device manufacturers on regulatory matters.
* Outline pre-approval inspection requirements for various sites.
* Lead discussions with regulatory agencies on device issues.
* Import/export issues for devices during development and marketing.
* Stability and biocompatibility study requirements.
* Support the protocol for ISO and human factor testing and interpreting agency requirements.
* Review of device product info and labels.
* Keep abreast of emerging global device regulations and trends including attendance at key device meetings.

Qualifications

Educational requirements:

* B.S. degree in a biological science, chemistry or related field with at least 8 years experience in regulatory affairs with a minimum of 5 yrs recent experience with delivery device development and approval.

Preferred:

* Advanced degree in a biological science, chemistry or related field with at least 8 years experience in regulatory affairs with a minimum of 5 yrs recent experience with delivery device development and approval.

Required Experience and Skills

* Good organizational, communication, interpersonal and negotiating skills.
* Experience with conducting agency meeting with health authorities.
* Regulatory experience with development / approval of biologic injectable delivery devices.
* General competency with drug development.

Preferred Experience and Skills:

* Participated in submission of marketing authorization applications worldwide resulting in approval of injectable delivery devices.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # REG000830.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Regulatory Affairs Generic

Primary Location: US-PA-Upper Gwynedd
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Upper-Gwynedd-Director-Regulatory-Affairs-Drug-Delivery-Devices-Job-PA-19436/1431789/143178914317892012-06-15Merck/MSDRegulatory Affairs Genericfull-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Oncology Clinical Science Liaisons serve as scientific liaisons to Merck investigators or physician/scientists with potential interest in participating in Merck studies (MRL sponsored trials, Merck Investigator Initiated Study Program (MISP), and Oncology Collaborative Study Program (OCSP). Clinical Science Liaisons report to the Manager, Oncology Clinical Science Liaisons in Global Medical Affairs.

**This position will be responsible for the Mid-Atlantic Territory**

Responsibilities include and are not limited to the following:

* Serve as Medical and Scientific Liaison supporting Merck studies through ongoing interaction with clinical investigators and potential investigators
* Maintain an expert level of scientific knowledge about the molecular biology of cancer and the rationale for current cancer therapies
* Work with Regional Director Medical Affairs, MRL Staff, and Global Clinical Trial Operations to understand the objectives and science around Merck studies
* Identify potential study sites and increase participation in studies of Merck compounds by increasing investigator awareness of the variety of research opportunities supported directly or indirectly by Merck Oncology
* Discuss relevant scientific issues with investigators that relate to actual or potential clinical oncology research activities
* Facilitate publication and early dissemination of Merck-sponsored study results
* Attend relevant oncology professional society meetings to support ongoing self-education, to maintain awareness of new science in Oncology and to interact with investigators in the same capacity in which they interact with them in other settings

Qualifications

Education:

* Required: Health Care Professional (MD, PharmD, RN, NP, PA) or scientist (PhD, MS)

Required:

* At least 3 years experience in clinical oncology, oncology basic science, oncology clinical trials, oncology scientific liaison function or other highly relevant clinical and scientific experience
* Must possess demonstrated ability to interpret and communicate complex scientific issues
* Must have significant prior oncology-related experience and possess a high level of understanding of the clinical and scientific challenges facing oncology researchers
* Strong interpersonal skills with ability to work independently and within a team
* Demonstrated Project Management Skills
* 50% Travel required for this position

Assets:

* Experience or working knowlege of cancer centers
* Previous experience as a Medical Science Liaison

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # REG000946.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-AW1

Job
: Regulatory Affairs Liaison

Primary Location: US-PA-Upper Gwynedd
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Upper-Gwynedd-Oncology-Clinical-Science-Liaison-Job-PA-19436/1866479/186647918664792012-06-15Merck/MSDRegulatory Affairs Liaisonfull-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Sr. Manufacturing Engineer is a member of the IPT (Integrated Process Team) and provides technical support to the vaccine bulk production area. The production includes media preparation, cell culture, viral and filtration processes as well as supporting area such as sterile goods/parts supplies and media preparation. This support will focus on investigation of manufacturing deviations, process improvement and optimization. Specifically, this individual will lead the deviation investigation to determine root cause, develop corrective actions to prevent reoccurrence and assess the impact on product quality. The incumbent will also be responsible for leading process improvement projects and implementation the productivity enhancement initiatives.

Responsibilities include, but are not limited to, the following:

* Lead in the identification and implementation of process improvement projects, productivity initiatives and corrective actions while focusing on equipment uptime, minimizing cost and maintaining process consistency
* Investigate deviations (both minor and major), with responsibility to interface with Operations, GVTE (Global Vaccine Technology & Engineering), Automation, and Quality approvers.
* Author and manage the investigations to meet key timing commitments, with well-investigated and well-documented deviation reports.
* Work with the Technology, Automation, and Quality Approvers to determine the breadth and scope of the investigation to identify the appropriate root cause, implement corrective actions, complete trending analysis, and determine product disposition.
* Foster a collaborative relationship with manufacturing floor personnel focused on high quality investigations, meaningful corrective actions, and reducing the deviation generation rate. Determine appropriate corrective actions to prevent reoccurrence of the deviation. Ensure corrective actions are effective and improve right first time (RFT).
* As part of the deviation management role, present and defend investigations during regulatory inspections, as required.
* Perform a thorough review of batch records and related GMP documentation, identifying and resolving discrepancies in a timely manner, and implementing corrective actions to improve the batch record execution/review process.
* Develop training material. Working with subject matter experts (SMEs), provide/track necessary training for operator qualification as assigned.
* Work alongside operations and lean six sigma team members to develop reliable, consistent manufacturing processes that meet cGMP requirements.
* The successful candidate must have strong problem solving skills and a hands-on approach to problem solving. The successful candidate should be able to examine an issue from diverse perspectives (safety, compliance, automation, equipment, process, and people) in order to best understand and resolve it at root cause.

Qualifications

Education:

BS/MS in engineering preferred in chemical or industrial engineering. Other fields in scientific disciplines can be considered provided the candidate has strong, relevant and hands-on work experience.

Required:

* A minimum of 5 years relevant experience
* Familiarity with cGMPs and vaccine regulatory requirements
* Experience in problem solving and troubleshooting
* Technical writing and deviation investigation experience
* Biological product manufacturing process improvement and optimization experience

Desired:

* cGMP experience in a sterile, bulk or finished pharmaceutical environment.
* Experience with formal problem solving techniques, such as root cause analysis (RCA), failure mode effects analysis (FMEA), and/or Lean Six Sigma tools.
* Experience in automation and manufacturing execution system (MES), process modeling and process improvement.
* Experience in deviation management, troubleshooting and resolving manufacturing anomalies.
* A minimum three year supervisory or project management experience.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAN001260.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Manuf./Operations Generic

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-Sr_-Manufacturing-Engineer-Job-NC-27701/1525481/152548115254812012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Quality Operations Laboratory Analyst performs laboratory testing on a variety of product samples, including bulk vaccine, filled vaccine, and media. The successful candidate may be assigned to work in any of the three main areas of the laboratory.

Biochemistry Laboratory

The emphasis is on ELISA and basic benchtop biochemistry, such as Karl Fischer moisture analysis, thermal stability, and restoration.

Microbiology Laboratory

The emphasis is on microbiological methods, such as compendial sterility, bacteriostasis/fungistasis, mycoplasma, and in-vitro mycobacteria.

Bio-analytical Methods

The emphasis is on cell-based and virological laboratory methods, such as tissue culture safety, cell-line maintenance, and infectivity titration (potency).

The successful candidate:

· Has knowledge of biochemical laboratory techniques and processes, and/or cell culture propagation and maintenance procedures, and/or microbiological laboratory procedures

· Authors standard operating procedures (SOPs) for the performance of laboratory methods

· Trouble-shoots equipment issues as needed

· Initiates and contributes to laboratory investigations as needed and follows site procedures in the documentation of Quality Notifications and CAPAs

· Collaborates with Durham Laboratory Compliance to ensure adherence to regulatory requirements

· Provides active support during audits and inspections (regulatory, internal, safety)

· Supports MMD divisional and Quality initiatives

Qualifications

Required:

· B.S. degree in a science field required, preferably biology, microbiology, or biochemistry

· Must have good technical writing skills and high attention to detail.

· Must be able to work independently and within a team environment

· Must possess good communication skills

Preferred:

· Knowledge of cGMPs

· Root cause analysis methodology

· Lean Laboratory knowledge and experience

· Experience in analytical method transfer

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # QUA002743.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality GMP Related

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-QO-Lab-Analyst-Biological-LabsMethods-Job-NC-27701/1650159/165015916501592012-06-15Merck/MSDQuality GMP Relatedfull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Supplier Development & Performance Management (SD&PM)

Overview / Basic Functions & Responsibilities:

Responsible for serving as the primary point of contact with Suppliers for MMD sites within the region. Responds to requests from SD&PM-Core and other MMD representatives outside of the region to manage Suppliers within the region.

Responsible for implementing procedures and best practices supporting Merck's Supplier Development & Performance Management program, under the direction of the SD&PM Relationship Manager. The incumbent will exercise leadership in monitoring and maintaining Supplier compliance with worldwide regulatory requirements, current Good Manufacturing Practices (cGMPs), MMD Quality Manual, and pertinent legal and / or business contract requirements. Key responsibilities include leading Supplier Deviation investigations, evaluation and execution of Supplier Change Management, upskilling Suppliers, and interfacing with MMD sites associated with Supplier issues within the region. The incumbent will assist the SD&PM Relationship Manager in calibrated Quality oversight and interfacing with Procurement and Technology colleagues.

The incumbent will work with an assigned SD&PM Relationship Manager for personnel-related requirements and workload balancing as well as a functional SD&PM Relationship Manager in a matrix organization for functional guidance.

The incumbent will possess Analytical, Scientific, Technical, Manufacturing, and / or Quality experiences in order to effectively administer and control Quality and Technical programs and projects needed to manage Suppliers, under the direction of the SD&PM Relationship Manager.

Primary Roles include, but are not limited to:

* Travels up to 50% of the time, to and from Supplier sites and MMD sites within the region.
* Serves as the primary point of contact to Suppliers in the region.
* Responsible for coordination, oversight and communication on matters related to the cGMP status with the Suppliers. Must understand worldwide regulatory requirements and current Good Manufacturing Practices associated with materials supply.
* Acts as a liaison between Suppliers and internal Merck site personnel.
* Travels to and from Suppliers' locations to resolve Manufacturing, Quality, Technical and supply issues as well as facilitating overall Quality improvements to proactively prevent Supplier issues.
* Provides support to the Suppliers to facilitate, qualify, and / or validate materials for new product introductions.
* Provides compliance input and support for implementation of analytical methodology and process development initiatives.
* Coordinates and evaluates Supplier-initiated or Merck-initiated Change Control associated with materials supply.
* Coordinates, communicates and oversees general technical matters pertaining to Suppliers, including understanding and optimizing component / material usage and upskilling Suppliers to provide improved materials and services.
* Partners with SD&PM Quality, Procurement and Technology colleagues to provide efficient and effective solutions and Corrective Actions / Preventative Actions (CAPAs) to Supplier and / or site issue resolution, including Deviation Management, response to Supplier audit issues and customer complaints.
* Provides technical consultation, review and execution of Quality Agreements, Change Control Agreements and Supply Agreements.
* Tracks and monitors Supplier operational and quality performance. Escalates issues to the SD&PM Relationship Manager, SD&PM Technology Managers, and to site personnel.
* Assists in development and delivery of Supplier metrics and scorecards.
* Participates in periodic Business and Relationship review meetings with Suppliers

Qualifications

Education:

* BS/BA degree in Engineering, Science or Business

Required:

* Minimum 5 years experience in Quality, Technical, Manufacturing Operations, or related Business Operations working with products or processes.

Preferred:

* Demonstrated Quality, Technical and / or Manufacturing experience in the areas of chemical, pharmaceutical and / or vaccine manufacturing or packaging.
* Six Sigma Black Belt, Green Belt or Yellow Belt certification
* Experience conducting technical investigations
* Ability to develop and / or improve commercial relationships
* Knowledge of cGMPs, technical writing, data management collection and analysis
* Facilitates business negotiations in a professional manner

Works independently with all levels of the organization, and has demonstrated the following skills:

* Rapid / Disciplined decisions
* Acts with courage and candor
* Drives results
* Escalation of issues / concerns to management, as appropriate
* Ability to Prioritize, Align and Simplify

*LI-AS2

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition QUA002866.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Qual Assurce - 3rd Party Manuf

Primary Location: US-NC-Durham
Other Locations: US-TN-Cleveland, US-FL-Miami Lakes, US-VA-Elkton, US-NC-Wilson
Employee Status: Regular
Number of Openings: 3

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Durham-SD&PM-Field-Generalist-Job-NC-27701/1809482/180948218094822012-06-15Merck/MSDQual Assurce - 3rd Party Manuffull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


As part of Merck's Quality Operations Organization, the Durham site Quality team is seeking highly motivated individuals for the role of Integrated Process Team Quality Assurance Coordinator responsible for providing on the floor Quality Assurance coverage, involing resolution/investigation of deviations and processing issues. These individuals will assist with executing/maintaining product release activities and review of supporting process documentation.

These individuals will partner with Manufacturing Operations, Automation and Technology as members of the demonstration team for the new Durham Vaccine Bulk Facility, focused on the demonstration of a new live virus bulk facility supporting VARIVAX® (Chicken Pox Vaccine) and ZOSTAVAX® (Shingles Vaccine) manufacturing. These individuals must embrace and be committed to working in an empowered team culture, with the goal of each employee reaching their fullest potential and having accountability and responsibility to one another, our community and our patients.

This role will allow you to use the Quality Assurance experience and expertise that you have gained and contribute directly to the successful manufacture of lifesaving Vaccine Products; additionally, you will be able to further develop your skills through partnering with Operations and Technical Support to successfully start up new vaccine facilities.

The Quality Assurance Coordinator will act as the primary contact working directly with the manufacturing team in a 24/7 operation.

Primary areas of responsibility:

* Partnering with Operations and Technical Support to resolve deviations and complex processing issues
* Managing deviations through the review of completed facility audits, noting deviation and trends and working to resolve
* Release of product through Batch Record Review and support process documentation review.
*
Review and provide guidance on investigations

*
Use your leadership skills to oversee special projects

*
Participate in Regulatory Inspections and Corporate Audits

* Support the Environmental Monitoring Program through sample collection and data evaluation

These positions require the incumbents to work a straight 12 hour day or 12 hour night shift.

Qualifications

Requirements:

* Bachelor Degree in an Engineering or Science Field
* These positions require the incumbent to work a 12shift that includes all days of the week and either a straight hour day or straight hour night shift.
* 5 Years of Experience within a Quality Assurance role supporting a GMP Manufacturing Process to include Batch Record Review and Deviation Management.
* Understanding of Aseptic Processing, Compliance Requirements, and Environmental Monitoring practices in a GMP environment

Preferred:

* Demonstrated leadership, teamwork and communications skills

* Knowledge or CFP, Eudralex and other regulatory guidance specific to the pharmaceutical industry

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # QUA002764.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality GMP Related

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 4

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/Durham-IPT-Quality-Assurance-Coordinator-Job-NC-27701/1689827/168982716898272012-06-15Merck/MSDQuality GMP Relatedfull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Production Associate performs various production and operations related tasks as part of an empowered team. Performs cleaning of Good Manufacturing Practice (GMP) space and equipment, operates and monitors equipment as deemed appropriate by skill level, provides materials and support needed to maintain equipment uptime, accurately and efficiently moves process materials in accordance with established procedures. Works in compliance with appropriate procedures, documentation, governmental regulations, safety programs, lean manufacturing principles and current good manufacturing practices (cGMPs).

Major Responsibilities:

Clean Room Cleaning/Materials Management (50% of time)

* Performs tasks that require aseptic gowning.
* Maintain clean rooms with appropriate cleaning and disinfection procedures. Includes mopping floors, walls and ceilings, wiping down equipment, removing trash and re-stocking supplies.
* Maintains the equipment prep area.
* Manages laundry including receipt and storage of clean garments, re-stocking of garments, and removal of dirty garments.
* May initiate purchase of cleaning chemicals, components and other consumables to ensure supply/inventory of production support items
* Move soiled equipment to equipment prep area for cleaning and/or sterilization.
* Manages inventory levels in Supermarkets/Kanbans.
* May coordinate w/ materials management and move filled vials from Vaccine Manufacturing Facility (VMF) staging area to cold storage in Materials Maintenance and Support Facility (MMSF).
* May move stoppers to equipment prep for sterilization, then to filling for use.
* Moves materials throughout Durham Facility and MMSF, as required. Includes operation of material handling equipment (forklifts, carts, hand trucks, etc).
* Expected to lift and move various items up to 50 lbs.
* In all work follows current good manufacturing practices (cGMPs), appropriate SOPs, safety programs, good documentation practices and other governmental regulations.
* Follows lean manufacturing principles.
* Performs CIP (Clean-In-Place) and SIP (Sterilization-In-Place) and associated skid activities in PSF (Pooling, Sonication & Filtration) Suite.
* Performs Shell Freezing/-70 Freezer activities to support downstream processing.
* Performs Grade A activities.
* Participates in and assists with the development and execution of personnel training.
* Demonstrates proficiency with Distributed Control System and other automated systems (including, but not limited to, SAP, MES, DeltaV, NG LIMS, HanDEL, Word, Excel)
* Performs sampling/in-process testing supporting the manufacturing and validation process for current process as well as developmental work for new products/processes as required.
* Schedules and performs environmental monitoring during processing and records results in the computerized database system.

Operations Support (40% of time)

* Operates and/or monitors production support equipment to include but not be limited to: parts washers, autoclaves, portable tank CIP/SIP/storage panels, stopper processor, heat sealer.
* Uses automated systems including MES and PLC based systems.
* Manages equipment flow (reusable parts, tubing machines, portable tanks, stoppers) through the equipment wash and prep area. Includes tracking soiled and clean hold times, proper labeling and inventory management of clean and sterile equipment using Kanbans and using the automated MES system to set QC status and expiry of sterile equipment.
* Picks-up, labels and delivers samples to appropriate sample storage locations.
* Performs tasks as needed to support continuous operations to include but not be limited to: emptying trash, handling and remediating spills, performing as-needed cleaning, assisting with Technician activities.

Information Transfer (10% of time)

* Receive training including safety, GMP, aseptic and process specific as required by the job
* Perform duties based on Star Model including: first level resource issue resolution, initiate quality improvement ideas, participate in quality, safety and environmental investigations, HECP, HAZOP and equipment challenges, support development of SOPs and training materials.
* Detect and communicate potential safety, environmental and compliance events
* Recommend improvements in equipment uptime and personnel efficiency
* May participate in regulatory inspections

Please note, this position requires the ability to work various shifts (evenings, overnights, weekends)

Qualifications

Education:

* High School Diploma or GED

Required:

* Prior experience cleaning equipments in a Good Manufacturing Practice (GMP) facility, OR have completed courses related to biotechnology (Bioworks).
* Basic computer skills, including knowledge of Microsoft Office applications.

Preferred:

* Prior experience working in a manufacturing environment.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PRO008901.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
ZZ5ML

Job
: Production / Maintenance

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/Durham-Production-Associate-Job-NC-27701/1528616/152861615286162012-06-15Merck/MSDProduction / Maintenancefull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The (Energy Center) Maintenance Mechanic will be responsible for the Energy Center operations and will provide maintenance support to the Vaccine Manufacturing Process. The Mechanic will operate all Plant Engineering utility generating equipment located throughout the entire site and take appropriate action to correct Plant Engineering maintenance problems. The mechanic will also be responsible for supporting departmental vision that provides for continuous improvement in all aspects of the operation. The Mechanic identifies and demonstrates a working knowledge of customers and or suppliers and their requirements.

Responsibilities include but are not limited to the following:

* Operate all Plant Engineering Equipment, which includes but not limited to air handling units, chillers, air compressors, boilers, and clean steam and WFI water systems.

* Sets up, adjusts, repairs, and maintains all vaccine process utility equipment

* Performs calibrations and maintains industrial instrumentation standards

* Prepares technical documentation (PMs, CIs, & validation procedures) on as needed basis

* Participate in the establishment of new equipment and the improvement of existing process equipment.

* Provides technical specifications and information to Quality, Manufacturing, Process-Project Engineers, and other MMD requestors

* Maintains Utility equipment by developing/performing PM's, developing/performing instrument calibrations, installing new equipment, completing validation protocols, documenting work using a computerized maintenance management system (SAP) and other duties as requested by the Utility Maintenance Coach.

* Performs preventative maintenance inspections and prepares inspection reports concerning operation of equipment and mechanical condition of equipment.

* Responsible for participating in new equipment installations by interfacing with equipment vendors and recommending spare parts, selecting lubrication processes and assisting process project engineers. Performing initial de-bug and redesign operations to make equipment operable.

* Responsible for performing assignments in conformance with appropriate Regulatory (GMP's) and department Standard Operating Procedures which assure the quality of our products.

Qualifications

Education:

* High school diploma/GED and 7 years maintenance experience with a focus on industrial utility systems management, troubleshooting & repair within an Energy Center environment OR a 2-year technical degree and 5 years maintenance experience with a focus on industrial utility systems management/troubleshooting & repair within an Energy Center environment

Required:

* Proficient in the use and knowledge of PCs (Hardware & Software) including project management, word processing, spreadsheet applications, and Microsoft Windows platforms

* Must be able to read electrical prints, P&ID's, and understand P&ID control loops

* Extensive industrial experience involving utility systems, with a strong knowledge of steam generation systems, air compressors, chillers, potable water systems, Building Automation Services, and HVAC systems

* Must have excellent documentation and verbal communication skills

* Must be able to function in a team-based empowered culture

* Must possess the ability to work independently and effectively with peers, and display strong interpersonal and organizational skill

* The ability to work a rotating schedule that includes weekend, holiday, evening and nights

Preferred:

* Knowledge of BAS (Building Automation System)

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

com/ to learn about the Durham Vaccine Facility and apply for this position and to create a profile and your resume for requisition# PRO008183. You can also request to be notified when future openings become available.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Job
: Production / Maintenance

Primary Location: US-NC-Durham
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/Durham-Energy-Center-and-Utilities-Technician-Merck-&-Co_%2C-Inc_-Durham%2C-North-Carolina-Job-NC-27701/963995/9639959639952012-06-15Merck/MSDProduction / Maintenancefull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career

The Sr. Manager, Regulatory Operations, Merck Consumer Care responsibilities include, but are not limited to the following:

· Lead all Regulatory Operations activities for Merck Consumer Care to enable regulatory submissions to Health Authorities on a global basis including:

o electronic document management

o submission planning and coordination,

o publishing and archiving

o ISI Writer template creation, maintenance and training

· Work collaboratively with Regulatory Affairs. Managers, Merck Consumer Care Regulatory Operations staff, Merck Research Labs colleagues and outside vendors to ensure quality, on time, regulatory submissions

· Keep current of CTD/eCTD requirements on a global basis

· Oversee Compliance activities related to commitment tracking and departmental SOPs and Work Practices

· Work with IT to evaluate submission and document management enabling technologies and ensure Merck Consumer Care requirements are considered as part of broader Merck technology initiatives.

Qualifications

Education:

* Bachelor's degree

Required:

* Minimum 8 years experience working in the pharmaceutical industry.
* Minimum 5 years of document management experience and submission preparation and publishing in a regulatory affairs department of a pharmaceutical company.
* Experience with CTD format as well as electronic submissions (XML and study tagging).
* Strong technical background and proficiency with documentum based electronic data management systems and electronic submission publishing tools; such as, CoreDossier or eCTDXpress.
* Strong written and verbal skills with customer service orientation.
* Ability to manage multiple projects simultaneously, work under pressure and adhere to deadlines.

Preferred:

* Familiarity with ISI Toolbox.
* Previous supervisory experience.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #REG000924.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-EF1

Job
: Regulatory Affairs Generic

Primary Location: US-NJ-Summit
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Summit-Sr_-Manager%2C-Regulatory-Operations%2C-MCC-Job-NJ-07901/1824621/182462118246212012-06-15Merck/MSDRegulatory Affairs Genericfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Project Manager leads the planning and implementation of complex global product launches and product changes on major consumer brands. Accountable for leading global project teams with minimal supervision, ensuring all launch and business criteria are achieved on multiple projects simultaneously. This includes the execution of projects to meet multiple project parameters, including project scope, market timing, cost, quality, multiple stakeholder expectations, and other defined and undefined requirements. Applies leading edge web-based project management processes and business/product development/supply chain knowledge, skills, tools, and techniques to commercialization project activities for complex new product launches and product changes in order to meet or exceed customer expectations and achieve on-time ship-to-trade delivery.

Major Activities/Responsibilities

* Leads with minimal supervision, and is accountable for, as one process, the planning, evaluation and implementation of complex global consumer product launch and product change projects. Projects include new product launches generated from the development of new technologies, health authority pre-submissions and acquisition activities around the globe.
* Assesses project requests from the business units or sales. Provides preliminary technical, logistical, cost, timeline, customer service, risk/benefit and other feasibility implications. Ensures launch success criteria are clearly defined.
* Develops project implementation plans, including resource allocation, critical path timelines and risk/contingency options. Ensures project timelines (MS Project) include cross-functional input and decision points. Oversees and ensures alignment of critical workflows with the project plan.
* Ensures that project activities/timelines for multi-faceted projects (e.g. new product launch, displays, print ads, etc.) are integrated.
* Leads multi-site, cross-functional commercialization implementation teams and oversees coordination/execution of activities. Manages project scope, cost, timing, and quality. Identifies and resolves team/project issues that may impact deliverables.
* Manages project communication to business teams across the organization. Assesses and facilitates critical project decisions with business teams and/or senior management to ensure project priorities are optimized.
* Manages project financial risk and contingency planning (COG's, capital, etc.)
* Tracks process metrics and project success criteria. Reports performance measures. Ensures post-launch reviews are conducted.
* Conducts or facilitates root cause investigations when project or process deviations occur, and identifies resolutions or corrective actions.
* Applies leading edge web-based project management processes and business/product development/supply chain knowledge, skills, tools, and techniques to commercialization project activities for complex new product launches and product changes in order to meet or exceed customer expectations and achieve on on-time ship-to-trade delivery.
* Utilizes and populates leading edge web based project management processes and tools with project data (timelines, agenda's, minutes and other critical project information).

Qualifications

Education:

* Required: BA/BS

Required:

* Minimum 3-5 years of project management experience
* Computer skills, including demonstrated experience with electronic project management, resource management and document workflow tools
* Advanced knowledge of Microsoft Project
* Demonstrated experience in team leadership/facilitation, decision-making, process management, analytical skills, negotiating and conflict-management skills, risk management, and written and oral communication

Preferred:

* Knowledge of global regulatory requirements
* PMP certification
* Six Sigma Green Belt certification
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PRO009586.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Product Dev Proj/Prog Mgmnt

Primary Location: US-NJ-Summit
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Summit-Project-Manager-Job-NJ-07901/1855927/185592718559272012-06-15Merck/MSDProduct Dev Proj/Prog Mgmntfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Associate Product Manager responsibilities includes leading or participating in all elements of the marketing mix including marketing plan development, advertising and promotion planning and execution, marketing research and consumer insights, new product development, market and competitive analysis, sales forecasting, budget and financial management, and manufacturing and operations interface. This position will include primary responsibility for several key areas of the marketing mix including digital advertising, consumer promotion and innovation under the supervision of a Product Manager on the brand.

Specific responsibilities will likely include:

* Manage digital advertising and communications including managing relationships with advertising and media agencies and development of creative
* Manage innovation projects from conception to launch including consumer insights, new product development and launch strategies.
* Manage consumer promotion initiatives both nationally and customer-specific
* Manage analytical needs of business including volume forecasting, budget management, and performance analysis
* Help develop and implement business plan including identifying key issues and developing strategies and initiatives to achieve the brand's volume goals
* Manage relationships with key customer teams to help brand deliver its volume goals and partner with Customer Marketing group to develop and implement relevant programming

Qualifications

Education:

* MBA required.

Required:

* A minimum of 2 years marketing/sales or business experience
* The candidate for this position must demonstrate strong general management skills in the areas of leadership, teamwork, innovation, executional excellence, strategic acumen, analytical skills, and project management.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. merck.com/careers to create a profile and your resume for requisition # PRO009635.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Product Management

Primary Location: US-NJ-Summit
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Summit-Associate-Product-Manager-Job-NJ-07901/1885958/188595818859582012-06-15Merck/MSDProduct Managementfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position will work collaboratively with Regional and Local Country Regulatory professionals and franchise research and development (R&D) and business colleagues to develop global regulatory strategies for new projects, to support the MCC Digestive Health and Women's Health Franchises.

Key activities include but are not limited to:

* Provide guidance and advice to R&D development teams, business partners, and to senior management on the regulatory requirements and milestones required for project success.
* Work closely with local country regulatory staff and MCC regulatory staff to ensure the production of dossiers that meet registration requirements in international markets
* Work cooperatively with Merck Research Laboratories (MRL) regional regulatory staff and Local country regulatory staff to ensure that MCC regulatory initiatives are executed as planned
* Monitor activities of trade group organizations and health authorities and advise MCC of new requirements and policies that affect MCC Digestive Health and Women's Health products
* Evaluate new business development and licensing opportunities

Qualifications

Education Requirement:

* Bachelors degree (preferably in a scientific discipline)

Required:

* Minimum of 10 years work experience
* Direct consumer or pharmaceutical regulatory experience (preferably including OTC and international experience).
* Demonstrated ability to influence organizational decision-making, experience in risk assessment and risk management together with sound business judgment.
* Must possess excellent strategic, collaboration, communication, organization and presentation skills.

Preferred:

* International Regulatory experience

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # REG000849.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-JN1

Job
: Regulatory Affairs Liaison

Primary Location: US-NJ-Summit
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Summit-MCC-Regulatory-Affairs-Franchise-Lead-Digestive-Health-Women's-Health-Job-NJ-07901/1525475/152547515254752012-06-15Merck/MSDRegulatory Affairs Liaisonfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Director of Corporate Accounts (DCA) is responsible for but not limited to:

* Managing our relationship with the major Poultry and Swine producers in USA and Latin America: Tyson, Smithfield and BRF.
* Working together with the Global Species groups and local commercial organizations where these clients are located
* The DCA will develop the relationship matrixes, establish regular contact and relationship with the key decision makers, develop and implement long-term plans to enhance our image as a trustworthy business partner, while maximize our Sales and wallet-share with these accounts.

Qualifications

Education Minimum Requirement:

* Bachelors Degree Required

Required Experience and Skills:

* 7 years of relevant experience
* Minimum of 2 years in sales or marketing of Swine or Poultry products in multicultural / multinational environment.
* Leadership and communication skills.

Desired Experience and Skills:

* Veterinarian and/or background in technical issues related to Poultry or Swine production or health

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ACC002418.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Account Management Generic

Primary Location: US-NJ-Summit
Other Locations: US-Iowa, BRZ-São Paulo, US-Arkansas
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Summit-Director-of-Corporate-Accounts-Job-NJ-07901/1881758/188175818817582012-06-15Merck/MSDAccount Management Genericfull-timeUSDstarting0BSSummit, NJ, US
Description

MSD in Switzerland is a Swiss subsidiary of the successful global pharmaceutical company Merck & Co. Inc. with its headquarters in USA. Approx. 90'000 employees are currently working for us globally and we are showing strong growth.

Our Swiss operations with currently 700 employees include MSD International GmbH, Merck Sharp & Dohme-Chibret AG, Essex Chemie AG, Schering Plough Central East AG, Werthenstein BioPharma GmbH and Veterinaria AG.

Veterinaria AG - the leading animal health company in the Swiss market - is dedicated to preserving and improving the health, well-being and performance of animals and offers veterinarians, farmers and pet owners a wide range of veterinary pharmaceuticals, vaccines and health management services. For Veterinaria AG we are currently looking to fill the position for a

Financial Business Support Manager Animal Health

Main tasks:

- Financial Planning/Forecasting and Analysis of Swiss Animal Health Business (AH)

- Preparation of Management Reports and Presentations to Senior Management

- Ongoing budget management and variance analysis

- Member of Animal Health Management Team

- Project Management: Financial Systems Integration and Financial input to projects as needed

- US GAAP and Entity book close in cooperation with Shared Business Services

- Provide guidance on Cost Center and Account set-up

- Review and monitor customer terms & conditions, credit limits and accounts receivables aging

- Manage internal & external audits

- Coordinate Financial Stewardship and Compliance activities

- Exploring potential opportunities for continuous process improvements within the function

The position will be part of the team which also supports the Swiss Human Health (HH) business and its supporting functions. While the position is initially and foremost to support the Animal Health business, there will be opportunities for synergies across the whole team to provide enhanced support to both HH and AH business

Qualifications

- Masters/Bachelor degree in Business Administration - MBA preferred

- Strong analytical skills and has sound knowledge of US + Swiss GAAP

- At least 5 years experience in Financial Planning & Analysis or in a similar position

- Strong communication skills as well as knowledge of financial accounting tools (e.g. SAP)

- Customer oriented and Close to the Business

- Flexible and multi-tasking person who prioritizes effectively and is skilled at conflict resolution

- Copes well with stressful situations and change demonstrating high degree of resilience

- Ability to work independently but also in a team

- Fluent (oral and written) in English and German and have basic knowledge of French

The job is initially located in Pfaeffikon/Schwyz and will move to Lucerne end of 2012 when the Animal Health office will relocate.

If this job profile raises your interest and you are searching for new professional challenges and growth opportunities as part of a highly motivated organization then please apply online.

For more information on the Animal Health Business please refer to the following webpages:

www.msd-animal-health.com

www.msd-animal-health.ch

Job
: Financial Analysis

Primary Location: CH-LU-Luzern
Employee Status: Regular

Travel
: No
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Financial-Business-Support-Manager-Job/1796560/179656017965602012-06-15Merck/MSDFinancial Analysisfull-timeUSDstarting0BSLuzern, LU, CH
Description

External Manufacturing Relationship Manager (ExMRM), in partnership with the respective functional representatives, is responsible for ensuring reliable supply of quality Merck product at a competitive cost from the applicable contract manufacturer(s) and appropriate integration in Merck's supply chain. The ExMRM is the owner and primary point of contact for all dealings between MMD and the external party and establishes boundaries and ground rules of engagement. The number of contract manufacturers that each ExMRM is accountable for will depend upon factors such as: product type, size and/or complexity of supply agreement, geography, etc.;

1. The External Manufacturing Relationship Manager (ExMRM) is the primary owner of Merck Manufacturing Division's relationship (MMD) with the contract manufacturer and point of contact for all dealings between the two parties. The ExMRM serves as the air traffic controller of all information between MMD and the contract manufacturer and establishes boundaries and ground rules of engagement.

2. The ExMRM is responsible for all operational related activities and be the focal point for:

* Dispute resolution (w/ appropriate escalation)
* Production Planning
* Materials Management (MRP entries, Logistics)
* Quality issues (Deviation Management, Product Release, Change Control)
* Technology issues
* Oversight of shop floor production (determining when an ExM functional rep should be deployed to the External Party's (EP) facility)
* OpEx and Continuous Improvement activities

3. The ExMRM partners with ExM Procurement, ExM Quality, and ExM Technology on commercial aspects of relationship, including Identify, Select, Negotiate and Re-negotiate/terminate, as required. ExMRM may not involved in all transactional interactions if they can be managed/delegated to a functional area but will be kept apprised of status/resolutions, etc.

4. The ExMRM participates on the cross-functional team that Product Source Management assembles following a Supply Chain Committee (SCC) approved siting/source change to an external party and assume primary ownership of the new source.

5. The ExMRM facilitates the collection of EP capacity information (e.g. stated capacity, firm capacity, future capacity plans, time horizon / lead times required, comments/concerns, etc.) in preparation for future Assumption Based Reviews (ABRs) and ensures template completion.

6. The ExMRM is responsible for maintaining the integrity of the Joint Service Procedure (JSP), ensuring alignment with the Supply and Quality agreements and appropriate document revision and distribution control.

7. The ExMRM is responsible for inventory control. Depending on the location of goods (at External Party or at Merck), ExMRM ensures adequate documentation of material disposition. In some markets, ExM Operations may need to witness the destruction of goods (to prevent counterfeiting) or have the External Party certify the destruction, per destruction procedures described in the JSP.

8. The ExMRM is responsible for ensuring contract terms agreed upon by MMD and the External Party are executed including purchase orders, forecasts, deliveries, and approving invoice payments.

9. The ExMRM partners with the ExM OpEx expert and ExMOrg Representatives (e.g. technical, quality, procurement, etc.) to identify External Party OpEx / continuous improvement opportunities and supports implementation once approved. The ExMRM may commit resources provided Merck and the EP would share in the costs and benefits of such operational improvements.
The ExMRM facilitates and participates in periodic Business and Relationship Review Meetings. The ExMRM also prepares an annual "state of the union" presentation for the relationships s/he manages which includes successes and failures in order to leverage across ExMOrg.

Qualifications

Education/Experience:

* Bachelors degree preferably in the Engineering, Science or Business
* a Minimum 7 years experience in commercial /business and manufacturing (operations, quality, technology, planning) function required (or equivalent combination of education/experience).

Skills:

* Excellent interpersonal, communication, collaboration, negotiation, analytical, and project management skills required.

* Has demonstrated strong leadership, problem solving, and team building abilities and sensitivity to diverse cultures.

* Must posses the ability to work independently with minimal coaching.

* Must be decisive in an ambiguous environment.

* Able to be the one face of MMD to the external party.

Job
: Qual Assurce - 3rd Party Manuf

Primary Location: CH-LU-Luzern
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-External-Manufacturing-Relationship-MgrSr-Manager-Job-LU/1824604/182460418246042012-06-15Merck/MSDQual Assurce - 3rd Party Manuffull-timeUSDstarting0BSLuzern, LU, CH
Description

Department

Analytical Development and Validation (ADV) is a scientific Center of Excellence responsible for advanced analytical characterization of protein products. Over 60 highly trained professionals support development of commercial manufacturing processes, develop and validate quality control assays and perform complex analytical characterization and trouble-shooting. The in-depth expertise on analyses of proteins is crucial to the MSD network and is truly unique in the Netherlands.



You provide leadership as an analytical project manager for the development and maintenance of recombinant protein products. Your main task is to deliver on project milestones by driving analytical activities, identifying scientific/quality/timing issues and developing creative solutions in close collaboration with with stakeholders. This includes participation in international CMC development teams and leadership of associated analytical teams.

Qualifications

Desired Skills & Experience

You are at least an MSc in (analytical) science with broad knowledge of chromatography, electrophoresis and spectroscopy. At least 3 years of industrial development experience. Knowledgeable of EU/US regulatory requirements and late stage drug development. Excellent interpersonal/communication skills and proven project management experience. Strong results orientation and can-do mentality. Fluent in English.

Information

For more information on the position please contact Henno van den Hooven, Section Head ADV; 0412 66 2986

Job
: Lab Technician

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Analytical-Project-Manager-Job-NB/1853555/185355518535552012-06-15Merck/MSDLab Technicianfull-timeUSDstarting0BSOss, NB, NL
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


We currently have a need for an experienced chemist for a Senior Analytical Chemist role at our Wilson, NC facility.

The Wilson facility, located at the intersection of I-95 and US 264 Alternate, is a 500,000 square foot solid dosage / packaging site on 225 acres. The facility packages over 95% of physician samples in the U.S. market, including SINGULAIR, FOSOMAX, and MAXALT, among many others. The facility has been in operation since 1983, and was recently selected as Merck's Packaging and Stability Centers of Excellence for North America. Wilson, NC is conveniently located approximately 2 hours from NC beaches and 45 minutes from the state capitol, Raleigh, NC. Wilson is home to Vollis Simpson's Windmill Farm, the only North Carolina Baseball Museum and the Wilson Botanical Gardens.

The Analytical Chemist performs quality sampling, testing, and data review for bulk raw materials, active pharmaceutical ingredients, water, microbiological limits, primary packaging components, annual compendia component testing and finished pharmaceutical products.

* Tests, documents, reports, and provides second chemist review for stability samples.
* Interprets compendia and internal monographs, NDAs and Merck Quality Standards. Leads and documents investigations according to established procedures and recommends corrective actions.
* Expert knowledgeable in cGMP, CFR and other regulations in order to assure laboratory compliance.
* Able to evaluate laboratory SOPs and recommend improvement opportunities to maintain compliance with corporate and regulatory guidelines. Develops or revises laboratory SOPs as required.

This position is 2nd shift.

Qualifications

Required:

* B.S. degree in a science field required, preferably Chemistry
* Minimum of 5 years experience in a pharmaceutical laboratory
* Expert knowledge of analytical instrumentation with strong technical and interpersonal skills (ability to work in a team environment)
* Must possess the ability to work independently, manage multiple priorities and interpret a broad range of policies, procedures, and regulations to ensure regulatory compliance
* Must have good technical writing skills and high attention to detail.
* Strong collaboration skills

Preferred:

* Lean Laboratory knowledge and experience
* Root cause analysis methodology

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # QUA002731.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality Lab Related

Primary Location: US-NC-Wilson
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 2nd]]>http://jobs.merck.com/job/Wilson-Senior-Analytical-Chemist-Job-NC-27893/1605058/160505816050582012-06-15Merck/MSDQuality Lab Relatedfull-timeUSDstarting0BSWilson, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck Sharp & Dohme Corp. currently has a Quality Assurance Analyst position opening at its Wilson, North Carolina facility. The Wilson facility, located at the intersection of I-95 and US 264 Alternate, is a 500,000 square foot facility on 225 acres. As a Packaging Center of Excellence for Merck, the facility packages a variety of finished goods types for both domestic and international supply. The Wilson facility also includes one of Merck's Global Stability Centers of Excellence, which completes stability testing for active pharmaceutical ingredients and finished goods which are manufactured and supplied around the world. The facility has been in operation since 1983, and is located in Wilson, NC. Wilson, NC is conveniently located approximately 2 hours from NC beaches and 45 minutes from the state capitol, Raleigh, NC. Wilson is home to Vollis Simpson's Windmill Farm, the only North Carolina Baseball Museum and the Wilson Botanical Gardens.

The primary responsibilities of the Quality Assurance Analyst include a variety of activities supporting our solid oral dosage manufacturing and packaging facility (packaging operations also includes secondary packaging of vial, syringe, and inhaler configurations). Main responsibilities include completion of production investigations, with a concentration of investigation of customer complaints. This analyst position must demonstrate solid leadership capability as demonstrated by, but not limited to, ensuring timely completion of investigation activities, establishing and maintaining knowledge and understanding of trends and changes within the production environment, as well as corrective action effectiveness. The Quality Assurance Analyst is knowledgeable in both domestic and international regulatory requirements, and ensures site compliance with all expectations.

Specific areas of responsibility include, but are not limited to the following:

* Complaint and production investigation root cause analysis and corrective action identification.
* Completion of documentation of investigations.
* Use of statistical methods in defect resolution.
* Participation in internal/external GMP audits and regulatory inspections.
* Policy/procedure development and interpretation.
* Review and approval of GMP-related SOPs.
* Knowledge of equipment/process validation/qualification activities.
* Regulatory documentation review.
* Monitoring of performance through tracking and trending to ensure compliant operations.

Qualifications

Required Skills:

* Bachelors required; Masters degree preferred.
* Minimum of 4 years experience in a Quality function that supports compliance activities within pharmaceutical manufacturing facility.
* Expert knowledge of regulatory requirements/cGMPs.
* Excellent written and oral communication skills (including technical writing).
* Experience in the development and management of metric/trend information.
* Excellent leadership skills, including collaboration and ability to identify and drive continuous improvement
* The candidate must also possess a high degree of problem solving ability (performance of root cause analysis) and have demonstrated ability to manage multiple priority
* projects/workload, ensuring timely completion.
* Strong knowledge of cGMPs and domestic and international regulatory requirements.

* Preferred Skills:

* Degree field in science, technical operations or engineering preferred.
* In-depth knowledge of domestic and international regulatory requirements.
* Experience designing and implementing lean business processes.
* SAP system experience.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # REG000860.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Regulatory Compliance

Primary Location: US-NC-Wilson
Employee Status: Regular
Number of Openings: 2

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Wilson-Quality-Assurance-Analyst-Job-NC-27893/1540440/154044015404402012-06-15Merck/MSDRegulatory Compliancefull-timeUSDstarting0BSWilson, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This role will be in the newly created Late Lifecycle Management Center of Excellence (COE) which is being established to work across the Merck organization to drive more systematic planning for the late lifecycle and loss of exclusivity (LOE) of all Merck brands. The COE will directly support the continued development and growth of the Diversified Brands Customer Business Line by developing and implementing a series of practical approaches ('toolkit') for management of the loss of exclusivity to maximize the value of an established brand over the later part of its lifecycle, with the objective of driving an industry-leading revenue-retention post-LOE across Merck's portfolio globally.

Following a new programmed approach, this individual will work with brands starting approximately 7 years before LOE in the first major market (US or EU) to develop and drive implementation of the plans for optimal revenue retention post-LOE (benchmarked with industry-average performance on a per market basis). The scope of planning will include commercial activities, product development (including Rx-OTC switch planning as appropriate), manufacturing, patent, pricing and market access and others as relevant. Around 4 years prior to LOE, the engagement process will move from being globally focused to being more market-driven in its planning activities. This work will be cross-functional in nature, involving the brand marketing teams, Regional Marketing Leaders (RMLs), market level teams, Merck Manufacturing Division, Merck Research Laboratories as well as support functions and others in Diversified Brands to develop and implement tailored strategies for products in this time window. The team (working with the brand teams and the markets) will undertake detailed planning and implementation for approximately 8 brands with high revenue potential, including SINGULAIR and MAXALT, with a more limited approach to the other ~14 brands in this planning window.

Responsibilities, beyond driving the systematic brand planning, include:

* Develop deep understanding of the market dynamics of LOE transitions, particularly in the US and EU
* Understand the drivers of market growth in the EM in the late-lifecycle
* Strong knowledge and understanding of drivers of product performance in LOE transitions, including but not limited to market dynamics, therapeutic/disease area needs, etc.
* Rapidly establish excellent working knowledge of Merck proprietary LCM model/tool to work with products/markets in the late-lifecycle
* Work with LCM Leader, LCM Analyst and support functions to continue to evolve standard models/approaches to undertake comprehensive product performance assessments for the peri/post LOE period. This will include involvement in periodic strategic re-assessment of all possible value/revenue levers across all relevant markets
* Contribute to ongoing development a broad toolkit of practical approaches (product and solution-based) for managing LOE transitions that allow tailored approaches to be developed for product portfolio, including guidance on when to apply what approaches/solution(s) (e.g., for what disease, patient type, geography, etc.)
* Develop deep practical and commercially focused expertise on impact of various approaches (i.e. tools or levers to influence product utilization in LOE transitions), and use knowledge to continue to enhance performance of products in late lifecycle
* Coordinate with internal and external experts in the field to supplement knowledge base
* Ensure appropriate education/training of brand teams

Qualifications

Education:

* Required: Bachelor Degree

Education:

* Bachelor Degree required

Required:

* A minimum of 10 years relevant experience in lifecycle management, marketing, market access / managed markets, or process/change management related role
* Well-developed interpersonal skills with experience in interacting with colleagues at various levels are required

Preferred:

* Familiarity and experience with peri/post LOE transitions (planning and execution).
* Strong track record in commercial program execution
* Superior analytical, problem solving, judgment, interpersonal skills.
* Strong strategic thinking skills, proven success working within large strategic initiatives
* Process development, analysis and improvement experience/skills.
* Strong leadership, communication and project management skills
* Innovative and be able to invent and create opportunities, self starter
* Superior written and oral communication skills

merck.com/careers to create a profile and your resume for requisition # PRO009211.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Product Management

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular
Number of Openings: 2

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Whitehouse-Station-Late-Lifecycle-Management-Planner-Job-NJ-08889/1658097/165809716580972012-06-15Merck/MSDProduct Managementfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Future Talent Program features paid internships targeted to start in June 2012 for 10 - 12 weeks and will include one or more projects. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals.

The Reporting & Analytics Summer Intern will work as a member of the Data Excellence and Analytics Team in executing various analytics and reporting projects designed to identify savings associated with process improvements, compliance and corporate policy optimization.

Qualifications

Education:

* Currently pursuing a Bachelor's degree

Required:

* Background in Information Systems / Information Technology

Preferred:

* Experience with Microsoft Office
* Knowledge of data mining and analysis
* Good oral and written communications skills and attention to detail
* Desire to participate in developing new ideas and opportunities to be analyzed

merck.com/careers to create a profile and your resume for requisition # BUS000472.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-NJ-Whitehouse Station

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Reporting-and-Analytics-Analyst-Job-NJ-08889/1855915/185591518559152012-06-15Merck/MSDInternfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the guidance of a Senior Director, Outcomes Research (OR), the incumbent has the primary responsibility for planning and managing outcomes research activities for in-line and developmental drugs on a worldwide basis. This includes all phases of outcomes research including design and implementation of retrospective database studies, assessment of patient reported outcomes, epidemiological studies and economic modeling. The incumbent works closely with Franchise Teams, Regional Product Directors, MSD affiliates, Public Affairs, MedEd and Merck Research Laboratories (MRL) to ensure OR programs are in line with marketing strategies in key countries. The incumbent also contributes to product development and marketing strategies to ensure that product value is defined and developed.

Responsibilites include and are not limited to the following:

* Chairs/Co-chairs product/franchise-specific OR Sub-teams and provides leadership in developing the OR strategies and plans for developmental compounds and obtains cross-divisional senior management approval.
* Critically assesses drivers and drivers to reimbursement and market access to provide input into clinical and market development programs.
* Implements programs to document the burden or unmet need, patient reported outcomes (PRO) components, and health economic aspects of disease and the value of drug therapy as outlined in the OR planning process and generates data on a worldwide basis to support pricing and reimbursement.
* Develops core deliverables (e.g., health economic evaluations) and their adaptation to generate country-specific data supporting pricing and reimbursement.
* Works closely with the Product Development Teams (PDTs) to develop OR plans for Merck in-line and developmental products based on the regulatory, marketing and reimbursement environments on a worldwide basis. Works with MRL, MSD affiliates and consultants to write, coordinate, and validate as required, study design, protocols, measurement questionnaires, case report forms, data analysis plans, and final reports/publications.
* Works with the Merck Investigator Study Program Committee to evaluate outcomes research study protocols for studies in local markets .
* Supports MSD affiliates to understand local needs, adapt health economic evaluations, customize OR documents lsuch as protocols and reimbursement dossier, which includes the development of the worldwide template document, design of data collection forms for customization to countries, and in collaboration with MSD affiliates, adaptation of the document according to local requirements.
* Works closely with other GHH departments (and Public Affairs to effectively develop/ communicate OR data and consistent messages throughout Merck and to external customers.
* Responsible for maintaining awareness of scientific developments within his/her areas of expertise, both in terms of new methodology and new activities to establish communications with key outcomes research opinion leaders.
* May travel on company business to ensure broad internal/external input into the OR planning process and to assure the timely completion of projects.
* Builds relationships with health economic and outcomes research experts worldwide.
* Presents outcomes research data at international/national congresses and publishes articles in scientific journals.

Qualifications

Education:

* Required: Masters Degree
* Preferred: Doctoral degree from a recognized school of medicine, public health, management, pharmacy, or economics

Required:

* Minimum of (5) years relevant experience
* Minimum of (2) years experience in the design and implementation of clinical, epidemiological, or health economic studies

Preferred:

* Demonstrated expertise in the field of outcomes research, epidemiology or health economics
* Excellent leadership and strategic thinking skills

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # OUT000174.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Outcomes Research -Health Econ

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Associate-Manager-GHO-Job-NJ-08889/1866475/186647518664752012-06-15Merck/MSDOutcomes Research -Health Econfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Qualifications

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ADM005073.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Administrative Svcs Generic

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Whitehouse-Station-Administrative-Assistant-III-Job-NJ-08889/1885957/188595718859572012-06-15Merck/MSDAdministrative Svcs Genericfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The incumbent is responsible for statistical planning and data analysis of clinical trials, in particular Early Phase and Clinical Pharmacology trials.

This position requires a solid knowledge of statistical methodology, experimental design, and some knowledge in computing software and data management. The knowledge must be sufficient to ensure that sound scientific principles and statistical methods are applied to designing and analyzing clinical trials in support of discovery and worldwide regulatory submissions.

This position involves interaction with Medical, Data Coordination, Merck scientists, and Regulatory staffs in designing and analyzing clinical trials and providing the statistical support for clinical drug projects.

Qualifications

Education:

* MS or PhD in statistics/biostatistics

Required:

* PhD or at least 3 years experience (for MS) in the design and evaluation of drug/vaccine discovery, non-clinical development or clinical trials.
* Knowledge of computers, statistical and data processing software.
* Excellent communication skills are required.

Preferred:

* Publications in peer reviewed statistical/medical journals
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003496.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Biostatistics

Primary Location: US-PA-Upper Gwynedd
Other Locations: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: N/A

Hazardous Materials
: No]]>http://jobs.merck.com/job/Upper-Gwynedd-Biometrician-Biostatistics-Job-PA-19436/1735587/173558717355872012-06-15Merck/MSDBiostatisticsfull-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Worldwide Regulatory Liaison is responsible for developing the global regulatory strategy for assigned Diabetes and Obesity products, in order to obtain the optimal product label and shortest time to approval by regulatory agencies.

In this position your responsibilities include but are not limited to:

* Independently manages the regulatory aspects of projects within Diabelets and Obesity therapeutic area; functioning as the single, accountable, global point of contact on those projects.
* Independently interacts with the Worldwide Regulatory Agencies and/or subsidiaries with regard to global regulatory strategy/registration requirements with one or more Merck investigational and marketed drugs/Biologics.
* Responsible for preparation, submission and follow-up contact with regulatory agencies and/or subsidiaries for all applications and submissions.
* Responsible for regulatory review and final approval of all submissions and associated documentation.
* Provides expertise as worldwide regulatory representative to Product Development teams.

Qualifications

Education:

* MD, PhD in biological science, pharmacology, chemistry or related discipline, or PharmD.

Required:

* MD with minimum of 4 years relevant experience
* PhD or PharmD with minimum of 7 years relevant experience
* General competency with drug development
* Good organizational, communication, interpersonal and negotiating skills are required

Preferred:

* MD preferred, particularly with experience in endocrinology

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # REG000952.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-EK1

Job
: Regulatory Affairs Liaison

Primary Location: US-PA-Upper Gwynedd
Other Locations: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: N/A

Hazardous Materials
: None]]>http://jobs.merck.com/job/Upper-Gwynedd-Assoc_-Dir_Director%2C-Worldwide-Regulatory-Liaison-Job-PA-19436/1868788/186878818687882012-06-15Merck/MSDRegulatory Affairs Liaisonfull-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


It is business critical that Merck negotiates global site contracts and budgets in late and early stage clinical trials in accordance with company policies, local laws and regulatory requirements in a timely manner. It is also imperative that Merck negotiates investigator initiated study contracts, consultant agreements, non-clinical agreements for marketed products, material transfer agreements, data transfer agreements, letters of delegation and authorization, master agreements and confidentiality agreements on time and within Merck's policies, local laws and regulatory requirements in a timely manner . This will be strongly supported by this role: Lead, Global Agreements Management.

Under the guidance of Head Global Site Ready and Clinical Quality Management (GSRCQM), the Lead, Global Agreements Management will oversee the end-to-end processes of global agreements.

* Leading directly a team of Subject Matter Experts (SMEs) in Global Agreements Management for Late and Early Stage Clinical Trials
* Leading directly a team of SMEs for Consulting Agreements and Investigator Initiated Studies
* Process Ownership for Global Agreements area
* Identifies and proposes strategies, procedures, and tools for the optimization of the processes. Applies creative solutions to complex site ready situations and demonstrates situational leadership within cross functional and global teams. Manages relationship with external partners for programmatic and functional sourcing
* Formulates analysis of complex problems considering all of the functional areas of management, including finance, operations, and human resources
* Recognizes and considers various solutions to problems or situations
* Anticipates the results of proposed course of action, including potential short and long-term benefits, risks involved, effect on customers, and resources and time required
* Execution: Works with internal/external partners to assure all required contracts and budgets are negotiated within policies, local laws and regulations on time; Monitors/tracks key performance indicators; Ensures the integrity of all in-scope contracts. Ensures compliant and efficient, customer focused process that helps to decrease overall spend on resources. Track compliance and on-time delivery and return of non clinical study site supplies.
* Strategic Development and Process Management: Identifies best practices and updates processes when appropriate; Addresses adverse trends in process following root cause analysis; Updates and maintains all in-scope supporting document templates.
* Internal/External Management: Ensures communication with external partners, stakeholders, and customers; Liaises with Global Study and Site Budget Management, clinical teams, country operations colleagues, Office of General Counsel, GSRCQM, Compliance and external partners to achieve site ready timelines; Interfaces with staff members to provide management, general leadership, and guidance.
* Performance Tracking: Identifies and reviews metrics to assure process remains efficient and effective; Collaborates with external partners to identify areas for delay and create mitigation strategies. Monitors industry trends, FDA regulations, ICH guidelines, etc. to keep abreast of any changes affecting documentation.
* Audit and Inspection Support: Works with clinical teams, GCQM, and GCC to ensure inspection process readiness. Assists in retrieval of documentation during sponsor monitor inspections; participates in mock inspections; participates in inspection training preparation and awareness. Supports the development of responses to audits and inspections and ensures appropriate implementation. Ensures that all actions and commitments are implemented in a timely manner

Position manages the following:

* 8 direct reports

* 4 indirect reports

* 65 non-merck positions reporting into this organization

Preferred location is Rahway, NJ or Upper Gwyned, PA, however, position can also be field based

Qualifications

Education:

* Bachelor's degree required
* Masters preferred.
* Degree in law would be of great benefit

Required:

* A minimum of 10 years of relevant experience in clinical research including global site contract and budget negotiation and management/oversight of such individuals, with a demonstrated record of accomplishments
* Knowledge of ICH-GCP, working knowledge of global local laws and customs and other relevant regulations to manage site contracts and budgets in addition to investigator initiated study contracts, consultant agreements and confidentiality agreements
* Must have a solid understanding of the functional area responsibilities associated with the clinical development process, trial management, and clinical trial management systems, as well as quality management and control tools
* Superior oral and written communication skills in an international environment.
* Excellent project management and organizational skills.
* Excellent teamwork and leadership skills, including conflict resolution expertise and discretion.

Demonstrated ability to

* lead, manage and motivate individuals responsible for the execution of regulatory documents specifically external vendors
* manage multiple projects with varying deadlines is also required
* lead cross-functional teams of business professionals.
* analyze, interpret, and solve complex problems.
* think strategically and objectively and with creativity and innovation.
* proficiently interact with all levels of management and exert influence to achieve results.

Preferred:

* Working knowledge of Clinical Trial IT systems is preferred

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PRO009618.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Proj Mgmnt-Clinical Research

Primary Location: US-PA-Upper Gwynedd
Other Locations: United States, US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1

Shift (if applicable)
: N/A

Hazardous Materials
: None]]>http://jobs.merck.com/job/Upper-Gwynedd-Lead-Global-Agreements-Management-Job-PA-19436/1877982/187798218779822012-06-15Merck/MSDProj Mgmnt-Clinical Researchfull-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The U.S. Outcomes Research Department is dedicated to conducting scientific studies and evaluations focused on outcomes research, quality of care, health technology assessment, and health policy research. Our research agenda is driven by the needs of both Merck and our U.S. based customers, including patients, their health-care providers, and payers, with the overall goal of developing programs to improve patient outcomes. Examples of current research activities include observational studies and health economic research in disease states such as hepatitis C, diabetes, cardiovascular disease, medication adherence, and other areas of interest to Merck.

Responsibilities

The department currently has a position opening that will have broad responsibility for supporting the outcomes research needs of key Merck brands. The responsibilities for this position include:

1. Directing and executing the planning, development, implementation, and communication of outcome research initiatives supporting Merck products.
2. Work within a matrix team of outcomes research, epidemiology, statistics, marketing and sales colleagues to provide guidance on the value of outcomes research techniques to address important topics to payers and health care providers.
3. Work with U.S. outcomes research colleagues to design and implement strategies in support of U.S. brand team objectives.

Qualifications

Education:

Ph.D. in a discipline related to health services research (Outcomes Research, Health Policy, Epidemiology, Health Economics, Biostatistics, etc.).

OR

Doctoral level clinical degree in medicine, pharmacy, or nursing (MD, PharmD, PhD) with a Masters degree in a discipline related to health services research (Outcomes Research, Health Policy, Epidemiology, Health Economics, Biostatistics, etc.).

Experience:

Candidates must have a minimum of three years relevant research experience and a demonstrated track record of scientific research and publication in peer-reviewed journals in areas related to health services research. Experience should also include the design and implementation of observational research studies, health economic evaluations, simulation models, or other examples of evaluations of health care technology. All candidates must be able to demonstrate:

· Excellent written and oral communication skills,

· The ability to work in a matrix environment,

· A thorough understanding of the U.S. health care system, and

· The ability to manage multiple projects, including budgets, contracts, and timelines.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. merck.com/careers to create a profile and your resume for requisition # OUT000170.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Outcomes Research -Health Econ

Primary Location: US-PA-Upper Gwynedd
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Upper-Gwynedd-US-Outcomes-Research-Scientist-Job-PA-19436/1733750/173375017337502012-06-15Merck/MSDOutcomes Research -Health Econfull-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Co-op student for the Medical Communications department will function as a fully-integrated member of the scientific writing team. Day-to-day activities will focus on translating scientific results of clinical trials from statistical reports into clear and comprehensible PowerPoint slides. The Co-op student may be asked to audit study results in slides against the statistical reports and source documents. The Co-op student will also attend team meetings to provide a wider perspective on the scientific writing and study summarization phase of clinical trial conduct. The Co-op student is responsible for accurate transfer of information, plotting simple graphics in Power Point and Excel, summarizing information in table format and ensuring accuracy compared to source materials. Co-op student will have the opportunity to gain further knowledge and skill set in understanding statistical aspects, trial conduct design and methodology and scientific writing. We are seeking candidates with strong academic performance, communication skills, teamwork, and the ability to work in a multi- functional environment.

This is a 6 month co-op that will begin Fall 2012 for 6 months. No housing will be provided.

Qualifications

Required:

*
Pursuing either Bachelor, Master, or PhD degree in a science or related field.

* Skills in Power Point and Microsoft and XL (graphing, and setting up formulas and equations) and writing/editing experience preferred, such as (depending on education level): newsletters, journal articles, presentation delivery.

*
Applicants must be currently enrolled in an academic program.

Preferred:

* Some exposure to clinical research.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #RES001312.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-PA-Upper Gwynedd

Job Type
: Co/Op
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Upper-Gwynedd-Medical-Communications-Co-op-Job-PA-19436/1885949/188594918859492012-06-15Merck/MSDCo/Opfull-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Quality Assurance Laboratory Analyst is responsible for supporting the Facility Environmental and Utility Monitoring programs that directly support the Durham Vaccine Manufacturing Facility Integrated Process Team (IPT) and the site value stream map, while actively supporting, participating in and embracing an empowered team culture.

Specific to Environmental and Utility Monitoring, the coordinator will be responsible for maintaining the EM program to include the following:

· Sample Receipt, Incubation and Enumeration of microbiological environmental samples from aseptic areas, personnel and utility systems

· Perform USP Water testing of pharmaceutical water systems including Bioburden, Endotoxin, Total Organic Carbon (TOC), Nitrates, pH and Conductivity

· Provide data entry and review as required

· Provide summaries of test results to appropriate personnel as needed.

· Perform growth promotion testing of media and agars

· Participate in media challenge execution and evaluation of units

· Troubleshoot applicable lab equipment as needed.

· Participate in resolving laboratory and production investigations as needed.

Other:

· SOP development and review

· Direct support of regulatory inspections and audits

· Direct support of validation activities and all other associated quality functions

Qualifications

Qualifications:

· Bachelors degree in Microbiology, Biological Sciences, Chemistry or relevant area.

Preferred:

* Some direct laboratory or environmental monitoring experience
* Previous experience in a laboratory position
* Specific assay experience in bioburden testing by membrane filtration, kinetic endotoxin testing, TOC or conductivity testing of pharmaceutical water samples
* Experienced in the methods and approaches of conducting environmental and utility monitoring
* Understanding of aseptic processing and compliance requirements would be beneficial.
* Experience with SAP, LIMS, electronic document management systems (EDMS) and
* Knowledge of Standard Methods for Water and Wastewater, USP, CFR, Eudralex and other regulatory guidance specific to the pharmaceutical industry.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAN001283.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

ZZ5ML

Job
: Manuf./Operations Generic

Primary Location: US-NC-Durham
Employee Status: Regular

Travel
: No
Number of Openings: 4

Shift (if applicable)
: 1st

Hazardous Materials
: BL2 Micro organisms]]>http://jobs.merck.com/job/Durham-Laboratory-Analyst-EM-Laboratory-Job-NC-27701/1553316/155331615533162012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


We currently have exciting positions as a Maintenance Production Technician at our Vaccine Manufacturing Facility (VMF) in Durham, NC.

The VMF Maintenance Production Technician role is a multi-faceted position. The succeesful candidates will use their maintenance expertise to ensure that the equipment is running at optimal levels at all times. The Maintenance Production Technician will be responsible for all aspects of product manufacturing and equipment maintenance to include preventive maintenance, troubleshooting and repair - this will involve true ownership. This is an excellent opportunity for experienced mechanics, recent graduates of technical degree programs, or mechanically talented persons with CGMP manufacturing and leadership experience. We are seeking candidates that desire to be responsible for all aspects of the manufacturing process and desiring to be a part of a diverse operations team with daily activities that go beyond typical roles of completing PM tasks and responding to equipment downtime. The role offers opportunities to obtain in-depth process / equipment knowledge and leadership experience in an empowered, team driven environment.

The Production Technician will troubleshoot, maintain, and operate process and process support equipment in support of vaccine manufacturing operations. The Merck Durham facility boasts an empowered culture and as such, the Production Technician is a self directed employee part of a team that is responsible for providing support, direction and training in operations areas (weigh/dispense, media prep, bulk formulation, filling, capping & inspection) in clean room conditions. Develops standard operating procedures (SOP's) and preventative maintenance (PM's) plans as requested. Conducts in-process testing as needed. May make calculations required for ususal dosage determinations and solution preparation and resolves variances as necessary. Performs check-in, set-up/preparation of equipment, cleaning/sterilization, changeover of lines and general housekeeping. Will perform general maintenance and troubleshooting. Follows proper procedures for maintaining equipment, supplies and facilities in a sterile environment. Responsible for written documentation of activities. Actively support, participate and embrace an empowered team culture including significant interaction with Quality, Technical Operations, Engineering and other groups as required.

Must be flexible to perform all of the following functions and other tasks as needed:

* Demonstrated ability to troubleshoot mechanical and electrical components
* Perform general troubleshooting and maintenance of equipment while maintaining production schedule
* Provide training to others
* Set-up and prepare equipment for ongoing operations
* Perform on-going cleaning/maintenance of sterile core
* Operate various computer controlled process support/process equipment (i.e. washer, autoclave, filling line, lyophilizer, cap/inspect machines, etc.)
* Follow instructions for completion of job tasks.
* Complete written documentation of work performed.

Responsible for working as part of an empowered team to achieve site mission, vision and goals through:

* Efficient and safe operation of equipment
* Compliance with current good manufacturing processes (cGMP)
* Effective communication

Qualifications

Education:

High School Diploma/GED

Required:

* 4 years Maintenance experience, applicable mechancial, electrical or control technician certificate or Bachelor's Degree in Mechanical Engineering
* Ability to work with and troubleshoot computer control equipment including Programmable Logic Controllers (PLC) and/or Distributed Control Systems( DCS)
* Basic computer fluency (internet browsers, e-mail, word processing)
* The ability to work a rotating schedule that includes weekend, holiday, evening and nights

Desired:

* Bioworks certificate
* Experience in clean room or GMP/regulated manufacturing environment

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merckmanufacturing-durham.com/ to learn about the Durham Vaccine Facility and apply for this position and to create a profile and your resume for requisition # MAN000604.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Job
: Manuf./Operations Generic

Primary Location: US-NC-Durham
Employee Status: Regular

Travel
: No
Number of Openings: 3

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/Durham-Vaccine-ProductionMaintenance-Technician-Job-NC-27701/900704/9007049007042012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Quality Assurance Laboratory Analyst is responsible for supporting the Facility Environmental and Utility Monitoring programs that directly support the Durham Vaccine Manufacturing Facility Integrated Process Team (IPT) and the site value stream map, while actively supporting, participating in and embracing an empowered team culture.

Specific to Environmental and Utility Monitoring, the coordinator will be responsible for maintaining the EM program to include the following:

· Sample Receipt, Incubation and Enumeration of microbiological environmental samples from aseptic areas, personnel and utility systems

· Perform USP Water testing of pharmaceutical water systems including Bioburden, Endotoxin, Total Organic Carbon (TOC), Nitrates, pH and Conductivity

· Provide data entry and review as required

· Provide summaries of test results to appropriate personnel as needed.

· Perform growth promotion testing of media and agars

· Participate in media challenge execution and evaluation of units

· Perform method qualification testing

· Troubleshoot applicable lab equipment as needed.

· Participate in resolving laboratory and production investigations as needed.

Other:

· SOP development and review

· Direct support of regulatory inspections and audits

· Direct support of validation activities and all other associated quality functions

Qualifications

Qualifications:

· Bachelors degree in Microbiology, Biological Sciences, Chemistry or relevant area.

· Minimum 3 years direct experience in a laboratory setting

Preferred:

· Previous experience in a laboratory position

· Specific assay experience in bioburden testing by membrane filtration, kinetic endotoxin testing, TOC or conductivity testing of pharmaceutical water samples

· Experienced in the methods and approaches of conducting environmental and utility monitoring

· Understanding of aseptic processing and compliance requirements would be beneficial.

· Experience with SAP, LIMS, electronic document management systems (EDMS)

· Knowledge of Standard Methods for Water and Wastewater, USP, CFR, Eudralex and other regulatory guidance specific to the pharmaceutical industry.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAN001284.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

ZZ5ML

Job
: Manuf./Operations Generic

Primary Location: US-NC-Durham
Employee Status: Regular

Travel
: No
Number of Openings: 4

Shift (if applicable)
: 1st

Hazardous Materials
: BL2 Micro Organisms]]>http://jobs.merck.com/job/Durham-Laboratory-Analyst-EM-Lab-Job-NC-27701/1553317/155331715533172012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Bio-Process Technician is an excellent entry level opportunity for recent university graduates as well as experienced individuals that are interested in a hands on opportunity to manufacture vaccines. The individual in this position will support the manufacturing process through hands on cell culture and purification activities as well as other production related activities. Key responsibilities for the Bio-Process Technician include aseptic practice and GMP (Good Manufacturing Practices) adherence, working in a team environment to accomplish departmental goals, as well as the ability to direct your own work through leadership.

Responsibilities include, but are not limited to:

Working in conjunction with all appropriate personnel, performs manual and automated operations, general maintenance and support functions necessary for the production of vaccines.

* Participates in and assists with the development and execution of personnel training.
* Revises and authors SOPs and GMP documentation.
* Serves on safety, quality and other committees as required.
* Provides all documentation and clerical functions necessary to allow proper accountability and traceability of product.
* Maintains, inventories, and transports all required equipment, materials, supplies and products. Ensures shipment criteria and timely availability and delivery.
* Demonstrates proficiency with Distributed Control System and other automated systems (including, but not limited to, SAP, MES, NG LIMS, HanDEL, Word, Excel)
* Performs general maintenance and assists in troubleshooting of equipment.
* Performs housekeeping in all work areas. Executes facility decontamination according to approved procedures.
* Performs sampling/in-process testing supporting the manufacturing and validation process for current process as well as developmental work for new products/processes as required.
* Provides process ownership through timely actions , related to equipment supplies, required maintenance/repairs, process concerns, safety concerns, and area for improvements.
* Identifies and addresses compliance, environmental, safety, and process deviations as appropriate while notifying appropriate personnel.
* Maintains, cleans and prepares equipment used in vaccine production.
* Schedules and performs environmental monitoring during processing and records results in the computerized database system.
* Performs all job functions of Production Associate as required.
* Provides timely delivery of sample and other materials as required to appropriate laboratories, coordinating with Quality and Logistics as required.
* Attends and actively participates in HAZOPS, waste walkthroughs, 5S, kaizen events, or any other operations, lean six-sigma, quality, safety or environmental training/initiatives as required.

Merck's Durham facility is growing tremendously and will be hiring for multiple opportunities in this role.

Qualifications

Education and Previous Work Experience Required:

* Bachelor degree in Life Science or Engineering OR
* Bachelor degree and a minimum of 2 years relevant experience (working in an FDA regulated industry) OR

* Associates degree in Life Science or Engineering with 2 years relevant experience (working in an FDA regulated industry.) OR
* Associates degree with 4 years relevant experience (working in an FDA regulated industry.) OR

* High School Diploma or Equivalent with at least 5 years relevant experience (working in an FDA regulated industry.)

Required:

* Must be willing to lift 50 lbs
* Must be willing to be vaccinated/blood tested for titer for products manufactured within the facility if needed
* Must be willing to work 12 hour shifts, including evenings(7pm - 7am)
* Must be willing to work a rotating 2-2-3 schedule (2 days on, 2 days off, 3 days on) which may include weekends.

Preferred:

* Experience in biological and/or vaccine processing
* Experience performing aseptic/sterile operations
* Experience with GMP's (Good Manufacturing Practices)
* Mechanical aptitude and ability to analyze equipment and take appropriate corrective action
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition MAN001237.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


ZZ5ML

Job
: Manuf./Operations Generic

Primary Location: US-NC-Durham
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/Durham-Bio-Process-Technician-Job-NC-27701/1770816/177081617708162012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Accountable for Quality Assurance (QA) operations of Active Pharmaceutical Ingredients including materials and product disposition, investigations, CAPAs, shop floor and in-process QA activities, product complaints, qualification and validation and audits. Leads and facilitates the integration of the quality operating systems, management infrastructure and colleagues' mindset and behaviors to achieve financial goals ensuring compliance of processes with regulatory requirements while promoting an environment that encourages creativity, innovative ideas, and engagement as well as a high performance culture.

In partnership with the QO Technical & Lean Operations Leader, incumbent will lead and facilitate the integration of all Quality Operations, compliance systems, management infrastructure and colleagues' mindset and behaviors. This will help leading the Durham site to achieve its financial goals ensuring compliance with all regulatory requirements while promoting an environment that encourages creativity, innovative ideas, and engagement as well as a high performance culture within the site and the immediate site network within Durham.

ESSENTIAL FUNCTIONS:

The essential functions of this position include, but are not limited to:

* Controls the manufacturing steps of Active Pharmaceutical Ingredients to assure adherence to cGMPs, corporate, plant policies and procedures, and regulatory requirements. Coordinates the activities and directs the efforts of QA personnel to meet quality standards.
* Primarily responsible for the timely release of products within plant and regulatory requirements.
* Establishes, improves and maintains quality programs, procedures and controls for the assigned areas.
* Assures full compliance of the following Quality systems: Change Management, Validation, Deviations, Commissioning and Qualification.
* Monitors and advises on the performance of the quality management system by producing data and reporting through measurement against set department indicators.
* Reviews product and/or process failures to evaluate and determine if added tests or manufacturing changes are required to prevent recurrence.
* Responsible for determining appropriate skilled staffing for tasks execution. Effectively delegates and assigns tasks according to the levels of support and direction needed. Allocate resources as needed to meet business demand and support the on time completion of area deliverables. Creates work plans and assigns tasks without leadership intervention. Assess the need for contracted or temporary resources.
* Provides leadership and guidance to drive balance between compliance and business needs in the resolution of quality and technical issues. Guides subordinates to resolve issues.
* Meets established priorities to maintain product supply.
* Liaises with other Leaders and staff throughout the organization to ensure that the QA system is functioning properly. Partners with other departments towards the resolution of technical issues.
* Supervises inspection, product disposition and QA technical support personnel to achieve established goals and standards.
* Trains and develops inspection, product disposition and QA technical support personnel to assure understanding and compliance with GMPs and other regulatory requirements.
* Assist in preparing, analyzing and controlling the Quality Assurance operating budget plan.
* Manages compliance with EEO safety guidelines established by plant management.
* Identifies and implements cost improvement projects.
* Supports the development of departmental objectives aligned with Company/Site/Department objectives.
* Responsible for assuring that colleagues are properly trained to execute their duties.
* Accountable for providing timely and appropriate counseling and feedback to employees as necessary to achieve department and site objectives.
* Develops a plan for short and long range development of colleagues under his/her responsibility.
* Responsible for performance assessments and salary recommendations.
* Promotes an environment conducive to creative/innovative ideas to improve areas performance.
* Promotes respectful and constructive relationships with direct reports and co-workers
* Versatile and willing to be assigned to different areas.
* Balances authority and influence to make things happen.
* Takes time to understand issues and address root causes. Analyzes, and makes adequate and quick decisions.
* Acts and leads in alignment with goals, improving collaboration and team work.
* Understands and accepts the impact of decisions without blaming others.
* Capable to provide and receive coaching. Manages conflicts effectively and is open to receive feedback.
* Deploys information and keeps direct reports communicated about plant strategies, vision and direction. Aligns colleagues and departmental actions and goals with Vision.
* Understands and enforce company policies.
* Creates an environment in which direct reports are open to provide feedback and ideas.
* Communicates effectively progress of department towards achievement of goals and indicators. Identifies vulnerable areas and creates/proposes plan to make sure situations are resolved.

Qualifications

*
Required:

Education Required:

* Bachelor degree in Science, Business Management or other related technical area.

Experience Required:

* At least 8 years in Pharmaceutical Manufacturing Industry
* At least 5 years of leadership experience
* Proven application of effective supervision principles
* Proven record of achievements in leading operational projects
* Demonstrated innovative mindset
* Keeps updated in latest industry regulatory trends and leading edge technologies

* Proven experience in Global Pharmaceutical Business
* Experienced in organizational positioning from remote locations

* Demonstrated cross cultural agility and resourcefulness
* Proven expertise of:
* Qualification and validation processes
* Root Cause Analysis
* Investigative methods
* Pharmaceutical industry and business nature
* Solid Dosage products process
* cGMPs, EHS, other related regulatory requirements and Controlled Substance
* Labor Laws
* Company policies
* Financial principles
* Knowledge of Lean, 6 Sigma, M1 tools

Preferred:

Master degree a plus

Yellow, Green or Black belt certification desirable

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # QUA002768.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality Operations

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Durham-Quality-Operations-Director-Job-NC-27701/1711014/171101417110142012-06-15Merck/MSDQuality Operationsfull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This New Leader is critical to proactively integrate the Quality Compliance functions to all the activities associated with Product Transfers to a new facility. This leader will assure BOH inspection readiness, product license conformance for the Durham site. This new leader reporting to the Site Quality Head, will provide governance, will establish and maintain managerial process all activities related with facilities and product licensing as well as all regulatory communications with FDA, EMA and other Global Health Authorities and the following:

* Will provide oversight to all the Quality Internal Audits, Corporate and BOH Regulatory readiness.
* Will coordinate context and content of the Durham site communications with global BOH.
* Will orchestrate an integrated meaningful site quality council as well as any quality issue escalation process. Will have direct responsibilities for the site master file, annual product review, customer complaints, and CAPA effectiveness program.

This role will provide leadership, focus and governance to the site compliance and regulatory requirements of the GMP live virus vaccines products operation. Facilities within the Vaccines will be transfrring new technology and expanding capacity in support of products.

Qualifications

Required Education/Certifications:

* Minimum Bachelor's degree required in applied sciences and technology: (i.e. BioChemistry, Pharmacy, Engineering or similar)

Education Preferred:

* J.D Law in Biotechnology - Pharmaceutical
* Master, or PhD degree in applied sciences and technology: (i.e. BioChemistry, Pharmacy, Engineering or similar)

Required Experience/Knowledge/Certifications:

* Minimum 10 years experience in the Pharmaceutical industry with significant experience in biologics, vaccines and/or biopharmaceuticals compliance
* Minimum 8 years experience with increasing responsibility.in Compliance and Regulatory Affairs
* Proven experience in Global Pharmaceutical Business - Working in FDA, EMA or other BOH is desirable
* At least 5 years of leading/managing experience
* Demonstrated knowledge of GMPs, compliance issues, inspectional trends, industry quality assurance practices and systems, and personnel management skills.
* Direct Exposure to Regulatory inspections including interactions with Board of Health representatives and responding to Board of Health observations
* Good understanding Global regulatory processes
* Proven application of effective supervision principles
* Demonstrated innovative mindset
* Keeps updated in latest industry regulatory trends and leading edge technologies
* Experienced in organizational positioning from remote locations
* Demonstrated cross cultural agility and resourcefulness
* Proven expertise with:
* Bio-Pharmaceutical Law and International Regulations
* Technical Writting and Presentations
* Investigative and Auditing methods
* Financial and Administration principles
* Lean 6 Sigma methodologies

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # QUA002949.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality Operations

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-Site-Quality-Compliance-Director-Job-NC-27701/1891873/189187318918732012-06-15Merck/MSDQuality Operationsfull-timeUSDstarting0BSDurham, NC, US
Description

MSD Ireland (Carlow) - where patients come first

Merck Sharp & Dohme Biologics (Ireland) Ltd. is a subsidiary of Merck & Co. Inc., New Jersey, USA, one of the leading healthcare companies in the world.

Located on the periphery of Carlow Town, Merck Sharp & Dohme Biologics (Ireland) Ltd. is our latest Irish facility, joining existing Merck Sharp & Dohme operations in Tipperary and Dublin. The vaccines, biologics and other products we will formulate in our new Carlow facility could ultimately be used by millions of people across the world.

We are now seeking applications from energetic, motivated and innovative people interested in becoming part of this exciting new phase in our global development. Working with likeminded individuals, you will join a growing dynamic team in a newly constructed, contemporary environment. Successful applicants in each of the positions outlined here will make an important contribution to our overall operations in Carlow, Ireland and worldwide.

This role is one of our exciting job opportunities right now:

Position Title - Material Handler

Reporting to the Logistics Coach, the Material Handler will be responsible for assisting in all aspects of delivering a lean, optimized and efficient logistics function within the Carlow facility.

Key to success in this role will be the candidate's ability to work well within a complex team environment, to make problems visible & to take direction to ensure performance excellence and compliance at all times.

The Logistics team are responsible all for inbound, outbound and on-site logistics including international shipping, therefore the successful candidate will provide support across all of these key areas.

Key Responsibilities

* Ensure the safe movement of materials in and around the facility on a daily basis
* Preparation & packaging of outbound product shipments & samples ensuring compliance with Merck, EHS and global trade requirements
* Provide input into the development of department documentation (e.g. SOP's, Risk Assessments and all other relevant documentation)
* Interact with the site inventory management system (including RF technology)
* Provide a high level of customer service to both internal & external customers
* Assist in ensuring that the site logistics team always pursue industry best practice & develop a culture of continuous process improvement
* Ensure the safe and efficient operation of site material handling equipment
* Ensure the safety of logistics equipment by participating in relevant daily/weekly audits/checks & flagging issues as appropriate

Qualifications

Key Experience
Essential

* 3-5 years working in a similar role in a challenging logistics environment
* Ability to work as part of a team in a challenging environment
* Good communication & interpersonal skills
* Good computer literacy & experience of working with RF technology
* Forklift training

Desirable

* SAP Experience
* Experience of dangerous goods compliance & chemical handling practices
* Knowledge of continuous improvement methodologies
* Prior knowledge of the healthcare/ pharmaceutical industry including cGMP's

Job
: Logistics

Primary Location: IE-Leinster-Carlow
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: N/A

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Carlow-Material-Handler-Job/1855917/185591718559172012-06-15Merck/MSDLogisticsfull-timeUSDstarting0BSCarlow, Leinster, IE
Description

The IT Analyst covers a variety of IT Operating Model (ITOM) job roles specifically in support of the scientific business functions and laboratories including those required to comply with regulatory requirements. These roles involve a combination of Client Services and Solution Delivery capabilities including primarily Business Analysis, but also Project / Program Management, Technical Analysis and Account Management on an a selected basis operating under the guidance of an MRL-IT Director. This role has responsibility for the continuity, availability, validation and authorized use of the applications in accordance with SOPs and GxP guidelines as well as the planning and installation of new applications under regulatory guidelines. The IT Analyst may also have budget responsibilities associated with specific projects.

MAIN ACTIVITIES/TASKS

* Partners with the business to develop the business case. Documents and verifies business and end user requirements for technology solutions.
* Ensures understanding among technology partners, contributes to training development, facilitates user acceptance testing and manages requirements change.
* Acts as a contact between the business and IT as needed. Helps to drive business innovation and value.- Leads local or global business change initiatives with responsibility for the overall implementation of a project or program managing scope, cost and schedule.
* Provides technical expertise in one or more defined IT solutions with an ability to solve, or refer appropriately for resolution technical fixes to applications or services.
* Responsible to maintain the quality and validated status of applications.

* Contacts:
Close contacts with key users in the relevant departments in Merck Research Labs(MRL) / Merck Manufacturing Division(MMD) business areas.
Occasional contacts with business process owner or delegate.

Qualifications

Bachelor's degree, preferably in sciences

Basic project management skills

Ability to work under change control procedures

Ability to work with cultural differences

Team worker

Fluency in spoken and written English

Previous experience

2-3 years experience working in scientific laboratory and/or clinical and regulatory environments involving the implementation or supporting of IT solutions.

Knowledge

Thorough knowledge of the Research business processes

Extensive knowledge of the applications in MRL

Ability to maintain application related documentation and training

Thorough knowledge of validation policies and practices including ability to write and execute test scripts

Understanding of formal user support processes (e.g. ITIL)

Job
: Information Technology

Primary Location: MX-Distrito Federal-Xochimilco
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Xochimilco-MRL-IT-Analyst-Job/1871144/187114418711442012-06-15Merck/MSDInformation Technologyfull-timeUSDstarting0BSXochimilco, Distrito Federal, MX
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position will lead design, product development and project management of insoles and devices. This position has regular interface with Marketing, Regulatory, Legal and Clinical groups within Merck Consumer Care, and with supplies and vendors outside of Merck Consumer Care. This position will design and develop new products for retail consumers and will also provide ongoing support for existing products including the global expansion of existing domestic products into international markets. This position supports device development in the area of footcare, but may also support skincare, women's health and upper respiratory.

Qualifications

Education:

* Bachelor's degree required (preferably in Science, Engineering or Industrial Design)

Required:

* Minimum of 3 years work experience.
* Product design and/or development experience in healthcare or consumer products company.
* Experience working in product teams.
* Excellent communication skills and organization skills required.

Preferred:

* 3D design experience (with AutoCAD, Rhino, ProE or similar).

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CHE003395.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-JN1

Job
: Chemistry

Primary Location: US-TN-Memphis
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Memphis-Senior-Scientist-Job-TN-37501/1737821/173782117378212012-06-15Merck/MSDChemistryfull-timeUSDstarting0BSMemphis, TN, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Sourcing Manager is responsible for managing Animals category of procurement which supports drug metabolism, safety assessment, and in-vivo pharmacology areas of the Discovery and Pre-Clinical Sciences organization. Responsible for establishing and leading cross-functional teams of stakeholders through the Sourcing Management Process to develop and implement sourcing strategies.

* Category Management - Direct responsibility for managing the Animals category of spend within the Discovery and Pre-Clinical Sciences organization
* Sourcing Management - Uses the Sourcing Management Process to manage assurance of supply, quality, service, cost, innovation and regulatory compliance within Global category of spend, resulting in breakthrough strategies which optimize value and ensure appropriate risk management. Understands the Sourcing Management Process and how to apply required tools in the creation and implementation of source plans.
* Proactive Cost Management: Achieves cost control, cost reduction, and cost containment targets, and adds value to area of expenditure through a strong total cost orientation.
* Market Knowledge and Insight: Uses thorough market knowledge and data analysis to gain critical insights that drive the selection of Sourcing Strategies and continuous improvement activities.
* Supplier Management and Conditioning: to ensure that appropriate supplier agreements and relationships have good supplier matrix embedded within them. Monitor, report, manage and continuously improve supplier performance
* Stakeholder Management and Business Sponsorship: Ensures appropriate stakeholders are identified and managed through stakeholder matrix. Engages assigned stakeholders and partners with them to define and meet or exceed business requirements and identify and manage profit plan savings targets. Understands strategic business requirements at 1-3-5 year horizon.
* Contract Negotiation and Management: to create detailed pre-negotiation plans, to lead and participate any prolonged negotiation sessions with suppliers and to conduct post negotiation debriefs and follow through plans
* People Management: Build talent within the organization through management of two direct reports

Qualifications

Qualifications:

Education:

Required:

* BS Chemistry, Biology, Engineering or other related subject required.

Preferred:

* MBA or advanced degree and/or other relevant certification are desirable.

Experience

Required:

* 3 to 5 years experience in strategic sourcing, or related role.
* Experience of Procurement related business process.

Preferred:

* Experience in in-vivo pharmacology.
* Experience managing direct reports.

*LI-AS2

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # TEC000496.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Technical Purchasing

Primary Location: US-NJ-Whitehouse Station
Other Locations: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Whitehouse-Station-Sourcing-Manager-Job-NJ-08889/1883042/188304218830422012-06-15Merck/MSDTechnical Purchasingfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Provide expertise to teams including:

* Apply OE methods such as Six Sigma, Lean, change management, and project management
* Utilize consultative skills
* Map, investigate and analyze business processes
* Conduct Kaizen events to improve manufacturing and business processes
* Coordinate benchmarking studies and identify and deploy external and internal best practices and technologies

Work with sponsors and team leaders supporting OE projects:

* Identify target areas for business process improvement
* Develop business cases and establish financial and non-financial project goals
* Assess business process efficiency and performance
* Develop recommendations of business process improvement projects
* Manage projects to ensure proper achievement of results

Educate, communicate, and excite the organization about OE:

* Promote a common OE language and methodology across MMD
* Provide leadership for OE knowledge management and sharing
* Share best practices across MMD sites
* Perform other duties as assigned

Qualifications

Education Minimum Requirement:

* BS in Science or Engineering
Required Skills & Experience:

* Consultative skills: ability to influence decision making, ability to interact with all levels of the business (senior leaders to working teams), project management skills (demonstrated experience in managing large teams), solid business acumen, proven team building skills, exceptionally good listening skills, results oriented, strong analytical skills, and prior process improvement experience.
* Hands-on experience with most of the following OE tools: DMAIC, voice of the customer, SMART problem and goal statements, SIPOC and process mapping, process capability analysis, failure mode and effects analysis, graphical methods, measurement systems analysis, hypothesis testing, analytical hierarchy process, benchmarking, design of experiments, quality function deployment, control charts
* Experience leading and mentoring successful Lean projects, strong command of Lean tools including value stream mapping, 5S/ visual factory, standardized work, mistake proofing, SMED, pull/ flow, Kaizens

Preferred:

* Six Sigma Black Belt certification or Lean Expert certification; excellent skills using IT applications to organize and analyze data (MS-Access, MS-Excel, Minitab, IGraphX, etc.).
* Proficiency in design for Six Sigma (DFSS) and single minute exchange of dies (SMED)
* Advanced academic degree(s) in a related technical or business discipline or equivalent experience and multiple years of demonstrated achievement or significant work accomplishment of the above skills. Experience working in a Six Sigma / Lean continuous improvement culture.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # OE/000299.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: OE/Six Sigma

Primary Location: US-NJ-Whitehouse Station
Other Locations: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Senior-Analyst%2C-MMD-Lean-Six-Sigma-Job-NJ-08889/1891866/189186618918662012-06-15Merck/MSDOE/Six Sigmafull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview

Sourcing Manager is responsible for managing complex clinical programmatic outsourcing projects on a global scale, through collaboration with regional sourcing professionals. Responsible to establish and lead cross-functional teams of stakeholders through the Sourcing Management Process to develop and implement sourcing strategies for the programmatic CRO area.

Primary activities are as follows:

* Category Scope: Direct responsibility for a portfolio of categories and supplier relationships that are Global or International in nature. Indirectly. In collaboration with stakeholders and Regional procurement professionals, creates and implements 1-3-5 year strategic sourcing strategies.
* Sourcing Management: Uses the Sourcing Management Process to manage assurance of supply, quality, service, cost, innovation and regulatory compliance within Global or International category of spend, resulting in breakthrough strategies which optimize value and ensure appropriate risk management. Understands the Sourcing Management Process and how to apply required tools in the creation and implementation of source plans.
* Proactive Cost Management: Achieves cost control, cost reduction, and cost containment targets, and adds value to area of expenditure through a strong total cost orientation.
* Market Knowledge and Insight: Uses thorough market knowledge and data analysis to gain critical insights that drive the selection of Sourcing Strategies and continuous improvement activities.
* Supplier Management and Conditioning: Responsible for building relationships with Global, International and Enterprise suppliers and managing supplier performance against business requirements using proven processes; ensures adequate inclusion of diversity suppliers in RFPs and contracts as applicable. Supports major Regional supplier relationships.
* Stakeholder Management and Business Sponsorship: Ensures appropriate stakeholders are identified and managed through stakeholder matrix. Engages assigned stakeholders and partners with them to define and meet or exceed business requirements and identify and manage profit plan savings targets. Understands strategic business requirements at 1-3-5 year horizon.
* Contract Negotiation and Management: Once strategy is approved, personally leads the sourcing including RFX, RFP, negotiations and contracting for Global and International categories to put in place the right suppliers. Negotiates at tactical and strategic levels to develop local, regional, global company contracts.
* People Management: May be responsible for selection, development, retention and performance management of one or more procurement analysts.

Qualifications

Education:

* Required: BS in Business, Finance, Clinical, or related field.
* Preferred: MBA or advanced degree and/or relevant certification

Required:

* 3 to 5 years experience in strategic sourcing, clinical or related role.
* Knowledge of Procurement related business processes.

Preferred:

* Strong Clinical outsourcing experience.
* Experience in international business.

*LI-AS2

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # TEC000470.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Technical Purchasing

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Whitehouse-Station-Sourcing-Manager-Global-Sector-Job-NJ-08889/1788669/178866917886692012-06-15Merck/MSDTechnical Purchasingfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Future Talent Program features paid internships targeted to start in June 2012 for 10 - 12 weeks and will include one or more projects. Housing is available for those interns meeting the housing distance guideline. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals.

In this role, the Analyst - Summer Intern will:

* Perform research as assigned
* Gather and validate corporate real estate portfolio data
* Perform multi-variable analyses
* Assist in development of presentations to management
* Assist in the identification of optimization opportunities

Qualifications

Education:

* Pursuing a B.S.
* Degree in Real Estate Finance preferred

Required:

* Demonstrated experience in data gathering and analyses
* High degree of proficiency with MS Excel
* Demonstrated skills in translation of large complex data sets into easily understood presentations
* High degree of interpersonal skills
* Demonstrated experience in corporate real estate finance
* Understanding of real estate terminology

Preferred:

* Demonstrated experience with advanced analytical / visualization tools

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # IT 000312.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-NJ-Whitehouse Station

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Analyst-Summer-Intern-Job-NJ-08889/1778458/177845817784582012-06-15Merck/MSDInternfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the direction of the Learning Lead, the individual will be responsible for design, development and delivery of instructional content to support training solutions. The incumbent will also be responsible for leading training projects throughout phases of the instructional systems design lifecycle. Responsibilities may also include overseeing the maintenance of training records and the generation of training reports as required.

• Utilize instructional design techniques in the development of training courses. Ensure that appropriate media are used for delivering training content, and address the varied learning styles of adult professionals.

• Deliver the training solution (stand up training) to end users.

• Design and program e-learning templates using current programming language used to develop e-learning. Work in conjunction with training coordination to schedule classes and ensure that employee training records are maintained in compliance with regulatory guidelines.

• In close coordination with the Metrics staff, may develop evaluation surveys to measure the effectiveness of the training courses for continual improvement.

• Develop any supporting documentation which may include on-line documentation or training job aides.

• Review and edit end-user training and eLearning documentation.

• Stay abreast of current trends in adult learning, learning technology and corporate training programs to ensure that the department utilizes best practices.

Qualifications

Education:

* Bachelor's degree, required, preferably in biomedical sciences, education or computer science.

* Advanced degree preferred

Required:

* A minimum of six years of business related experience, preferably the pharmaceutical/healthcare industry.

* A minimum of two years of training experience.( i.e. classroom, one on one , elearning).

* Must have strong presentation, written communication and interpersonal skills.

* Experience having managed and/or lead a team on project initiatives.

* Proven ability to work independently or as part of a team.

* Must be detail oriented, have good problem solving abilities and strong computer skills.

Preferred:

* Pharmaceutical Industry experience

* Experience designing and delivering training solutions and using e-learning development tools.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # EMP000441.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Employee Dev./Training Generic

Primary Location: US-PA-Upper Gwynedd
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Upper-Gwynedd-Learning-Specialist-Job-PA-19436/1895225/189522518952252012-06-15Merck/MSDEmployee Dev./Training Genericfull-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Functions as lead epidemiology support for a major project area, working with other groups to identify epidemiologic research needs, translate these into protocols, secure approval, execute studies, and report results with a high degree of independence as to methodology and approach. Works closely with Clinical Research, Regulatory Affairs, Biostatistics, and components of the Human Health Division and investigators at external sites to coordinate activities and studies in epidemiologic research programs.

* Serving as lead epidemiology support for a major project area, designs and coordinates all aspects of epidemiologic research programs, including protocol preparation, study design, supervising the ordering and shipping of all equipment and supplies, directing design and preparation of data collection forms and data tabulations, preparing data summaries/reports for regulatory submissions, publications and technical reports with delegation of certain tasks where possible. Directs maintenance of up-to-date reference documents and study manuals. Conducts or directs site visits.
* Directs data management activities to ensure high quality. Writes complex programs to process and summarize epidemiologic data. Determines own approach to tasks and independently applies basic and more complex techniques. Recognizes when additional statistical and programming consultation is needed and communicates requirements effectively. Maintains awareness of external data resources and identifies appropriate studies for addressing questions of interest, recognizing the limitations and strengths of the databases. Provides consultation to other groups on the validity of studies based on prescription and diagnostic information in databases. Independently performs data queries and summarizes epidemiologic information tabularly and graphically.
* Proactively works with other groups to identify epidemiologic research needs for projects and works interactively to develop research studies to address such needs. Develops and validates new measurement techniques, including but not limited to new instruments for measurement of health-related quality of life. Critiques internally and externally written manuscripts/published literature. Provides epidemiologic consultation on clinical trial design, analysis, and interpretation.
* Prepares reports to communicate epidemiologic study results to Merck management, internal committees, external investigators, and regulatory agencies. Collaborates with other groups at Merck in preparing documentation for regulatory agencies, reimbursement agencies or other organizations.
* Maintains professional knowledge by reading journals and textbooks, attending internal and external courses, and undertaking methodologic research. Presents at professional scientific meetings, publishes research findings, teaches courses, collaborates with external investigators, communicates with scientific personnel at regulatory agencies. Participates in training new department members.

Qualifications

Education:

* Doctoral degree in Epidemiology, or related discipline, with three years of related research experience with demonstrated ability to conduct independent research
* Master's degree in Epidemiology or related discipline with at least seven years' experience, with demonstrated ability to conduct independent research.

Required:

* Understanding of fundamental principles of biostatistics, epidemiology, human biology, and basic medical sciences.
* Knowledge of health care delivery systems and health care databases.
* Facility in use of computer systems and data processing software.
* Strong communications and organizational skills.
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # EPI000197.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Epidemiology

Primary Location: US-PA-Upper Gwynedd
Other Locations: US-NJ-Springfield, US-NJ-Kenilworth, US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: None]]>http://jobs.merck.com/job/Upper-Gwynedd-Senior-Epidemiologist-Job-PA-19436/1799265/179926517992652012-06-15Merck/MSDEpidemiologyfull-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the general direction of the Clinical R&D Head, Respiratory & Immunology, Infectious Disease, and Oncology, Emerging Markets (EM), the candidate has overall responsibility to design clinical plans and clinical protocols, to execute clinical studies, to produce clinical study reports and publications in collaboration with internal and external experts. The primary disease area focus will be infectious disease to include the development of new (particularly fixed dose combinations, new delivery forms, and novel formulations), and life cycle management for existing Diversified Brands in EM countries. The candidate will also serve as the clinical research representative for compounds he/she is responsible between Diversified Brands, innovative products, as well as the scientific, technical and commercial leads.

Specific Responsibilities:

* Collaborates with medical and operational teams in HQ and EM countries to design and execute clinical programs that are customized for EM countries;
* Interprets and summarizes study results leading to EM filings (new drug applications (NDAs), supplemental NDAs, abbreviated NDAs (aNDAs) and/or the equivalent) or to post-marketing study publications;
* Authors the clinical sections of regulatory filings, and supports Regulatory Affairs in filing activities and interactions with regulatory agencies;
* Supports licensing and evaluates Business Development opportunities in EM;
* Maintains close working relationships with clinical research scientists in various Merck franchises and leverages that relationship to access disease-specific knowledge as required;
* Maintains close working contacts with the Marketing colleagues and supports them with competitive issues and marketing strategies;
* By virtue of his/her extensive drug development experience and product knowledge, serves as a source of advice for management and colleagues;
* May serve on expert committees outside Merck, on editorial boards, or on planning committees or major scientific meetings

Performance expectations for this position, within areas of assigned responsibility, for the first year are:

* Develops and maintains lean and efficient processes for clinical research execution in EM;
* Progresses the compounds rapidly and efficiently through clinical development to support regulatory filings.

Location: Merck facilities in Rahway NJ, Kenilworth, NJ or Upper Gwynedd, PA.

Qualifications

Education Requirements:

* MD and/or PhD required

Required:

* At least 3 or more years experience working as a trial physician in clinical research in the pharmaceutical or biotechnology industry;
* Have completed a number of clinical studies (or fewer if some are large multicenter studies) which have yielded clear-cut results;
* Demonstrated ability to establish satisfactory interpersonal relationships with internal and external collaborators;
* Creativity and innovativeness are clearly expected
* A recognized expert for outstanding scientific and leadership ability
* Outstanding leadership characteristics exemplified through clarity of goal setting;
* Ability to inspire others, to set a positive example by providing assistance, recognition, and encouragement.

Preferred:

* Experience with infectious diseases, e.g., virology and antibiotics, is strongly preferred, experiences with respiratory and inflammatory disease is preferred
* Experience with international studies and filings especially in EM countries is desirable
* Experience in managing outsourced clinical trial in collaboration with CROs is desirable

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CLI002566.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Clinical Research Generic

Primary Location: US-PA-Upper Gwynedd
Other Locations: US-NJ-Kenilworth, US-MA-Boston, US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Upper-Gwynedd-Director-Clinical-ResearchLead-Infectious-Disease-Emerging-Markets-Job-PA-19436/1596741/159674115967412012-06-15Merck/MSDClinical Research Genericfull-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck's Experimental Medicine group seeks an individual to provide leadership and experience in translational sciences in Cardiovascular Disease, Respiratory & Immunology or Infectious Diseases. However, qualified individuals with a focus in other therapeutic areas of medicine may be considered.

The mission of Experimental Medicine is to enable drug development through the qualification of biomarkers and clinical trial methodologies. These tools will be used to help guide decision making in early clinical development, to prioritize our pipeline of new compounds, and support target-specific approaches to proof of concept. The ultimate goal of our work is to provide an early assessment of efficacy or safety, thus ensuring that we bring forward into late development those candidates that have the highest likelihood of becoming new and valuable medicines.

We partner closely with our discovery colleagues to provide clinical guidance for the development of clinically translatable, practical biomarkers which may include molecular profiling, imaging and biochemical biomarkers, and this position will interact with experts in this disciplines that support the therapeutic area. The input is intended to span planning for preclinical biomarkers through the clinical demonstration of proof-of-concept. Biomarkers are applied to develop evidence that compounds successfully engage the target in humans or exert downstream pharmacodynamic effects. Biomarkers may also be deployed to identify patient groups with the best chance to benefit from a particular therapy. We align our activities with plans to develop new compounds in Clinical Pharmacology and later in Clinical Development, transferring successful biomarkers and technologies to these colleagues to support rapid clinical study execution. Experimental Medicine also works along the development continuum to identify opportunities to add value, including rapid proof-of-concept paradigms, and development of clinical platforms that provide product differentiation. We collaborate with colleagues in academia, medical practice, and industry so as to be able to identify promising technologies and scientific results applicable to Merck's pipeline.

This position will recommend the use of Experimental Medicine resources to support the therapeutic area. Whenever Experimental Medicine designs a clinical study the clinical monitor is expected to drive study design, and collaborate with biostatisticians, drug metabolism, regulatory affairs, and other relevant disciplines to construct a high quality clinical study. We place high value on efficient, cost effective and rapid study execution, necessitating careful collaboration with operational experts. The clinical monitor will interpret, prepare clinical study reports, and present results in order to maximize their impact, both within Merck and at external scientific meetings.

This position will require effective collaboration with those in the therapeutic area that set strategy (the Franchise), creating a strong scientific link in order to translate strategic goals into useful results and decisions that influence drug development. This position will assist in the prioritization of other biomarker work through collaboration with biomarker specialists in areas such as imaging, molecular profiling, genomics and proteomics.

The position will supervise the data-to-day work of clinical scientists in Early Stage Development working on Experimental Medicine clinical studies. When appropriate, the position will supervise the work of other physician or post-doctoral scientists in Early Stage Development.

Through supervision, and through their role on drug development teams, this position will build the leadership capabilities, team effectiveness skills and knowledge of Franchise business objectives of early development employees.

Qualifications

* Candidates will generally hold an MD or MD and PhD degrees, plus subspecialty board certification or eligibility, and potentially may hold other advanced training or qualifications.
* While candidates are usually new to industry or relatively early in their pharmaceutical career, they are expected to bring substantial prior experience in academia or industry.
* A record of scientific scholarship and achievement, a proven track record in clinical medicine, and a background in biomedical research will be demonstrated by peer reviewed publication record and successful research grant applications.
* Candidates will generally possess the academic rank at the Assistant Professor level (or higher) or up 2 to 5 years of drug development experience in industry.
* As required in a team-centered environment, the candidate should demonstrate capable leadership, communication, and project management skills.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CLI001447.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Clinical Research (M.D.)

Primary Location: US-PA-Upper Gwynedd
Other Locations: US-NJ-Kenilworth, US-NJ-Rahway
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Associate-Director%2C-Clinical-Research-Experimental-Medicine-Job-NJ-07065/1326413/132641313264132012-06-15Merck/MSDClinical Research (M.D.)full-timeUSDstarting0BSGwynedd, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck is seeking a talented scientist to join the Product Value Enhancement group in Summit, New Jersey. The successful candidate will execute formulation and process development activities using DOEs for life cycle management opportunities, carry out due diligence/paper feasibility on new product concepts, coordinate development activities with Process Chemistry, Preformulation group, Analytical Sciences, Molecule & Material Characterization, outsource/co-ordinate formulation development or clinical manufacturing at CROs/CMOs, if necessary, facilitate manufacturing, packaging and release of clinical supplies for bio-comparison and or bioequivalence studies, assist in scale up activities at pilot and commercial scale, and summarize results in technical reports and presentations.

Qualifications

Education Minimum Requirement:

* PhD in Pharmaceutics, Chemical Engineering or any life sciences with up to or around 3 years of experience in pharmaceutical industry

Required Experience and Skills:

* Experience performing early phase formulation/process development of a wide range of dosage forms for small molecule new chemical entities (NCEs)
* Proven ability to identify and develop innovative ideas using sound statistical experimental designs and multivariate analysis
* Demonstrated ability to apply the principles of physical/organic chemistry & materials science to formulation development
* Prior hands-on experience with various pharmaceutical unit operations
* Successful at working effectively and comfortably in a multi-disciplinary team seeking innovation under accelerated timelines
* Strong verbal and written communication skills

Preferred:

* Prior experience in product life cycle management including development of fixed dose combination bi/tri-layer drug products, novel drug delivery systems, solubilization/bioavailability enhancement and modified release technologies
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # RES001276.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Research Pharmacy

Primary Location: US-NJ-Summit
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 2

Hazardous Materials
: Handling of new/marketed chemical entity]]>http://jobs.merck.com/job/Summit-Sr-Research-ChemistPharmacistEngineer-Job-NJ-07901/1711011/171101117110112012-06-15Merck/MSDResearch Pharmacyfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position is for a Senior Development Engineer in Pharmaceutical Commercialization Technology (PCT). This group is responsible for pharmaceutical process development of solid oral, liquid oral, and topical drug products from Phase IIb through regulatory filings, process validation, and into the first few years of commercial launch. The group's work is facilitated by a Global, Science, Technology, and Commercialization's (GSTC) network of commercialization sites run by Global Pharmaceutical Commercialization (GPC). These sites, which are currently located in Ballydine, Ireland and Las Piedras, Puerto Rico, coupled with pilot plants in West Point, PA and Summit, NJ, form the foundation of our manufacturing and development capabilities.

This role works independently to plan, conduct, evaluate, and interpret pharmaceutical process development studies, including scale up, design space development, clinical and formal stability batch manufacture, and process validation. Problem-solving skills are essential and knowledge of concepts of Quality by Design, including risk-based approaches to development, design of experiments, and process modeling, are desired. Proficiency in writing and documentation practices is required to prepare experimental protocols and technical reports in support of product registration and launch efforts. Strong oral communication skills are needed to effectively collaborate within teams and across organizations on product development efforts.

Other responsibilities include physical testing, data analysis, technology evaluation, compliance with applicable safety and current good manufacturing practices, external publications (as appropriate), and patent applications. Guidance, training, and/or supervision of lower level colleagues may be necessary.

Qualifications

Education:

* BS, MS, or PhD degree in Chemical Engineering, Materials Science/Engineering, Pharmaceutical Sciences, or a related discipline.

Required:

* PhD with no prior industry experience necessary, or BS/MS with approximately 8 to 12 years of relevant industry experience.
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition PRO009564.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Process Engineering

Primary Location: US-NJ-Summit
Other Locations: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1

Hazardous Materials
: Active Pharmaceutical Ingredients and Pharmaceutical Powders]]>http://jobs.merck.com/job/Summit-Senior-Development-Engineer-Job-NJ-07901/1877981/187798118779812012-06-15Merck/MSDProcess Engineeringfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The primary function of this Clinical Research Associate position is to assist in the design, coordination, monitoring, and reporting of pharmaceutical product development activities in companion animal and livestock studies to obtain U.S. Food and Drug Administration (FDA) approval to market selected Intervet pharmaceutical products in the U.S.A. The position will require the candidate to participate in Good Clinical Practice (GCP) field studies, as well as Good Laboratory Practice (GLP) studies. The candidate will report to a Manager of Clinical Research. This CRA position will have colleagues located in NJ and KS.

The CRA is a member of a Field Study Team (FST) and works under the supervision and the leadership of the Field Study Team Leader (FSTL). The CRA is involved in most aspects of the conduct of the studies. The CRA is accountable to the FSTL for assigned FST responsibilities. Key roles and responsibilities of the CRA include but are not limited to:

* Overall Leadership
* possesses a working knowledge of applicable VICH/GCP regulations and SOPs, as well as applicable regulations and guidelines (i.e., for a study specific region)
* assists the FSTL to ensure that all necessary actions are taken for a successful study outcome
* works with the FSTL to ensure that study timelines are met
* assists FSTL in resolving any Quality Assurance audit finding

* Study Planning
* participates in the creation of study protocols
* contributes to the design and preparation of CRFs and all other study documents in cooperation with the FSTL, the Data Manager (DM) and the statistician (ST)
* prepares study notebooks
* co-ordinates activities related to the overall drug supply, including drug ordering and importation, labeling, as well as sponsor/site inventory and drug accountability
* works with the FSTL to identify potential study Investigators
* participates in the preparation of study budgets as appropriate
* translates study protocols and CRFs when appropriate
* assists the FSTL in the preparation of the study contracts as appropriate
* prepares study files

* Study Conduct
* ensures that the Investigational Veterinary Products are shipped to the Investigator sites
* assists with management of clinical drug room (receipt, shipment, return and destruction of IVP)
* ensures study sites have all study related supplies
* conducts or participates in site initiation, monitoring, and close out visits, ensuring site compliance with protocol, VICH / GCP, SOPs, and local regulations (Study sites will consist of small animal veterinary hospitals and clinics, as well as farms)
* communicates with all assigned study sites regarding protocol conduct, enrollment and retention, protocol amendments and deviations, regulatory documentation, drug inventory and accountability, as well as timelines
* collects, reviews, and monitors all study documentation
* verifies CRFs against medical records where applicable
* ensures that all monitoring queries are resolved
* prepares monitoring visit reports
* ensures that all monitoring visits reports are promptly provided to the FSTL
* communicates regularly with the FSTL and assists FSTL in tracking all study activities
* acts as a point of contact for operational questions, drug and study supplies
* identifies site performance and quality issues and works with the FSTL to assess and resolve these issues
* ensures that adverse events and serious adverse events are reported to the FSTL according to our department SOP and pharmacovigilance requirements
* compiles study documentation / notebook
* maintains study file

* Data Management
* ensures good data quality by thorough monitoring of raw data and study documentation
* ensures that all raw data are made available for data entry once fully monitored and all monitoring queries have been resolved
* may participate in data management activities such as creation of databases, data entry, and QC verifications, or be designated as the DM for the study

* Study Reporting
* assists FSTL in preparing, addressing review comments and finalizing the FSR in co-operation with the FST the preparation of the FSR
* works with the FSTL to ensure that the study file is closed once the FSR is signed
* assists in the preparation of the study package for regulatory submission
* works with FSTL to transfer the study file to the archivist

Qualifications

Education Minimum Requirement:

* Minimum of a Bachelor in arts or science

Required Education and Skills:

* Working knowledge of GCP regulations. Knowledge of GLP regulations is preferred.
* Ability to understand and implement CVM regulations and Company Procedures.
* Must be able to travel nationally up to 50% of the time. Travel requirements will vary greatly depending on study activities, from 0 to 50 % and may require weekend travel.
* Ability to work independently and efficiently, as well as to work in a project team environment
* Excellent organization skills.
* Excellent communication skills (oral, written).
* Must be proficient in MS Word, Excel. Knowledge of Power Point, SharePoint, and Adobe Acrobat applications preferred.

A successful candidate for this position must be enthusiastic, self driven and highly motivated to excel as a Clinical Research Associate. Flexibility in task assignments and multi-tasking are a must. Candidates with experience in animal production or animal research are encouraged to apply.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CLI002634.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Clinical Research Monitor(CRA)

Primary Location: US-NJ-Summit
Other Locations: US-KS-DeSoto
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Summit-Clinical-Research-Associate-I-Job-NJ-07901/1732165/173216517321652012-06-15Merck/MSDClinical Research Monitor(CRA)full-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Future Talent Program features paid internships targeted to start in June 2012 for 10 - 12 weeks and will include one or more projects. Housing is available for those interns meeting the housing distance guideline. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals.

The Customer Solutions Intern will work with a cross-functional team to develop category plans and strategies for the assigned project, which are aligned with Marketing objectives and Customer needs.

As part of their assignment, the Intern will assist the Customer Solutions Team in the following:

* Pull and analyze syndicated and customer POS data
* Develop recommendations based on the analysis of data from various sources
* Provide assistance to the Customer Solutions team to enhance and improve business results

During the course of the internship, the individual will interact with Merck Consumer Care (MCC) colleagues in a variety of job functions including, Sales, Marketing, Retail Operations, Display Operations and Category Development.

Qualifications

Education:

* Junior, pursuing a college degree

Required:

* Pursuing a marketing, business or liberal arts degree
* Available June - August 2012

Preferred:

* 2013 Graduate
* Demonstrate strong management skills in the areas of leadership, teamwork, innovation, analytical skills and project management

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #SAL002742.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-NJ-Summit

Job Type
: Intern
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/Summit-Customer-Solutions-Intern-Job-NJ-07901/1729526/172952617295262012-06-15Merck/MSDInternfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The selecected individual will be responsible for but not limited to:

* Review and approve adverse event reports for pharmaceutical, pesticide and biological animal health products from all Merck/MSD locations.
* Determine case validity and enter into validated database as appropriate.
* Initiate and coordinate investigations into pharmacovigilance reports.
* Provide guidance to national pharmacovigilance teams regarding cases.
* Prepare aggregate reports for EPA-regulated products.
* Serve on internal teams to develop and implement procedures to ensure regulatory compliance is maintained.

Qualifications

Education Minimum Requirement:

* DVM

Required Experience and Skills:

* At least 5 years of experience in Pharmacovigilance or Regulatory Affairs in an industrial setting.
* Excellent interpersonal, communication and negotiating skills.
* Must be able to work effectively as a team member in a highly interactive and collaborative environment.

Desired Experience and Skills:

* Knowledge of animal health regulations of major regulatory agencies (FDA, EPA, USDA, and/or EMA).
* Experience with Microsoft Office.
* Strong organizational, written and oral skills.
* Ability to manage several projects simultaneously strongly desired.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # DRU000172.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Drug Safety Surveillance (MD)

Primary Location: US-NJ-Summit
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Summit-Senior-Regulatory-Affairs-Manager-Pharmacovigilance-Job-NJ-07901/1868785/186878518687852012-06-15Merck/MSDDrug Safety Surveillance (MD)full-timeUSDstarting0BSSummit, NJ, US
Beschreibung
Merck Sharp & Dohme-Chibret AG ist die Schweizer Niederlassung der Merck & Co., USA. Merck entwickelt, produziert und vertreibt weltweit innovative Medikamente und gehört international zu den führenden Pharmaunternehmen. Weltweit arbeiten ca. 100'000 Mitarbeiter für uns.

Die Schweizer Organisation beeinhaltet die Unternehmungen MSD International GmbH, Merck Sharp & Dohme-Chibret AG, Essex Chemie AG, Schering Plough Central East und Werthenstein BioPharma GmbH mit gesamthaft 700 Mitarbeitern.

Für die Werthenstein BioPharma in Schachen LU suchen wir zur Verstärkung des Teams im GMP/Comparator Labs per sofort oder nach Vereinbarung eine/n

Analytiker-/in

Aufgabenbereich:

· Organisation, Koordination sowie selbständige Durchführung aller analytischen Aktivitäten im Zusammenhang mit Stabilitätsstudien und Freigaben von pharmazeutischen Vergleichsprodukten

· Entwicklung, Validierung und Transfer von analytischen Methoden für die Freigabe und Stabilität von pharmazeutischen Vergleichsprodukten

· Unterstützung der Laboranten bei ihrer Arbeit

· Mitarbeit bei globalen Projekten

· Geräteverantwortung

Qualifikationen

· Akademiker/in (Hochschulabsolvent/in oder Fachhochschulabsolvent/in in Chemie oder parmazeutischer Analytik) mit praktischer Erfahrung in der instrumentellen Analytik Erfahrung in GMP-Richtlinien wünschenswert

· Sehr gute Englischkenntnisse

· Hohes Qualitätsbewusstsein und Sinn für eine effiziente Arbeitsweise

· Ausgeprägte Lernbereitschaft und Selbständigkeit

· Teamorientierte und offene Persönlichkeit

*LI-DR1

Job
: Forschung, allgemein

Primärer Standort: CH-Luzern
Mitarbeiterstatus: Permanent
Reisebereitschaft: Ja, 10 % der Zeit
Anzahl offener Stellen: 1
Externes Job Ausschreibungsportal: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-Analytiker-in-Job/1881755/188175518817552012-06-15Merck/MSDForschung, allgemeinfull-timeUSDstarting0BSLuzern, CH
Description

Afdeling:

Quality Assurance Biotech is verantwoordelijk voor de vrijgifte van grondstoffen, halffabrikaten en eindprodukten van de Biotechnologische productie processen voor zowel eindprodukten t.b.v klinische studies als commerciele produkten. Waarborgt het GMP nivo volgens geldende procedures en wet en regelgeving.

Functie

· De Release & Validation Officer neemt deel aan een team van 6 QA medewerkers.

· Is (mede) verantwoordelijk voor de vrijgifte van grondstoffen, hulpmaterialen, halffabrikaten en Drug Substance (API) voor klinische en commerciele biotech producten, met een sterke focus op vrijgifte en compliance t.b.v nieuwe producten

· Reviewed/beoordeeld productie en process development documenten, (master) batch record, afwijkingen , wijzigingen (incl. implementatie)

· Neemt deel aan- en initieert verbeterprojecten t.b.v. kwaliteit waarborging volgens de wereldwijde standaard van Merck.

· Schrijft en onderhoud interne procedures en stemt deze af op de wereldwijde procedures.

· Rapporteert aan Quality Assurance Lead

Qualifications

· HBO

· Ervaring in Quality Assurance en GMP in pharmaceutical manufacturing is een pre

· Engelse communicatieve vaardigheden in woord en geschrift

· Passie voor Lean Six Sigma en continue verbeteren.

· Kennis en ervaring in BioTechnologische industrie is een pre.

· Een teamspeler (met coachingsvaardigheden is een pre)

· 32- 40 uur beschikbaar

Job
: Qual Assurance & Ops Generic

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Release-&-Validation-Officer-Job-NB/1866483/186648318664832012-06-15Merck/MSDQual Assurance & Ops Genericfull-timeUSDstarting0BSOss, NB, NL
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the direction of the MPS Team Leader, the Manager will work as a: 1) Coach, teacher and partner for plant managers and their leadership teams to develop plans and execute performance improvement activities that directly contribute to the business 2) Develop Lean management and people development processes and plans 3) manage processes and projects to realize intended people and business benefit, 4) utilize various Lean , six sigma , coaching, collaboration and engagement tools and techniques to analyze and improve people and business processes 5) provide teaching and coaching to effectively transfer Lean mindsets, behaviors and skills into the organization.

MMD MPS Manager will be responsible & have capability for the following:

* Process and Value Stream mapping.
* Defining and applying measurement systems to processes.
* Apply Lean techniques and "Way of Thinking" to processes to solve moderately complex system (multiple processes) problems (building quality in, continuous flow, kanban, heijunka, pull). Integrate this work with SAP.
* Apply scientific problem solving (PDCA), standardized work, and six sigma to solve process and system (full value stream) problems.
* Lead, teach, coach and develop Lean Experts in training and development of others.
* Coach and develop people mgrs/supervisors, teams and individuals to apply Lean management principles in problem solving, process improvement and standardized work.
* Develop and manage continuous improvement processes (Visual Work Place, Lean Experts Selection & Development Process, etc..)
* Apply coaching and consequence management techniques to influence decision making, guide continuous improvement activities and ensure sustainability.
* Partner and collaborate with others to prioritize, align, integrate and implement Lean and other efforts to the best benefit of functions, sites, etc.

Qualifications

Education:
Required: Bachelor's degree in a related field

Required: Hands-on experience with application of most of the following Lean & Six Sigma and techniques: Standardized Work, Scientific Problem Solving, value stream mapping, SMED, mistake proofing, 5S-Visual Factory, DMAIC

Coaching,Teaching and Inclusion skills: ability to influence decision making, ability to interact with all levels of the business (senior leaders to working teams), project management skills (demonstrated experience in managing large teams), solid business acumen, proven team building skills, exceptionally good listening skills, results oriented, strong analytical skills, and prior process improvement experience. Proven experience in coaching and teaching others to think, behave and apply lean methods and tools. Experience enabling and leveraging diverse perspectives, talents, etc to achieve business outcomes.

Preferred:

Extensive Lean application experience, Six Sigma black belt certification; excellent skills using IT applications to organize and analyze data (MS-Access, MS-Excel, Minitab).

*LI-AS2

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition OE/000311.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: OE/Six Sigma

Primary Location: US-NC-Durham
Other Locations: US-NC-Wilson
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Durham-MMD-Sigma-Manager-Job-NC-27701/1864339/186433918643392012-06-15Merck/MSDOE/Six Sigmafull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Technical Support Engineer is a member of the IPT (Integrated Process Team) and provides technical support to the vaccine formulation/filling production area. This support will focus on investigation of manufacturing deviations and review of GMP batch records. Specifically, this individual will lead the investigation of deviations to determine root cause, will develop corrective actions to prevent reoccurrence, and will assess the impact of the deviation on product quality. Routine review of batch records and associated data required for release is also a key role in this position.

Primary responsibilities include, but are not limited to the following:

* Investigation of deviations (both minor and major), with responsibility to interface with Operations, GVTE (Global Vaccine Technology & Engineering), Automation, and Quality approvers.
* Manages the investigations to meet key timing commitments, with well-investigated and well-documented deviation reports.
* Works with the Technology, Automation, and Quality Approvers to determine the breadth and scope of the investigation to identify the appropriate root cause, implement corrective actions, complete trending analysis, and determine product disposition.
* Fosters a collaborative relationship with manufacturing floor personnel focused on high quality investigations, meaningful corrective actions, and reducing the deviation generation rate. Determines appropriate corrective actions to prevent reoccurrence of the deviation. Ensures corrective actions are effective.
* As part of the deviation management role, presents and defends investigations during regulatory inspections, as required.
* Performs a thorough review of batch records and related GMP documentation, identifying and resolving discrepancies in a timely manner, and implementing corrective actions to improve the batch record execution/review process.
* Leads process improvement projects, productivity initiatives, change requests, implementation of corrective actions, and execution of investigational test protocols, as required.

Qualifications

Education:

B.S./M.S degree in engineering/scientific field required.

Required:

* Minimum 2 years experience in a manufacturing or process support role.
* Working knowledge of cGMPs and of regulatory requirements as they apply to the vaccine/pharmaceutical industry.
* Experience in deviation management, troubleshooting and resolving manufacturing anomalies.
* Technical writing experience related to investigations of manufacturing process variation.

Desired:

* cGMP experience in a sterile, bulk or finished pharmaceutical environment.
* Experience with formal problem solving techniques, such as root cause analysis and/or Lean Six Sigma tools.
* Execution/review of manufacturing batch records

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAN001073.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Manuf./Operations Generic

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/Durham-Technical-Support-Engineer-Job-NC-27701/1281991/128199112819912012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Manufacturing Engineer is a member of the IPT (Integrated Process Team) and provides technical support to the vaccine bulk production area. The production includes media preparation, cell culture, viral and filtration processes as well as supporting area such as sterile goods/parts supplies. This support will focus on investigation of manufacturing deviations, training, process and system improvement. Accountabilities include leading investigation of deviations to determine root cause, developing corrective actions to prevent reoccurrence, and assessing impact of the deviation on product quality, training operations staff, and being part of the improvement efforts.

Primary responsibilities include, but not limited to, the following:

* Engage with the suite operations and provide support on training program, deviation management, process and system improvement.
* Lead process improvement projects, productivity initiatives, change requests, implementation of corrective actions, and execution of investigational test protocols, as required.
* Develop training material
* Working with subject matter experts (SMEs), provide/track necessary training for operator qualification as assigned.
* Investigate deviations with responsibility to interface with Operations, GVTE (Global Vaccine Technology & Engineering), Automation, and Quality approvers.
* Author and manage the investigations to meet key timing commitments, with well-investigated and well-documented deviation reports.
* Work with the Technology, Automation, and Quality Approvers to determine the breadth and scope of the investigation to identify the appropriate root cause, implement corrective actions, complete trending analysis, and determine product disposition.
* Foster a collaborative relationship with manufacturing floor personnel focused on writing high quality investigation, carry-out effective training, implementing meaningful corrective actions, and reducing the deviation generation rate. Determine appropriate corrective actions including training, process and system improvement to prevent reoccurrence of the deviation. Ensure corrective actions are effective and improve right first time (RFT).
* As part of the deviation management role, present and defend investigations during regulatory inspections, as required.
* Perform a thorough review and gather accurate information related to deviation and GMP documentation, identifying and resolving discrepancies in a timely manner, and implementing corrective actions.

Qualifications

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

BS/MS in engineering/scientific field

Required:

* 0-2 years relevant experience
* Experience in problem solving and troubleshooting
* Technical writing experience

Desired:

* cGMP experience in a sterile, bulk or finished pharmaceutical environment.
* Experience with formal problem solving techniques, such as root cause analysis (RCA), failure mode effects analysis (FMEA), and/or Lean Six Sigma tools.
* Execution/review of manufacturing batch records
* Experience in deviation management, troubleshooting and resolving manufacturing anomalies.
* A minimum one year supervisory or project management experience.

merck.com/careers to create a profile and your resume for requisition QUA002937.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Qual Assurance & Ops Generic

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-Manufacturing-Engineer-Job-NC-27701/1874868/187486818748682012-06-15Merck/MSDQual Assurance & Ops Genericfull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Durham Vaccine Facility is looking for a highly skilled Energy Center Utilities Technician. The Energy Center Technician is responsible for the Energy Center operations. The technician will have experience and knowledge of boiler operation, air compression, industrial chillers, refrigeration and water systems, steam generation, Human Interface Systems (HMI) and Building Automation Systems (BAS).

The technician will navigate between multiple PC screens to monitor for building alarms for various critical parameters.

The technician will operate all Plant Engineering utility generating equipment located throughout the entire site and take appropriate action to correct Plant Engineering maintenance problems.

The technician will perform the job duties per Standard Operating Procedures and cGMP's.

The technician will also be responsible for supporting departmental vision that provides for continuous improvement in all aspects of the operation.

The Mechanic identifies and demonstrates a working knowledge of customers and or suppliers and their requirements.

This position requires the incumbent to work 12 hour shifts and work five days in a row; the incumbent will switch shifts every 90 days.

Qualifications

Required Qualifications:

* High School Diploma and 10 years utility operation or utility maintenance OR 2 year technical degree and 7 years maintenance experience

* Experience with Utility System Generation, Boilers, Industrial Chillers, Distribution Systems, Control Systems

* Knowledge or Steam, Compressed Air, Water and Electrical Systems

* Use of Human Interface Systems and Building Automation Systems

* Experience navigating between multiple PC screens to monitor Building Alarms

* Experience with Industrial Refrigeration Systems that include DX systems, Cascade Refrigeration systems and Adsorption systems

* Abiliy to troubleshoot refrigeration and instrumentation systems

* Ablity to read electrical prints, P&ID's and understand P&ID control loops

Preferred Qualifications:

* Experience working in a facility that is regulated

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition PRO009448.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Production / Maintenance

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/Durham-Refrigeration-and-Utility-Plant-Engineering-Technician-Job-NC-27701/1764633/176463317646332012-06-15Merck/MSDProduction / Maintenancefull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This new leader role will mainly be providing direct oversight to the Quality Systems as described in Regulatory expectation documents such as ICH Q10. Reporting directly to the Site Quality Head, this leader will be responsible for overall QO performance metrics and Quality Projects associated with product Quality, process improvements and automated technologies (SAP, EBR, etc.). This role will create value by taking charge of building internal cost effective asset capabilities for product quality, GMP testing facility and will assure efficient quality process sustainability.

In alignment with ICH Q10 Objectives 2 and 3,this role will impact our ability to establish and maintain a state of control and to facilitate continual improvements

* Establish and Maintain a State of Control
* To develop and use effective monitoring and control systems for process performance and product quality, thereby providing assurance of continued suitability and capability of processes. Quality risk management can be useful in establishing the monitoring and control system.
* Facilitate Continual Improvement
* To identify and implement appropriate product quality improvements, process improvements, variability reduction, innovations, and pharmaceutical quality system enhancements, thereby increasing the ability to consistently fulfil quality needs. Quality risk management can be useful to identify and prioritise areas for improvement.

Qualifications

Education Required:

* Minimum Bachelor's Degree

Education Preferred:

* Master, or PhD degree in applied sciences and technology: (i.e. BioChemistry, Pharmacy, Engineering or similar)

Experience/Knowledge/Certifications Required:

* Minimum of 10 years experience in the Pharmaceutical industry with significant experience in biologics, vaccines and/or biopharmaceuticals.
* Minimum of 8 years experience in QA/QC with increasing responsibility.
* Proven experience in Global Pharmaceutical Business - Working in functions outside Quality & Compliance, e.g. Technology, Validation, Regulatory
* At least 5 years of leading/supervisory/managerial experience
* Demonstrated knowledge of GMPs, compliance issues, inspectional trends, industry quality assurance practices and systems, and personnel management skills.
* Exposure to Regulatory inspections including interactions with Board of Health representatives and responding to Board of Health observations
* Good understanding Global regulatory expectations
* Proven application of effective supervision principles
* Demonstrated innovative mindset
* Keeps updated in latest industry regulatory trends and leading edge technologies
* Experienced in organizational positioning from remote locations
* Demonstrated cross cultural agility and resourcefulness
* Proven expertise with:
* Qualification and validation processes
* Root Cause Analysis
* Investigative methods (such as KT, DMAIC)
* Financial principles
* Lean, 6 Sigma

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #QUA002950.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality Operations

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-Quality-Systems-&-Bus-Proc-Excellence-Director-Job-NC-27701/1891872/189187218918722012-06-15Merck/MSDQuality Operationsfull-timeUSDstarting0BSDurham, NC, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position is the second rung of the Customer Logistics Ladder. It provides more advanced analytical work and increased direct customer responsibility. This position builds from the existing CSCA roll. This role is responsible for driving customer and organizational performance improvement through analysis, communication and process improvement. Investigates and understands customer specific supply chain goals, metrics and processes to design and implement business building execution plans working cross-functionally with the Sales Teams. Directly responsible for ensuring supply chain optimization on a specific customer set. The activities will include day to day management of sales, customer service, transportation and logistics interaction to ensure successful execution of customer performance requirements. This position will also provide enterprise level analysis for assigned projects and process improvement opportunities.

Responsibilities:

* CPFR / Customer Collaboration: Organizing and leading customer collaboration meetings, both with the customer and within the Merck account team; sales and demand planning forecast alignment; order flow monitoring and trouble shooting; general management day to day activity of account operations.
* Analytical Activity: Customer specific and organizational analysis of ongoing trends; preparation, presentation, and implementation of process improvements.
* Business Planning / Customer Development: Customer scorecard reporting and presentations; customer penetration through travel; customer specific project implementation and execution; seasonal activity planning.
* Administration: Internal reporting on accounts and activities; departmental projects; meeting recaps; travel expenses, etc.

Qualifications

*LI-AS2

Education:

* Required: Bachelors Degree required

Required:

* 5-10 years experience, preferably in a Sales, Customer Service, Logistics or Transportation role.
* Strong Customer Orientation
* Excellent oral and written communication skills
* Strong analytical skills
* Self-Starter
* High work capacity

Preferred:

* Ability to successfully deal with diverse people, projects and requirements.
* Problem solving/decision making skills.
* Consumer Products experience
* Candidate should have exposure to multiple aspects of the supply chain and have a well-rounded background.
* Deals well with stress
* Demonstrated time management and prioritization skills
* Leadership
* Team Building

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition SUP000339.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Supply Chain Dev&Optimization

Primary Location: US-TN-Memphis
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Memphis-Sr_-Customer-Supply-Chain-Analyst-Job-TN-37501/1868783/186878318687832012-06-15Merck/MSDSupply Chain Dev&Optimizationfull-timeUSDstarting0BSMemphis, TN, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Drug Safety Surveillance Specialist is responsible for preparation, analyses, and follow-up of adverse event (AE) and serious adverse event (SAE) reports for domestic and international OTC products in compliance with company Standard Operating Procedures and applicable guidelines. Assure data accuracy, clinically valid case assessment and regulatory reporting status assessment. May serve as a primary point of contact for specific projects, in addition to providing Safety support and expertise on cross-functional project teams.

Duties include and are not limited to the following:

* Triage of incoming adverse event reports for completeness, legibility and validity. Assessment of case reports for seriousness, causality and expectedness.
* Writing case narratives.
* Process and perform medical assessment and reviews for medical/regulatory content.
* Assure accuracy per protocol requirements, requesting follow-up as necessary.
* Assess and triage of literature and media reports.
* Interact with Regulatory Affairs on issues pertaining to submission of appropriate reports to FDA and with Quality department on issues pertaining to quality investigation requests.
* Assist with developing project specific safety database customization and data entry guidelines.
* Acts as a liaison internally and with external collaborators to develop programs and processes to meet regulatory reporting requirements.
* Alert manager to potential signals, such as an unusual number of similar reports.
* Bring serious or potentially serious adverse event complaints and any Drug Safety-related issues to the attention of management as necessary and appropriate.
* Participate in professional and departmental meetings providing medical input and recommendations for improvement.
* Act as the Medical Monitoring Representative in project teams, as appropriate.
* Act as mentor, and direct workflow as appropriate to Drug Safety Surveillance Coordinators and Drug Safety Surveillance Specialists.
* Assist in supporting inspections and audits.
* Assist with staff training and mentoring. Accountability for delivery of results.
* Recognize potential or impending problems and work with manager to implement solutions.

Qualifications

Education:

* Requried: Associate's degree (or LPN), preferably in scientific field.

Required:

* Minimum (2) years pharmacovigilance related or healthcare work experience.
* Knowledge and/or experience in drug safety and the drug development process.
* Excellent verbal / written communication skills.
* Decision-making skills.
* Experience with computer applications including database management and pharmacovigilance related computing systems.
* Excellent team / project leadership and delegation skills.
* Proactive approach/uses own initiative appropriately.

Preferred:

* Applied knowledge of global regulations and global compliance timeline desired.
* Strong understanding of and ability to interpret and apply global safety regulations.
* Flexibility and adaptability with a positive attitude.
* Proficient in Microsoft Excel and Word.
* Experience in MedDRA coding.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # DRU000170.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Drug/Dvcs Sfty Survnce (NonMD)

Primary Location: US-TN-Memphis
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Memphis-Drug-Safety-&-Surveillance-Specialist-Job-TN-37501/1781664/178166417816642012-06-15Merck/MSDDrug/Dvcs Sfty Survnce (NonMD)full-timeUSDstarting0BSMemphis, TN, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Senior Scientist position works under the direction of an Associate Principal Scientist in the Analytical Method Development group. This position will perform development and optimization of analytical methods for pharmaceutical and cosmetic formulations. The Senior Scientist will collaborate both within the department and cross functionally on product development projects. The position will be involved with method validation and transfer, GMP testing, laboratory automation, technical training on analytical methodology, and laboratory software.

In addition, the Senior Scientist will use chemical and physical analytical techniques to support new formulations development, characterization, elucidation of degradation pathways, and impurity identification. This individual functions with minimal supervision to plan and execute projects and investigations. The candidate must be able to participate as a team member as well as an individual performer.

Major Activities and Responsibilities:

* This is a hands on laboratory position responsible for development and optimization of analytical methods for pharmaceutical and cosmetic formulations.
* This position provides analytical support to new formula development, characterization, elucidation of degradation pathways, and impurity identification in a pharmaceutical drug product development environment.
* This position works closely with formulations groups to plan and execute experiments.
* This position works with other scientists within the analytical group to recommend new equipment or techniques.

Qualifications

Education:

* Required: B.S. in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Science, or equivalent from an accredited college/university
* Preferred: MS / PhD in Chemistry

Required:

* 5 - 8 years in the pharmaceutical industry
* Minimum (5) years recent hands on method development experience (60-80% on the bench) working in a GMP, FDA regulated, and pharmaceutical/biotechnology drug product development company.
* Provide analytical support to new formulations development, characterization, elucidation of degradation pathways, and impurity identification primarily in a pharmaceutical drug product development industry environment.
* Advanced computer skills using Excel, Word and Statistical and experimental design skills
* Excellent oral and written communication and interpersonal skills
* Good collaboration and team work.
* Organize work and time to manage multiple project responsibilities and clients.
* Adapts to and performs well under changing priorities and deadlines.

Preferred:

* Experience with analytical method development of small molecules, specifically with pharmaceutical drug product formulations.
* Thorough knowledge with hands on experience with HPLC, UV/Vis, FTIR, Dissolution, LCMS, GCMS, degradation assessment/pathways, structural and physical characterization.
* Working knowledge of chromatography software (preferably Empower or Millennium).
* Understands, applies and can supervise advanced analytical practices
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CHE003473.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-EF1

Job
: Chemistry

Primary Location: US-TN-Memphis
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Memphis-Senior-Scientist-Chemical-Research-Job-TN-37501/1862525/186252518625252012-06-15Merck/MSDChemistryfull-timeUSDstarting0BSMemphis, TN, US
Description

The role of the Sr. Principal Packaging Engineer is to manage a portfolio of primary and secondary packaging projects for launch in global markets.

Expectation:

* Lead complex package design proposals.
* Identify, benchmark, develop and incorporate best engineering practices.
* Lead evaluation and selection of packaging technologies and suppliers. Perform exploratory work for packaging materials and design to support product innovation.
* Partner with Marketing, Manufacturing, Regulatory Affairs and other departments to meet all packaging requirements, including but not limited to; USP Testing, regulatory requirements, engineering studies and line qualification, storage and distribution testing.
* Assemble and lead cross functional teams of packaging suppliers, external parties and manufacturing sites to support development and commercialization activities.
* Prepare and execute development plans, technical procedures and testing protocols.

Scope of work:

* Package concept approval, drawing approval, tooling qualification, child-resistant / senior-friendly testing, specification generation and approval.
* Primary package types include tubes, sprays, aerosols, bottles, closures, foil sachets, etc.
* Secondary package types include pressure sensitive labels, shrink sleeves, folding cartons, club store trays, thermoforms, shipping cases, etc.
* Responsible for all package specifications to the pallet level to support new product launches.

Qualifications

Education:

* BS in Package Engineering (or other engineering degree)

Required:

* A minimum of 10-15 years experience in Package Development for consumer products in a regulated environment.
* Must be able to manage multiple projects that span different timelines.
* Risk-based decision making skills without knowledge of all the inputs.
* Must be able to work seamlessly in a team based environment.
* Clear communication skills (oral, written).
* Working knowledge of FDA regulations and guidance documents.
* Write, review, approve and route specifications in an electronic-based system.

Preferred:

* Design Thinking experience/Creative skills to fuel product/package innovation pipeline.
* Consumer testing experience to guide decision making.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PAC000119.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-EF1

Job
: Packaging Engineering

Primary Location: US-TN-Memphis
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Memphis-Senior-Principal-Packaging-Engineer-Job-TN-37501/1891870/189187018918702012-06-15Merck/MSDPackaging Engineeringfull-timeUSDstarting0BSMemphis, TN, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Develop new primary and secondary packaging for new product launches in global markets.

Responsibilities include and are not limited to the following:

* Package concept approval, drawing approval, tooling qualification, child-resistant / senior-friendly testing, specification generation and approval.
* Primary package types include tubes, sprays, aerosols, bottles, closures, foil sachets, etc.
* Secondary package types include pressure sensitive labels, shrink sleeves, folding cartons, club store trays, shipping cases, etc.
* Responsible for all package specifications to the pallet level to support new product launches.

* Perform exploratory work for packaging materials and design to support product innovation. This includes technology networking, laboratory work and testing, exploratory design and testing, consumer research, etc.
* Work with Marketing, Manufacturing, Regulatory Affairs and other departments to meet all packaging requirements, including but not limited to; USP Testing, regulatory requirements, engineering studies and line qualification, storage and distribution testing.
* Prepare/review/approve packaging protocols for developmental and pre-market stability packaging runs.
* Travel to sites to lead/assist in execution of these protocols.

Qualifications

Education:

* Required: BS in Package Engineering

Required Experience:

* Minimum (6) years experience in Package Development for consumer products in a regulated environment
* Must be able to work independently with little to no supervision on multiple projects that span different timelines
* Risk-based decision making skills without knowledge of all the inputs
* Must be able to work seamlessly in a team based environment
* Clear communication skills (oral, written)
* Working knowledge of FDA regulations and guidance documents
* Write, review, approve and route specifications in an electronic-based system
* 20% Travel

Preferred Experience:

* Design Thinking experience
* Creative skills to fuel product/package innovation pipeline
* Consumer testing experience to guide decision making
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PAC000116.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-EF1

Job
: Packaging Engineering

Primary Location: US-TN-Memphis
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Memphis-Senior-Packaging-Engineer-Job-TN-37501/1866481/186648118664812012-06-15Merck/MSDPackaging Engineeringfull-timeUSDstarting0BSMemphis, TN, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Future Talent Program features internships that last 10-12 weeks and will include one or more projects. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals.

For Biology majors, these include opportunities in process validation and manufacturing technical areas. Opportunities are also available in analytical, biological, and vaccine development. Projects can include research on assigned problems in the above listed areas, including applied development, problem solving, process / product improvement and laboratory testing in the above listed areas. Many analytical techniques are used, including both in vivo and in vitro methods, to characterize complex biological products and systems

For Chemistry and related majors, these include opportunities in synthetic, organic, analytical, physical chemistry and biochemistry. Projects include chemical laboratory work on assigned problems in the above listed areas, including applied development, problem solving, process / product improvement and laboratory testing in the above listed areas. Techniques that might be applied NMR, HPLC, near IR, immunoassays, wet chemistry techniques, CZE, physical property testing, and other analytical techniques. Course and lab work in instrumental methods is a plus.

Each of these opportunities provides a challenging environment to learn and contribute. The intern will be expected to work in a team environment. Responsibilities will also include the analysis and interpretation of data for problem solving and predictive purposes.

LOCATIONS: West Point, PA; Elkton, VA; Durham, NC; Rahway, NJ

Specific internship openings in MMD are as follows:

* Analytical Chemistry in Development and Supply (West Point, PA, Rahway, NJ) performs analytical development and support for new chemical, biological and pharmaceutical processes;
* Global Vaccines Technology and Engineering (West Point, PA, Elkton, VA, Durham, NC) is responsible for process implementation, validation and maintenance for biological processes;
* Biologics Manufacturing Science & Commercialization (Rahway, NJ, West Point, PA) is responsible for the development and implementation of vaccine and therapeutic protein processes;
* Vaccine Operations (West Point, PA, Elkton, VA, Durham, NC) is responsible for oversight and continuous improvement for vaccine manufacturing.

Qualifications

Requirements:

Education:

* Working toward BS in Biology, Microbiology, Virology, Chemistry or Biochemistry

Requirements:

* Available for 10 week internship beginning June 2012
* Strong personal character and ethics
* Superior Communication and Interpersonal Skills
* Excellent Academic Achievement, Analytical Ability
* Ability to work effectively with others as well as independently
* U.S. citizen or lawful permanent resident of U.S.
* Laboratory experience is preferred
* Titers may be required

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ADM004844.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-NJ-Summit
Other Locations: US-PA-West Point, US-NC-Durham-RTP, US-NJ-Rahway

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1

Relocation Provided
: None]]>http://jobs.merck.com/job/Summit-MMD-Science-Intern-2012-Job-NJ-07901/1729523/172952317295232012-06-15Merck/MSDInternfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position will be responsible for managing and supporting assigned Device Development MBV (Merck Bio-Ventures) projects from early design concept definition through commercialization. This position will interact with cross functional development teams and within Device Development. The incumbent must be able to work well with all levels of employees and be able to effectively coordinate the execution of Device Development and MBV strategies. In addition, he / she must be experienced in the field of injection molding, specifically in understanding of mold design and construction, and developing and validating injection molding processes.

Support of Device Development:

* Manage and provide leadership to device development teams of low to high complexity
* Ensure effective execution of assigned projects while adhering to management approved strategic plans, corporate policies, and providing clear communication within and external to the team.
* Monitor progress of project plans and communicate variances to plan within device development and to appropriate parties as needed
* Participate in preparation of materials for presentation of programs for management
* Work effectively with Device Development and MBV professionals to ensure successful execution of device development project plans
* Support the development, implementation and continuous improvement of Design Control processes and procedures
* Provide expertise with product design, development and commercialization
* Support Device Development, MBV and external groups in activities related to mold design, construction and validation
* Participate in troubleshooting manufacturing issues at the supplier site

Travel = 35%

Qualifications

Education:

* Bachelors degree in an engineering discipline.
* Advanced degree (MS) and / or Project Management Certification is a plus.

Required:

* At least 5 years relevant experience including in pharmaceutical/ engineering / academia / project management
* Direct project management experience with medical device development
* Demonstrated ability to work effectively in teams and develop plans which translate strategic objectives into executable actions and results
* Proven ability to effectively keep teams, projects, and assignments on track and raise issues in a timely faction to ensure that projects / assignments either stay on track or are properly re-scoped with management approval
* Strong knowledge in the field of injection molding, specifically in understanding molds' design and construction, and developing and validating injection molding processes
* Experience working with the suppliers on troubleshooting manufacturing issues at the supplier site
* Effective interpersonal skills and ability to work collaboratively across diverse teams and networks; able to foster cooperation in others
* Effective written and oral communicator
* Able to speak up & contribute in team forums
* Able to apply prior experiences and learning's in new settings, even if these are unfamiliar

Preferred:

* Working knowledge of medical device regulations with experience in their application is an asset.
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MEC000112.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-MG1

Job
: Mechanical Engineering

Primary Location: US-NJ-Summit
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: none]]>http://jobs.merck.com/job/Summit-Senior-Enginer-Job-NJ-07901/1737832/173783217378322012-06-15Merck/MSDMechanical Engineeringfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Senior Product Manager (SPM) for the MiraLAX® business is the general manager of the MiraLAX brand and interacts with every part of the organization that touches the brand. The SPM identifies key issues and opportunities for the brand, strategies and tactics and an action plan and investment needed to impact the short and long term growth of the brand. The SPM would have one direct report, an Associate Product Manager.

The SPM is responsible for but not limited to:

* Product and Brand Knowledge: Be an expert on the brand and the category and draw on that knowledge to make recommendations to further the business. Find ways to maximize our claims to tap into consumer insights and address competitive pressures. Leverage strong knowledge of brand and category to educate cross functional team members so they can finds ways to add value. Leverage knowledge to develop effective marketing plans.
* Facilitating External Market Analysis: Lead gathering of data inputs to answer key strategic questions about category dynamics and brand performance. Guide direct report and cross functional team members in analysis of market trends, sales, shipments, inventory flow, forecasts, etc. Provide input and direction to Market Research Department for the development and execution of all consumer market research. Analyze Market Research data to uncover new consumer insights, find ways to leverage those insights and disseminate learning and action plan to cross functional team.
* Strategic Thinking and Planning: Lead marketing plan process including establishing key issues, objective strategies and tactics. Develop multi year growth strategies and provide input on innovation vision.
* Marketing Communications: Lead development of all marketing communication with outside agencies to develop effective advertising, PR, consumer promotion and packaging. Recommend marketing communication strategies for the brand. Oversee development of creative briefs to ensure creative work is on strategy. Lead development of annual media plan and adjust when appropriate.
* Financials: Manage brand P&L and oversee management of marketing budget. Examine ROI of all projects and benchmark against best practices, similar brands and or programs.
* Facilitating Customer Relationships: Lead annual communication of brand plans to sales, align brand objectives and strategies with customer objectives, be the key interface with field sales.
* New Product Management: leverage product and brand knowledge and consumer insights to identify product improvements and cost savings opportunities, develop and champion new product business cases through IMT, lead cross functional teams to develop marketing support to achieve new product objectives, oversee development of sales materials. Provide input to Global Franchise group on the certain new product initiatives being handled by that team.
* Project Management: oversee and challenge project teams to ensure the execution of product plans that enhance brand value and deliver brand objectives and strategies. Manage advertising and other promotional/PR agencies, working with more senior levels, to ensure the development of appropriate strategies and tactics to achieve band objectives.

The SPM must be able to exhibit these behaviors:

* High degree of comfort making rapid decisions with uncertain or incomplete information
* Excellent project management and planning skills to execute a high volume of projects on time and with excellence
* Ability to set priorities and adjust given changes in market conditions or internal resources, etc
* Build effective teams by providing developmental support to the Associate Product Manager reporting directly to him or her and by working well with all cross functional team members.
* Excellent communication and presentation skills (both oral and written)

Qualifications

Education:

* Bachelor's degree required; emphasis in marketing desired.
* MBA preferred.

Required:

* Minimum 4 years marketing/sales experience

Preferred:

* Experience working on consumer products in a marketing or sales capacity.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PRO009454.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-EF1

Job
: Product Management

Primary Location: US-NJ-Summit
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Summit-Senior-Product-Manager%2C-GI-Business-Job-NJ-07901/1818570/181857018185702012-06-15Merck/MSDProduct Managementfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position will work collaboratively with Regional and Local Country Regulatory professionals and franchise research and development (R&D) and business colleagues to develop global regulatory strategies for new projects, to support the MCC Footcare and Skincare Franchises.

Key activities include :

* Provide guidance and advice R&D development teams, business partners, and to senior management on the regulatory requirements and milestones required for project success.
* Work closely with local country regulatory staff and MCC regulatory staff to ensure the production of dossiers that meet registration requirements in international markets
* Work cooperatively with Merck Research Laboratories (MRL) regional regulatory staff and Local country regulatory staff to ensure that MCC regulatory initiatives are executed as planned
* Monitor activities of trade group organizations and health authorities and advise MCC of new requirements and policies that affect MCC footcare and skincare products
* Evaluate new business development and licensing opportunities

Qualifications

Education:

* Bachelor's degree required (preferably in scientific discipline)

Required:

* Minimum of 10 years work experience
* Direct consumer or pharmaceutical regulatory experience (including OTC and international experience).
* Demonstrated ability to influence organizational decision-making, experience in risk assessment and risk management together with sound business judgment.
* Must possess excellent strategic, collaboration, communication, organization and presentation skills.

Desired:

* Medical device regulatory experience

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # REG000823.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-JN1

Job
: Regulatory Affairs Liaison

Primary Location: US-NJ-Summit
Other Locations: US-TN-Memphis
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Summit-MCC-Regulatory-Affairs-Franchise-Lead-%28SkincareFootcare%29-Job-NJ-07901/1385043/138504313850432012-06-15Merck/MSDRegulatory Affairs Liaisonfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Senior Customer Business Manager (SCBM) is responsible for developing and executing retail sales and promotional strategies in a top-tier customer account to achieve sales and profit objectives. The incumbent cultivates strong customer relationships and influences key internal and external decision makers to drive mutually-beneficial business opportunities. The incumbent develops, executes, tracks, and adjusts a retailer-specific business plan designed to achieve MCC and customer business objectives. The SCBM leads customer-focused projects and partners cross-functionally to execute strategic and tactical selling solutions based on marketplace knowledge and retailer trends. The SCBM maintains strong marketplace and retailer understanding and applies this knowledge to capitalize on customer opportunities.

Key responsibilities include and are not limited to the following:

* Manages top-tier, high-volume customer accounts to achieve MCC sales and profit goals, including market share and growth
* Leads the development of a strategic account business plan that integrates and optimizes MCC and customer business objectives
* Utilizes strategic selling and negotiation skills to maximize sales growth, promotional effectiveness, and long-term partnership
* Influences MCC's strategic business plan by providing field intelligence on emerging account and industry opportunities and trends. Provides "future-view" perspective of retail partnership to senior management in order to facilitate sustained growth
* Cultivates multi-level retailer relationships to understand short and long-term customer needs
* Influences, builds rapport, and negotiates with top-tier customer decision makers and internal management, resulting in increased distribution, shelving, merchandising, and improved marketing
* Analyzes both financial and logistical risks and implications during top-tier account decision making
* Differentiates MCC from competition as a proactive and innovative "thought leader" for retailer through analysis of MCC product, industry, and competitive developments and associated recommendations
* Leads the process to proactively provide insight-driven innovative solutions which meet customer needs and drive innovative growth
* Leads and continuously improves innovative merchandising and promotional programs which drive incremental volume, profit, and distribution for MCC brands, while maximizing ROI of trade budget and fund allocations
* Leads and continuously improves innovative merchandising and promotional programs which drive incremental volume, profit, and distribution for MCC brands, while maximizing ROI of trade budget and fund allocations
* Partners with Forecasting to analyze volume for sales and displays while planning corresponding budget long-term. Facilitates regular communication between groups to ensure alignment across teams on forecast attainment
* Manages budgets, including trade allocation, promotional funds, and display
* Partners with MCC headquarters to drive the development of custom products, packaging, displays, promotions, and launch of new product introductions to meet customer needs
* Partners with internal team members to develop and execute strategies for enhancing margin
* Manages shelving, promotion, and accrual fund to maximize sales growth, while also maximizing trade promotional tools
* Integrates multiple data sources to delivers customer presentations that maximize impact of resources
* Represents "voice of the customer" within MCC to drive profitable short and long-term results that align to customer needs and opportunities
* Manages communication, prioritization, and information flow with cross-functional teams, including Customer Solutions, Marketing, Customer Marketing, Logistics, Finance, Replenishment, and Analytics/Insights, while facilitating the sharing of best practices
* Influences retail execution through marketplace and retailer knowledge to ensure customer-focused resolution of operations challenges, optimization of retail opportunities, and competitiveness of innovations and programs

Qualifications

Education:

* Required: Bachelor's Degree

Required:

* (6+) years of work experience
* 20% travel required for this position
* Cross-retailer business experience
* Strong computer proficiency, including MS Office and database resources
* Excellent negotiation and consultative selling skills
* Ability to influence, motivate, and coach other
* Industry and product knowledge and experience
* Ability to manage and resolve conflict
* Ability to solve complex problems
* Ability to think strategically
* Strong analytical skills
* Strong interpersonal skills
* Proven ability to partner cross-functionally
* Knowledge of financial reporting
* Strong financial acumen
* Executive-level presentation and strong verbal & written communication skills

Preferred:

* Experience in CPG Sales
* Cross-Functional experience

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # DIR004257.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Direct Sales - Nondurable Goods

Primary Location: US-NJ-Summit
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Summit-Senior-Customer-Busness-Manager-Job-NJ-07901/1835828/183582818358282012-06-15Merck/MSDDirect Sales - Nondurable Goodsfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the guidance of a Senior Director, Outcomes Research (OR), the incumbent has the primary responsibility for planning and managing outcomes research activities for in-line and developmental infectious disease drugs on a worldwide basis. This includes all phases of outcomes research including design and implementation of retrospective database studies, assessment of patient reported outcomes, epidemiological studies and economic modeling. The incumbent works closely with Franchise Teams, Regional Product Directors, MSD affiliates, Public Affairs, MedEd and Merck Research Laboratories (MRL) to ensure OR programs are in line with marketing strategies in key countries. The incumbent also contributes to product development and marketing strategies to ensure that product value is defined and developed.

* Chairs/Co-chairs product/franchise-specific OR Sub-teams and provides leadership in developing the OR strategies and plans for developmental compounds and obtains cross-divisional senior management approval.
* Critically assesses drivers and drivers to reimbursement and market access to provide input into clinical and market development programs.
* Implements programs to document the burden or unmet need, patient reported outcomes (PRO) components, and health economic aspects of disease and the value of drug therapy as outlined in the OR planning process and generates data on a worldwide basis to support pricing and reimbursement.
* Develops core deliverables (e.g., health economic evaluations) and their adaptation to generate country-specific data supporting pricing and reimbursement.
* Works closely with the Product Development Teams (PDTs) to develop OR plans for Merck in-line and developmental products based on the regulatory, marketing and reimbursement environments on a worldwide basis. Works with MRL, MSD affiliates and consultants to write, coordinate, and validate as required, study design, protocols, measurement questionnaires, case report forms, data analysis plans, and final reports/publications.
* Works with the Merck Investigator Study Program Committee to evaluate outcomes research study protocols for studies in local markets.
* Supports MSD affiliates to understand local needs, adapt health economic evaluations, customize OR documents such as protocols and reimbursement dossier, which includes the development of the worldwide template document, design of data collection forms for customization to countries, and in collaboration with MSD affiliates, adaptation of the document according to local requirements.
* Works closely with other GHH departments (and Public Affairs to effectively develop/ communicate OR data and consistent messages throughout Merck and to external customers
* Responsible for maintaining awareness of scientific developments within his/her areas of expertise, both in terms of new methodology and new activities to establish communications with key outcomes research opinion leaders.
* May travel on company business to ensure broad internal/external input into the OR planning process and to assure the timely completion of projects.
* Builds relationships with health economic and outcomes research experts worldwide.
* Presents outcomes research data at international/national congresses and publishes articles in scientific journals.

Qualifications

Education:

* Required: Masters Degree
* Preferred: Doctoral degree from a recognized school of medicine, public health, management, pharmacy, or economics

Required:

* Minimum (3) years experience in the design and implementation of clinical, epidemiological, or health economic studies
* Travel of 15% is required for this position

Preferred:

* Masters Degree with (5+) years relevant experience or doctoral training and (3)+ years relevant experience
* Demonstrated expertise in the field of outcomes research, epidemiology or health economics
* Excellent leadership and strategic thinking skills
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # OUT000172.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Outcomes Research -Health Econ

Primary Location: US-NJ-Whitehouse Station
Other Locations: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Whitehouse-Station-Associate-Director-Director-Global-Health-Outcomes-Research-Job-NJ-08889/1807380/180738018073802012-06-15Merck/MSDOutcomes Research -Health Econfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the direction of the Manager, Global Trade Compliance COE, responsible for providing analytical support to Global Trade Compliance COE to include HTS Classification determinations ,Global Trade Compliance database and SAP/GTS system support, project management in support of trade compliance programs globally. Provides support to the Export Compliance Program as needed. Additionally ensures adherence to policies and procedures while continually striving to improve trade compliance level.

Primary responsibilities to include: Primary activities include, but are not limited to:

* Assist in the development, implementation and review of policies and procedures to ensure a strong global trade compliance management system.
* Assist in the development and update of trade compliance training materials and provide training to involved Employees with the best possible training methods.
* Perform risk analysis and determine trade compliance impact for Global Logistics sourcing changes as needed.
* Provide guidance on valuation, assists, royalty, and reconciliation.
* Provide guidance on Country of Origin and Trade Preference Programs.
* Classifies items for Export Classification Control Number (ECCN), determines licensing requirements, applies for export licenses where applicable.
* Advise management of regulatory changes and additions that may impact the business.
* Provide timely support for site trade compliance activities.
* Propose ways to utilize the trade laws and regulations to get the most benefit for the company.
* Continuously improve company trade compliance level.

Qualifications

Education:

* Required: Bachelors Degree
* Preferred: Advanced Degrees

Required:

* Minimum 4 years functional expertise with international trade or equivalent.

Preferred:

* Trade related certificate
* Licensed Customs Broker desirable
* Export Compliance Experience
* Advanced Computer / Technical skills to include SAP
* Strong project management and process improvement skills
* Strong leadership and teamwork skills, collaboration, and facilitation skills

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # REG000925.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Regulatory Affairs Generic

Primary Location: US-NJ-Whitehouse Station
Other Locations: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Whitehouse-Station-Sr_-Trade-Compliance-Analyst-Job-NJ-08889/1807382/180738218073822012-06-15Merck/MSDRegulatory Affairs Genericfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the direction of the Head, Emerging Markets Strategy and Commercial Innovation, the incumbent will work in a project-focused organization as a leader of divisional and cross divisional teams to champion commercial innovation projects, manage and prioritize innovation portfolios and facilitate execution of key initiatives via shaping the charter of projects, gathering data, analyzing and developing improvements, and preparing presentations to communicate project status and business results. He/she will assist with implementing the innovative ideas across EMs.

The incumbent will:

* Drive a culture of innovation across emerging markets.
* Utilize various approaches in external analysis such as benchmarking, assessing industry, and provide insights as needed to test internal and external innovative ideas
* Translate vision into actionable plans via objectives, strategy and roadmaps
* Utilize portfolio management techniques to aggregate, filter, prioritize and manage various innovation projects
* Provide quantitative and qualitative analytics and reporting as needed
* Work with the project sponsors and senior management to develop recommendations of innovation initiatives
* Partner with other innovation leaders across Merck to ensure learnings, best practices, and cross fertilization of innovative ideas
* Assist with expansion and implementation of successful commercial innovation pilot projects across emerging markets
* Perform other operational duties as assigned by the manager

Qualifications

Education:

* Bachelor's degree required
* Master's degree (MBA) preferred

Required:

* Minimum of 8 years work experience
* Demonstrated portfolio/project leadership
* Practical experience and proven results on commercial innovation initiatives
* 25-30% travel is required for this position

Preferred:

* Global work experience (particularly with or within Emerging Markets)

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAR004181.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-JN1

Job
: Market/Segment Development

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Whitehouse-Station-Director%2C-Commercial-Innovation-%28Emerging-Markets%29-Job-NJ-08889/1824623/182462318246232012-06-15Merck/MSDMarket/Segment Developmentfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck Global Services delivers requested services and makes recommendations on ways to enhance the workplace and the experience of working at Merck. We also collaborate with our colleagues to deliver the right level of services and solutions that help everyone to be more productive and enable innovation. Operating as a business partner, we are able to propose new ideas and innovative solutions to our internal clients that enable new business capabilities.

Merck Global Services has four core functional areas in which opportunities exist:

Information Technology

The Information Technology group provides technology leadership and innovation for business solutions that support Merck's divisions including Research and Development (R&D), Manufacturing, Sales and Marketing, Consumer Care, Animal Health and Corporate functions such as Finance and Human Resources.

Shared Business Services

Shared Business Services (SBS) supports Merck clients as well as suppliers and customers. In some cases, SBS is the primary face of the company to our health care partners. Delivering innovative services and business-focused solutions is a foundational element of SBS. All six core functional areas of the organization work together to deliver business-focused solutions.

Global Security

Global Security works with analysts, law enforcement agencies, intellectual property enforcement organizations, and pharmaceutical industry anti-counterfeiting efforts, to protect Merck people, assets and facilities. On-the-job training will be provided to the intern on basic and advanced structured analytic techniques, and the use of analytic tools. Staff members develop, implement and manage strategic initiatives to identify and mitigate security risks across Merck which may focus on individuals, groups, events, locations, or special associations, based on the program needs.

Facilities Management

Facilities Management is comprised of Site Operations and Centers of Expertise. Site Operations provides site services to all research, sales, marketing, and corporate company sites and to some sites where multiple divisions reside. Centers of Expertise provide strategic direction to the company on global real estate and workplace planning, aviation and fleet, energy and sustainability, dining services, maintenance, lab asset management, strategic sourcing governance and program realization for facility services.

Potential Locations: Whitehouse Station, NJ; Rahway, NJ; Summit, NJ; Union, NJ; Branchburg, NJ:, Lebanon,NJ; Springfield, NJ; West Point, PA; Upper Gwynedd, PA; Lansdale,PA; Elkton, VA; Durham, NC, Charlotte, NC; Boston, MA; Memphis, TN

Qualifications

Required:

* Currently enrolled in a Masters level or PhD program in: Computer Science, Computer Engineering, Business, Engineering, Mathematics, Statistics, Management Information Systems or a related discipline.
* Ideal candidate will possess superior communication and interpersonal skills.
* Must graduate program between May 2011 and August 2012 and be able to begin work in either January 2012 or June/July 2012
* U.S. citizen, lawful permanent resident of U.S. or otherwise authorized to work in U.S.

Preferred:

* GPA of 3.0 or higher

Our employees are key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # (IT 000294). Open to U.S. Residents & Citizens only.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-NJ-Whitehouse Station
Other Locations: US-TN-Memphis, US-NJ-Rahway, US-PA-Upper Gwynedd, US-NJ-Branchburg, US-PA-West Point, US-VA-Elkton, US-NJ-Springfield, US-MA-Boston, US-NJ-Summit, US-NJ-Lebanon, US-NC-Durham-RTP, US-NJ-Union, US-NC-Charlotte

Job Type
: Full Time
Employee Status: Regular
Number of Openings: 4]]>http://jobs.merck.com/job/Whitehouse-Station-Global-Services-Associate-Analyst-Job-NJ-08889/1689830/168983016898302012-06-15Merck/MSDFull Timefull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Future Talent Program features paid internships targeted to start in June 2012 for 10 - 12 weeks and will include one or more projects. Housing is available for those interns meeting the housing distance guideline. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals. The projects that you work in can be in one of the following areas:

PROCESS DEVELOPMENT, SCALE UP AND LAUNCH

* Work in teams to bring research discoveries to full production scale by applying engineering, biology, chemistry and pharmaceutics skills to bench-scale processes.
* Conceive, develop and implement new processing and manufacturing technologies
* Work with teams to develop processes for new products, using chemically- or biologically- derived products
* Support process development and product development with pilot plant scale up, drug supply preparation and technology transfer to operations groups

EQUIPMENT AND FACILITIES DESIGN

* Design and build advanced manufacturing plants, laboratory and office facilities
* Involvement with all phases of project management from the first engineering drawing to the last phase of project start up

MANUFACTURING

* Support line production and maintenance operations
* Maintain manufacturing processes at high levels of performance
* Engineer plant site improvements to enhance safety, quality and the environment
* Optimize existing processes to achieve improvements in process quality, yield and efficiency.

LOCATIONS:: Rahway, NJ; West Point, PA; Cokesbury, NJ; Summit, NJ; Elkton, VA; Durham, NC

Specific internship openings in MMD are as follows:

* Center for Material Science & Engineering (West Point, PA; Rahway, NJ; Summit, NJ) performs analytical evaluation of raw materials, intermediates, and final products to aide in investigation and process improvement evaluations
* Chemical Process Development & Commercialization (Rahway, NJ) and Pharmaceutical Commercialization Technology (West Point, PA, Summit, NJ) groups perform process development and demonstration for new chemical and pharmaceutical processes;
* Global Vaccines Technology and Engineering (West Point, PA, Elkton, VA, Durham, NC) is responsible for process implementation, validation and maintenance for biological processes;
* Biologics Manufacturing Science & Commercializaton (Rahway, NJ, West Point, PA) is responsible for the development and implementation of vaccine and therapeutic protein processes;
* Global Technical Operations (West Point, PA, Elkton, VA) is responsible for continuous improvement of existing processes.
* Global Engineering Services (Cokesbury, NJ with projects at other sites) is responsible for designing and project management for capital projects;
* Vaccine Operations (West Point, PA, Elkton, VA, Durham, NC) is responsible for oversight and continuous improvement for vaccine manufacturing.

Qualifications

Education:

* Working toward BS in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field

Requirements:

* Available for 10 week internship beginning June 2012
* Strong personal character and ethics
* Superior Communication and Interpersonal Skills
* Excellent Academic Achievement, Analytical Ability
* Good team player and ability to work independently
* U.S. citizen or lawful permanent resident of U.S.
* Titers may be required for this position

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ADM004817.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-NJ-Whitehouse Station
Other Locations: US-NC-Durham-RTP, US-NJ-Rahway, US-PA-West Point, US-NJ-Summit, US-VA-Elkton

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1

Relocation Provided
: None]]>http://jobs.merck.com/job/Whitehouse-Station-MMD-Engineering-Intern-2012-Job-NJ-08889/1729521/172952117295212012-06-15Merck/MSDInternfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

1. Product Promotion:

- Drive opening of new business avenues for Critical care in own territory hospitals through promotion of BU products to respective Medical fraternity in order to generate the business of the CC product portfolio
- Use detail aids to support scientific selling and Liaison with the HOD's , Purchase committee and Drug Committee doctors at the institutions for inclusion of the CC Products in the pharmacopoeia

2. Territory Sales:

- To prepare a target list of customers as per therapy profile. Understand and implement marketing strategies to medical fraternity to generate prescriptions for the cc products.
- To maintain and balance right distribution of products to the Pharmacy.

3. Market Intelligence/ Sales Reporting

-Interact with paramedical staff in hospitals to seek inputs on competitor activities, patients moving on MSD products, new products in the hospital etc. to maintain intelligence on MSD and competitor activity in the hospital
- Provide field reports in terms of FIRM, Tracker and Sales statement etc. in order to update the sales MIS

4.Customer Relationship Management:

- Organizing and conducting CME's with the user department at the institution in coordination to create and build the market for MSD products
- Manage the relationship with KOL's. Build, maintain and grow new KBL's and support CRM-Scientific activities with KOL's

Qualifications

BSc/ B Pharma with 3+ years of total sales experience in the Pharmaceutical sector

Job
: Direct Sales Generic MAH

Primary Location: IN-KA-Bangalore
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Bangalore-Territory-Business-Manager-Bangalore-%28HIV%29-Job-KA/1868790/186879018687902012-06-15Merck/MSDDirect Sales Generic MAHfull-timeUSDstarting0BSBangalore, KA, IN
Description

The Supply Chain / Order to Cash Analytics Lead defines and implements strategies around the use of supply chain / order management information to drive business value. Understands business needs around SCM/OTC analytics and defines solutions that map those needs to available solutions / data sources. Works with appropriate delivery organizations to ensure successful delivery of analytical solutions.

Provides leadership to Merck employees and contractors who are engaged in delivery of analytic solutions including rapid prototyping / analysis. Works closely with multiple Merck organizations to ensure that the business needs are met around the use of supply chain / order management information for analysis purposes. Develops strong relationships with key organizations such as operational support, ERP COE, and key business COEs such as Shared Business Services.

Develops knowledge of industry trends / external solutions and applies this knowledge to continuously improve the solutions / processes leveraged by the organization.

Participates in the process of demand management (e.g. cost/effort estimation, advisory services to refine / understand business need) associated with programs or projects that require financial information to be used for analytical purposes.

This position has global accountability - approximately 20% travel, which includes travel to international locations, is required.

Qualifications

Education

BA or BS in Supply Chain Management, Business Management, or Computer Science required

Experience

* 5-10 years of experience either in business or IT roles supporting Supply Chain / Order Management is required
* 5-10 years of experience with SAP (order management/supply chain management area) is required
* Prior leadership position that required either the definition and execution of a strategy in a complex global organization AND/OR that required operational leadership of a business or IT function in a complex global organization

Skills/Capabilities

* Demonstrated leadership skills in the following areas: written / verbal communications, negotiation / influencing, define / drive strategy, innovation
* Knowledge of Cognos, Spotfire, SAP BI or similar business intelligence technology is preferred.
* Knowledge of data warehousing technology (SAP BW, Oracle, Teradata or similar) is preferred

Job
: Accounts Payable/Receivable

Primary Location: IE-Leinster-Dublin
Other Locations: Belgium
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Supply-Chain-Order-to-Cash-Analytics-Lead-Job-L/1729552/172955217295522012-06-15Merck/MSDAccounts Payable/Receivablefull-timeUSDstarting0BSDublin, Leinster, IE
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


We are looking for a scientist with experience in the discovery and /or preclinical development of biopharmaceuticals. This position is a leadership position for a group of scientists responsible for the development, implementation and interpretation of in vitro pharmacology assays and in vivo efficacy models for therapeutic proteins focusing on Biosimilars. The candidate will be expected to provide scientific leadership to move programs through pre- clinical and clinical development including support for regulatory submissions. The candidate will serve as a member of cross functional teams and is expected to develop interactions strong working relation ships with, Discovery, Bioprocess, Toxicology and Clinical development.

Qualifications

Education:

* Ph.D. in an area of the Biological Sciences is required.

Required:

* 10+ year's relevant experience. Industry in biotherapeutic development is desirable.
* Previous experience managing scientists and research associates.
* Experience in development of a variety cell-based in vitro pharmacology assays using both cell lines and primary cells for mechanism of action and immune functions.
* Experience with establishment use and interpretation of preclinical efficacy animal models.
* Experience with report wring and the ability to effectively present technical/scientific communications to both project teams and senior management.
* Previous experience in participation and/or leadership of cross functional teams is desirable.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # RES001306.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Research Science Generic

Primary Location: US-NJ-Union
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Union-Pharmamcolgy-Group-Leader-Biopharmaceuticals-Job-NJ-07083/1828435/182843518284352012-06-15Merck/MSDResearch Science Genericfull-timeUSDstarting0BSUnion, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The team member within the Neuroscience Drug discovery group will employ in vitro and in vivo pharmacology techniques to enhance understanding of neurological disease processes, identify and validate novel therapeutic targets, and support the discovery and preclinical development of drug candidates. It is expected that the team member will spend >75% of their time generating primary data at the bench.

The responsibilities of the team member include:

* Responsible for the identification and validation of drug discovery targets for Alzheimer's and Parkinson's disease. Define, optimize, and implement a research operating plan suitable for advanced development of small molecule leads. Together with a medicinal chemistry lead, identify and optimize potential therapeutics (small molecule, biologic, RNAi) for validated Neurology targets.
* Fully understand mechanism of action and key points of differentiation for supported target relative to other targets in the same therapeutic area.
* Design and execute preclinical studies, including biomarker studies, to support the clinical development small molecule candidates
* Collaborate with members from other functional groups including In Vitro Pharmacology, In Vivo pharmacology, Medicinal Chemistry, Basic Pharmaceutical Sciences, and Exploratory and Translational Sciences
* Work with external academic, biotech, and contract research organizations.
* Monitor the external research environment and helping establish collaborations that are consistent with Neuroscience franchise and functional strategies.
* Manage internal and external resources to accomplish scientific goals in a rigorous and cost effective manner

Additional responsibilities of the team member include:

* May represent N&O franchise biology on cross-functional project teams
* May work with and communicate program progress with all levels of individuals within MRL basic research
* May have scientific management responsibilities of other scientists

Qualifications

Education:

* PhD in Neuroscience or related areas (example: Pharmacology, Cell and Molecular Biology, Biochemistry, etc) with approximately three (3) years postdoctoral experience or previous pharmaceutical industry experience.

Required:

* Subject matter expertise in the biology and pathophysiology of neurological disorders as demonstrated by strong publication record
* Expert knowledge of both biological principles, concepts and theories
* Strong hands-on technical expertise
* Demonstrated ability to thrive in a team environment
* Ability to communicate clearly and candidly
* Demonstrable leadership skills
* Proven ability to create and work within high performance teams in a matrix organization

Preferred:

* Subject matter expertise in Alzheimer's disease or other neurodegenerative conditions
* Experience in preclinical discovery of drug candidates
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003587.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Biology-Discovery

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Radioactive material, human and non-human primate samples]]>http://jobs.merck.com/job/West-Point-Neuroscience-Biology-Team-Member-Job-PA-19486/1862510/186251018625102012-06-15Merck/MSDBiology-Discoveryfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Medical Education Lead's responsibilities include but are not limited to the following:

* Oversee the work process and projects managed by a team of contract medical education promotion managers, supporting products globally across multiple therapeutic categories. Ensure the delivery of consistent, high quality medical education content (non CME) aligned with customer learning needs and business objectives across the Merck portfolio of products, vaccines and healthcare solutions.
* Monitor the outsourced staffing model, making adjustments based on business needs and work allocation.
* Develop and oversee execution of product launch support and transition plans for launch promotion managers and in-line promotion managers.
* Oversee Annual Planning process collaborating closely with the brand marketing teams to ensure medical education plans support brand and customer strategies, are adequately funded, and align with the overall Integrated Marketing Communications Plan.
* Implement new and innovative approaches to medical education content and program types and leverage best practices across brands and CBLs.
* Track and analyze marketing effectiveness of medical education tactics through the use of new and existing measurement tools to ensure optimal allocation of resources aimed at creating the greatest value for customers and delivering the highest return on investment.
* Oversee scientific agency scopes of work, budget planning, forecasting, and invoice management for content development budget across supported products globally; realize efficiencies and savings where possible.
* Partner with Legal, Regulatory and GEMS leadership as part of an ongoing assessment of medical education content, program types, and speaker/program owner training.
* Foster a culture of customer engagement, integration and revenue generation within the global medical education department and across GMC&CS.

Qualifications

Education:

* Required: Bachelor's degree
* Preferred: Advanced degree

Required:

* Minimum 2 years experience in pharmaceutical Marketing/Marketing Communications
* Strong scientific background
* Demonstrated planning and project management skills
* Experience working within teams

Preferred:

* Sales and/or marketing experience across multiple therapeutic areas and customer segments (PCP, Specialty and Thought Leader)
* Prior experience developing peer-to-peer medical marketing communications or promotional resources
* Previous experience managing or leading a team
* Previous experience managing an agency or vendor partnership
* Previous experience with PRT (Product Review Team for Medical/legal review)

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAR004195.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Marketing Communications

Primary Location: US-PA-West Point
Other Locations: US-PA-Upper Gwynedd
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Medical-Education-Lead-Job-PA-19486/1871151/187115118711512012-06-15Merck/MSDMarketing Communicationsfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The incumbent will lead the Customer Strategy market research team. The Team Leader will work directly with the Management Teams for Vaccine Customer Strategy Initiatives on business issues.

Team Leader

* Leads (effectively manages, coaches and mentors) a team of market researchers
* Proactively communicates and facilitates discussion with Marketing/Commercial Teams to ensure that insights are considered in decision-making and planning; provides consultative guidance to Marketing/Commercial Team(s)
* Understands marketing/ business needs at both a strategic and tactical level, encompassing local as well as global issues and cross portfolio issues.
* Has a solid understanding of the customer area, relevant therapeutic areas, market research methods and their appropriate application, and varied data sources
* Challenges business partners, your team and yourself about the business issues
* Understand the broader issues with the US Market, across Customer Areas, across Merck entire portfolio and applies knowledge to that to the Customer Strategy business
* Drive transformational changes and supports team during the transformation
* Has ability to manage through ambiguity and to provide clarity to the team on how to manage through ambiguity

Main tasks are:

* Planning and mobilizing resources to ensure key growth drivers receive appropriate resourcing investment in primary and secondary market research and analytic efforts
* Responsible for creation and effective application of relevant market, business and competitor insights in support of his/her assigned Marketing/Commercial Team(s).
* Directs and closely monitors his/her team in conducting market research projects where outputs/ recommendations will provide guidance for the development, monitoring and refinement of commercial and brand strategies and tactical implementation decisions. May personally lead such efforts if required based on business needs.
* Working differently with agencies to deliver on the business in new ways
* Implementing and adhering to service level agreements
* Prioritizes work and business issues across Vaccine Customer Initiatives
* Partner with Global Customer to align on customer strategies and initiatives for Merck
* Increases functional and leadership competencies across the team
* Ensures the budget and resources are aligned to business priorities
* Creates and shares a compelling vision for the Vaccine Customer Initiatives and translates the vision into strategies and priorities
* Model, lead and enable transformational change
* Proactively analyzes the Vaccine Customer Strategic business issues and recommends courses of action
* Ensures all primary/secondary research has a action standard and provides recommendations and implications
* Works with Commercial Management to ensure that GMRA support for their Marketing/Commercial Team(s) is effectively and efficiently managed, including:
* Ensures appropriate resources (plan, budget and people) supporting business objectives through the profit plan process
* Manages/ tracks research plans (primary and secondary) and budgets to meet objectives in a cost-effective, efficient and innovative manner; integrates plans with relevant stakeholders (e.g. Managed Markets & Policy, USRMLs, Global Marketing Communications, Global Marketing Team, Customer Engagement, Customer Marketing, etc.).
* Proactively directs the design, recommendation, implementation and presentation of comprehensive primary and secondary research.
* Ensures integration/coordination of research across global, regional, and country teams and internal working groups.
* Ensures rigorous, efficient and effective development of SCOPE tools, in order to develop marketing insights and support strategy development for assigned Marketing Team(s).
* Cultivates and applies strong understanding of market background, trends, geographic/country-level differences and the implications of such on the business.
* Manages a team of individual contributors that may include Market Research Managers (M04), Associate Managers (MO5) and Analysts (MO6); demonstrates appropriate situational leadership skills.
* Responsible for full range of career development and performance management activities, including recruiting, career planning, employee development/training, compensation planning and performance evaluation
* Allocates workload among team members to assure optimal use of resources, while balancing developmental objectives of the employee with the needs of the business.
* Coaches team members on all research project deliverables to ensure business needs are addressed, results are high quality and presented clearly, and recommendations are actionable and appropriate.
* Trains research team members on appropriate methods and use of data sources to address business needs.

Qualifications

Education:

* Required: University (bachelor's) degree from accredited institution
* Preferred: Master's degree (MBA)

Required:

* Minimum of 8 years work experience (preferably in pharmaceutical industry, consumer package goods or in market research agency)
* Prior customer strategy experience
* Excellent command of written and spoken English

* Knowledgeable of Brand Marketing - knowledgeable of multiple therapeutic areas, applies knowledge of the healthcare environment, leads strategic choices for brands/portfolio
* Mastery of functional market research skills - frames business decisions, provides business insights, synthesizes findings and delivers a story
* Innovative and strategic thinking
* Strong analytical and statistical skills and able to create databases
* Excellent communication skills
* Strong leadership and negotiation skills
* Comfort in collaborating with Senior Mgmt
* Fosters collaboration, embraces and drives new ideas
* Ability and comfort in leading in a complex and ambiguous environment of a global matrixed organization

Preferred:

* Prior vaccines experience
* Prior people management experience

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAR004138.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Market Research/Intelligence

Primary Location: US-PA-West Point
Other Locations: US-NJ-Whitehouse Station
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Team-Leader-Vaccine-Customer-Market-Research-Job-PA-19486/1742687/174268717426872012-06-15Merck/MSDMarket Research/Intelligencefull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The team member within the Neuroscience Drug discovery group will employ in vitro and in vivo pharmacology techniques to enhance understanding of neurological disease processes, identify and validate novel therapeutic targets, and support the discovery and preclinical development of drug candidates. It is expected that the team member will spend the majority of their time generating primary data at the bench.

The responsibilities of the team member include:

* Conducting experiments to support preclinical drug discovery efforts at different stages of development including target identification and validation, lead identification and lead optimization.
* Designing and executing preclinical research studies to support the clinical development of small molecule candidates
* Generating and integrating data from in vitro and in vivo experiments towards the discovery and validation of target engagement, pharmacodynamic, efficacy and safety biomarkers of drug candidates.
* Collaborating with members from several functional areas including In Vitro Pharmacology, In Vivo pharmacology, Medicinal Chemistry, Basic Pharmaceutical Sciences, Safety Assessment, and Exploratory and Translational Sciences.
* Fully understand mechanism of action and key points of differentiation for supported target relative to other targets in the same therapeutic area.

Additional responsibilities of the team member include:

* Managing the design of research protocols and execution of experimental studies using standard and innovative scientific approaches and techniques
* Oversight of summarization and consolidation of experimental data
* Ensuring that study objectives and results are communicated in a concise and clear manner to the appropriate teams and committees

Qualifications

Education:

* BA/BS or MS in Biology or Biochemistry or related field with a minimum of five (5) years of previous pharmaceutical industry experience.

Required:

* Strong hands-on technical expertise
* Experience in preclinical discovery of drug candidates
* Experience working with and administering therapeutics to rodents
* Demonstrated ability to thrive in a team environment
* Ability to communicate clearly and candidly
* Demonstrable leadership skills
* Proven ability to create and work within high performance teams in a matrix organization

Preferred:

* Subject matter expertise in the biology and pathophysiology of neurological disorders
* Subject matter expertise in Alzheimer's disease or other neurodegenerative conditions
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003588.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Biology-Discovery

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Radioactive material, human and non-human primate samples]]>http://jobs.merck.com/job/West-Point-Neuroscience-Biology-Team-Member-Job-PA-19486/1862508/186250818625082012-06-15Merck/MSDBiology-Discoveryfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Sales Planning Manager (SPM) is responsible for establishing and leading the MCC sales planning process.

* Maps, monitors, and measures key sales planning decisions, milestones, and data to support the MCC sales teams and meet customer expectations and needs.
* Leads the development of sales and spending plans while partnering with Sales Strategy Managers and cross-functional areas to achieve MCC business goals.
* Leads the long-term business planning process for top customers in alignment with MCC strategy and vision.

Qualifications

Education:

* Bachelor's degree required

Required:

* Minimum (5) years work experience
* Project management experience
* Consumer products industry work experience

Preferred:

* Sales planning experience

Job
: Channel Sales Generic

Primary Location: US-NJ-Summit
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Summit-Manager%2C-Sales-Planning-%28Merck-Consumer-Care%29-Job-NJ-07901/1774608/177460817746082012-06-15Merck/MSDChannel Sales Genericfull-timeUSDstarting0BSSummit, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview

The successful candidate will oversee the Global Ergonomics program for Merck & Co., Inc. The Global Ergonomics Leader will work closely with regional and site Environmental, Health and Safety (EHS) personnel to implement effective ergonomic practices at manufacturing and research locations. The leader will coordinate the implementation of policies and procedures which will provide for continuous improvement of the program while maintaining the flexibility required by the company's research and manufacturing activities. This position will also oversee the development and implementation of training for both EHS professionals and operations supervisors. The successful candidate will also be expected to support the EHS audit program section on ergonomics.

Additional responsibilities are as follows:

* Develop policies, procedures, tools, and training programs to improve ergonomic practices and reduce injuries.
* Provide support and expert advice to divisions and sites in the control of ergonomic hazards for manufacturing, research and office personnel.
* Make recommendations for changes in work environments based on interpretations and principles of professional practice.
* Assist in the evaluation and interpretation of current international, federal, and industry ergonomic regulations and guidelines.
* Provide technical assistance and guidance on basic and complex ergonomic problems.
* Conduct ergonomic program reviews of Merck facilities at international and domestic sites.
* Audit records and prepare supporting data for required government, industry and management reports.

Qualifications

Educational requirements:

* Bachelor's degree in safety, ergonomics or related field.

Preferred:

* Master's degree.

Required skills and Experience:

* A minimum of 10 years practical experience in ergonomics.
* Experience in pharmaceutical or other related industry.
* Strong communication skills, and a demonstrated ability to work both independently and as part of a larger group.

* An understanding of how ergonomics fits into the overall EHS program.

Preferred:

* Certified Professional Ergonomist (CPE) certification strongly recommended.
* Experience with international regulations and guidance.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. merck.com/careers to create a profile and your resume for requisition # IND00132.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-BR1

Job
: Industrial Hygiene & Safety

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Whitehouse-Station-Global-Ergonomics-Lead-Job-NJ-08889/1542239/154223915422392012-06-15Merck/MSDIndustrial Hygiene & Safetyfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Recruiting & Staffing Lead is responsible for delivering a comprehensive talent acquisition strategy to support all divisions / functions in the region. He/She will work with the global Centers of Expertise - COE's (Executive Recruiting, Recruiting Solutions and University Recruiting) to deliver the most effective solutions on talent resourcing commitments to drive the business. He/She will work with the country HR leaders to ensure alignment on appropriate local, regional and global tools and resources to support our business clients. He/She will work with the other regional CoE's (Talent Management, Learning and Compensation) to ensure an integrated approach to Talent that supports the business needs across the region. He/She will also be a member of the senior Merck Recruiting and Staffing leadership team.

Core Responsibilities:

* Demand planning & talent acquisition strategy - maintain contact with the business leaders in the region to have an ongoing view of business strategy/plans and impact upon human capital requirements (hiring, redeployment, downsizing, etc.). Understand the capability gaps, succession plan gaps and internal talent pools to develop optimal talent plans and solutions for the business - as part of an integrated talent strategy.
* Infrastructure - Building a recruitment infrastructure (internal and external resources) to cost effectively fill vacancies with the talent that the business requires. Leverage recruitment sourcing efforts across and between region(s). Build the right recruiting models according to the combined needs of individual countries and the broader needs of the global business.
* Recruitment Process - Apply appropriate global approaches, combined with sensitivity to local needs. Emphasize good local practice so it can be shared across the region/globally. Recruitment process, technology implementation and rollout of Taleo for region, continually improving the efficiency and effectiveness of global processes. Interview and selection methodology/process/tools improvement
* People Management - manage and develop the team of recruiters and managers under direct line management to achieve business targets. Coach and develop the team to develop leadership bench strength for the regional and global future staffing roles.
* Leadership, direction and coordination for recruitment priorities in region and influence those doing dual HRBP/Recruiting roles to align to company and regional strategy.
* Executive Recruiting - this role also serves as the Executive Recruiter for the region as needed. Coordination of executive recruiting, interviewing, selection and offers in the region, in partnership with Executive Recruiting and senior HR leaders. Retained and contingent search firm coordination and contract management for the region
* Branding - Oversight of recruiting advertising agency and employment brand strategy, in partnership with the Recruiting Solutions group.
* University and Diversity recruiting strategy and delivery for the region. Working in partnership with the Global University recruiting team, deliver on the future talent requirements for the region.
* Metrics, reporting and business outcome coordination for the region. Contribute to the enhanced analytics need at a global level - and the need to support decision making at the local level. Support the evolution of quality of hire metrics as we develop towards a measurement of both efficiency and effectiveness of hiring.
* Change management - as the Recruiting and Staffing function outside the US is still relatively new, there is a strong change management and change leadership component to this role at this stage in its existence - transforming the way we support our recruiting and staffing needs within HR and specifically on redefining roles / relationship between the HR Business Partner, the Recruiter and the Hiring Manager.

Please note: This is position will be based out of the Asia / Pacific Region, Desired Locaton is Singapore

Qualifications

Education Requirements:

* Bachelors degree required

Required Experience / Skills:

* Minimum 10 years related experience
* Minimum 3 years of Staffing leadership experience preferred, including direct sourcing experience either in-house or in a search firm
* Change management experience - having led change across multiple client groups
* Strong consulting and negotiation skills required
* Proven ability to persuade and influence others using communication and diplomacy skills with colleagues in other areas and at all levels of the organization including executive level.
* Systems to business translation - to understand what tools are available and effective for the business red
* Ability to work effectively with many different cultures and styles, including with a US corporate environment
* Excellent verbal and written communication skills
* People Management experience required

Preferred Experience / Skills:

* MBA preferred
* HR business partner experience prefer

Please note: This is position will be based out of the Asia / Pacific Region

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # HR 000308.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: HR Generic/Consultant Generic

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Recruiting-&-Staffing-Leader%2C-Asia-Pacific-Job-NJ-08889/1874870/187487018748702012-06-15Merck/MSDHR Generic/Consultant Genericfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Work closely with Global Transportation Team functional leads to ensure alignment on business case assumptions as well as participate in the implementation of the solutions as an advisor

Under the direction of the Manager for Network Modeling & Optimization, the incumbent is responsible for performing analysis of potential transportation, logistics, and distribution network/model configurations. The position requires close collaboration and communication with Global Tranportation functions, Global Logistics operations, and other functions such as planning, procurement, finance, and manufacturing. The incumbent will coordinate with cross functional global teams, internal as well as external stakeholders, to complete the collection of data, analysis and recommendation of best alternatives to senior leadership of Global Logistics. The position requires sound understanding of logistics outsourcing operations, technology, as well as general understanding of financial, business, and quality areas. In performing these functions and responsibilities, the incumbent will comply with all Company and Divisional policies, ethical business practices and all relevant laws and regulations.

The Logistics Engineer will lead analysis, design, and continuous improvement projects of Merck's Logistics Network. The incumbent will:

* Conduct analysis of potential transportation & distribution network/model configurations
* Construct & utilize reusable models or modeling tools for periodic analysis and evaluation of the Global Transportation Network and Logistics operations
* Lead process definition or redesign projects & facilitate solution design workshops
* Provide Global Logistics and other areas with analytical and modeling expertise
* Provide evidence of best practices and key trends that will assist in shaping the decisions to design an efficient and agile Transportation Network
* Interface with regional stakeholders to ensure voice of customer, data, as well as benchmark information is gathered to formulate business case

Qualifications

Required:

* Minimum of a Bachelors Degree
* 5+ years of experience in logistics/supply chain or relevant field.
* Proficient in the use of tools such as Excel & Access for data analysis
* Skilled in formulating process diagrams using tools such as Visio

Preferred:

* Prior experience working on a global network modeling project prefered
* Knowledge of Supply Chain modeling packages preferred (e.g. JDA SCS, IBM LogicNet+, Infor SCD, Lammasoft
* Knowledge of computer programming and experience with building reusable modeling/analysis tools
* Prior experience in designing a global supply chain/logistics network

LI-AS2

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # LOG000162.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-NJ-Whitehouse Station
Other Locations: US-PA-West Point, US-NJ-Summit, US-NJ-Rahway

Job Type
: Full Time
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Logistics-Engineer-Job-NJ-08889/1742688/174268817426882012-06-15Merck/MSDFull Timefull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck Corporate Audit and Assurance Services' (MCAAS) primary purpose is provide value-added independent and risk based audit and assurance services. The Senior IT Auditor conducts audits and assessments of information technology resources across all Merck divisions and functions to evaluate the adequacy of internal controls and to develop recommendations for improvement. Information technology resources include business critical applications as well as the related technology infrastructure, data, facilities, organizations, and processes.

Senior IT Auditors are responsible for the audit of complex IT environments and may serve as the In-Charge on certain assignments. In addition, they frequently perform audits with limited supervision from the IT Audit Managers. Audit activities include: gathering and analyzing information to identify key risks and controls; systematically testing and evaluating controls to verify efficiency and effectiveness of operation; reliability of information and compliance with applicable laws and regulations; recommending control improvements; communicating findings and recommendations to management; documenting audit work using automated audit management tools; and following-up on the status of corrective actions. As part of the audit process the Senior IT Auditor identifies internal control best practices and promotes their adoption across the enterprise. In addition, Senior IT Auditors provide training to other members of the department and to affiliate organizations and lead MCAAS improvement projects using appropriate methodologies.

Qualifications

Education Requirement:

* Bachelor's degree preferably in computer science or equivalent education and/or job experience.

Required:

* Knowledge of audit methodology and internal IT controls.
* A minimum of 3 years of Information Technology and/or IT Audit experience.
* A strong understanding of IT processes and technology, with demonstrated proficiency in one or more of the following areas is required: program/project management, ERP systems (SAP), information security, and/or infrastructure services (operating systems, databases, network, hardware).
* Willingness to travel domestically and internationally (up to 40%).

Preferred:

* A professional security, audit, or control certification, control-related professional certification, such as CISA, CIA, CRISC or CISSP.
* Experience in the assessment of internal controls and communicating findings and recommendations to others clearly and accurately in non-technical terms is desirable.
* Experience with Sarbanes-Oxley compliance is a plus.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # FIN000748.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-PD1

Job
: Fin/Bus Cntrls & Audit Generic

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 3]]>http://jobs.merck.com/job/Whitehouse-Station-Senior-Internal-Auditor-IT-Job-NJ-08889/1655963/165596316559632012-06-15Merck/MSDFin/Bus Cntrls & Audit Genericfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Senior Sourcing Analyst, Direct Materials - Packaging Components

Position overview:

The Senior Sourcing Analyst will support the implementation of global category strategies across our internal and external manufacturing network. Packaging components scope includes approximately $500 MM of spend across secondary packaging (folding cartons, inserts, and labels), primary packaging (plastic bottles & closures, film & foil, aluminum tubes, bulk drums), drug delivery systems and cold chain components. The Global Packaging Team works with our internal and external sites and other stakeholders globally in a fast-paced dynamic environment. Strong interest and desire to excel/develop in Supply Chain Management required. Job responsibilities include but are not limited to:

* Compiles and synthesizes both business requirements and external market conditions to support optimal category strategy development
* Develops and compiles Request for Information (RFI), Request for Quotation (RFQ) or Request for Proposal (RFP) to facilitate development of sourcing strategy
* Supports implementation of sourcing strategy (competitive bidding, eSourcing tools, reverse auctions, etc.).
* Applies financial analyses to address Strategic Sourcing challenges
* Conceives and develops complex analytical & pricing models, including analysis of financial statements and industry cost drivers
* Develops detailed analyses of financial statements and cost structures
* Conducts comprehensive supplier analysis (strategic direction, financial health, market position, power within industry, capabilities & capacity, risk assessment)
* Supports negotiation strategies, contract analyses, and sourcing communications and meetings

Reporting structure and Location:

* Director Global Procurement - Packaging Components
* Please note that this position can be located in US or Europe at the Merck local sites. There is no international relocation offered. Local candidates are considered.

Qualifications

Education:

* Required: BS/BA degree in Finance/Business/related field

Required Experience:

* Four to seven years of relevant experience (examples include but not limited to; manufacturing, technical R&D or process engineering, finance, consulting, business operations, external manufacturing, supply chain management etc.)
* Ability to conduct a comprehensive analysis of data from multiple sources and to present the conclusions in an easy to understand and actionable manner
* Three to five years experience in Project Management demonstrating the ability to successfully complete large, complex and international projects
* Demonstrated strong problem solving, negotiation, and conflict management skills
* Drive results while dealing with ambiguity
* Excellent oral and written communication skills; able to influence at all levels in the organization
* Thorough knowledge of MS-Office (Word, Excel, PowerPoint, Access, Project, Outlook);
* Advanced MS Excel Skills (Vlook Ups, Macros, & Pivot Tables) and Access (for analysis and report creation)

Experience and Skills:

* Demonstrated capabilities in Sourcing & Supplier Strategies, Sourcing Methodology, Cost Optimization, Supplier Relationship Management, Negotiation Skills, Financial/Legal Aspects with Procurement, and Supplier Risk Management
* Demonstrated strong interpersonal skills, inclusion and diplomacy in all interactions - particularly when interacting with people from different cultures/countries and all levels of management. Must be a team player and relationship builder and have the ability to interface with senior management in a professional yet courageous manner
* Demonstrated experience in leading complex analysis including the ability to analyze large sets of data
* Candidate must have proven skills in prioritizing and multitasking utilizing strong organizational skills. Must possess strong attention to detail and follow up. Ability to be consistently poised under pressure and the ability to keep an objective perspective
* Strong financial and business acumen
* Strong quantitative, analytical and problem resolution skills
* Ability to lead cross-functional teams
* Strong attention to detail
* Demonstrated competence, achievements and ability to work independently in a fast paced environment

*LI-AS2

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition TEC000491.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Technical Purchasing

Primary Location: US-NJ-Whitehouse Station
Other Locations: US-NJ-Rahway, US-PA-West Point, US-VA-Elkton, US-NC-Durham, US-NJ-Summit, US-NC-Wilson, Netherlands, CH-Lucerne
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Whitehouse-Station-Sr_-Procurement-Analyst-Job-NJ-08889/1871152/187115218711522012-06-15Merck/MSDTechnical Purchasingfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

1. Product Promotion:

- Drive opening of new business avenues for Critical care in own territory hospitals through promotion of BU products to respective Medical fraternity in order to generate the business of the CC product portfolio
- Use detail aids to support scientific selling and Liaison with the HOD's , Purchase committee and Drug Committee doctors at the institutions for inclusion of the CC Products in the pharmacopoeia

2. Territory Sales:

- To prepare a target list of customers as per therapy profile. Understand and implement marketing strategies to medical fraternity to generate prescriptions for the cc products.
- To maintain and balance right distribution of products to the Pharmacy.

3. Market Intelligence/ Sales Reporting

-Interact with paramedical staff in hospitals to seek inputs on competitor activities, patients moving on MSD products, new products in the hospital etc. to maintain intelligence on MSD and competitor activity in the hospital
- Provide field reports in terms of FIRM, Tracker and Sales statement etc. in order to update the sales MIS

4.Customer Relationship Management:

- Organizing and conducting CME's with the user department at the institution in coordination to create and build the market for MSD products
- Manage the relationship with KOL's. Build, maintain and grow new KBL's and support CRM-Scientific activities with KOL's

Qualifications

BSc/ B Pharma with 3+ years of total sales experience in the Pharmaceutical sector

Job
: Direct Sales Generic MAH

Primary Location: IN-WB-Kolkata
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 2]]>http://jobs.merck.com/job/Kolkata-Territory-Business-Manager-Kolkata-%28Critical-Care%29-Job-WB/1672534/167253416725342012-06-15Merck/MSDDirect Sales Generic MAHfull-timeUSDstarting0BSKolkata, WB, IN
Descripción
MSD es un líder global en el cuidado de la salud con una diversificada cartera de medicinas de prescripción, vacunas y productos de consumo para la salud, así como productos para la salud animal. Hoy en día, nos encontramos construyendo un nuevo tipo de compañía de salud - que esté listo para ayudar a crear un futuro más sano para todos nosotros.

Nuestra capacidad de superación depende de la integridad, conocimiento, imaginación, habilidad, diversidad y trabajo en equipo de gente como usted. Con este fin, nos esforzamos en crear un ambiente de respeto mutuo, estímulo y trabajo en equipo. Como parte de nuestro equipo global, usted tendrá la oportunidad de colaborar con colegas talentosos y dedicados, mientra su carrera se desarrolla y expande.

El Director de Asuntos Regulatorios es responsable de cumplir con los requerimientos sanitarios locales y las políticas de la compañía para la comercialización de los productos de MSD Venezuela.

PRINCIPALES RESPONSABILIDADES:

- Obtener de las autoridades venezolanas el registro sanitario necesario para la comercialización de los productos elaborados o importados por la Organización.
- Preparar las solicitudes de registro de nuevos productos, nuevas indicaciones y posologías de manera que cumplan con todas las regulaciones sanitarias locales, seleccionando, evaluando y organizando la documentación técnico - científica que se obtiene de la Casa Matriz. Mantener actualizados los productos comercializados por la e de acuerdo a las regulaciones sanitarias venezolanas y las políticas de registro de la compañía.
- Obtener de las autoridades sanitarias la aprobación para realizar en Venezuela cada estudio de investigación clínica que se decida llevar a cabo con los productos, sometiendo la documentación y estudios requeridos.
- Hacer seguimiento al registro en Venezuela de las marcas de fábrica de la compañía, necesarias para la comercialización de sus productos en el país y mantener actualizados los listados de las marcas disponibles
- Suministrar a subsidarias de la compañía de otros países la documentación legal necesaria para el registro de productos fabricados por la subsidiaria de Venezuela que se exportan a esos países.
- Revisar y aprobar conjuntamente con el Director Médico el arte final de todo el material promocional de los productos, de acuerdo a la política de mercadeo de la compañía y a las condiciones del registro sanitario local.
- Supervisar y controlar al personal a su cargo asegurando que cumplan con las políticas y normas de la compañía.

Cualificaciones
Educación: Farmaceútico (Grado en Farmacia en reconocida Universidad Nacional)
Registrado en el Ministerio de Salud.

Miembro del Colegio de Farmacéuticos de Venezuela.

Registrado en el Instituto de Previsión Farmacéutica

Idiomas: Español (nativo), Inglés ( Intermedio alto).

Experiencia Laboral: Más de siete años en posiciones similares.

Conocimientos requeridos: Experiencia en manufactura, aseguramiento y control de calidad de productos farmcéuticos.

Habilidades: dinamismo, organización, proactividad, responsabilidad, compromiso con el trabajo, orientado a trabajo en equipo.

Nuestros empleados son la clave del éxito de nuestra empresa. Demostramos nuestro compromiso con nuestros empleados ofreciéndoles un programa de recompensas competitivo y valioso. Los beneficios en MSD están diseñados para apoyar la amplia gama de objetivos, necesidades y estilos de vida de nuestros empleados y de muchas de las personas que constituyen lo más importante en sus vidas.

*LI-KT1

Puesto
: Asuntos regulatorios genéricos

Ubicación principal: VE-Caracas Capital District-Caracas
Tipo de acuerdo laboral: Fijo(a)
Viajes: Sí, un 25% del tiempo
Cantidad de vacantes: 1]]>http://jobs.merck.com/job/Caracas-Director-de-Asuntos-Regulatorios-Job/1853558/185355818535582012-06-15Merck/MSDAsuntos regulatorios genéricosfull-timeUSDstarting0BSCaracas, Caracas Capital District, VE
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The incumbent is responsible for the completion of financial, operational and/or computer audits, integrated audits and process audits, and for the delivery of an audit report that adds value to the business unit audited. Under the direction of the Client Audit Director and/or the Auditor-in-Charge, the incumbent is responsible for the effectiveness and efficiency of the audit that he/she is assigned to. You are responsible for expediting all stages of the writing and review of reports, which accurately reflect facts and recommendations of an objective appraisal of Merck operations. You will maintain the highest standards of professionalism and independence in the execution of your duties, always with the Company's best interests in mind. You will lead by personal behavior and ethics that are also of the highest standard. The incumbent should embody the Corporate Audit Group (CAG) values and vision, and is cognizant of the CAG Policies and Procedures, and adheres to them and applies them.

Participate in achieving the Corporate Audit's annual audit plan according to established schedules. The primary role will be to lead small teams of auditors on various assignments. Incumbent will be expected to lead complex, large and/or sensitive audits with limited management supervision in addition to actively participating in the audit and performing audit work. Incumbent will have overall responsibility for the preparation and quality of workpapers for the team as defined in the CAG's Policies and Procedures. Incumbent is expected to effectively partner and communicate with the client, support groups, internal resources and external organizations.

Complete audit programs and workpapers within the parameters set forth for performing audit work. Use of AutoAudit is required to document audit findings, evaluations, work programs, test results, evidential matter, and audit reports. The incumbent is expected to meet deadlines as set forth by Corporate Audit's Polices and Procedures and comply with established internal and external workpaper standards and procedures.

Apply elements of the Corporate Audit Group Vision and Values to assist in maintaining a strong internal control environment throughout Merck. Integrate and maintain both the stewardship and consultative roles into all assignments. Follow the standards of conduct defined for the profession and as defined in Corporate Audit's Policies and Procedures.

Participate in the assigned roles for specific projects and ensure the realization of the specified results. Support Corporate Audit management in the sharing of best practices and establishment of a best practices database that will support line management in enhancing the stewardship practices across geographical areas. Incumbent will accomplish this by maintaining client relationships, completing tasks efficiently and according to established milestones, encouraging positive team interactions and providing progress reports.

Demonstrate proactive commitment to the "Know and Develop Yourself" principle of Merck's leadership model. When acting in a leadership capacity, demonstrate proactive commitment to the "Know, Support and Develop Your People" principle of the Merck leadership model

Qualifications

Education Requirement:

* BS/BA required preferably in Accounting or Finance.

Required:

* Knowledge of audit methodology and internal controls.
* A minimum of 3 years of prior internal audit and or public accounting and or general accounting experience.
* Willingness to travel within assigned regions/entities both domestically and internationally to complete testing; estimated travel up that 40% of the time.

Preferred:

* Excellent interpersonal skills, including the ability to interact effectively with client/business process owners
* Effective oral and written communication, computer, and time management skills and the ability to work with limited supervision
* Knowledge of SAP.
* MBA, CPA or CIA.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #GEN000110.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means

Job
: General Audit

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Senior-Internal-Auditor-Job-NJ-08889/924196/9241969241962012-06-15Merck/MSDGeneral Auditfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The incumbent is responsible for the completion of financial, operational and/or computer audits, integrated audits and process audits, and for the delivery of an audit report that adds value to the business unit audited. Under the direction of the Client Audit Director and/or the Auditor-in-Charge, the incumbent is responsible for the effectiveness and efficiency of the audit that you are assigned to. You are responsible for expediting all stages of the writing and review of reports, which accurately reflect facts and recommendations of an objective appraisal of Merck operations. You will maintain the highest standards of professionalism and independence in the execution of your duties, always with the Company's best interests in mind. You will lead by personal behavior and ethics that are also of the highest standard. The incumbent should embody the Corporate Audit Group (CAG) values and vision, and is cognizant of the CAG Policies and Procedures, and adheres to them and applies them.

Participate in achieving the Corporate Audit's annual audit plan according to established schedules. The primary role will be to lead small teams of auditors on various assignments. Incumbent will be expected to lead complex, large and/or sensitive audits with limited management supervision in addition to actively participating in the audit and performing audit work. Incumbent will have overall responsibility for the preparation and quality of workpapers for the team as defined in the CAG's Policies and Procedures. Incumbent is expected to effectively partner and communicate with the client, support groups, internal resources and external organizations.

Complete audit programs and workpapers within the parameters set forth for performing audit work. Use of AutoAudit is required to document audit findings, evaluations, work programs, test results, evidential matter, and audit reports. The incumbent is expected to meet deadlines as set forth by Corporate Audit's Polices and Procedures and comply with established internal and external workpaper standards and procedures.

Apply elements of the Corporate Audit Group Vision and Values to assist in maintaining a strong internal control environment throughout Merck. Integrate and maintain both the stewardship and consultative roles into all assignments. Follow the standards of conduct defined for the profession and as defined in Corporate Audit's Policies and Procedures.

Participate in the assigned roles for specific projects and ensure the realization of the specified results. Support Corporate Audit management in the sharing of best practices and establishment of a best practices database that will support line management in enhancing the stewardship practices across geographical areas. Incumbent will accomplish this by maintaining client relationships, completing tasks efficiently and according to established milestones, encouraging positive team interactions and providing progress reports.

Demonstrate proactive commitment to the "Know and Develop Yourself" principle of Merck's leadership model. When acting in a leadership capacity, demonstrate proactive commitment to the "Know, Support and Develop Your People" principle of the Merck leadership model.

Qualifications

Education Requirement:

* BS/BA required preferably in Accounting or Finance.

Required:

* Knowledge of audit methodology and internal controls.
* A minimum of 2 years of prior internal audit and or public accounting and or general accounting experience.
* Willingness to travel within assigned regions/entities both domestically and internationally to complete testing; estimated travel greater that 50% of the time.

Preferred:

* Excellent interpersonal skills, including the ability to interact effectively with client/business process owners
* Effective oral and written communication, computer, and time management skills and the ability to work with limited supervision
* Knowledge of SAP
* MBA, CPA or CIA

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # FIN000601.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Financial Analysis

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Internal-Auditor-Job-NJ-08889/1211082/121108212110822012-06-15Merck/MSDFinancial Analysisfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Market Research Associate Director will be the first point of contact for the Vintafolide Marketing/Commercial Team within the Oncology Franchise. The position will plan, manage, and execute a worldwide market research launch plan within a tight timeframe. Responsible for providing strategic input to the extended team by proactively identifying global issues, answering key business questions, and applying all available resources to produce actionable global solutions and recommendations. Requires a strong understanding of primary and secondary market research methodologies, particularly related to a new product launch and multiple customer segments within the specialty segment. Experience in oncology is preferred. This individual is expected to be a strong team player, to interact with multiple internal and external groups, to influence decision-making, and to pro-actively identify business opportunities for both Vintafolide and the Oncology Franchise, while working closely with the Team Leader. The Associate Director will have demonstrated consistently strong leadership skills with an ability to work independently in a rapidly changing environment, while exhibiting a transformational mindset, cultural awareness, and resilience to effectively produce results.

Primary activities include, but are not limited to:

* Develops and oversees the global market research plan and timeline, both US tactical and global, for Vintafolide across multiple indications with a strategic mindset and minimal supervision, based on understanding wide range of business issues.
* Manages all aspects of primary market research for Vintafolide including leadership in framing critical business questions, identification of information needs, and development of research/analysis plans and management of the research process to deliver an objective understanding of key customers, competitors, products and current/future market developments.
* Implements research studies & monitors budget; briefs agencies to deliver what is Required -
understands vendor capabilities, quality requirements, and recommends innovative options.
* Articulates the rationale, hypotheses, and methodology of research approaches to both the manager and the franchise/client team proactively and ensures the business objectives are met and communicated in an effective way.
* Explores alternative/creative ways of meeting an information need, considering new techniques alongside more traditional approaches to more quickly and efficiently address business requests.
* Completes complex analyses using available secondary data, syndicated reports and databases and integrates findings into primary market research efforts to tell and evolve the "story".
* Proactively communicates and facilitates discussion with Marketing/Commercial Teams to ensure that insights are considered in decision-making and planning; integrates a variety of sources/studies to present strategic options to the extended team; provides consultative guidance to Marketing/Commercial Team(s).
* Leads implementation of all administrative aspects of research studies using available resources.
* Collaborates proactively with cross-functional business partners including marketing communications, market access colleagues, and the advertising agency to ensure optimal integration for the launch.
* Assists with analysis to inform the strategic assumptions that are built into brand forecasts.
* Independently manages competing priorities and demands from within a product team/franchise applying best practices and innovative techniques maximize value and actionable output.
* Takes full ownership of understanding the business challenge/information needs, considers alternatives, proposes appropriate method/approach, applies best practices, and proactively considers and/or develops new techniques and innovations to meet objectives.
* Works on and leads adhoc franchise wide initiatives and/or projects as needed.

Qualifications

Education:

* Bachelor's Degree

Required:

* Minimum of 8 years of work experience including marketing-related positions (e.g. research, forecasting/ analytics, marketing, sales, and support) with at least 2 years experience in pharma market research.
* Well developed analytical skills, strong problem-solving, and demonstrated ability to think strategically and objectively.
* Can apply market research methods and models, is proficient and has directly worked with a variety of methodologies.
* Orientation toward collaboration/ team work, ability to lead teams in execution of market research, interest in ongoing learning.
* Demonstrates strong leadership skills around customer focus, decision making, courage & candor, and fostering collaboration.
* Ability and comfort in leading in a complex and ambiguous environment of a global matrixed organization.
* Ability to communicate effectively and a strong desire to lead change in terms of developing Best Practices.

Preferred:

* Experience in oncology and/or the specialty segment highly desired.
* Solid understanding of marketing strategy and the Monitor process preferred.
* MBA or other advanced degree desirable.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. merck.com/careers to create a profile and your resume for requisition # MAR004203.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Market Research/Intelligence

Primary Location: US-NJ-Whitehouse Station
Other Locations: US-PA-Upper Gwynedd
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-GMRA-Oncology-Job-NJ-08889/1885954/188595418859542012-06-15Merck/MSDMarket Research/Intelligencefull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Director, HR Communications is responsible for developing and delivering strategic internal HR communication plans to inform employees of HR initiatives, to heighten employee morale and engagement, to attract and retain employees and to strengthen the employee brand. This position will report to the Head of Corporate Communications within the Global Communications function.

Responsibilities:

* Oversee strategic HR communication projects and plans, detailing goals, creative strategy, media strategy, schedule, budget and measurement, to create a positive tone for the entire organization and facilitate change in support of company and HR long-term goals.
* Manage the activities of outside consultants, freelance talent and vendors to ensure projects are up to the Company's quality and brand standards and are completed on time and within budget.
* Develop innovative approaches to increase adoption and impact of HR programs and resources by reaching a diverse (geographic and level) audience using technology as well as traditional methods of communications.
* Provide communications counsel and executive communications support to Executive Vice President of HR.
* Work with HR, internal and external partners to assimilate business objectives and develop communications strategies to achieve those objectives and engage employees.
* Provide business partnership and consultation to clients, regional communication teams, and team members. Influence others, including senior leaders, to buy into new concepts and methodologies.
* Implement measures to determine effectiveness of communications programs with the goal of tracking and improving results.
* Manage diverse projects and activities into a cohesive and strategic program.
* Provide corporate communications strategy and support, as needed.

Qualifications

Education:

* Bachelor's Degree

Required:

* 8 years experience in corporate communications (including internal and/or human resources communications).
* 2 years experience directly managing people including hiring, developing, motivating, and directing people as they work.
* Superior writing skills across a variety of mediums (e.g., print, presentation, web).
* Proven track record in working with subject matter experts to effectively communicate complex ideas to a broad range of audiences.
* Excellent organizational skills and an ability to handle multiple tasks and competing priorities.
* Problem-solving skills with a high degree of diplomacy and teamwork.

Preferred:

* Working knowledge of HR disciplines including: compensation, employee benefits, organizational communication, employee relations, diversity programs, performance management and learning and development.
* Demonstrated excellence in partnering effectively and influencing senior executives on communication strategy.
* Experience in corporate communications at a Fortune 100 company or an organization with over 25,000 employees.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # INT000135.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Internal/Employee Comms

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-HR-Communications-Lead-Job-NJ-08889/1895228/189522818952282012-06-15Merck/MSDInternal/Employee Commsfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck for Mothers is our commitment to join the global effort to create a world where no woman has to die from complications of pregnancy and childbirth. This new 10-year initiative will harness the company's financial resources, expertise in science and business, and legacy of taking on tough global health challenges to help reach Millennium Development Goal 5 - reduce the global rate of maternal mortality by 75%. Merck is committed to discovering smart, sustainable ways to expand access to healthcare around the world. As we learn how to bring maternal health solutions to countries and regions with extremely limited resources, we will become more relevant as a global healthcare company and better deliver on our mission of saving and improving lives.

The primary activities include, and are not limited to the following:

* General Secretarial/Clerical duties constitute approximately 75% of job responsibilities.
* Work requires the coordination and performance of multiple tasks while understanding the project principles and technical skills related to own work assignments.
* Work priorities and activities are reviewed with little supervision.
* Schedules complex, multi-leg domestic and international travel
* Communication Skills must be at a level to effectively interact with Merck executives and internal/external clients both on-site and remotely to maintain workflow.
* May coordinate special projects within the division/area

Qualifications

Education:

* Required: High School Diploma or equivalent
* Preferred: Advanced education or certifications desirable (e.g. Certified Administrative Professional, Project Management Professional Certification, Professional in Human Resources Certification)

Required

* Minimum eight (8) years Administrative Assistant experience
* Minimum three (3) years Administrative experience supporting Sr. Directors / Executives
* Advanced computer skills (MS Outlook, Word, Excel, Power Point) and operation of other peripheral devices
* Advanced knowledge of the SAP involving (Expense Reports, Vendor Add Forms, Purchase Orders)
* Manages all aspects of coordinating/scheduling multi-leg domestic and international travel which includes processing Visa/Passport applications
* Coordinates domestic/international meetings and teleconferences with both internal and external clients
* Demonstrated use of analytical, critical thinking and problem solving skills
* Advanced secretarial/clerical skills with a history of high performance
* Knowledge of HR reporting tools, policies and procedures

Preference:

* Working knowledge of Merck and familiarity with the various divisions and functions.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ADM005053.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Administrative Svcs Generic

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Whitehouse-Station-Administrative-Associate-IV-Job-NJ-08889/1774612/177461217746122012-06-15Merck/MSDAdministrative Svcs Genericfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position will lead research, product development and project management through commercialization of Class I and Class II medical devices. This position has regular interface with Marketing, Regulatory, Legal and Clinical groups within Merck Consumer Care, and with supplies and vendors outside of Merck Consumer Care. This position will develop new products for retail consumers and will also provide ongoing support for existing products including the global expansion of existing domestic products into international markets. Products will generally consist of Footcare products, non FDA regulated articles, Class I OTC medical devices and Class II OTC medical devices. This position may also support device development in other areas of the Merck Consumer Care such as skincare, women's health, and upper respiratory.

Qualifications

Education:

* Bachelors degree required (preferably in Engineering).
* Advanced degree (MS or PhD) preferred.

Required:

* Minimum of 7 years experience.
* Medical device and product development experience.
* Experience working in product teams.
* Excellent communication skills and organization skills required.
* Knowledge of Federal regulations regarding Class I and Class II medical devices.

Preferred:

* 3D design experience (with AutoCAD, Rhino, ProE or similar)

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PRO009283.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Project Management Generic

Primary Location: US-TN-Memphis
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Memphis-Assoc-Principal-Scientist-%28Chem-Research%29-Job-TN-37501/1737828/173782817378282012-06-15Merck/MSDProject Management Genericfull-timeUSDstarting0BSMemphis, TN, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck Consumer Care is seeking candidates to lead a team of development scientists in the Oral Dosage Development Group. The successful candidate will direct the formulation activities both internally and externally for global new product development in support of the Upper Respiratory franchise. The position requires working within a matrix organization of development, regulatory, medical and marketing functions to bring consumer-relevant products to market.

Primary responsibilities include but are not limited to:

* Directs and monitors multiple projects internal and external to the company in support of Divisional goals. Works collaboratively within group and with research counterparts to establish tools to aid in formulation design including formulation, pharmacokinetic and statistical modeling.
* Works with R&D and Marketing franchises to identify opportunities and outline resources needed for new product development.
* Evaluates outside development options and external product opportunities where appropriate and makes recommendations to upper management on external pathways.
* Works with various departments within Merck Consumer Care to establish strategy and tactics for global development and submissions. Provides project outlines, briefing packages and dossier support as needed. Represents formulation group at Health Authority meetings asking and addressing questions to drive to acceptable development and approval standards.

Qualifications

Education Requirement:

* PhD degree

Required:

* Minimum of 10 years work experience in product development.

Preferred:

* People management experience
* Relevant experience in Consumer Healthcare
* Experience with global development and registration requirements

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CHE003296.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-JN1

Job
: Chemistry

Primary Location: US-TN-Memphis
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Memphis-Team-Lead-Development-Allergy-Job-TN-37501/1522574/152257415225742012-06-15Merck/MSDChemistryfull-timeUSDstarting0BSMemphis, TN, US
Description

Under the direction of the PV Manager/Director, the Manager is responsible to lead part of the Pharmacovigilance Data Management Center operation.

Promotes and supports the comprehensive development of the staff under his/her supervision by reviewing and evaluating their performance plans and leadership principles. Besides, he/she should encourage the interaction inside MRL to achieve common objectives.

Primary Activities:

Develops career plans for 2-15 direct reports, makes work assignments, conducts periodic skill assessments as well as annual performance appraisals, coaches for performance, provides ongoing feedback on performance, provides rewards and recognition, and sets priorities.

Provides developmental opportunities for employees, including challenging growth assignments. Develops promotion strategies and prepares promotion recommendations. Ensures employees receive appropriate training and mentoring to be successful in their assignments.

Maximizes staff effectiveness by working with employees to ensure a realistic work load that supports value-added work and work-life balance, estimating length and difficulty of tasks and projects, anticipating and adjusting for obstacles and setbacks, and elevating complex issues to the appropriate management level.

Increases functional effectiveness by supporting departmental efforts to simplify and standardize procedures to the greatest extent possible, sharing best practices and leading continuous improvement efforts.

Qualifications

· Professional title in Medicine, Nursing, or health careers related.

· Experience at least 5 years' experience in data management, years of supervisory or management experience in CROs or Pharmaceutical Industry.
· Exceptional Communication skills in English (oral and written)

Job
: Clinical Data Management

Primary Location: CO-Distrito Capital de Bogotá-Bogotá
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/Bogot%C3%A1-Data-Managment-Center-Manager-Job/1855923/185592318559232012-06-15Merck/MSDClinical Data Managementfull-timeUSDstarting0BSBogotá, Distrito Capital de Bogotá, CO
Description

MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career

The Marketing Manager will be in charge of developing and implementing the marketing plans, providing strategic leadership and execution for different the different species (Poultry/Ruminant/Companion animal & Swine). He/she will also responsible for market research and customer databases.

Duties, Responsibilities, Activities:

* Manage and administer the annual marketing plan allocating the activities to each one of the species. Prepare marketing plan activities for the next year. Present quarterly forecast revision to the different BUMs.
* Market research. Maintain an updated database with information about competitors related with sales, new products launching, prices increases, comparative retail prices vs main competitors, evolution index.
* Analyze market trends, competitive landscape and identify opportunities for increasing customer and business value through product differentiation.
Ensure all product road maps address potential synergies and leverage integration opportunities with the rest of line in the BU.
Business development: analyze the segments and search for opportunities to crease our business in the ruminant area
Go to the field. Spend at least 20% of his/her time identifying opportunities with our customers

Qualifications

Education:

Required: Bachelor's Degree. Master's Degree will be a plus.

Preferred area of study: Veterinarian, Agronomist, Business Administration/Marketing

Minimum required 3 years of experience leading a marketing area, a line or a product. Preferred in a Animal Health Laboratory or in a company closely linked to the farmers activities.

Skills

Rapid and discipline decision making, driven to deliver quality results on time, customer focus, high degree of ethics and integrity, influential leadership, advise and counseling skills.
Strong communication skills as well as problem solving and organizational effectiveness skills are necessary.
The ability to see new business opportunities and develop strong working relationships will be required for success.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. MSD's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

*LI-KT1

Job
: Marketing Generic

Primary Location: AR-Buenos Aires-Vicente López
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Vicente-L%C3%B3pez-Marketing-Manager-Job/1891868/189186818918682012-06-15Merck/MSDMarketing Genericfull-timeUSDstarting0BSVicente López, Buenos Aires, AR
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


A key feature of Sourcing Management is a high volume requirement for strategic analysis of suppliers, supply markets and supply chains in selected categories of spend. This role will work for the Sourcing Director for API and custom intermediate sourcing area and provide high quality analytical analysis, strategic analysis and insight to suppliers and markets. In addition the analyst prepares and conducts pre-negotiation planning, live negotiations as well as leading and conducting RFIs, RFP/Qs, e-auctions and quotation analysis and cost modeling. Scope of spend impacted will be >$50million for this category (APIs and custom Intermediates) and requires active management of several suppliers within external manufacturing network. This category for a senior analyst will be strategic in nature and highly complex and require a wide breadth of skills.

* Supplier and Supply Market Analysis - to conduct detailed supplier and supply market analyses looking at facts and data analysis, reports and changes in technology and to provide deep and meaningful insight to Sourcing Management teams
* Cost Modeling / Cost reduction - to construct detailed cost models/purchase price analysis of goods and services that are supplied to Merck, typically this will require supplier visits to create a complete understanding of the cost structure of suppliers and develop cost reduction opportunities.
* Strategic Analysis - to conduct up to six separate forms of project analysis which turns the information gathered from 1) and 2) above into insightful, well structured breakthrough options and opportunities. Examples include Portfolio Analysis, Supplier Preferencing and Day One Sourcing.
* Negotiation Planning and Execution - to create detailed pre-negotiation plans, to lead and participate any prolonged negotiation sessions with suppliers and to conduct post negotiation debriefs and follow through plans
* Sourcing - to facilitate cross functional team through strategic sourcing steps (SMP), create and execute RFIs, RFPs, together with subsequent structured information analysis wherever possible using electronic procurement processes
* Reverse Auctions - to prepare, lead, conduct and implement Reverse Auctions on selected leverage categories
* Contract Management - to prepare, finesse and implement appropriate forms of contract and commitment with suppliers
* Supplier Value Management - to ensure that appropriate supplier agreements and relationships have good supplier matrix embedded within them. Monitor, report, manage contractual spend and continuously improve supplier performance for the assigned set of suppliers within external manufacturing network
* Category Team Membership - to be an active member of one or more category teams using the techniques and content created in 1) to 8) above as input in the creation of breakthrough strategies delivering cost reduction targets
* Risk Assessment and mitigation - to conduct effective risk assessment & establish appropriate risk mitigation plans within the supply-base in compliance with MMD risk management frame-work
* Sharing of Learning's - As a senior analyst the incumbent will be expected to generate work of a world class quality and share and transfer this to colleagues throughout procurement.

Qualifications

Education:

* Required: Bachelors degree

Experience:

* Required: Four to seven years of relevant experience (examples includes but not limited to; manufacturing, technical R&D or process engineering, finance, business operations, external manufacturing, supply chain management etc.)

Preferred:

* Two to four years of Procurement strategic sourcing experience, strong project management & analytical skills.

*LI-AS2

Our employees are the key to our company's success.

We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition TEC000489.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-NJ-Whitehouse Station
Other Locations: US-PA-West Point, US-NJ-Rahway

Job Type
: Full Time
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1

Relocation Provided
: None]]>http://jobs.merck.com/job/Whitehouse-Station-Senior-Procurement-Analyst-Job-NJ-08889/1858704/185870418587042012-06-15Merck/MSDFull Timefull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck Corporate Audit and Assurance Services' (MCAAS) primary purpose is provide value-added independent and risk based audit and assurance services. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

The Information Technology Audit Manager leads complex audits and assessments of information technology resources across all Merck divisions and functions to evaluate the adequacy of internal controls and deliver audit reports that add value to the area audited. Information technology resources include business applications as well as the related technology infrastructure, data, facilities, organizations, and processes. Information technology controls include Information Technology General Controls and Application Based Controls.

In addition to leading complex, large and/or sensitive information technology audits under direction of the Senior Audit Director, you will actively participate in the audit and performance of audit work. You will have overall responsibility for the preparation and quality of workpapers for the team and expediting all stages of the writing and review of reports, which accurately reflect facts and recommendations of an objective appraisal of the areas audited. Incumbent is expected to effectively collaborate and communicate with the client, support groups, internal resources and external organizations. You will maintain the highest standards of professionalism and independence in the execution of your duties, and lead by personal behavior and ethics that are of the highest standard.

The Information Technology Audit Manager may participate and lead specific projects and support MCAAS management in its efforts to drive continuous improvement and efficiencies. The incumbent will accomplish this by completing tasks efficiently and according to established milestones, encouraging positive team interactions and providing periodic progress reports.

The incumbent is expected to provide technical guidance and consultation on information technology security and control issues to the client and audit staff, as well as coach, mentor and train new members of the department.

Qualifications

Education Requirement:

* Bachelor's degree preferably in computer science or equivalent education and/or job experience.

Required:

* An in-depth knowledge of information systems audit principles and techniques.
* A minimum of 5 years of Information Technology Audit experience (internal audit and / or public accounting).
* The incumbent must demonstrate superior communication skills (verbal, written), interpersonal skills and the maturity to interact with the highest levels of business and technical management at local, divisional, and corporate sites.
* The incumbent must also demonstrate strong leadership, high ethical standards at all times when representing the Company/department to both internal clients and external organizations.
* Willingness to travel within assigned regions/entities both domestically and internationally to complete testing; estimated travel up to 40% of the time.

Preferred:

* A professional security, audit, or control certification such as CPA, CISA, CIA, CRISC or CISSP.
* Experience with Sarbanes-Oxley compliance.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # FIN000805.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-PD1

Job
: Fin/Bus Cntrls & Audit Generic

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Audit-Manager-IT-Job-NJ-08889/1782780/178278017827802012-06-15Merck/MSDFin/Bus Cntrls & Audit Genericfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the guidance of a Senior Director, Global Health Outcomes, the incumbent has the primary responsibility for planning and managing outcomes research (OR) activities for in-line and developmental drugs on a worldwide basis. This includes all phases of Outcomes Research (OR) including design and implementation of retrospective database studies, assessment of patient reported outcomes, epidemiological studies and economic modeling. The incumbent works closely with the Global Franchises, Regions, and MSD affiliates to ensure OR programs are in line with marketing strategies in key countries. The incumbent also contributes to product development and marketing strategies to ensure that product value is defined and developed.

Primary Activities:

* Co-chairs product/franchise-specific OR sub-teams and provides leadership in developing the OR Strategy and Plan for developmental compounds and obtains cross-divisional senior management approval.
* Critically assesses drivers and barriers to pricing, reimbursement, and market access to provide input into clinical and market development programs.
* Implements programs to document the burden of disease or unmet need, patient reported outcomes (PRO) components, and health economic aspects of disease to define the value of drug therapy as outlined in the OR planning process.
* Develops core deliverables (e.g., health economic evaluations) and their adaptation to generate country-specific data supporting pricing and reimbursement.
* Works closely with the Product Development Teams (PDTs) to develop OR plans for Merck in-line and developmental products based on the regulatory, marketing and reimbursement environments on a worldwide basis. Works with MRL, MSD affiliates and consultants to write, coordinate, and validate as required, study design, protocols, measurement questionnaires, case report forms, data analysis plans, and final reports/publications.
* Works with MRL for inclusion of outcomes research related measures (e.g., PROs, resource consumption) into clinical trials.
* Supports MSD affiliates by understanding local needs, adapting health economic evaluations, customizing OR documents according to local requirements (e.g., protocols and reimbursement dossiers, data collection forms).
* Is responsible for maintaining awareness of scientific developments within his/her areas of expertise, both in terms of new methodology and new activities to establish communications with key OR scientific leaders.
* May travel on company business to ensure broad internal/external input into the OR planning process and to assure the timely completion of projects.
* Builds relationships with health economic and OR experts worldwide.
Presents OR data at international/national congresses and publishes articles in scientific journals.

Qualifications

Education:

* At least Masters Required
* Doctoral (preferred) degree from a recognized school of medicine, public health, management, pharmacy, or economics and with demonstrated expertise in the field of outcomes research, epidemiology or health economics preferred.

Required:

* Minimum of 5 years experience in the design and implementation of clinical, epidemiological, or health economic studies

Preferred:

* Excellent leadership and strategic thinking skills

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # OUT000175.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-AW1

Job
: Outcomes Research -Health Econ

Primary Location: US-NJ-Whitehouse Station
Other Locations: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Whitehouse-Station-Outcomes-Research-Leader-Immunology-Job-NJ-08889/1877975/187797518779752012-06-15Merck/MSDOutcomes Research -Health Econfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Future Talent Program features paid internships targeted to start in June 2012 for 10 - 12 weeks and will include one or more projects. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals.

The Enterprise Portal & Support Services intern will work with a diverse team to implement content and process solutions for our Service Partners across Global Services as well as for end-users (Merck employees and non-Merck persons) globally.

As part of their assignment, the Intern will assist the Support Services team in various activities, including but not limited to the following:

* Analyzing and fulfilling requests for the creation and maintenance of support groups and self-service forms
* Analyzing usage trends of self-service tools and provide recommendations for process or content improvement
* Providing assistance to the Enterprise Portal & Support Services team to enhance and improve business results

During the course of the internship, the individual will interact with Global Services colleagues in a variety of job functions including IT Operations, HR Content Management, Help Desk Operations and Shared Business Services.

Qualifications

Education:

* Pursuing a Bachelors degree

Required:

* Available full-time from June 2012 through August 2012
* Pursuing a Bachelors degree in Information Technology, Business, or Liberal Arts

Preferred:

* Ability to demonstrate strong management skills in the areas of leadership, teamwork, innovation, analytical skills and project management.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requistion #IT000295.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations

.

Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-NJ-Whitehouse Station

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Support-Services-Intern-William-Griggs-Job-NJ-08889/1864344/186434418643442012-06-15Merck/MSDInternfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Beschreibung

Merck Sharp & Dohme-Chibret AG ist die Schweizer Niederlassung der Merck & Co., USA. Merck entwickelt, produziert und vertreibt weltweit innovative Medikamente und gehört international zu den führenden Pharmaunternehmen. Weltweit arbeiten ca. 100'000 Mitarbeiter für uns.

Die Schweizer Organisation beeinhaltet die Unternehmungen MSD International GmbH, Merck Sharp & Dohme-Chibret AG, Essex Chemie AG, Schering Plough Central East und Werthenstein BioPharma GmbH mit gesamthaft 700 Mitarbeitern.

Für die Werthenstein BioPharma in Schachen LU suchen wir zur Verstärkung des Teams im GMP/Comparator Labs per sofort oder nach Vereinbarung eine/n

Analytiker-/in

Aufgabenbereich:

· Organisation, Koordination sowie selbständige Durchführung aller analytischen Aktivitäten im Zusammenhang mit Stabilitätsstudien und Freigaben von pharmazeutischen Vergleichsprodukten

· Entwicklung, Validierung und Transfer von analytischen Methoden für die Freigabe und Stabilität von pharmazeutischen Vergleichsprodukten

· Unterstützung der Laboranten bei ihrer Arbeit

· Mitarbeit bei globalen Projekten

· Geräteverantwortung

Qualifikationen

· Akademiker/in (Hochschulabsolvent/in oder Fachhochschulabsolvent/in in Chemie oder parmazeutischer Analytik) mit praktischer Erfahrung in der instrumentellen Analytik Erfahrung in GMP-Richtlinien wünschenswert

· Sehr gute Englischkenntnisse

· Hohes Qualitätsbewusstsein und Sinn für eine effiziente Arbeitsweise

· Ausgeprägte Lernbereitschaft und Selbständigkeit

· Teamorientierte und offene Persönlichkeit

*LI-DR1

Job
: Forschung, allgemein

Primärer Standort: CH-Luzern

Mitarbeiterstatus: Permanent

Reisebereitschaft:: Ja, 10 % der Zeit

Anzahl offener Stellen: 1

Externes Job Ausschreibungsportal
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Luzern-Analytiker-in-Job/1881750/188175018817502012-06-15Merck/MSDForschung, allgemeinfull-timeUSDstarting0BSLuzern, CH
Description

MSD heeft beheer van electrische installaties ondergebracht in een Center of Excellence (CoE) Operational Excellence, die verantwoordelijk is voor continue verbetering. Activiteiten omvatten de implementatie van Lean Six Sigma, verbeterprojecten en investeringsprojecten. Binnen het CoE bevindt zich de groep Maintenance & Process Engineering. De groep fungeert als kenniscentrum voor onderhouds- en procestechnologie. De groep ondersteunt de (bio)chemische fabrieken betreffende beleid, verbeteringen, investeringsprojecten, start-up, kwalificatie en trouble-shooting. Voor dit CoE zoeken wij 2 installatieverantwoordelijken, die gaan werken voor POO of API.

Productie, verpakking en logistiek vindt op de locatie Oss plaats bij Pharmaceutical Operations (POO). Naast tabletten en injectievloeistoffen worden hier ook speciale producten gemaakt, zoals NuvaRing® en Implanon®. Dat gebeurt onder meer in de hypermoderne nieuwe faciliteit voor de productie van parenterals (injectievloeistoffen). Daar wordt gewerkt in ultramoderne cleanrooms, volgens verregaand geautomatiseerde processen.

Active Pharmaceutical Ingredients (API's) zijn de grondstoffen voor geneesmiddelen, die op (bio)chemische wijze geproduceerd worden. De faciliteiten van API Operations in Oss produceren in totaal ruim 100 verschillende actieve grondstoffen. Naast 'eigen' grondstoffen produceert API Operations ook producten voor externe partijen.

De Installatie Verantwoordelijke ben je:

* Verantwoordelijk voor elektrotechnische veiligheid conform het veiligheidsvoorschrift EVV
* Je beoordeelt nieuwe ontwerpen en wijzigingen van E-installaties en apparatuur
* Je bent verantwoordelijk voor aanwijsbeleid en opleidingseisen van personen die E- werkzaamheden verrichten
* Je Initieert verbeteringen
* Treedt op als SME (Subject Matter Expert) en adviseert / coordineert als zodanig collega's elders in de organisatie mbt regelgeving, techniek, compliance en ontwikkelingen.

Qualifications

* Afgeronde HBO opleiding Elektrotechniek of vergelijkbaar.
* Inhoudelijk deskundig met minimaal 5 jaar aantoonbare ervaring met nieuwbouw en onderhoud van elektrische installaties
* Kennis van Proces-industrie; Machineveiligheid; NEN 1010; NEN 3140; Aardingsinstallaties en EMC
* API werkt met chemische processen en vraagt om specifieke kennis van ATEX richtlijnen
* Ruime ervaring met het inspecteren van installaties
* Sterke persoonlijkheid die in staat is zelfstandig besluiten te nemen
* Goede beheersing van het Engels
* Green Belt & ervaring en kennis mbt SIL/CE strekt tot aanbeveling.

MSD is een aantrekkelijke werkgever en biedt mogelijkheden op het gebied van Research & Development, productie en stafafdelingen voor een groot spectrum van disciplines zoals biologie, chemie, procestechnologie, techniek, mechatronica, farmacie en operators. MSD is altijd op zoek naar de beste medewerkers op alle niveaus. We verwachten veel van onze medewerkers maar we hebben ook veel te bieden. Samenwerken, ondernemerschap, integriteit, leiderschap en communiceren op alle niveaus zijn eigenschappen die MSD waardeert en beloont.

Houd je ervan te worden uitgedaagd, steeds weer, dan is MSD een goede keuze als werkgever. We hebben uitstekende arbeidsvoorwaarden en je krijgt er alle mogelijkheden om je verder te ontwikkelen en door te groeien. MSD geeft je veel ruimte voor eigen initiatief en je krijgt veel verantwoordelijkheid. We hebben een speciaal netwerk voor onze jonge professionals die regelmatig workshops en bijeenkomsten organiseren waaronder ook sociale evenementen, die je de gelegenheid geven je collega's en het bedrijf te leren kennen.

Informatie en sollicatie

Voor meer informatie over over de vacature Installatieverantwoordelijk API neem je contact op met Guus Bekker (0412 66 5113). Voor vragen over Installatieverantwoordelijk POO contacteert je René Ploegmakers (0412 66 2658).

Job
: Electrical Equip Engineering

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/Oss-Verantwoordelijke-Electrische-installaties-APIPOO-%282x%29-Job-NB/1881753/188175318817532012-06-15Merck/MSDElectrical Equip Engineeringfull-timeUSDstarting0BSOss, NB, NL
Description

Department

Analytical Development and Validation (ADV) is a scientific Center of Excellence responsible for advanced analytical characterization of protein products. Over 60 highly trained professionals support development of commercial manufacturing processes, develop and validate quality control assays and perform complex analytical characterization and trouble-shooting. The in-depth expertise on analyses of proteins is crucial to the MSD network and is truly unique in the Netherlands.



You Develop and optimize analytical methods for the identification and characterization of complex glycoproteins/antibodies. Provide analytical support tot the development of drug substance and drug product manufacturing processes. You perform critical evaluation of analytical data against scientific standards. Implement new technologies that increase/improve the output (e.g. high throughput technologies). You identify scientific issues and assist in root cause investigations. Prepare and deliver oral and written technical reports for regulatory purposes. Participate in analytical project teams

Qualifications

Desired Skills & Experience

· MSc in analytical (bio)chemistry (or BSc with more than 5 years of relevant laboratory experience)

· Practical experience with liquid chromatography and/or capillary electrophoreris (preferably to identify and characterize complex glycoproteins/antibodies)

· Knowledgeable of statistical data evaluation

· Demonstrated ability to independently plan and execute tasks

· Excellent interpersonal and communication skills

· Fluent in English (oral and written)

· Strong results orientation and can-do mentality

· Expercience with assay automation (high throughput formats)

· Familiarity with late stage drug development

· Familiarity of Quality by Design principles

· Has shown ability to work with matrix teams

· Percentage in service 100

Information

For more information about this role, please contact Corné Stroop, Section Head ADV; 0412 66 3140.

Job
: Lab Technician

Primary Location: NL-NB-Oss
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Oss-Analytical-Scientist-%28Non-GMP%29-Job-NB/1855913/185591318559132012-06-15Merck/MSDLab Technicianfull-timeUSDstarting0BSOss, NB, NL
Description

Responsible for implementing Quality Assurance policies, procedures and guidelines supporting Merck's Suppliers, under the direction of, or on behalf of, the Director, Supplier Development & Performance Management (SD&PM). The incumbent will exercise a leadership role in monitoring and maintaining the Supplier's compliance with world-wide regulatory requirements, current Good Manufacturing Practices (cGMPs) and other pertinent legal and business requirements. Key responsibilities include developing Quality standards, AQLs, Quality Agreements, MMD Procedures, Quality Bulletins, Supplier Quality system remediation including calibrated quality oversight, interfacing with Procurement and Technology counterparts in Supplier Development & Performance Management and managing the SD&PM Field Generalist staff.

Possesses unique combination of analytical/scientific/Quality skills as well as excellent managerial skills in order to effectively manage and control all activities necessary to support a SD&PM - Quality program governing Suppliers in conjunction with and under the direction of the Director, Supplier Development & Performance Management.

* Along with SD&PM counterparts in Procurement and Technology, serves as the primary point of contact to the Suppliers and MMD sites. Responsible for coordination, oversight, and communication on matters related to the GMP status, operational and quality performance (metrics) with the Suppliers. Must be conversant with all regulations and compendia (domestic and foreign) governing the Supplier's operations.
* Assures that the SD&PM organization operates within established Merck policies/procedures and complies with all applicable governmental regulations.
* Manages activities associated with the SD&PM Field Generalists.
* Assures the development and maintenance of a Quality Agreements, specifications, standards and AQLs with Suppliers. Provides input into the development of Supplier contractual agreements.
* Works directly with senior management at the Suppliers to resolve quality and supply issues as well as providing overall quality improvements.
* Executes a program of calibrated Quality oversight based on the component/raw material risk profile, capabilities, and quality/compliance performance of the Suppliers.
* Responsible for Quality Assurance and control functions to include direct support to Suppliers, coordination and oversight for component and/or raw material testing for qualification purposes, and on behalf of the MMD sites, provides assistance to Suppliers for Deviation investigations and Change Control management.
* Responsible for maintenance and oversight of ongoing performance management to include regulatory inspection support and monitoring, internal complaint management, internal customer feedback coordination, and review of annual product reviews.
* Monitors efforts to improve the Suppliers' quality and reliability through ongoing oversight, upskilling, and formal communication programs and forums.
* Provides support to the Suppliers to facilitate and validate new product introductions. Provides compliance input and support, as appropriate for implementation of analytical methodology and process development initiatives.
* Leads coordination of significant investigations including Fact Findings and regulatory communications.
* Participates in external benchmarking and internal voice of customer analyses for best practices management.

Qualifications

* Education Minimum Requirement: BS/BA degree in Engineering, Science, or Business
* Minimum of 6 years experience in commercial, business, quality, technical or manufacturing operations functions
* Fluent in Dutch as well as English

Possesses the following Experience and skills:

* cGMPs and technical writing skills
* Data management, collection and analysis is desired
* Must have demonstrated interpersonal and communication skills
* Must have demonstrated networking and relationship building skills
* Ability to work independently with all levels of the organization is required

*LI-LVG1

Job
: Qual Assurce - 3rd Party Manuf

Primary Location: NL-NH-Haarlem
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Haarlem-Manager-Supplier-Development-&-Performance-Management-Job-NH/1871153/187115318711532012-06-15Merck/MSDQual Assurce - 3rd Party Manuffull-timeUSDstarting0BSHaarlem, NH, NL
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck's Global Recruiting & Staffing organization seeks a Staffing Consultant to support hiring (primarily US based) within the Merck Manufacturing Division and other organizations. Merck's staffing function believes in developing its team members through exposure over time to a variety of roles and to that end is seeking a multi talented Staffing Consultant that is able to plug and play over time in various roles including Full Life Cycle Recruiting, Executive Recruiting, University & Diversity Relations & Global Recruiting Solutions.

The Staffing Consultant will act as a Talent Advisor developing and fostering strong relationships with line clients and HR colleagues to ensure understanding of organizational need and develop strategies to effectively source talent internally and externally where growth and/or vacancies occur. Primary alignment will be divisional and functional with secondary emphasis on supporting initiatives on a plug and play basis as capacity permits and business need requires. The Staffing Consultant will be responsible for the development and delivery of creative, efficient, and effective sourcing and recruitment campaigns in response to clients' needs. Incumbent will act as a resource to clients by providing creative methods of building prospect pools, pre-screening and interviewing candidates, and facilitating the staffing process.

Responsibilities include but are not limited to:

* Coordinates, develops, and implements formal staffing plans and strategies with hiring managers and Human Resources Business Partners.
* Coordinates, facilitates and/or participates in interview days and job fairs.
* Identifies a diverse pool of candidates to ensure Merck & Co., Inc's diversity commitment.
* Reduces cycle time while maintaining or improving quality of hire.
* Contributes to process improvement initiatives and drives efficient process adherence.
* Manages relationship with third party vendor.
* Provides leadership and support of cross-functional and cross-divisional teams to implement an array of staffing initiatives, ensuring stakeholder participation, support and pull-through.
* Reports on recruiting activities as required or requested by the client as well as responsible for insuring compliance to EEO/OFCCP regulations.
* Delivers behavioral-based interview training to client groups across business.
* Position will focus on a majority of production roles in an extremely fast paced / high volume role
* Position will also have the opportunity to work on higher level, more technical roles

The position is in support of the Merck Manufacturing Division supporting Operations, Quality and other Technical groups.

The position requires up to 15% travel.

Qualifications

Education Requirements:

* Bachelor's degree required.

Experience Requirements:

* At least 5 years of recruiting/staffing experience required, preferably in a large, matrixed organization
* Experience with direct sourcing and qualification of candidates, including use of the Internet, conducting telephone and on-site interviews utilizing behavioral-based interviewing techniques required.
* Experience working in a fast paced - high volume Manufacturing environment is required
* Requires thorough knowledge of recruiting/staffing database systems (experience using Taleo a plus).
* Requires working knowledge of Microsoft Office Suite (Excel, PowerPoint, Word).
* Demonstrated strength in written and verbal communication as well as strong relationship building/maintenance, facilitation and influencing skills required.

Preferred Requirements:

* Pharmaceutical/Biotechnology industry recruiting experience is a plus.
* Project management expertise in a deadline driven environment is a plus.
* Global recruiting experience is also a plus.
* Behavioral based interview certification is a plus.
* Demonstrated success in use of social media such as LinkedIn, Facebook, Twitter, etc…to drive company branding as well as source and drive candidate pipelines desired.
* Agency and Corporate experience Desired
* Proven track record of successful recruiting experience in a fast paced environment is required

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # REC000147.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-PD1

Job
: Recruitment Generic

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Staffing-Consultant-Job-PA-19486/1871146/187114618711462012-06-15Merck/MSDRecruitment Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Chemistry Modeling & Informatics group is seeking creative, self-motivated individuals with exceptional interpersonal and problem solving skills to join our scientific team in West Point, Pennsylvania.

The successful candidate will be responsible for the design and optimization of novel drug candidates using advanced computational techniques. In addition to participating in Merck's medicinal chemistry and biology programs, the applicant would be expected to continue research in new areas of molecular modeling relevant to the drug discovery and development process.

Candidates must have a Ph.D. in chemistry, biochemistry, biophysics or equivalent with a computational emphasis and 5 years of relevant experience . Strong communication skills along with the ability to work well in multidisciplinary teams is essential. Evidence of creative application of computational approaches to problems of biological or chemical interest is necessary.

Qualifications

Education:

* PhD in chemistry, biochemistry, biophysics, or equivalent with a computational emphasis

Required:

* 5 years relevant experience
* Strong communication skills
* Evidence of creative application of computational approaches to problems of phamaceutical interest
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CHE003446.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Chemistry

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 2

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Central-Chemistry-Team-Member-Job-PA-19486/1790672/179067217906722012-06-15Merck/MSDChemistryfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The successful candidate will apply engineering, science, and business skills to help Merck carry out its core functions in one of the following areas. A number of different entry points are possible for a new hire, in either our research or our manufacturing division.

PROCESS DEVELOPMENT, SCALE UP AND LAUNCH

- Work in teams to bring research discoveries to full production scale by applying engineering, biology, chemistry and pharmaceutics skills to bench-scale processes.

- Conceive, develop and implement new processing and manufacturing technologies

- Work with teams to develop processes for new products, using chemically- or biologically- derived products

- Support process development and product development with pilot plant scale up, drug supply preparation and technology transfer to operations groups

EQUIPMENT AND FACILITIES DESIGN

- Design and build advanced manufacturing plants, laboratory and office facilities

- Involvement with all phases of project management from the first engineering drawing to the last phase of project start up

MANUFACTURING

- Support line production and maintenance operations

- Maintain manufacturing processes at high levels of performance

- Engineer plant site improvements to enhance safety, quality and the environment

- Optimize existing processes to achieve improvements in process quality, yield and efficiency.

Engineering at Merck has the vital role of bridging the gap between new pharmaceutical and vaccine discoveries and commercial products.

Chemical processes produce in bulk form, the high quality complex chemicals used in Merck's most valuable human health, animal health and agricultural products. We then convert these basic chemicals into safe effective pharmaceuticals through formulation and packaging processes. Biologically derived products follow a similar path.

Those who join Merck can look for substantial early responsibility, the opportunity to develop and apply state-of-the-art technologies, chances for growth and advancement in an informal, varied work environment.

Potential openings in MMD are as follows in West Point, PA; Danville, PA; Rahway, NJ; Summit, NJ; Cokesbury, NJ; Elkton, VA; Durham, NC:

* Chemical Process Development & Commercialization (Rahway, NJ) and Pharmaceutical Commercialization Technology (West Point, PA, Summit, NJ) groups perform process development and demonstration for new chemical and pharmaceutical processes;
* Global Vaccines Technology and Engineering (West Point, PA, Elkton, VA, Durham, NC) is responsible for process implementation, validation and maintenance for biological processes;
* Biologics Manufacturing Science & Commercialization (Rahway, NJ, West Point, PA) is responsible for the development and implementation of vaccine and therapeutic protein processes;
* Global Technical Operations (West Point, PA, Elkton, VA) is responsible for continuous improvement of existing processes.
* Global Engineering Services (Cokesbury, NJ with rotations to other sites) is responsible for designing and project management for capital projects;
* Vaccine Operations (West Point, PA, Elkton, VA, Durham, NC) is responsible for oversight and continuous improvement for vaccine manufacturing.

At Merck we believe you can develop faster if we give you real challenges right from the onset. In MMD, we encourage you to move between functional groups so that you get hands-on experience in many aspects of our operations.

Qualifications

Candidate Requirements:
* BS in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Mechanical Engineering or related field
* Strong personal character and ethics
* Superior Communication and Interpersonal Skills
* Excellent Academic Achievement, Analytical Ability
* Good team player and ability to work independently
* Willingness to travel and foreign language skills desirable for domestic and international assignments
* U.S. citizen or lawful permanent resident of U.S.

At Merck we believe you can develop faster if we give you real challenges right from the onset. In MMD, we encourage you to move between functional groups so that you get hands-on experience in many aspects of our operations.

The successful candidate will apply engineering, science, and business skills to help Merck carry out its core functions in one of the following areas. A number of different entry points are possible for a new hire, in either our research or our manufacturing division.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CHE003376.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Associate Engineer: CHE003376

Primary Location: US-PA-West Point
Other Locations: US-NC-Durham-RTP, US-NJ-Rahway, US-NJ-Summit, US-VA-Elkton, US-PA-Danville

Job Type
: Full Time
Employee Status: Regular
Number of Openings: 1

Relocation Provided
: None]]>http://jobs.merck.com/job/West-Point-Associate-Engineer-BS-Job-PA-19486/1729504/172950417295042012-06-15Merck/MSDFull Timefull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Area Head in the Biotechnology Manufacturing area at the West Point, PA facility will direct the day to day activities for the Recombivax Fermentation, Purification and Buffer areas ensuring compliance with all Safety and cGMP rules, as well as providing guidance to the Manufacturing Supervisors regarding efficient work flow and optimal throughput.

Additional responsibilities include reporting metrics for the business unit, ensuring compliance with policies around the framework of the local agreement, supporting initiatives for continuous improvement, and collaborating with the supporting Centers of Excellence (Technical, Quality, Maintenance). Must also provide accurate financial forecasting, revise cost standards as needed, and assist with departmental budget preparation. Works closely with the Director on a day-to-day basis to ensure alignment with the overall strategy for the department.

Qualifications

Education Minimum Requirement:

* Bachelor Degree

Required:

* Six years of experience in manufacturing or equivalent support.
* Excellent analytical, organizational, and project management skills
* Good written and verbal communication skills
* Ability to work independently as a team leader or team member
* Strong leadership and interpersonal skills

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BUS000503.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Business Consulting

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: None]]>http://jobs.merck.com/job/West-Point-Manufacturing-Area-Head-Job-PA-19486/1868786/186878618687862012-06-15Merck/MSDBusiness Consultingfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the direction of the Director, Global Supply Network Planning, the incumbent is responsible for managing the end-to-end supply chains for assigned Vaccine products in the tactical planning time horizon. Individual will lead, coordinate and integrate the functional/tactical planning activities for assigned supply chains in close collaboration with Product Leaders and Regional Hub Planning Analysts. Individual will be a member of the Value Chain Management Team for assigned products and will be the MMD lead for Global S&OP. The incumbent will also be responsible for collaborating with other GSNPs for best practice sharing and Standard Business Process development.

The Global Supply Network Planning Manager:

* Develops adequate supply options to manage and resolve supply/demand imbalances and optimization and executes product allocations in an effective manner.
* Executes consistent and robust planning processes
* Leads Global Supply Team for assigned products with all applicable regional planning hubs and site planning representatives.
* Owns Vaccine Profit Plan and Inventory Plan processes for assigned products
* Interfaces with MV (Merck Vaccines) on a routine basis regarding supply and allocations
* Executes Supply Chain Line Design - identifies and implements supply chain productivity and innovation opportunities
* Manages manufacturing events that have a global supply impact
* Leads process for tender evaluation and management
* Represents end-to-end value chain at Global Supply Review

Qualifications

Education:

Required:

* Bachelors Degree

Preferred:

* Advanced degree highly desirable.

Experience:

Required:

* Minimum of 5 years experience in planning, materials management, manufacturing or related positions.
* Basic understanding of vaccine operations is beneficial.
* Must possess strong interpersonal and communication skills, a proven ability to lead cross-functional teams, and the ability to anticipate and solve problems.
* Must be able to manage multiple priorities.
* Prior experience with MRP systems, practices/principles is beneficial.

merck.com/careers to create a profile and your resume for requisition SUP000348.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Supply Chain Mgmnt Generic

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Global-Supply-Network-Planning-Manager-Job-PA-19486/1895224/189522418952242012-06-15Merck/MSDSupply Chain Mgmnt Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Research Associate in the Applied Mathematics and Modeling group, within Informatics IT, develops mathematical models and computational solutions using optimization, simulation, pattern recognition, discrete algorithms, knowledge representation, data mining, automated induction and inference, decision analysis, and related techniques. Project areas include safety assessment, toxicity profiling, experimental design and analysis, disease and biochemical kinetics/systems biology modeling. Work is objective-related and requires the efforts of a skilled scientist.

Qualifications

Education Minimum Requirement:

* Must currently possess a PhD or expect to earn a PhD within the next 12 months OR must have a Master's Degree with at least 5 years of research experience and 2 first-author publications.
* A degree in one of the following fields: computer science, computational biology, statistics, or another computational area with an emphasis on the use of machine learning and informatics to solving problems in biology or chemistry.

Required Experience and Skills:

* The position requires advanced and thorough scientific knowledge related to the above-mentioned areas of expertise.
* Must have the ability to plan, recommend and complete research programs of major divisional importance
* The incumbent must be capable of motivating and training junior scientists and offering counsel to peers within the Division
* Experience in several and extensive knowledge in one or more of the following areas is Required: optimization, discrete and numerical algorithms, machine learning and automated pattern recognition, signal and/or image processing, computational biology, mathematical analysis and modeling, probability, stochastic processes, stochastic optimization, scientific software engineering, parallel algorithms, complexity theory, or knowledge representation
* Strong communication and interpersonal skills are required
* Plans and schedules daily computing, research and reporting activities in order to meet established timetables and objectives
* Develops the technical expertise that enables proprietary positions to be established. Participates in strategic research planning at the department level
* Enhances individual and corporate reputation through one or more of the following activities: Preparing and publishing or presenting technical papers to internal and external audiences
* Prepares basic patent applications in support of patent coverage of divisional research efforts.

Preferred Experience and Skills:

* Advanced, thorough scientific understanding of one or more of: cell biology, vaccine and antibody discovery, genetics, biochemistry
* A strong publication record as part of a research team
* Post-graduate research experience or some combination of directly relevant R&D work and training, especially if relevant to solving problems in the pharmaceutical, biotechnology, or biomedical industries.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BUS000434.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-PD1

Job
: Business Analysis

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Research-Associate%2C-Safety-Assessment-Applied-Mathematics-&-Modeling%2C-Informatics-Job-PA-19486/1577195/157719515771952012-06-15Merck/MSDBusiness Analysisfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Currently, we are sourcing candidates for full time union positions for Support Associate - Level 1 for the Merck Manufacturing Division at our West Point, PA site.

Openings may be for 1st, 2nd or 3rd shift positions which may include working on weekends.

* Some positions require aseptic gowning during performance of job duties.
* Successful candidates will be required to obtain all required titers prior to start date, including but not limited to Mumps, Measles, Rubella, Varicella and Hepatitis A.

Position Overview:

In alignment with operations staff and reporting to Management or others assigned oversight responsibilities, performs general support functions and troubleshooting necessary to facilitate efficient and cost effective production activities. Duties include but are not limited to:

* Maintains areas in compliance with Current Good Manufacturing Practices and applicable regulatory guidelines by performing all necessary housekeeping, disinfection, and waste management of assigned production environments.
* Adheres to Merck safety guidelines and procedures
* Monitors facility conditions during activities defined above and performs general tasks to ensure the environment and equipment are maintained in full regulatory compliance. Tasks include, but are not limited to equipment cleaning and minor surface repairs using common hand tools.
* Assists others in removing used process equipment or with the break down of equipment following completed operations.
* Maintains appropriate GMP documentation for all responsible activities and ensures compliance with all training requirements.
* Using data management systems, manages and ensures inventory of production and support supplies.
* Performs environmental sampling and sample management.
* Achieves and maintains job proficiency throughout training.
* Must achieve the skill set to advance to Support Associate - Level 2

Qualifications

Education:

* Must have a minimum of a High School Diploma or a G.E.D.

Required:

* All qualified candidates must pass a computer-based Skills Assessment
* Successful candidates may be required to lift up to 50 pounds, periodically work on ladders and handle trash, perform disinfection, etc.
* Support Associates required to work in an aseptic processing area must successfully demonstrate and maintain proficiency in aseptic gowning by passing monitoring tests.
* No relocation or work authorization sponsorship will be offered for these positions.

Preferred:

* 6 months or more experience working in a manufacturing environment
* Experience working in a cGMP, clean room, and/or aseptic environment
* Experience operating automated washers/sterilization equipment
* Previous forklift experience

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #USW000824. Open to U.S. Residents & Citizens only.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means

Job
: USW, LOCAL 2-86

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Support-Associate-Level-1-%28continuous-recruitment%29-Job-PA-19486/1703539/170353917035392012-06-15Merck/MSDUSW, LOCAL 2-86full-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The function of this position is to assure that products manufactured within the Integrated Process Team (IPT) comply with cGMPs, operating procedures, and other applicable regulations. The responsible person will manage the direct processing of materials and supervise the associated hourly workforce within the integrated process team. The position has specific responsibility for motivating the workforce, work performance, scheduling, task coordination, equipment and area preparation, complying with MPD requirements, and administration of personnel policies and procedures.

Ensure materials receiving and verification in the work area, equipment cleaning and set-up, and area cleaning and verification are completed according to procedures. Assure that materials are properly handled and equipment is properly operated according to SOPs, guidelines, and regulations. Maintain control of processes and product quality by developing appropriate procedures and ensuring compliance with cGMPs, safety and environmental regulations. Monitor the manufacturing processes during the shift.

Enforce the compliance with safety and environmental practices, cGMPs and OSHA regulations in work area. Participate in external and internal audits and inspections. Initiate the investigation when a quality or safety event occurs during the shift. Work with IPT members from Quality and Technical Operations to properly handle unplanned events. Ensure that corrective actions are implemented.

Ensure that personnel under his/her supervision are properly trained in cGMPs, procedures, good documentation practices and regulatory matters. Monitor personnel practices to ensure compliance with SOPs, practices and regulations. Participate in design and implementation of training and development programs. Supervise and motivate hourly employees. Perform performance management and disciplinary process.

Collaborate with IPT members in the identification and implementation of continuous improvement initiatives and action plans. Support activities in the areas of cost containment, efficiency, productivity, energy conservation, waste minimization, operational excellence and lean practices.

This is a 1st shift Monday through Friday position.

Qualifications

Education:

* Associate's degree.

Required:

* Minimum of 6 months experience in responsible line or staff position related to pharmaceutical production or 2 years supervisory experience or 1 to 2 years experience as an Associate Supervisor or Associate Engineer/Scientist.
* Working knowledge of manufacturing processes
* Ability to focus on and obtain business results
* Ability to effectively collaborate with and manage a work team
* Ability to enact conflict resolution
* Ability to effectively respond to change
* Excellent analytical and organizational skills
* Excellent oral and written communication skills
* Leadership and interpersonal skills to motivate direct reports and peers toward the achievement of production goals
* High personal integrity, credibility and energy
* Flexibility to perform related tasks to support the business

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition MAN001729.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Manuf./Operations Generic

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Manufacturing-Supervisor-Job-PA-19486/1862507/186250718625072012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck's Biological Sterile Validation (BSV) department, located in West Point, PA, is currently seeking a Senior Engineer/Scientist. BSV serves as a center of excellence for process/equipment validation supporting the manufacture of vaccine and sterile pharmaceutical products manufactured at Merck's West Point site.

The basic function of this position is to serve as a project lead to design and implement varied technical projects requiring knowledge of engineering and/ or the biological/ physical sciences. Job focus is on project life cycle of initiating, planning, design, execution, and closeout of cleaning validation, sterilization validation, filter validation, container closure integrity, controlled temperature units, and process validation activities, and may include relevant lab work.

Position Expectations

* Apply sound scientific principles, theories, concepts, and techniques in validation processes.
* The incumbent is expected to collect and interpret information and conceive, develop and implement solutions to projects of a more general scope.
* Able to collaborate across multiple departments, prioritize tasks to meet project demands, and possess project leadership/management experience which preferably includes supervisory experience managing contract personnel.
* While the ability to work independently is desirable, routine guidance and direction will be employed by the supervisor to review soundness of technical judgment and the status/schedule of the candidate's work.
* Able to author technical documents (validation protocols, final reports etc) and communicate intent and results in a clear and concise manner.
* Provide validation subject matter guidance to junior staff and act as source of validation technical knowledge.

Qualifications

Education:

* Required: B.S. in Engineering or Biological Sciences or equivalent industry experience
* Preferred: M.S. in Engineering or Biological Sciences or equivalent industry experience

Required:

* Minimum of (5) years relevant work experience required; at least
* Minimum of (3) years of work experience specifically in the field of validation
* Demonstrated project management, leadership, and teamwork skills
* Excellent analytical abilities
* Established written and verbal communication skills

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CHE003478.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-AW1

Job
: Chemical Engineering

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Senior-Engineer-Job-PA-19486/1840116/184011618401162012-06-15Merck/MSDChemical Engineeringfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview

Biologics Manufacturing Commercialization and Sciences (BMSC), Merck Manufacturing Division (MMD) is responsible for the commercialization of biological processes (novel therapeutic proteins and follow-on biologics) from Phase III through launch and transfer to supply. Activities include process development, scale-up and optimization, late-stage analytical support. Process and analytical activity include, interfacing with a network of facilities for product manufacturing and subsequent optimization, process and assay validation, analytical technical transfer, BLA filing documentation, and transfer to supply network. The incumbent will be responsible for coordinating the analytical interface between Merck and external partners and/or contract manufacturing and research organizations (CMO/CRO) in the area of biologics manufacture. He/she will coordinate with analytical and process development groups to prepare for and coordinate trouble-shooting, assay validation and analytical transfers between Merck, external partners and CMO/CROs. The incumbent will have experience in analytical development and quality control (QC), with a working knowledge of current Good Manufacturing Practices (cGMP). At any given time, the individual could be responsible for contributing to and coordinating analytical activities across multiple projects. He/she will also ensure alignment with late-stage analytical strategies and Quality Systems.

Additional Responsibilities Include:

* Coordinate analytical issue resolution as needed via subject matter experts within the global biologics network.
* Prepare and execute analytical method transfers and assay method validations - write and coordinate review of protocols and reports.
* Co-author and coordinate reviews of analytical comparability protocols and reports.
* Provide on-going support to external partners/CMOs/CROs to resolve analytical issues and trouble-shooting.
* Assist in the development and execution of critical reagent qualification protocols and stability studies.
* Act as the BMSC representative on cross-functional analytical sub-teams.
* Assist with the technical review of analytical change requests, atypical analytical results, Out-Of-Specification results, and analytical methods.
* Contribute as author and reviewer to regulatory submissions including marketing applications.

Qualifications

Educational requirements:

* B.S. with 8+ years of relevant industry experience.

Preferred educational requirements:

* Ph.D. in Biochemistry/Biological Sciences or equivalent, with 2+ years of relevant late-stage industry experience.

Required experience and skills:

* Experience with assay development, validation, technical transfer, and trouble-shooting.
* Late stage analytical experience.
* Experience preparing and executing biochemical assay validation and transfers protocols and reports.
* Experience in effectively managing analytical development and testing activity at external vendors such as CMOs
* Experience with drug substance and drug product release, stability and extended characterization testing for biologics.
* Experience developing analytical comparability protocols and reports.
* Strong organizational and project management skills.
* Strong oral and written communication skills.
* Ability to work independently with minimal supervision.
* Effectively identify and communicate risks.
* Experience with deviation management and change control processes.

Preferred experience and skills:

* Experience operating as part of cross functional/cross divisional teams.
* Experience with analytical support for process development activities.
* Experience working with contract laboratories and contract manufacturing organizations, and managing relationships with other external partners.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition CHE003491.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-AS1

Job
: Chemical Engineering

Primary Location: US-PA-West Point
Other Locations: US-NJ-Rahway
Employee Status: Regular

Travel
: No
Number of Openings: 3

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Senior-Engineer-Scientist-Job-PA-19486/1866488/186648818664882012-06-15Merck/MSDChemical Engineeringfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position is in the Regulated Bioanalytical Group of the Pharmacokinetics, Pharmacodynamics and Drug Metabolism Department of Merck Research Laboratory. Primary responsibilities of the position include the validation and application of bioanalytical methods to the quantitative determination of xenobiotics in biological fluids obtained from clinical and pre-clinical studies.

Candidates will be expected to be able to:

* Assemble, set up and operate any necessary experimental equipment or apparatus.
* Conducts laboratory procedures in compliance with established protocols/plans and in compliance with regulatory and laboratory requirements.
* Perform limited analysis, evaluation and interpretation of technical data under the close supervision of a manager.
* Document experimental data in technical notebooks or approved electronic files including activities undertaken, existing conditions, observed results, and variation from expected data patterns.
* With guidance from management, maintain a level of technical knowledge and understanding in his/her assigned area of responsibility.
* Interact with other personnel within the department and key support groups within the research labs to develop a network of resources to facilitate completion of assignments.
* Participate in recommended educational and training opportunities to further develop technical competence in his/her area of assigned responsibilities.
* Understand and comply with safety, good laboratory practice and company policies and procedures as appropriate.

Qualifications

Education:

* B.A./B.S. Science related degree

Required:

* Quantitative analysis of drug candidates and metabolites from biological fluids using liquid chromatography tandem mass spectrometry (LC-MS/MS).
* Experience in a laboratory setting utilizing automated sample handling instrumentation.
* Comfortable handling biological fluids. Prepare various solutions and solvent mixtures as per validated methods.

Preferred:

* 0-3 years
* Knowledge of GLP laboratory and documentation requirements a plus.
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PHA001082.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Pharmacokinetics/Drug Metab

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Hazardous Materials
: Human and Animal Biological fluids (plasma, blood, urine, cerebral spinal fluid etc.)]]>http://jobs.merck.com/job/West-Point-Chemist-Job-PA-19486/1895232/189523218952322012-06-15Merck/MSDPharmacokinetics/Drug Metabfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Future Talent Program features paid internships targeted to start in June 2012 for 10 - 12 weeks and will include one or more projects. Housing is available for those interns meeting the housing distance guideline. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals. The projects that you work in can be in one of the following areas:

PROCESS DEVELOPMENT, SCALE UP AND LAUNCH

* Work in teams to bring research discoveries to full production scale by applying engineering, biology, chemistry and pharmaceutics skills to bench-scale processes.
* Conceive, develop and implement new processing and manufacturing technologies
* Work with teams to develop processes for new products, using chemically- or biologically- derived products
* Support process development and product development with pilot plant scale up, drug supply preparation and technology transfer to operations groups

EQUIPMENT AND FACILITIES DESIGN

* Design and build advanced manufacturing plants, laboratory and office facilities
* Involvement with all phases of project management from the first engineering drawing to the last phase of project start up

MANUFACTURING

* Support line production and maintenance operations
* Maintain manufacturing processes at high levels of performance
* Engineer plant site improvements to enhance safety, quality and the environment
* Optimize existing processes to achieve improvements in process quality, yield and efficiency.

LOCATIONS:: Rahway, NJ; West Point, PA; Cokesbury, NJ; Summit, NJ; Elkton, VA; Durham, NC

Specific internship openings in MMD are as follows:

* Center for Material Science & Engineering (West Point, PA; Rahway, NJ; Summit, NJ) performs analytical evaluation of raw materials, intermediates, and final products to aide in investigation and process improvement evaluations
* Chemical Process Development & Commercialization (Rahway, NJ) and Pharmaceutical Commercialization Technology (West Point, PA, Summit, NJ) groups perform process development and demonstration for new chemical and pharmaceutical processes;
* Global Vaccines Technology and Engineering (West Point, PA, Elkton, VA, Durham, NC) is responsible for process implementation, validation and maintenance for biological processes;
* Biologics Manufacturing Science & Commercializaton (Rahway, NJ, West Point, PA) is responsible for the development and implementation of vaccine and therapeutic protein processes;
* Global Technical Operations (West Point, PA, Elkton, VA) is responsible for continuous improvement of existing processes.
* Global Engineering Services (Cokesbury, NJ with projects at other sites) is responsible for designing and project management for capital projects;
* Vaccine Operations (West Point, PA, Elkton, VA, Durham, NC) is responsible for oversight and continuous improvement for vaccine manufacturing.
* Titers may be required for this position

Qualifications

Requirements:

Education:

* Working toward BS in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field

Requirements:

* Available for 10 week internship beginning June 2012
* Strong personal character and ethics
* Superior Communication and Interpersonal Skills
* Excellent Academic Achievement, Analytical Ability
* Good team player and ability to work independently
* U.S. citizen or lawful permanent resident of U.S.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ADM004867.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-PA-West Point
Other Locations: US-NC-Durham-RTP, US-NJ-Rahway, US-NJ-Summit, US-VA-Elkton, US-NJ-Whitehouse Station

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1

Relocation Provided
: None]]>http://jobs.merck.com/job/West-Point-MMD-Engineering-Intern-2012-Job-PA-19486/1729522/172952217295222012-06-15Merck/MSDInternfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under direction from a Manager or Director, the Sr. Regulatory Coordinator is responsible for developing and implementing CMC regulatory strategies for Merck's vaccine products in accordance with domestic and international regulations and guidances, and is responsible for the preparation and submission of CMC sections for new biological products. Primary responsibilities include, but are not limited to:

Project Responsibilities:

* Works to compile data and information in support of new and in-line biological product license/registration worldwide. Prepares license supplements to existing biological product license applications (BLAs) or marketing authorization applications (MAAs) for US, Europe or ROW. Authors Annual Reports for licensed biological products.

Technical Competence:

* Demonstrates an understanding of regulatory affairs and applies this understanding to the benefit of the company to ensure the continued market supply of Merck Biological products worldwide.

Quality Responsibilities:

* Responsible to have a working understanding of the domestic and international regulations that govern the licensure of biological products and provides Regulatory input and support during time of governmental inspections of the site.

Qualifications

Education Minimum Requirement:

* Minimum of a BS/BA in a biological science or a related field. Preferred fields of study include Microbiology, Virology, Molecular Biology, Biochemistry, or Biochemical Engineering.

Required Experience and Skills:

* At least three (3) years of relevant experience, including biological/pharmaceutical research; manufacturing, testing, or licensure of biological or pharmaceutical products; or related fields.
* Demonstrated sound understanding of related fields (e.g., manufacturing, analytical, quality assurance) and the ability to be creative and imaginative in the approach to new and diverse problem solving.
* Proven experience in critically reviewing detailed scientific information and assessing whether technical arguments are presented clearly and conclusions are adequately supported by data.

Preferred Experience and Skills:

* The ideal candidate will possess strong technical writing skills with the ability to take complicated scientific data and present it in a clear format.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition REG000939.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Regulatory Affairs Generic

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Senior-Regulatory-Coordinator-Job-PA-19486/1864341/186434118643412012-06-15Merck/MSDRegulatory Affairs Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Contribute significantly to the design, implementation, and management of the Merck Institute for Science Education (MISE) professional development initiatives for teachers, administrators, and other leaders in partner school districts. This includes the Academy for Leadership in Science Instruction, Professional Development Design Workshops and Peer Teacher Workshops. Develop assessment instruments to measure impact of MISE initiatives on student learning and contribute to the evaluation of MISE programs. Represent MISE on local, state, and national levels. Work under minimal supervision with extensive latitude for the use of initiative and independent judgment.

Primary Activities:

* Collaborate with MISE staff in the planning, implementation and management of all MISE professional development programs.
* Facilitate sessions, support school- and district-based teams, and assist in the development of tools for the Academy for Leadership in Science Instruction.
* Collaborate with MISE staff in the design and implementation of the Professional Development Design Workshops to build the capacity of districts to provide effective professional development to all teachers.
* Design and provide professional development for teachers in order to equip and support them to bring about improved instruction at partner school sites.
* Apply detailed and deep understanding of science content, assessment principles and theory, and superior management and communications skills to develop, pilot and evaluate multiple student assessment instruments.
* Work closely with district assessment personnel and external experts to interpret, manage and communicate student assessment results to diverse and key audiences.
* Assist with all aspects of the evaluation of MISE initiatives, including contributing expertise to the evaluation.
* Apply advanced training in science content and curriculum theory to identify, collect and disseminate effective teaching materials.
* Assist the Executive Director with strategic planning and decision-making for expanding MISE's partnership to include a large urban district.
* Assume a significant role in building the capacity of the new partner school district to support the continuous improvement of their science education program.
* Plan, organize and facilitate meetings, conferences and workshops, both internally and externally.
* Develop and deliver presentations to key stakeholder groups in partner organizations, as well as statewide and nationally.
* Create and review manuscripts, articles, reports, and other documents to summarize evaluation findings and disseminate lessons learned.

Qualifications

Education:

* A Master's degree in science or education

Required:

* A minimum of 8 years' full-time experience in precollege education are required. Broad understanding of education policy and systemic reform is necessary, with an emphasis on issues as they pertain to science education, and to urban schools.
* The position requires excellent oral and written communication skills, program management skills and highly developed interpersonal, team-building, organizational/time management and computer skills.

Preferred:

* Strong background in the physical sciences.
* Familiarity with new technologies or strategically-relevant trends in social media.
* Experience using various social media channels such as Facebook, Twitter; YouTube and Google Plus.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # COR00159.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-PD1

Job
: Corporate Resp./Philanthropy

Primary Location: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Manager%2C-Education-Programs-Merck-Institute-for-Science-Education-%28MISE%29-Job-NJ-07065/1877979/187797918779792012-06-15Merck/MSDCorporate Resp./Philanthropyfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Merck Diabetes and Endocrinology Department is searching for a dynamic leader with proven experience in drug discovery and development. The candidate will have >10 years experience in the area of metabolic diseases, especially Type 2 Diabetes and its related co-morbidities. The candidate will be an experienced people leader who manages well across a complex multidisciplinary organization and who can lead drug development programs from target identification to the clinic. The candidate will have an in depth understanding of appropriate models with which to develop new drugs. He/she will have a deep understanding of whole body physiology as it pertains to Type 2 Diabetes and metabolic disease in general. The ideal candidate will have experience in small and large molecule drug development, with expertise in peptide drug development. Experience with insulin and insulin analogs is a plus, particularly in the development of novel potentially breakthrough insulins such as glucose-responsive, novel basal, or oral insulins.

The Scientific Lead will:

* Report to the D&E site lead as a member of the D&E leadership team
* Have the desire and ability to grow and to achieve more senior levels within the organization
* Contribute intellectually and strategically to multiple programs within the Department
* Interact cross-functionally with other therapeutic areas such as cardiovascular
* Be accountable for driving one or more drug discovery/development programs to ensure project delivery of milestones through proper allocation of resources and technologies
* Interact seamlessly across a complex multidisciplinary organization
* Play a major role in helping to guide Franchise strategy and foster innovation as it pertains to new areas of research
* Serve as a role model for enthusiasm, commitment, hard work and entrepreneurial thinking to the department
* Serve as a mentor for more junior colleagues

Qualifications

Education:

* Ph.D or MD or related discipline

Required:

* At least 10 years experience the area of metabolic diseases, especially Type 2 Diabetes and its related co-morbidities.
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003544.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Biology-Discovery

Primary Location: US-NJ-Rahway
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: None]]>http://jobs.merck.com/job/Rahway-Diabetes-Team-Lead-5-Job-NJ-07065/1776654/177665417766542012-06-15Merck/MSDBiology-Discoveryfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Assistant Engineer - Co-op for Pilot Facilities Engineering, Equipment Development & Maintenance will gain hands-on experience through assisting with maintenance activities and capital projects from the initial concept through construction and startup. The Assistant Engineer is responsible for:

* Interfacing between process operations and facility maintenance personnel
* Have exposure to all facets of Merck Pilot Plant operations, facility maintenance, and capital upgrades developing practical application skills as an engineer
* Working closely with process operations to support Merck Research Labs (MRL) drug development through the execution of process setups and facility maintenance, while complying with all Merck standards for current Good Manufacturing Practices (cGMP) and safety.
* Assisting in the management of predictive and preventive maintenance programs to ensure minimal processing downtime and efficient drug development

Other working relationships may be required with Global Engineering Services, site operations, architectural and engineering firms, construction management firms, and other outside consultants.

Qualifications

Education:

* Pursuing B.S. degree in Chemical or Mechanical Engineering

Required:

* U.S. Citizen or lawful permanent resident of U.S.
* Available full-time for a period of 6 months beginning June, 2012

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #ADM004959.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-NJ-Rahway

Job Type
: Co/Op
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Assistant-Engineer-Co-op-Job-NJ-07065/1840112/184011218401122012-06-15Merck/MSDCo/Opfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Sourcing Manager ("SM") is responsible for global category management and sourcing leadership of Secondary Market research and US Commercial Operations which account for ~$50 million annual spend. Secondary Market Research (which can be loosely defined as sources of information such as data or syndicated materials used to support business decisions) is a key focus. The SM must be able to identify, lead, and source secondary market research. Must collaborate closely with the GMRA (Global Market Research & Analytics) teams to help develop and execute secondary market research initiatives Proactively communicates and facilitates discussion with GMRA Analytics & Forecasting Teams to ensure marketing/ business needs at both a strategic and tactical level, encompassing local as well as global. Planning and conducting secondary market research sourcing strategies is a key job function.

* Category Scope -Responsible for commercial support of Marketing Services categories. In collaboration with stakeholders and Regional and local procurement professionals, creates and implements 3-5 year strategic sourcing strategies.
* Global Category Team: Participates on teams of regional & local representatives to develop and implement strategic source plans as well as to ensure alignment on key initiatives and priorities for Marketing services categories.
* Sourcing Management - Uses the Sourcing Management Process to manage assurance of supply, quality, service, cost, innovation and regulatory compliance within Marketing services categories resulting in strategies which optimize value and ensure appropriate risk management. Understands the Sourcing Management Process and how to apply required tools in the creation and implementation of source plans.
* Proactive Cost Management: Achieves cost control, cost reduction, and cost containment targets, and adds value to area of expenditure through a strong Total Cost of Ownership (TCO) orientation and process management.
* Market Knowledge and Insight: Uses thorough market knowledge and data analysis to gain critical insights that drive the selection of Sourcing Strategies and continuous improvement activities. Actively participates in relevant industry conferences and events as appropriate.
* Supplier Management: Responsible for building relationships with Global, International and Enterprise suppliers and managing key supplier performance against business requirements using proven processes (i.e. SVM) ; ensures adequate inclusion of diversity suppliers in RFPs and contracts as applicable. Supports major Regional supplier relationships
* Stakeholder Management and Business Sponsorship: Ensures appropriate stakeholders are identified and managed through stakeholder matrix. Engages assigned stakeholders and partners with them to define and meet or exceed business requirements and identify and manage profit plan savings targets. Understands strategic business requirements at 1-3-5 year horizon.
* Contract Negotiation and Management: Once strategy is approved, personally leads the sourcing including RFX, RFP, negotiations and contracting for Global and International categories to put in place the right suppliers. Negotiates at tactical and strategic levels to develop local, regional, global company contracts.

Qualifications

LI-AS2

Education:

* Required: BS in Business, Finance, Marketing or related field strongly preferred.
* Preferred: MBA or advanced degree and/or relevant certification is desirable.

Experience:

Required:

* 5+ years experience in strategic sourcing (global category management) or in role related to secondary market research.

Preferred:

* Knowledge of Procurement related business processes.
* Knowledge of secondary market research suppliers and information including; data, information, licenses & syndicated materials highly desirable.
* Demonstrates solid leadership capabilities at the Manager level, with particular strengths in collaboration, written and verbal communications, and cross-functional teamwork

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition GOO999126.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Goods Purchasing

Primary Location: US-PA-West Point
Other Locations: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Sourcing-Manager-Secondary-research-Job-PA-19486/1858702/185870218587022012-06-15Merck/MSDGoods Purchasingfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


We currently have an exciting opportunity for an experienced engineer or scientist to support the life cycle management of Merck's vaccine portfolio. The position is solid line to Vaccine Manufacturing Science and Commercialization (VMSC) and dotted line to Sterile Liquid Commercialization (SLC). The role will primarily focus on the formulation and filling processes associated with the drug product. Key responsibilities may include process enhancements, development of new images and product value extensions, and new technology development. This is a unique opportunity to make a significant impact to life saving vaccines.

The specific activities associated with this position may include:

* Participate on drug product working groups responsible for project implementation
* Apply drug product understanding and manufacturing expertise to develop robust and scalable manufacturing processes
* Support process risk assessments to guide and prioritize development work
* Design, plan and execute process development studies for sterile solutions, suspensions, and/or lyophilized products
* Analyze and document experimental results and make recommendations for path forward, communicating key findings to both project teams and area management
* Facilitate the preparation of materials for clinical trials and/or stability studies by collaborating with a network of pilot plants and launch facilities
* Contribute to the technology transfer of processes into commercial supply sites, enabling the execution of validation lots and contribute to regulatory filing documentation
* Demonstrate the feasibility of new technologies and the potential application to vaccine products

Qualifications

Education:

* Required: BS in Chemical Engineering, Materials Engineering/Science, Pharmaceutics or related field

Required:

* 0-3 years post-bachelors degree experience in manufacturing, process development, or a related field
* Previous experience working with sterile drug products with a pharmaceutical or biotechnology company

Preferred:

* Experience with aseptic techniques and manufacture of sterile products
* Experience with viral vaccines
* Knowledge of cGMPs and experience working in a GMP environment

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition CHE003486.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Chemical Engineering

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Staff-Scientist-Job-PA-19486/1868794/186879418687942012-06-15Merck/MSDChemical Engineeringfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Currently, we are sourcing candidates for a union position for Lab Technician -Level 1 for the Merck Manufacturing Division at our West Point, PA site.

Position Overview:

Under supervision of the Laboratory Supervisor, Senior Supervisor, Area Head or Laboratory Manager, consults with supervisor to plan and perform testing on raw materials, culture media, production intermediates, manufactured bulks, finished products and/or other samples in compliance with written procedures. Testing may be performed in one or more of the following scientific disciplines: Microbiology, Biochemistry, and/or Virology.

Essential functions of this position include, but are not limited to the following:

* Read, record, review and calculate test results. May be required to assist in approval/validation of test data generated according to written procedures.
* Participate in performing investigational testing as needed and directed by supervisor for product evaluation and assist supervisor in conducting and authoring atypical investigations.
* Assist in the revision/implementation of control procedures (CPs) and standard operating procedures (SOPs) within the department and assist in training and orientation of other Laboratory Technicians.
* In compliance with operating practices, company policies, government regulations and current Good Manufacturing Practices (cGMPs), assures that quality of our products and services are of highest priority and meet associated safety and compliance requirements.
* Responsible for performing assay specific procedures associated in one or more scientific functional disciplines for products requiring testing.
* Maintain complete records of testing conducted and record test observations. Using approved statistical methods, read, record, review and calculate test results and may assist in the approval/validation of test data generated according to written procedures. Notifies supervisor of potential atypical testing results.
* Assist supervisor to plan daily work schedules and maintain laboratory documentation according to departmental policies and procedures.
* Maintain stock of equipment, glassware, supplies, etc. and notify supervisor when inventories are low.
* Perform computer analysis and enter test data into appropriate system. (i.e. LIMS, Excel).
* Participate in regulatory activities and may be responsible for assisting in or leading internal compliance initiatives (i.e. External and Divisional Audits, Shop Floor Activities).
* Assist area supervisor in orientation and training of other departmental technicians as part of process specific training and maintain a clean, safe, and orderly work area while adhering to departmental, safety and regulatory policies and procedures.
* Attend and actively participate in HAZOPS, waste walkthroughs, kaizen events, or any other operations, Lean Six-Sigma, Quality, Safety or Environmental training/initiatives as required.
Please note, Union position that may require 2nd or 3rd shift and/or weekend work.

Qualifications

Education:

* Bachelor's degree in Biological Science or related discipline.

The following minimum courses are Required:

* Eight semesters of biological science course work to include but not limited to: General Biology, Microbiology, Bacteriology, Immunology, Virology, Parasitology, Physiology, Mycology or Molecular Biology.
* A minimum of two laboratory courses.
* Four semesters of chemistry including General Chemistry with laboratory, Organic Chemistry and/or Biochemistry.
* Two semesters of college level mathematics

Required:

* The incumbent must satisfactorily complete a skills assessment evaluation and/or specific qualification training
* Ability to lift and move various items weighing up to 45 pounds
* Proficiency in cell culture techniques

Desired:

* One year prior working experience with analytical laboratory methods.
* 1 year experience with small volume liquid handling.
* One year working experience with aseptic technique.
* Previous experience with Polymerase Chain Reaction (PCR) and/or quantitative PCR.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PRO00303.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Production / Operator

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/West-Point-Laboratory-Technician-Level-1-%28continous-recruitment%29-Job-PA-19486/1807386/180738618073862012-06-15Merck/MSDProduction / Operatorfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview

We are establishing a Global Manufacturing Operations and Quality Systems Effectiveness function within Quality to create and manage an on-going assessment program to drive compliance improvements throughout our network. The candidate will be responsible for a program to gather and manage data from global regulations and regulatory inspections, and other data inputs selected from throughout the network to provide assessments of this information, and develop corrective actions to be enacted across the network. This position will oversee the management and tracking of global commitments and corrective actions. They will provide quarterly reports to Global Quality Leadership Team (GQLT) and Merck Leadership Team (MLT). The candidate will manage direct reports.

Additional responsibilities are as follows:

* Proactively tracks and interprets global regulator observations and researches changes or proposed changes in global CGMP regulations and other regulations applicable to Merck's Quality Management System that affect company procedures and practices.
* Plans and conducts analysis of data, identifies risk and utilizes rapid disciplined decision making to recommend courses of action that have broad or global regulatory compliance impact across the network. Resulting actions must maintain compliance and drive consistency in application of requirements across multiple sites, multiple technologies, multiple geographies and businesses world wide, including but not limited to HH, AH and CHC.
* Develops, implements, and manages a continuous improvement program to collect & analyze internal and external data that assures that activities related to manufacturing, testing and holding of products are performed according to drug, device and biologics CGMP regulations using risk management principles and lean six sigma tools.
* Selects, manages and leads cross functional committees and teams and in concert, analyzes the data with the team to drive improvement to the Quality Management System and operations across the network.
* Prepares, provides and delivers high quality presentations and high quality reports to Global Quality Leadership Team including status updates and reports to Divisional Quality Council and to Merck Leadership Team.
* Oversees, participates and approves the interviewing, hiring, and training of departmental employees; conducts performance evaluations for direct reports; and assists direct report managers with performance evaluation process for their units.
* Reports quarterly to GQLT and MLT.
*
Drives development of global Quality compliance infrastructure in accordance with the overarching Quality Management System (QMS) strategy.

*
Assists in the development of strategies, tactics, trainings, programs and activities related to assuring compliance with regulations.

*
Identify and drive compliance improvements throughout network.

*
Ability to accurately interpret and apply regulator expectations and regulations to the QMS in a drug, device and biologics manufacturing and quality environment.

* Stay abreast of changes and proposed changes to all regulations by networking both internally and externally to research best practices and deliver pragmatic recommendations and solutions to Executive Management. Candidate must be capable to influence at all levels of the organization and across the network in order to successfully design and manage cross functional network wide teams to gather and analysis data efficiently.

Qualifications

Education:

* B.S. Degree.

Preferred:

Advanced degree in Physical Science, Chemistry, Life Science, or Biological Sciences.

Required:

* Minimum of 10 years experience managing and supervising others which demonstrates proficiency in selecting, motivating and retaining a superior team, and effectively managing personnel issues.
* Minimum of 10 years of manufacturing and/or quality operation management experience within an FDA and/or EU pharmaceutical, device and biologics environment.
* Proven ability to successfully manage multiple teams and projects simultaneously.
* Experience working with regulating groups and networking, participating in expert panels. Must have a presence in the industry.
* Prior experience managing inspections performed by FDA and foreign Regulatory Authorities.
* Excellent project management, communication, technical writing and presentation skills.
* Computer Skills: Microsoft Outlook, Internet Explorer, MS Project, MS Excel, MS Word, Powerpoint.
* Strong collaboration and presentation skills with ability to concisely articulate and deliver recommended courses of action to Executive Management. Must have demonstrated ability to defend the recommended courses of action and influence and drive change all at levels of the organization.
* Expert in interpretation and practical application of regulations for Drug, Device and Biologics and interpretation and application of ICH Q8,9,10 principles to Quality Systems that include oral, sterile (Aseptic and Terminal), API, clinical and packaging technologies & operations. Must have strong analytical skills in order to develop and recognize appropriate action plans and how they will impact operations and compliance.
* Thorough understanding of Quality Management Systems for drugs, devices, biologics including risk management.
* Energy, self-motivated, proactive and endurance to stay focused on the task at hand and thrives on the challenge.
* Adaptable to a fast paced, complex and ever changing business environment, flexible, proactive and decisive.
* Model and reinforce behaviors consistent with Merck's Leadership behaviors, values and culture.
* Required to attend industry related conferences to stay current with regulator expectations and requirements. Travel to manage remote staff, attend required internal or external divisional, staff or other meetings.

Preferred:

* Prior FDA and/or EU experience preferred-minimum 7 years.
* Lean Six Sigma belt certified.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition QUA002927.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-BR1

Job
: Qual Assurance & Ops Generic

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Director-of-Quality-Compliance-Job-PA-19486/1858705/185870518587052012-06-15Merck/MSDQual Assurance & Ops Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview

Under the direction of a Manager or Director, the Senior Regulatory Coordinator is responsible for implementing CMC regulatory strategies for Merck's vaccine product franchise in accordance with domestic and international regulations and guidances, and is responsible for the preparation and submission of CMC sections for new vaccine products.

Primary responsibilities include, but are not limited to:

Project Responsibilities:

* Works to compile data and information in support of new and in-line vaccine product license/registration worldwide.
* Prepares license supplements to existing vaccine product license applications (BLAs) or marketing authorization applications (MAAs) worldwide.
* Authors Annual Reports for licensed vaccine products.

Technical Competence:

* Demonstrates an understanding of regulatory affairs and applies this understanding to the benefit of the company to ensure the continued market supply of Merck vaccines worldwide.

Quality Responsibilities:

* Working understanding of the domestic and international regulations that govern the licensure of vaccines and provides Regulatory input and support during time of governmental inspections of the site.

This position is in the Viral Vaccine Franchise which supports M-M-R®II, RotaTeq®, VARIVAX®, ProQuad®, ZOSTAVAX®, VAQTA® and ANTIVENIN. Primary responsibility for this position is support of the Japanese registration for RotaTeq®.

Qualifications

Education:

* B.S. in a biological science or a related field.

Preferred:

* M.S. in a biological science or a related field. Preferred fields of study include Microbiology, Virology, Molecular Biology, or Biochemistry.

Required:

* At least three (3) years of relevant experience, including biological/pharmaceutical research; manufacturing, testing, or licensure of biological products; or related fields.
* Demonstrated sound understanding of related fields (e.g., manufacturing, analytical, quality assurance) and the ability to be creative and imaginative in the approach to new and diverse problem solving.
* Proven experience in critically reviewing detailed scientific information and assessing whether technical arguments are presented clearly and conclusions are adequately supported by data.
* Demonstrated superior oral and written communication skills in multicultural settings and ability to communicate complex issues in a succinct and logical manner. Strong listening skills.
* Demonstrated flexibility in responding to changing priorities or dealing with unexpected events.
* Demonstrated effective leadership, communication, interpersonal and negotiating skills.
* Demonstrated ability to generate innovative solutions to complex regulatory problems and effectively work with and communicate to key stakeholders.

Preferred:

* Understanding of viral vaccine manufacture and/or general understanding of vaccine requirements in Japan.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition REG000956.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-BR1

Job
: Regulatory Affairs Generic

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Sr_-Regulatory-Coordinator-Job-PA-19486/1871150/187115018711502012-06-15Merck/MSDRegulatory Affairs Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Clinical Innovation Lead, Global Clinical Trial Operations (GCTO) will identify new, novel and innovative ways to execute clinical trials. He/She will be the primary point of contact within operations for awareness and knowledge of industry trends in clinical innovation. In collaboration with internal, academic or other external research innovators in the Clinical area he/she will create and manager innovation experiments aimed at exploring, understanding, and identifying the application of promising new processes, services, and technologies to yield a positive impact on clinical development. The person in this position will define and initiate projects which allow piloting the application of promising new processes and technologies arising from innovation experiments. They will interface with external knowledge leaders and represent Global Clinical Trial operations on key external industry consortium and collaborations.

The successful conduct of clinical trials necessitates using new, emerging methods to focus on: 1) coordinating disease care and wellness efforts for patients, and 2) increasing the overall quality and efficiency of clinical trials. Physicians have increasingly embraced the use of technological tools, and some of these new methodologies and technologies are also starting to be applied to the clinical development domain, such as using social media for patient recruitment and experimenting with remote clinical trials and risk-based monitoring. Against this changing backdrop, innovation in the operational execution of clinical trials is required to speed the current overall system of drug development, so that new medicines can be delivered safely and more quickly to those who need them. This position will work to transform clinical development approaches, processes and technologies in a way that will fit with emerging trends and also serve to define the future state of clinical trial execution, by interacting with and engaging investigators, patients, government agencies, other industry representatives and academic institutions in improving clinical research and development.

Qualifications

Education:

* MS

Required:

* At least 15 years in clinical operations and/or a strategic, innovative field.
* At least 5 years in a leadership role.
* Strong working knowledge of the clinical development and operations processes.
* Experience designing and implementing innovative solutions in the clinical development arena.
* Strong knowledge of industry operational and technical trends.
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CLI002684.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-MG1

Job
: Clinical Research (Non-M.D.)

Primary Location: US-NJ-Rahway
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: None]]>http://jobs.merck.com/job/Rahway-Clinical-Innovation-Lead-Job-NJ-07065/1871155/187115518711552012-06-15Merck/MSDClinical Research (Non-M.D.)full-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Modeling and Simulation at Merck is characterized by a wide range of expert areas including but not limited to Statistical, PK/PD, Pharmaceutical, Mathematical and Physiological modeling within the "M&S Network". The M&S Dept has a key integrating function. The internshiop is part of this M&S Dept and plans and conducts advanced modeling and simulation to enable decisions, which enhance and accelerate research programs across the pipeline from discovery to late-stage development and mature products support and/or contributes to the development and implementation of new M&S capabilities, standards, and approaches, using techniques such as:
* PK and PK/PD modeling
* Mechanistic/Disease modeling
* Comparator modeling
* Absorption and biopharmaceutical modeling
* Biological pathway analysis
* Physiological modeling
* Statistical modeling
* Trial simulation
* Quantitative decision analysis
* Data creation and data mining

The Modeling and Simulation group in Merck Research Labs located in Rahway, NJ is seeking highly motivated and skilled graduate interns. Below are the descriptions of the intern projects:

Project #1 -

The student will investigate (global and local) sensitivity analysis as a diagnostic tool for covariate selection during PK/PD modeling (I3-capability enhancement). One of the key challenges in PK/PD modeling is covariate selection: poor choice of covariates can lead to covariance-step failure, which is difficult to troubleshoot, as well as over/under-fitting of the data. Based on the experience gained during the JACOBIAN evaluation project, we believe that sensitivity analysis can be used as a diagnostic tool to (a) investigate the cause of covariance-step failure; and (b) guide introduction of random-effect variables (ETA's). The effort can reduce the time for model refinement, improve the PK/PD modeling workflow, and lead to a publication.

The student should have some knowledge of ordinary differential equations and sensitivity analysis; and be experienced in MATLAB, R, or Mathematica. Experience in NONMEM is a definite plus. The student will gain knowledge and experience in PK/PD modeling and may be able to publish the findings.

Project #2 -

Modeling tumor growth is integral to quantifying drug response and predicting survival. The majorities of models currently used in drug development are oversimplified and are largely based on single growth and death parameters. Moreover, they do not explicitly account for important physiological factors that may affect tumor growth, e.g. spatial distribution of tumor cells, angiogenesis, and metastasis. A more mechanistic model can (a) improve the predictions of tumor response; (b) leverage existing imaging data, which would inform key components of the model; (c) facilitate translation of the model across different tumor types and species; and (d) inform tumor size-survival modeling. The objective of this project is to implement one such model based on qualitative mechanisms and assess its usefulness in drug development.

The student should have some ability to perform independent research and to implement difference equations and Monte Carlo simulations in R, MATLAB, or Mathematica. The student will gain knowledge in oncology modeling and its use in drug development.

Project #3 -

In order to optimize fixed-dose combination therapy development, the M&S department has developed a statistical model to streamline the biocompatibility (BE) and bioequivalence (BE) trials. This project is a follow-up effort to validate the statistical model and to answer important questions in the quantitative PVE space. Specifically, the student will (a) validate the developed statistical model by looking at historical BC/BE trial data; (b) incorporate correlation between biomarkers, e.g. AUC and Cmax, and/or compounds; and (c) investigate optimal strategy to maximize probability of success when more then two formulations are considered-whether a single pick-the-winner multiple-formulation crossover study or a sequence of 2-by-2 crossover studies is better given a fixed budget. The effort will guide future BC/BE trial designs, improve probability of success, and reduce cost.

The student should have experience in performing Monte Carlo simulations in R and will learn how Monte Carlo simulations are used in clinical trial design as well as some software engineering skills.

Project #4 -

The student would work on enhancing trial enrollment models by performing data analysis of prior studies to establish correct distributions and set parameters. The student would work on integrating models with CTMS system to draw on historical data directly from prior studies. The student should be able to perform statistical analyses, have a good working knowledge of R or Splus, and have experience in designing and performing Monte Carlo simulations. In addition, the student should be in a PhD program, and completed at least 1 year of study.

The internship is targeted to start in June 2012 for 9 - 11 weeks.

Qualifications

Required:

* Currently enrolled in a PhD or MS degree program in Pharmacometrics, Clinical Pharmacology, Mathematics, Pharmaceutical Sciences, Bioengineering, Chemical Engineering or Computer Science
* Programming skills in Matlab, WinNONlin, C/C++, Fortran, Java, and/or Mathematica
* Strong linear algebra, differential equations (ordinary and partial) & Multivariate calculus
* Applicant must be returning to school to complete their degree upon the completion of the internship

Preferred:

* Knowledge in statistical data analysis and stochastic processes and knowledge of statistical shape modeling methods
* Basic knowledge in clinical trials simulations
* Knowledge of scientific computing/numerical analysis, finite element methods; ANSYS and/or ABAQUS

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #RES001265.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-NJ-Rahway

Job Type
: Intern
Employee Status: Regular

Travel
: No
Number of Openings: 2

Relocation Provided
: Domestic (within country)]]>http://jobs.merck.com/job/Rahway-Modeling-&-Simulation-Research-Internship-MS-or-PhD-Job-NJ-07065/1729529/172952917295292012-06-15Merck/MSDInternfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Responsibilities include and are not limited to the following

* Development and execution of the Clinical Pharmacology strategy for a given program from preclinical candidate approval through the worldwide marketing application.
* Key member of the early development team, providing a leadership role on the team with regard to design and execution of early clinical development strategy.
* Clinical Pharmacology activities for a given program
* Authors initial program clinical plans, the early development plan, Clinical Pharmacology Phase I studies through Phase Ib
* Timely and safe execution of CP program studies.
* Ensure appropriate technical transfer of experimental medicine qualified platforms.
* Interact closely with internal and external clinical study support staff and scientists (including discovery research, biostatistics, drug metabolism, regulatory affairs, and global clinical trials operations).
* Provide Clinical Pharmacology support for programs through the worldwide marketing application filing including supportive registration documents and presentations.
* Clear, timely communication and interpretation of Clinical Pharmacology results Franchise, Function, and governance committees.

Qualifications

Education:

* M.D or M.D./Ph.D

Required:

* Demonstrated record of scientific scholarship and achievement.
* Proven track record in clinical medicine and background in biomedical research is essential.
* Prior specific experience in clinical research and prior publication is desirable but not necessary.
* Strong interpersonal skills, as well as the ability to function in a team environment are essential.

Preferred:

* Board Certification or Eligibility

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CLI002471.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Clinical Research (M.D.)

Primary Location: US-NJ-Rahway
Other Locations: US-PA-Upper Gwynedd, US-MA-Boston
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Rahway-Associate-Director%2C-Clinical-Research-Clinical-Pharmacology-Job-NJ-07065/1401647/140164714016472012-06-15Merck/MSDClinical Research (M.D.)full-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This position will be responsible for Biometrics imaging and bio-signal biomarkers projects including analysis of preclinical, early clinical, and experimental medicine imaging and EEG data. Responsibilities include all phases of data analysis from processing of raw imaging and EEG data to derivation of endpoints. Part of the responsibilities is development and implementation novel statistical methods and software for analysis of imaging and bio-signal data. This position will closely collaborate with MRL Imaging and Clinical Pharmacology departments; Experimental Medicine; Early and Late Stage Development Statistics; and Department of Modeling and Simulation. Publication and presentation of the results is highly encouraged as is collaboration with external experts.

Qualifications

Education:

* PhD in Statistics, Applied Mathematics, Physics, Computer Science, Engineering, or related fields

Required:

* Education should include Statistics related courses or, equivalently, working experience should involve data analysis and statistical modeling for at least 1 year.
* Excellent computing skills, R and/or SAS , MATLAB n Linux and Windows environment; working knowledge of parallel computing; C, C++, or Fortran programming.
* Dissertation or experience in at least one of these areas: statistical image and signal analysis; data mining and machine learning; mathematical modeling in medicine and biology; general statistical research

Preferred:

* Education in and/or experience with EEG and Imaging data analysis; stochastic modeling; functional data analysis; familiarity with wavelet analysis and other spectral analysis methods
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003546.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-MG1

Job
: Biostatistics

Primary Location: US-NJ-Rahway
Employee Status: Regular
Number of Openings: 1

Hazardous Materials
: None]]>http://jobs.merck.com/job/Rahway-Biometrician-Biostatistics-Job-NJ-07065/1777429/177742917774292012-06-15Merck/MSDBiostatisticsfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck's Clinical Development Laboratory is accountable for target engagement, pharmacodynamic, and patient segmentation biomarker assays supporting Merck clinical studies from early clinical development through registration. Along with physicians in Clinical Pharmacology (ClinPharm) and Experimental Medicine (EM), the laboratory conducts bioanaltyical science and develops novel biomarker platforms. It develops and validates biomarker assays using a wide variety of bioanalytical techniques including IHC, immunoassay, flow cytometry and genomic assays, and it works with vendors and internal groups when assays are sourced to external vendors. The primary role of the Genomics Capability Scientist will be meet the growing number of genomics assays required to support early phase clinical studies.


DUTIES:

* Applies technical expertise in the development, validation and clinical application of genomic PD and patient stratification biomarker assays. Collaborates with scientists and physicians in both early and late stage clinical development, ClinPharm and EM to facilitate implementation of biomarker strategies in clinical trials.
* Reviews and challenges proposed biomarker plans at internal review committees. Drives validation strategy for high complexity and regulated genomic assays. Analyzes and draws conclusions from genomic assay data independently and in connection with statistician colleagues.
* Develops and validates high value and novel genomic assays internally. Responsible for all technical aspects of assigned genomic assays from sample collection through clinical sample analysis. Prepares or reviews validation reports, laboratory SOPs, sample collection procedures, batch spec sheets, final reports and peer-reviewed publications.
* Responsible for outsourcing activities through close interactions with the Operations Lead. Interacts and develops relationships with external vendors. Creates work plans for assay development. Assists in developing the external vendor assay contracts with procurement. Selects vendors based on reviewing validation reports. Guides external vendors during assay development and validation.

Qualifications

Education Minimum Requirement:

* PhD in a life sciences discipline (such as Biochemistry, Immunology, Molecular Biology, Cell Biology, Computational Biology, etc.) or Chemistry with broad knowledge of biomarker science.

Required Experience and Skills:

* A minimum of 6 years of direct experience in genomic assay development on multiple expression, sequencing and genotyping platforms
* 1 year experience in outsourcing of genomic assays (including writing RFPs, vendor audits, vendor relationship management) OR 1 year experience at a CRO (working with biopharma partners)
* Outstanding interpersonal, verbal and written communication skills.
* Demonstrated record of scientific achievement (publications, patents, etc).
* Strong leadership and collaborative skills.
* Excellent data analysis skills, including ability to use SAS, Spotfire or analogous applications.

Preferred:

* 1 yr experience in biosample analysis in a clinical laboratory
* Experience with assay automation
* Experience in sample collection logistics in a clinical setting
* General project management skills or six sigma certification (e.g. green belt)
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003402.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Bio/Immuno Assay Development

Primary Location: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Bloodborne pathogens]]>http://jobs.merck.com/job/Rahway-Research-Fellow-Genomics-Job-NJ-07065/1542238/154223815422382012-06-15Merck/MSDBio/Immuno Assay Developmentfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Pharmaceutical Packaging and Development department is offering co-op positions available at our West Point, PA location. The Pharmaceutical Packaging and Development Co-op will be responsible for:

* Execution of planned activities on the evaluation of container systems for supporting stability and marketing suitability studies for new pharmaceutical products in both solid and liquid dosage forms.
* Laboratory work includes determination of moisture sorption isotherms (MSI) for various products and packaging components, novel head-space analysis, installation of custom-made apparatus, design and implementation of various product characterization studies quantifying the interaction of moisture and oxygen with labile products, thermal characterization of materials, and use of non-destructive techniques to evaluate package integrity.
* Non- laboratory tasks include compilation and analysis of data, and mathematical modeling (Math-CAD) of packaging systems.

This is a full-time co-op position anticipated to start March/April of 2012. Housing subsidy is not available as part of this program and if required by the student must be funded 100% by the student.

Qualifications

Education:

* Candidate must be pursuing a degree (BS/MS) in Chemical Engineering, Mechanical Engineering or a related engineering field.
* Completion of at least freshmen year of a BS degree is required.

Required:

* Ideal candidate will be proficient with MS Office programs.
* Candidate must be available for full-time employment for 6 months starting March/April 2012.
* Currently enrolled in an academic program and returning to school following this assignment.
* U.S. citizen and permanent residents required

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ADM004955.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-PA-West Point

Job Type
: Co/Op
Employee Status: Regular
Number of Openings: 3]]>http://jobs.merck.com/job/West-Point-Pharmaceutical-Packaging-and-Development-Co-op-%28West-Point%2C-PA%29-Job-PA-19486/1729515/172951517295152012-06-15Merck/MSDCo/Opfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Vaccine Manufacturing Sciences & Commercialization (VMSC) is seeking a highly motivated individual to partner with Vaccine Product & Technology Operations, Merck Research Laboratories, Bio-Sterile Validation and Regulatory groups to meet targeted process development and commercialization initiatives. VMSC is the process steward and provides technical support and process improvements for bulk manufacturing processes. The processes supported represent viral, recombinant, and bacterial bulk vaccines both in traditional and emerging markets. Within the VMSC group, there are leadership opportunities to develop new products and innovate new processes for the current vaccine portfolio.

The Staff Biochemical Engineer will be responsible for various activities necessary for existing product support projects and technical support on new facility start-ups. The primary focus of this position will be as follows:

* Investigational and laboratory support for existing products
* Discovery and innovation of new platforms for existing products
* Ensuring successful technology transfer for new products

This work may support future GMP (Good Manufacturing Practices) manufacturing activities, so work in a GMP environment is a plus. Due to the nature of the job, extensive lab scale upstream and/or downstream purification experience is a desired qualification. Other projects and responsibilities to be defined based on manufacturing and compliance needs.

Responsibilities include, but are not limited to the following:

* Managing key process development and manufacturing improvement projects for viral, recombinant, or bacterial vaccines
* Establishing, leading, and executing laboratory scale processes
* Intermittent analytical testing/assay development to support viral, recombinant, or bacterial vaccines
* Execution of projects against key timing commitments, with appropriate documentation and change control
* Support complex investigation / troubleshooting teams
* Provide technical leadership and ownership of assigned unit operations
* Identify and initiate process improvements using Quality by Design (QbD) and Design of Experiment (DoE) methodology
* Work with production, automation and engineering groups on process improvement projects

Qualifications

Education:

* Required: B.S. degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering or Biological Sciences
* Preferred: M.S. degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering or Biological Sciences
* Preferred: Biology, Biochemistry, or Chemistry

Required:

* Experience in upstream and/or downstream process development and/or manufacturing technical support and/or technology transfer
* Excellent communication (both written and oral), scientific, and teamwork skills
* Demonstrated track-record of technical problem-solving abilities
* Strong collaboration and leadership skills.

Preferred:

* Minimum of (2) years experience in the pharmaceutical industry
* Direct experience with cell culture or fermentation or purification unit operations
* Project management experience
* Proven ability to work independently in hands-on laboratory setting
* Experience in planning and executing statistically designed experiments
* Experience evaluating and implementing new technologies in a vaccines or biologics manufacturing setting
* Experience collaborating with teams in a matrix environment
* Knowledge of cGMPs and experience working in a GMP environment

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition BIO003590.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Bio Process-Ferment/Cell Cultr

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Staff-Biochemical-Engineer-Job-PA-19486/1885947/188594718859472012-06-15Merck/MSDBio Process-Ferment/Cell Cultrfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Sourcing Manager ("SM") is responsible for global category management and sourcing leadership of Merck's Global Contact Center needs (in coordination and collaboration with regional and/or local sourcing professionals. SM will responsible for the development and implementation of sourcing strategies for Contract Centers globally. In this role, the SM will help drive and implement regional and global supplier optimization activities, will find strategic partners to help grow and expand our global outbound contact center capabilities and mature our outsourcing strategies and relationships. Responsible to establish and lead cross-functional teams through the Sourcing Management Process and to provide strategy oversight for Local and Regional components of the category. Responsible for identifying and managing savings targets and other key metrics to established targets. Responsible for supplier management through Procurements Supplier Value Management program

* Category Scope -Responsible for commercial support of Marketing Services categories. In collaboration with stakeholders and Regional and local procurement professionals, creates and implements 3-5 year strategic sourcing strategies.
* Global Category Team: Participates on teams of regional & local representatives to develop and implement strategic source plans as well as to ensure alignment on key initiatives and priorities for Marketing services categories.
* Sourcing Management - Uses the Sourcing Management Process to manage assurance of supply, quality, service, cost, innovation and regulatory compliance within Marketing services categories resulting in strategies which optimize value and ensure appropriate risk management. Understands the Sourcing Management Process and how to apply required tools in the creation and implementation of source plans.
* Proactive Cost Management: Achieves cost control, cost reduction, and cost containment targets, and adds value to area of expenditure through a strong Total Cost of Ownership (TCO) orientation and process management.
* Market Knowledge and Insight: Uses thorough market knowledge and data analysis to gain critical insights that drive the selection of Sourcing Strategies and continuous improvement activities. Actively participates in relevant industry conferences and events as appropriate.
* Supplier Management: Responsible for building relationships with Global, International and Enterprise suppliers and managing key supplier performance against business requirements using proven processes (i.e. SVM) ; ensures adequate inclusion of diversity suppliers in RFPs and contracts as applicable. Supports major Regional supplier relationships
* Stakeholder Management and Business Sponsorship: Ensures appropriate stakeholders are identified and managed through stakeholder matrix. Engages assigned stakeholders and partners with them to define and meet or exceed business requirements and identify and manage profit plan savings targets. Understands strategic business requirements at 1-3-5 year horizon.
* Contract Negotiation and Management: Once strategy is approved, personally leads the sourcing including RFX, RFP, negotiations and contracting for Global and International categories to put in place the right suppliers. Negotiates at tactical and strategic levels to develop local, regional, global company contracts.

Qualifications

Education:
* Required: BS in Business, Finance, Marketing or related field strongly preferred.
* Preferred: MBA or advanced degree and/or relevant certification is desirable.

Experience:

Required:

* 5+ years experience in strategic sourcing (global category management) or in role related to contact center strategy development and execution.
* Knowledge of Procurement related business processes.
* Demonstrates solid leadership capabilities at the Manager level, with particular strengths in collaboration, written and verbal communications, and cross-functional teamwork.

Preferred:

* Experience in outsourcing, strategic supplier management, contract centers and international business also desirable.

LI-AS2

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition GOO000125.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Goods Purchasing

Primary Location: US-PA-West Point
Other Locations: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Sourcing-Manager-Contact-Centers-Job-PA-19486/1858703/185870318587032012-06-15Merck/MSDGoods Purchasingfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The RNA Therapeutics Bioinformatics Co-op will work closely in a team environment at our West Point, PA site with Merck scientists in the exciting new discipline of RNAi therapeutics. Merck is committed to developing RNAi therapy for treatment of diseases with unmet needs.

The responsibilities of this position include:

* Contributing to the development of potential targeted delivery reagents and RNA therapeutic and tool compound candidates through analysis of in vitro and in vivo assay data, microarray data.
* Data management, and maintenance and development of informatics and statistical tools and workflows.
* Utilizing basic statistical and programming skills to support research projects, including data management and maintenance of informatics tools and workflows.

This is a paid 6 month co-operative assignment. Housing or housing subsidy is not available as part of this program and if required by the student must be funded 100% by the student.

Qualifications

Education:

* Pursuing Bachelor's degree in biochemistry, biological sciences, biomedical engineering, computer sciences on a bioinformatics track or a related field.

Required:

* Available for full-time employment for 6 months with a targeted start date in September 2012
* Currently enrolled in an academic program and will be returning to school following this assignment
* General computer knowledge, good communication skills, solid problem-solving skills and attention to detail and to quality control are required.

Preferred:

* Some programming experience (any language)
* Basic laboratory skills are preferred.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #RNA000173.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-PA-West Point

Job Type
: Co/Op
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-RNA-Therapeutics-Bioinformatics-Co-op-Job-PA-19486/1883039/188303918830392012-06-15Merck/MSDCo/Opfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck is seeking a Bioinformatics and Information Technology Intern for our R&D facility in Rahway, New Jersey. In this role, you will help the Genetically Engineered Models (GEM) group further develop and update their DataBase Portal and Web Site to provide current data and content for the global Merck community and our network of CROs (contract research organizations) in Europe. The GEM department mission is to provide cutting edge rodent genetic models and phenotyping/pharmacology data in support of drug discovery programs by generation and utilization of models to provide target validation, efficacy, and compound data as part of Basic Research.

The professional in this position will become part of the GEM department by working to update our Merck internal database portal for GEM data (called MouseTrap) which allows 24/7 access to Genetically Engineered Models data and documents. In addition, you will work to update the GEM dept internal website (called MyMouse) for information and content, and develop ideas for continued database and Website sustainability and ease of use. You will be required to work both in a team setting as well as independently as part of and with the GEM dept, with Merck's IT support personnel, and with specific external international scientific staff. You will be asked to provide opinion and insight as well as learn, as DataBase Portals as well as Websites are meant to dynamically change and improve over time.

This is a 9-11 week, paid internship beginning in June 2012. Housing will be provided to those who meet distance requirement.

Qualifications

Required:

* Currently enrolled in Bachelor, Master's or PhD program in a BioInformatics, Computer Science, Biology or Genetics
* Available June 2012 for 10-12 weeks
* Good communication skills
* Ability to work independently

Preferred:

* Strong Bio Database knowledge or interest
* Strong knowledge of website technologies
* Experience with PHP, MySQL, and/or UNIX
* Knowledge of Biology or Genetics

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #PHA001050.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-NJ-Rahway

Job Type
: Intern
Employee Status: Regular

Travel
: No
Number of Openings: 1

Relocation Provided
: Domestic (within country)]]>http://jobs.merck.com/job/Rahway-Bioinformatics-and-Information-Technology-Research-Internship-2012-Job-NJ-07065/1729548/172954817295482012-06-15Merck/MSDInternfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Entry level position. Processes the sites outbound shipments and/or orders ensuring that all materials are handled, packaged, and documented in compliance with the applicable government agencies regulations while providing excellent service to the site's customers. Serves as order fulfillment and customer service agent for customers and Merck personnel in support of research and MMD supply orders to include distribution, invoicing and shipment delivery. Responsible for the preparation of documentation, order entry, and acknowledgement. Individual processes customer orders and addresses customer inquiries to support on-time delivery of the correct product in the specified quantity

* Domestic and international order fulfillment. Position may or may not include the activity of pick, pack, and shipping depending on the site the position is located.
* Ensures the preparation of all documentation related to shipments including: proformas, any local documents and invoices within select timelines.
* Role includes problem solving and customer service support; including coordinating shipping arrangements, proactive review to ensure timely shipment and respond/investigate customer inquires.
* Communicates any changes to order status to all appropriate individuals/ customers along the supply chain.
* Responsible and accountable for accuracy in invoicing (proforma/ pre-invoicing) and assures all required documentation is generated and accompanies each domestic or international shipment.
* Maintains knowledge of current procedures and business issues so as to facilitate effective and practical solutions to all customer orders, complaints and inquiries.
* Responsible for inputting and maintaining metrics to report monitor and improve customer service.
* Responsible for follow-through with customer's complaints,
* Identifies and supports the implementation of business process changes which are consistent with departmental and/or Merck continues improvement initiatives.
* Supports the review and creation of departmental SOPs.
* Adherence to DOT, IATA and other various regulatory agency requirements

Qualifications

Education:

* Required: High School Diploma or equivalent.
* Preferred - Bachelor's degree may be accepted in lieu of some work related experience.

Experience:

Required:

* Shipping experience.
* Must possess strong interpersonal and communication skills (both written and verbal) as well as a demonstrated ability to anticipate and solve problems.
* Must be able to manage multiple priorities simultaneously.
* Excellent performance in the areas of attention to detail, accuracy, organization and follow-up.
* Must demonstrate exceptional judgment and a genuine willingness/ desire to develop successful business relationships with customers.
* Practical experience in customer service, warehousing, distribution or related activities.
* Experience with computer systems/ databases are also desirable.

Preferred:

* DOT/IATA certification
* 1-2 years of shipping experience

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #TRA000603.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Transportation

Primary Location: US-NJ-Rahway
Employee Status: Regular

Travel
: No
Number of Openings: 2

Hazardous Materials
: Packing and Shipping only, various]]>http://jobs.merck.com/job/Rahway-Transportation-Specialist-Job-NJ-07065/1891867/189186718918672012-06-15Merck/MSDTransportationfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Utilizing the technologies of immunochemistry, mass spectroscopy, genomics, molecular pathology and flow cytometry the Clinical Development laboratory (CDL) is responsible for biomarker assay development, fit-for-purpose validation, clinical biomarker sample analysis and for coordinating the overall strategy and technical efforts in the development and regulatory approval of companion diagnostics at select diagnostic partners.

Job Responsibilities

* Develop, validate and implement clinical flow cytometry biomarker assays to support biomarker strategy.
* Perform in-house clinical sample analysis and manage flow cytometry assay outsourcing to support both US and global clinical studies.
* Evaluate & interprets analytical/scientific data. Perform assay trouble shot to ensure successful assay implementation.
* Write Assay Validation Reports and Clinical Sample Analysis Summary Reports
* Serve as CDL representative to clinical development teams and biomarker teams

Qualifications

Education:

* BS with 6-8 years of flow cytometry lab experience
* Ph.D. in Immunology, Cell Biology or related areas with at least 1 years of additional research or industry experience
* MS in Biomedical Science with 4-6 years of flow cytometry lab experience

Required:

* Scientific background in Cell Biology or Life Science research with broad knowledge of biomarker technologies
* Extensive hand-on experience in flow cytometry, cell-based assays and cell culture
* Capability of initiating, leading, and successfully completing scientific projects with strong problem solving skills
* Capability to follow SOPs, keep files and documentations well-organized and pay attention to the details
* Willingness to multitasking with a goal-oriented working style
* Desire to work in a collaborative team environment
* Strong verbal/written communication skills to clearly communicate scientific objectives and results

Preferred:

* Experience in clinical Flow Cytometry lab leading clinical assay development and validation
* Experience in managing clinical biomarker assay outsourcing
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003582.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-MG1

Job
: Bio/Immuno Assay Development

Primary Location: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Human tissue and Chemicals]]>http://jobs.merck.com/job/Rahway-Research-Biochemist-Job-NJ-07065/1835819/183581918358192012-06-15Merck/MSDBio/Immuno Assay Developmentfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Reporting to the Senior Director / Director of Biologics Analytical Sciences, the incumbent will be responsible for defining and managing the analytical development, method transfer and quality control functions in support of in-process, release and stability testing of drug substance and drug product for multiple late-stage biopharmaceutical development programs; will provide oversight and participate in the management and monitoring of cGMP-compliant contracted manufacturing and product and stability testing activities; and will work with quality assurance, compliance and regulatory functions to meet project demands and contribute to submissions to regulatory authorities.

The Associate Director of Biologics Analytical Sciences will be responsible for but not limited to the following:

* Supervise and guide development/optimization of analytical methods for testing and characterization of biopharmaceutical products, including biochemical assays, HPLC, CE, electrophoretic and immunochemical methods and methods related to drug product safety. Collaborate guide and influence assay development team members (internal and CRO/CMO-based) during development of new methods, method optimization and feasibility studies.
* Manage method transfer and preparation and approval of SOPs, validation protocols and method validation reports; review and revise SOP's; review and contribute to regulatory filings.
* Monitor analytical deviations/OOSs, lead laboratory investigations and participate in manufacturing-related investigations. Proactively incorporate learnings to improve and influence method development and optimization.
* Perform on-site representation (person-in-the-plant) during testing of drug substance/product.
* Manage and guide drug substance/product stability programs and drug product expiration/retest date notifications.
* Where appropriate, serving as primary contact with CROs/CMOs responsible for in-process, release and stability testing and bioanalytical testing in support of manufacturing development, production, preclinical and clinical activity.
* Expected to participate in the management and control of document/records for GMP and GLP operations.

Qualifications

Education:

* Ph.D. in a scientific discipline, i.e. biology, chemistry, engineering, etc. and a minimum of 8 years experience in the biotechnology/pharmaceutical industry, including at a minimum of 4 years experience involving quality control laboratories in a facility manufacturing clinical drug substance and/or drug product for US and/or EU studies.

Required:

* Thorough knowledge of biochemistry, bioassay and microbiological methods and associated instrumentation; knowledge of protein stability assessment
* Experience in validation and transfer of methods used for characterization of biological products
* Working knowledge of current Good Manufacturing Practices (cGMPs) for the US and EU, Good Laboratory Practices (GLPs), and ICH guidelines as they relate to testing and characterization efforts for late phase clinical and commercial drug supply and/or biopharmaceutical production
* Ability to prioritize and successfully manage complex and competing projects
* Excellent communication and organizational skills
* Experience interacting with contract manufacturers and/or partners
* Ability to proactively mitigate quality/regulatory risks
* Motivated team player with proven leadership abilities

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PRO009263.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Process Engineering

Primary Location: US-NJ-Rahway
Other Locations: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Associate-Director-Biologics-Analytical-Sciences-Job-NJ-07065/1708752/170875217087522012-06-15Merck/MSDProcess Engineeringfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview:

Responsible for providing comprehensive financial & economic analysis support to Research and Development (R&D) Division. Responsibilities include development of financial/economic analyses in support of executing business strategy, operating model changes, site shutdowns, site/function expansion, integration and restructuring activities. All financial analysis related to major capital investment and financing decisions fall within scope. Incumbent must be an effective problem-solver across a broad array of functions and responsibilities. Must possess exceptional business acumen and modeling skills.

Primary Activities

* Prepares financial analyses and valuation models to evaluate business proposals or opportunities in support of Merck Research Labs (MRL), including risk assessment , sensitivity analysis and monte carlo simulation. Maintains and updates MRL business case model to reflect implementation plan, and inform realization metrics.
* Develops decision frameworks for assessing multiple business opportunity scenarios including, but not limited to, cycle time valuations, alternative development model valuations, out licensing opportunties, and operating model changes..
* Interacts with area heads, department heads, and administrative personnel throughout the Division, and with various corporate support Personnel to develop business cases and economic analyses.
* Develops economic models of new R&D operating models & strategies.
* Incumbent will be required to analyze complex issues, identify business opportunities and risks, present findings and/or results to MRL/Finance senior management, and manage complex activities involving staff of various levels.
* Reviews and financially analyzes major Capital Projects, including economic assessment of alternatives (NPV/NPC, IRR, payback, etc.), and financing decisions where appropriate.
* Continuously work to benchmark and improve financial evaluation and modeling methodologies

Qualifications

Education Requirements:

* BS/BA (Finance/Economics/Science/Engineering Preferred)

Required

* Knowledge of corporate finance and statistical concepts as it relates to valuation, analysis and decision models.
* A minimum of 3 years of demonstrated experience in a business or financial analysis related role.
* Strong business acumen

Preferred

* MBA/CFA
* Understanding of Pharma R&D preferred to help frame key business questions, and to construct appropriate tools and decision frameworks
* Technical knowledge in advanced modeling and monte carlo simulation.

·

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. merck.com/careers to create a profile and your resume for requisition # FIN000726.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Financial Analysis

Primary Location: US-NJ-Rahway
Other Locations: US-PA-North Wales, US-PA-Upper Gwynedd, US-PA-West Point, US-NJ-Whitehouse Station, US-Pennsylvania
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Finance-Manager%2C-Merck-Research-&-Development-Job-NJ-07065/1889117/188911718891172012-06-15Merck/MSDFinancial Analysisfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


* Under the general direction of an Area Head or Manager, the incumbent is responsible for providing guidance and supervision to hourly employees in completing process, production, maintenance, or production support activities. Responsible for motivation, training, and problem resolution for subordinates.
* Uses team work and good communications to administer personnel policies and the local agreement.
* Ensure the area adheres to Good Manufacturing Practices, approved process steps, SOPs, quality procedures, safety, and environmental standards while operating within the profit plan.

The function of this position is to assure that products manufactured within the integrated process team (IPT) comply with cGMPs, operating procedures, and other applicable regulations. The responsible person will manage the direct processing of materials and supervise the associated hourly workforce within the IPT. The position has specific responsibility for motivating the workforce, work performance, scheduling, task coordination, equipment and area preparation, and administration of personnel policies and procedures.

* Maintain control of processes and product quality by developing appropriate procedures and ensuring compliance with cGMPs, safety and environmental regulations.
* Monitor the manufacturing processes during the shift.
* Participate in internal sub-teams focused on process improvements by using lean methodology.
* Work with IPT members from Quality and Technical Operations to properly handle unplanned events and ensure that corrective actions are implemented.
* Ensure that personnel under his/her supervision are properly trained in cGMPs, procedures, good documentation practices and regulatory matters.
* Monitor personnel practices to ensure compliance with SOPs, practices and regulations.
* Participate in design and implementation of training and development programs.
* Supervise and motivate hourly employees.
* Collaborate with IPT members in the identification and implementation of continuous improvement initiatives and action plans.
* Support activities in the areas of cost reduction, efficiency, productivity, operational excellence and lean practices.

Qualifications

Education:

* Required: HS Diploma with at least 5 years of manufacturing experience
* Preferred: B.S. or B.A. degree in Science, Engineering, Business or equivalent.

Required:

* Ability to focus on and obtain results.
* Ability to effectively collaborate with and manage a work team.
* Ability to enact conflict resolution.
* Ability to effectively respond to change.
* Excellent analytical and organizational skills.
* Leadership and interpersonal skills to motivate direct reports and peers toward the achievement of production goals.
* High personal integrity, credibility and energy.
* Flexibility to perform related tasks to support the business.

Preferred:

* Experience in responsible line or staff support position related to manufacturing.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition MAN001699.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Manuf./Operations Generic

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Associate-Manufacturing-Supervisor-Job-PA-19486/1871143/187114318711432012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Administration of eSTARS, Merck's electronic supplier tracking and reporting system for Supplier Management. Administration includes managing global supplier data changes, managing/controlling access to eSTARS, clean-up of eSTARS data and system enhancements.

* Conducting Supply chain mapping.
* Identifying trends and/or root cause(s) to help develop new initiatives and process improvements. This may include assisting in the preparation, coordination and delivery of Quality and/or Procurement Senior Management presentations at management conferences, training programs, Quality Council, Supplier Development & Performance Management leadership meetings.
* Serving as a primary contact for Supplier Development and Performance Management regulatory database searches, internal/external surveillance information, analysis, and communication.
* Maintaining various Supplier Quality Assurance databases and internal website.
* Leading projects for supplier quality improvements and/or supplier efficiencies using lean six sigma tools.

Qualifications

Required:

* BS/BA in Engineering, Science, Business or related field.
* Minimum 5 years experience in commercial, business, quality, technical or manufacturing operations

Preferred:

* Knowledge of six sigma methodology
* Microsoft Access, Visio and Project
* A thorough knowledge of cGMP's, technical writing skills, data management, collection and analysis.
* A strong knowledge of and broad experience in Quality Assurance.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition QUA002946.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Qual Assurce - 3rd Party Manuf

Primary Location: US-PA-West Point
Other Locations: US-NJ-Whitehouse Station, US-NJ-Summit
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-SDPM-Data-Co-ordinator-Job-PA-19486/1883043/188304318830432012-06-15Merck/MSDQual Assurce - 3rd Party Manuffull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview

As part of the Vaccine Product & Technology Operations (VAPTO) organization, Global Vaccine Technology & Engineering is seeking a highly motivated individual to partner with the Operations, Vaccine Manufacturing Sciences & Commercialization, Merck Research Laboratories, Quality Operations, Bio-Sterile Validation and Regulatory groups to meet the targeted supply and compliance initiatives within VAQTA Manufacturing. Specifically, you will be responsible for providing scientific support in the production of VAQTA Bulk Vaccine in the Global Vaccine and Sterile Manufacturing organization.

In this role you will be:

* Supporting the design, shakedown and start up of a new VAQTA bulk manufacturing suite. Responsibilities include supporting process development, facility start-up, process validation, product comparability and licensure activities.
* Providing technical support for manufacturing, including resolution and reduction of process deviations, support for regulatory filings and inspection activities, development and implementation of process improvements, and supporting complex technical investigations.
* Executing bench and full-scale developmental studies associated with the demonstration of new products/processes or the transfer of in-line products/processes to new manufacturing facilities.
* Executing projects against key timing commitments, with appropriate documentation and change control.

Qualifications

Education:

* B.S. in Chemical Engineering or Biological Science.

Preferred:

* M.S. in Chemical Engineering or Biological Science.

Required:

* Minimum of 5 years post-bachelors degree experience in the biological/pharmaceutical/chemical manufacturing industry (can be obtained through a combination of post-graduate education and work related experience).

Preferred:

* Demonstrated ability to work both independently and as a part of a team.
* Strong technical problem-solving abilities.
* Demonstrated effective written and verbal communication skills.
* Strong collaboration and leadership skills .
* Experience in technical support or production of sterile pharmaceutical products, bulk biological products or general aseptic manufacturing environments.
* Experience in process validation, facility start-up and facility licensure activities.
* Experience with one or more of the following biological manufacturing operations:
* Cell culture processes.
* Production scale chromatography and purification equipment.
* Viral inactivation.
* Alum adsorption processes.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition PRO009624.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Process Engineering

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Senior-Engineer-Job-PA-19486/1883046/188304618830462012-06-15Merck/MSDProcess Engineeringfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Manufacturing Engineer is responsible by assignment for the:

* Development, design , construction, qualification, or initial and sustained operation of vaccine and pharmaceutical, packaging processes, equipment, components, and facilities using new or existing technologies for new and in-line human and vaccine products.
* Analysis of packaging related processing, equipment, component, and facility problems through analytical thinking and the execution of laboratory/line testing.
* Development of sound scientific justification for planned packaging related process,equipment, component, and facility changes.
* Technology transfer of products and packaging processes to or from MMD West Point Packaging Operations.
* Begin to develop working relationship with MRL on technology transfer issues and significant packaging issues.
* Development of working relationship with MMD West Point Packaging Operations and with architectural and engineering firms, construction management firms, outside equipment vendors, and state and federal agencies (FDA, EPA, etc.) with whom Merck interfaces.
* Analysis of current safety/environmental and drug and/or biological product regulatory requirements and determination of the impact on Merck packaging operations.
* Assistance in the development of corporate engineering, quality and/or environmental policies/standards and in the assessment of compliance status for MMD West Point Packaging Operations.
* Assists in documentation preparation, maintenance, and review including SOP's, process descriptions, atypical process reports, customer complaint investigations, and change requests.
* Participates in the Profit Improvement Program by executing test plans and implementing project plans.
Responsible for printed component design (labels, cartons, circulars, films, shipper end labels) using ArtiosCAD and non-printed component design (shippers) in support of vaccine packaging operations.

* Responsible for interfacing with printed component vendors to investigate quality related deviations, including root cause analysis, corrective action/preventive action development, and quality impact assessment.
* Responsible for the initiation and execution of IOQ document and/or test protocols for the use of new or revised printed components on packaging equipment, or qualification of new vendors.
* Responsible for the initiation of change control documentation for the development of new printed component templates.

Qualifications

Education Minimum Requirement:

* Engineering (Packaging Engineering is 1st preference; Mechanical Engineering is 2nd preference)

Required Experience and Skills:

* Printed component design experience (labels, cartons, circulars, films, shipper end labels)
* ArtiosCAD experience
* Technical writing experience, specifically deviation management, change control, corrective action/preventive action development, test protocols, IOQ documentation, etc.

Preferred:

* Non-printed component design experience (shippers)
* Familiarity with industry standards for packaging component design testing, such as label adhesion, distribution/thermal, print scuffing, etc.
* Interfacing with supplier and vendors

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAN001350.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Manuf./Operations Generic

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: No]]>http://jobs.merck.com/job/West-Point-Manufacturing-Engineer-Job-PA-19486/1703544/170354417035442012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Reporting to the Senior Director / Director / Associate Director of Biologics Analytical Sciences, the incumbent will be responsible for managing the analytical development, method transfer and quality control functions in support of in-process, release and stability testing of drug substance and drug product for 1 - 2 late-stage biopharmaceutical development programs; will participate in the management and monitoring of cGMP-compliant contracted manufacturing and product and stability testing activities; and will work with quality assurance, compliance and regulatory functions to meet project demands and contribute to submissions to regulatory authorities.

Responsibilities include:

* Supervise development/optimization of analytical methods for testing and characterization of biopharmaceutical products, including biochemical assays, HPLC, CE, electrophoretic and immunochemical methods and methods related to drug product safety. Collaborate closely with assay development team members (internal and CRO/CMO-based) during development of new methods, method optimization and feasibility studies.
* Manage method transfer and preparation and approval of SOPs, validation protocols and method validation reports; review and revise SOP's; contribute to regulatory filings.
* Monitor analytical deviations/OOSs, lead laboratory investigations and participate in manufacturing-related investigations.
* Perform on-site representation (person-in-the-plant) during testing of drug substance/product.
* Manage drug substance/product stability programs and drug product expiration/retest date notifications.
* Where appropriate, serve as primary contact with Contract Research Organizations (CROs)/Chief Medical Officers (CMOs) responsible for in-process, release and stability testing and bioanalytical testing in support of manufacturing development, production, preclinical and clinical activity.
* Expected to participate in the management and control of document/records for GMP and GLP operations.

Qualifications

Education:

* Ph.D. in a scientific discipline, i.e. biology, chemistry, engineering, etc., with a minimum of 3 years experience in the biotechnology/pharmaceutical industry, including at least 1 - 2 years experience involving quality control laboratories in a facility manufacturing clinical drug substance and/or drug product for US and/or EU studies; or
* B.S. in a scientific discipline and a minimum of 6 years experience in the biotechnology/pharmaceutical industry, including at least 2 - 3 years experience involving quality control laboratories in a facility manufacturing clinical drug substance and/or drug product for US and/or EU studies

Required:

* Thorough knowledge of biochemistry, bioassay and microbiological methods and associated instrumentation; knowledge of protein stability assessment
* Experience in validation and transfer of methods used for characterization of biological products
* Working knowledge of current Good Manufacturing Practices (cGMPs) for the US and EU, Good Laboratory Practices (GLPs), and ICH guidelines as they relate to testing and characterization efforts for late phase clinical drug supply and/or biopharmaceutical production
* Ability to prioritize and successfully manage complex and competing projects
* Excellent communication and organizational skills
* Experience interacting with contract manufacturers and/or partners
* Ability to proactively mitigate quality/regulatory risks
* Motivated team player with proven leadership abilities

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PRO009265.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Process Engineering

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 2]]>http://jobs.merck.com/job/West-Point-Principle-Analytical-Scientist-Biologics-Analytical-Sciences-Job-PA-19486/1708753/170875317087532012-06-15Merck/MSDProcess Engineeringfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Responsibilities include and are not limited to the following:

* Planning and execution of assigned clinical programs on new or marketed drugs - includes all phases of clinical development, study design, and study monitoring.
* Includes initiation and monitoring of clinical trials.
* Preparation of clinical operational plans and protocols for clinical research trials.
* Analysis and summarization of clinical data from studies to which he/she is assigned.
* Preparation of progress reports and summaries regarding drug safety and efficacy
* Presentation of research findings at national and international scientific meetings.
* Participation in preparation of manuscripts for publication in peer-reviewed journals.
* Preparation of regulatory agency documents and participation in regulatory agency meetings.

Qualifications

Education:

* M.D or M.D./Ph.D, plus Board Certification or Eligibility is preferred

Required:

* Strong interpersonal skills, as well as the ability to function in a team environment are essential

Desired:

* Board certification/eligibility in endocrinology, with special emphasis in diabetes
* Experience in industry or academia
* Demonstrated record of scientific scholarship and achievement
* Prior specific experience in clinical research
* Prior publication is desirable, however not necessary

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CLI002440.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Clinical Research (M.D.)

Primary Location: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Rahway-Associate-DirectorDirector%2C-Clinical-Research-DiabetesEndocrinology-Job-NJ-07065/1299128/129912812991282012-06-15Merck/MSDClinical Research (M.D.)full-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Coordinate closely with Neurosciences Franchise Head, Merck Senior Leadership, and other internal as well as external partners to define requirements for Knowledge Discovery/Knowledge Management (KD/KM) capabilities. This position also maintains strong relationships with leaders across all Merck Research Laboratory (MRL) functions, and is recognized as an industry leader in the field of information science/knowledge management. This position also leads cross-divisional/functional teams to develop new information/knowledge management capabilities, and collaborates with KD/KM Leadership on development and delivery of the One Merck Digital Library.

* Coordinate with Research Heads for franchise/disease area of responsibility and respective Licensing committees, and to proactively provide Knowledge Discovery/Knowledge Management (KD/KM) support.
* Develop and execute a KD/KM Research Services strategy to deliver Scientific and Competitive Intelligence in support of strategic decision-making in areas of responsibility.
* Coordinate with the KD/KM Leadership Team, and internal and external partners to design and deliver industry-leading Research Services capabilities.
* Provide Information Science Leadership and Subject Matter Expertise for strategic MRL Initiatives (e.g., Connectivity) and contribute to content evaluation processes for the One Merck Digital Library.

· Provide scientific and project leadership on multiple KD/KM projects in support of research activities (e.g., target identification/validation and prioritization; lead identification & optimization; preclinical development; and identification of potential external partnership opportunities).

· Leverage KD/KM tools, databases, systems and other knowledge resources to provide optimal support to R&D project teams, in areas of interest including migraine, pain, Alzheimer's disease, Parkinson's disease, psychiatric diseases, sleep disorders, and ophthalmology.

· Manage direct reports including other KD/KM scientists, contractors/consultants, and cross-functional project teams to deliver high quality results to impact decision making in R&D.

Qualifications

Education:

* Minimum of a Masters Degree required, Ph.D., M.D., D.V.M. or other equivalent educational background in one of the Life Sciences areas or equivalent educational experience

Required :

* Requires excellent oral and written communication skills.
* Ability to partner effectively with senior management,
* Demonstrated experience managing a team of scientists and contract/contingent resources,
* Ph.D. level knowledge and expertise in the Life Sciences with an ability to define and execute a Research Services Strategy that will enable decision-making within, and collaboration between all levels of the organization.
* Analytical (natural language processing, text mining, data visualization, etc.) skills are also critical for this position.
* Minimum (10) years of experience in successfully conducting and managing drug research and development projects in the biotechnology/pharmaceutical industry

Preferred:

* Project consulting and partnering experience with senior leaders of drug R&D.
* Recognized as an industry leader in the field of information science/knowledge management.
* Deep knowledge of at least one Life Sciences area, plus broad drug R&D knowledge.
* Demonstrated ability to take on new projects and successfully deliver results in fast-paced, dynamic and multifunctional environments.
* Demonstrated proficiencies in the application of KD/KM and informational sciences technologies to impact drug R&D (e.g., Linguamatics, STN, Dialog, Pipeline Pilot, Spotfire, Pathway Analysis tools and pipeline databases such as TPharma or Prous).
* Proven record of innovative and critical thinking, and excellent problem-solving ability.
* Proven track record of high quality scientific publications in peer-reviewed journals.
* Proven skills in managing cross-functional project teams to deliver impactful results

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # COR000150.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Corp. Dev. & Licensing Generic

Primary Location: US-NJ-Rahway
Other Locations: US-NJ-Kenilworth, US-PA-West Point, US-MA-Boston
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Research-Services-Group-Lead-Job-NJ-07065/1598880/159888015988802012-06-15Merck/MSDCorp. Dev. & Licensing Genericfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck Manufacturing Division's Global Science, Technology & Commercialization (GSTC) organization is accountable for stewardship of manufacturing technologies within Merck and either directly accountable or supporting the late stage product and process development, commercialization, launch and support of Merck's pharmaceuticals, consumer care, vaccines and biologics. It also oversees a commercialization network of sites across the globe that directly manufactures experimental and commercial supplies for Merck. GSTC is almost 2000 people strong with people at almost every site globally in the Merck network. The creation, organization, retention and purposeful dissemination and reuse of all product, process and organization knowledge is a cornerstone of GSTC's competitive capabilities. The Knowledge Management mission is to manage Merck's existing & future assets (our competitive advantage); Sustain Merck's knowledge both within and across projects and functional boundaries for the full product life cycle, Help people find, organize, and share the knowledge they already have; Increase collaboration and knowledge sharing & Get the right information to the right people, in the right context and at the right time in ways that will measurably improve the performance of our business.

The Scientific Knowledge Management Specialist will promote knowledge sharing throughout the organization's operational business processes and systems. A seamless exchange of information will be accomplished by strengthening links between knowledge sharing and the information systems and improving integration among the organization's information systems. The Knowledge Management (KM) Specialist plays a vital role in the successful installation and realization of the GSTC KM initiative, which is currently in the design phase. These KM Specialists will report to the KM Program Leader or Sponsor and be part of the KM Office, which will provide a center of expertise on knowledge management for GSTC. Their responsibilities include facilitation of the design and implementation for existing and new KM projects.

The Specialists would be responsible for appropriately documenting any KM approaches in templates suitable for replication and serve as the owners of the general KM solutions. Their ongoing role would include serving as the focal point and key team member / facilitator for all replication activities, trainer of new users, advisor /monitor for implemented KM projects, and facilitator of new KM projects.

Key Responsibilities:

* Facilitates, monitors, and maintains the use and improvement of common knowledge management processes and approaches across the organization.
* Monitor and report progress of KM initiatives to the Knowledge Management Leader
* Work with business leaders and stakeholders to identify areas of opportunity and gaps in knowledge flow
* Support the design, implementation and enhancement of core knowledge management approaches used to support critical knowledge flow within and across the business and knowledge domains
* Promote knowledge management approaches (e.g., Communities of Practices, Transfer of Best Practices, Lessons Learned, common knowledge flow processes, and collaborative tools) to facilitate sharing of ideas, practices, and lessons learned and work among internal teams and external partners
* Monitor the effectiveness, maintenance, and use of the IT tools and systems as they apply to KM, and implement improvements.
* Help disseminate information about the organization's knowledge management program to internal and external audiences, including organizing knowledge-sharing events (such as knowledge fairs, site visits, interviews), maintaining communications on knowledge sharing across the organization, participation in orientation and training sessions, and preparation of brochures/presentations

Competencies:

* An understanding of the principles of knowledge management.
* Promotes knowledge management and knowledge-sharing behaviors across the organization.
* Up to date with the latest technology/social tools that supports knowledge management.
* Experience in chartering and sustaining communities of practice is highly desirable.
* Clear understanding of business processes and good working knowledge of organizational and business strategy.
* Strong project management oversight and also "hands-on skills" as needed.
* Strong facilitator, agent of change, and communicator.
* Works effectively as a team member.
* Ability to achieve consensus and collaboration across many business units.
* Ability to think strategically in terms of culture, behavior, business processes, and tools.
* Ability to manage differences and bring people together to share knowledge in terms of culture and behavior, business processes and technological tools.
* Good appreciation of customer needs, at both operational and strategic levels.
* Ability to travel domestically and internationally if necessary.

Qualifications

Education:

* Bachelor's degree required.
* Degree field in Engineering, Chemistry, Natural Sciences, Applied Sciences or Pharmaceutical Sciences preferred Master's or PhD highly preferred.

Required:

* 8 years of experience in one or more of the following: pharmaceutical/biotech industry, GMP manufacturing, Technical Operations, Process Development, Product Lifecycle Project Management within an FDA regulated organization, Regulatory Agency focusing on Pharmaceuticals/Biologics, and/or Knowledge Management function within an FDA regulated organization required.
* If a Master's or PhD is completed will consider experience less than 10 years (ie; Master's with 5 years and PhD with 2 years of above experience)

Preferred:

* Experience with Virtual Information Networks, keeping like organizations aligned with proper information sources or the Retention of Critical Knowledge across an organization. Both are highly preferred
* Experience in Knowledge Management preferential

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition BUS000487.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-AS1

Job
: Business Consulting

Primary Location: US-NJ-Rahway
Other Locations: US-PA-West Point, US-NJ-Summit
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Scientific-Knowledge-Mgmt-Specialist-Job-NJ-07065/1812617/181261718126172012-06-15Merck/MSDBusiness Consultingfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Process Development and Commercialization (Biologics) is responsible for the commercialization of biological processes (novel therapeutic proteins and follow-on biologics) from Phase III through launch and transfer to supply. Activities include process development, scale-up and optimization, interfacing with a network of facilities for product manufacturing and subsequent optimization, validation and filing documentation, and transfer to supply network. PDC is part of the Merck Manufacturing Division.

Under the general scientific and administrative direction of the Principal Engineer in Downstream Processing within PDC and working in conjunction with internal and external partners, this individual will support late stage bulk process development, characterization, technology transfer, clinical manufacturing, and validation studies associated with the development and implementation of bulk processes, systems and facilities related to therapeutic proteins (TPs). The individual will need advanced tech transfer and experimental skills, focusing on downstream processing.

Technical Scope:

* Participates in late stage process development, characterization, and validation with line-of-sight for licensure and commercialization. Primary focus will be on downstream processing, but with a working knowledge of the various aspects of product manufacture and functional area interdependencies, including upstream processing (e.g., cell culture, harvest), analytical, and site readiness.
* Actively interacts with internal and external counterparts with tech transfer and GMP site readiness activities. May represent functional area on cross-functional and cross-divisional teams.
* Responsible for process characterization and process validation studies to be performed either in-house or externally (including external partners, CROs and CMOs). Provides technical leadership and either execution of (internal), or management of (external) the design of experiments supporting characterization.
* Authors required regulatory and technical documentation, according to standard Merck practices.

Culture and Interactions with Others:

* Shows flexibility and agility in responding to changing needs across PDC and Merck.
* Actively listens and participates in discussions and is appropriately assertive in expressing own ideas. Gives timely constructive feedback when appropriate.
* Delivers what is needed on-time and holds self and team accountable for commitments, decisions, actions and behaviors.

Qualifications

Education:

* BS or MS in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry with at least 4 (for BS) or 2 (for MS) years relevant experience.

Required:

* Technical expertise in large scale downstream processing of biological molecules from mammalian- and/or microbial based expression systems, including lab based systems for scaled-down experimentation
* Excellent oral and written communication skills and ability for independent project leadership
* Experience with technology transfer and scale-up of manufacturing processes for biologics manufacture
* Strong organizational skills; ability to prioritize tasks, track and communicate progress as needed
* Experience with downstream process development of biological molecules

Preferred:

* In-depth knowledge of chromatography, ultrafiltration (UF/DF), and viral filtration of therapeutic proteins desired
* Prior experience in late stage bulk process development, process characterization, process validation, site readiness, batch record reviews, authoring regulatory BLA sections and/or working with external contract organization for development and or manufacturing is a plus
* Working understanding of analytical methods to characterize biologics and /or US/EU regulatory requirements and / or working knowledge of cGMPs is a plus
* Demonstrated ability to lead and collaborate within cross-functional and/or remote teams

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition BIO003538.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-AS1

Job
: Bio Process-Purif/Recovery

Primary Location: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Project-Engineer-Scientist-Job-NJ-07065/1760780/176078017607802012-06-15Merck/MSDBio Process-Purif/Recoveryfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Process Development and Commercialization (PDC) (Biologics) is responsible for the commercialization of biological processes (novel therapeutic proteins and follow-on biologics) from Phase III through launch and transfer to supply. Activities include process development, scale-up and optimization, interfacing with a network of facilities for product manufacturing and subsequent optimization, validation and filing documentation, and transfer to supply network. PDC is part of the Merck Manufacturing Division.

Under the general scientific and administrative direction of the Principal Engineer in Downstream Processing within PDC and working in conjunction with internal and external partners, this individual will support late stage bulk process development, characterization, technology transfer, clinical manufacturing, and validation studies associated with the development and implementation of bulk processes, systems and facilities related to therapeutic proteins (TPs). The individual will demonstrate advanced skills to optimize business and technical processes. The individual will be a scientific leader within the department, and will mentor junior staff as well as serve as a subject matter expert (SME) on cross-functional teams. The individual may also be responsible for management of the interface between Merck and external partners for particular programs.

Technical Scope:

* Participates in late stage process development, characterization, and validation with line-of-sight for licensure and commercialization. Primary focus will be on downstream processing, but with a working knowledge of the various aspects of product manufacture and functional area interdependencies, including upstream processing (e.g., cell culture, harvest), analytical, and site readiness.
* Actively interacts with internal and external counterparts. Represents functional area on cross-functional and cross-divisional teams, and communicates the basis and implications of various process and project decisions from within the functional area to outside stakeholders.
* Responsible for process characterization and process validation studies either in-house or externally (including external partners, Contract Research Organization (CROs) and Chief Medical Officer (CMOs). Provides technical leadership for the design of experiments supporting characterization. Capable of managing remote teams for the execution of lab-based experiments with the ability to conduct hands-on experimentation as needed.
* Authors required regulatory and technical documentation. Ensures that process/product are developed and documented according to standard Merck practices.
* Provides technical support and leadership for Merck's manufacturing processes. Responsibilities include supporting technical due diligence, technology transfer and technical oversight of clinical manufacturing to external partners, including process monitoring, troubleshooting and continuous process improvement.

Culture and interactions with others:

* Shows flexibility and agility in responding to changing needs across PDC and Merck.
* Actively listens and participates in discussions and is appropriately assertive in expressing own ideas. Gives timely constructive feedback when appropriate.
* Applies new functional and core competencies in a manner that adds value to the organization and shows understanding of the links between individual and team performance.
* Identifies and utilizes appropriate communications channels to most effectively make contact with key customers, including internal and external partners, and keeps relevant parties informed on progress or issues.
* Delivers what is needed on-time and holds self and team accountable for commitments, decisions, actions and behaviors.

Qualifications

Education:

* BS or MS in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry with at least 6 years relevant experience.
* Or, Ph.D. in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry with at least 1-3 years experience.

Required:

* Technical expertise in downstream processing of biological molecules from mammalian- and/or microbial based expression systems.
* Excellent oral and written communication skills and ability for independent project leadership.
* Experience with technology transfer and scale-up of manufacturing processes for biologics manufacture
* Strong organizational and project management skills; ability to prioritize tasks, track and communicate progress as needed

Preferred:

* Experience with downstream process development of biological molecules required, with an in-depth knowledge of chromatography, ultrafiltration (UF/DF), and viral filtration of therapeutic proteins desired.
* Prior experience in late stage bulk process development, process characterization, process validation, site readiness, batch record reviews, authoring regulatory Biological License Application (BLA) sections and/or working with external contract organization for development and or manufacturing is a plus.
* Working understanding of analytical methods to characterize biologics and /or US/EU regulatory requirements and / or working knowledge of cGMPs is a plus.
* Demonstrated ability to lead and collaborate within cross-functional and/or remote teams.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CHE003388.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-AS1

Job
: Chemical Engineering

Primary Location: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Senior-EngineerScientist-Job-NJ-07065/1708743/170874317087432012-06-15Merck/MSDChemical Engineeringfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career

The position is an internship within the Global Clinical Trial Operations organization.

This person will work closely with analysts in the Integrated Development Platform (IDP) group on various technical projects and proof of concepts utilizing their strong analytical skills and computer science background.

The Future Talent Program features paid internships targeted to start in June 2012 for 10 - 12 weeks and will include one or more projects. Housing is available for those interns meeting the housing distance guideline. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals.

Open to U.S. Residents & Citizens only.

Qualifications

Education:

* Currently enrolled in college program in a computer science (or related) capacity

Required:

* Available June 2012 for 10-12 weeks
* Good communication skills

* Ability to work independently
* Able to work independently and with good communication skills

Preferred:

* Strong Java and XML skills
* Strong Database knowledge
* Strong UNIX and Shell scripts skills especially Linux
* Entry level person with strong knowledge of database technologies
* Strong analytical skills with Computer science background
* Knowledge in Oracle technologies and PL/SQL scripting
* Knowledge of C#, RDF, N-Triples, Linux experience
* PL/SQL

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # IT000255.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-NJ-Rahway

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-IDP-Services-Integration-Intern-Job-NJ-07065/1729549/172954917295492012-06-15Merck/MSDInternfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This is a six (6) month co-op position in the Chemical Process Development and Commercialization Group. This group is responsible for the: process development for new, organically synthesized pharmaceutical products.

During the first co-op term, the student assignments can include independent laboratory-scale development experiments, process design, and equipment evaluation, among others.

In the second term, students are usually assigned to work in a development team in the pilot plant, where they are exposed to large scale pharmaceutical chemical processing on a variety of projects and problems.

Qualifications

Education:

* Major in Chemical Engineering or Biological Engineering

Required:

* Strong personal character and ethics
* Academic achievement and analytical ability
* Good communication and interpersonal skills
* Good team player and able to work independently
* U.S. citizen, lawful permanent resident of U.S. or otherwise authorized to work in U.S.

**Please provide a resume that lists your GPA, both in your major and overall.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #ADM004958.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-NJ-Rahway

Job Type
: Co/Op
Employee Status: Regular
Number of Openings: 1

Hazardous Materials
: No]]>http://jobs.merck.com/job/Rahway-MMD-Co-op-Chemical-Process-Development-and-Commercialization-Job-NJ-07065/1729518/172951817295182012-06-15Merck/MSDCo/Opfull-timeUSDstarting0BSRahway, NJ, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Director of Device Quality Assurance will be responsible to develop and establish Quality business processes in support of the global device strategy for the entire portfolio of injectable proteins /biologics / device combination products (Merck BioVentures).

The Director of Devices Quality Assurance responsibilities include but not limited to:

* Establish a Quality plan and strategy
* Establishing the QA methodology, processes and procedures to follow by MMD
* Work in partnership across the organization (MRL, MMD, Commercial) and management levels to understand the requirements for each device and document the appropriate test accordingly.
* Partner with Device teams in the evaluation, selection and management of third party testing resources supporting devices
* Prepare regular management progress reports for QA devices
* Partner with Device Regulatory Lead and Sr Director of Device for determining and recommending to Sr. Management when a device is ready for different stages (sourcing, testing, manufacturing)
* Participate in audits of device component manufacturer. Make coordination with Division accordingly. Qualify and monitor Device component manufacturer
* Involve and provide input with Quality Agreements with device component manufacturer in partnership with Procurement
* Establish requirements for device specs and internal/external device validation.
* Partner with sites to oversee quality assurance for Final assembly & quality control
* Establish Quality test plan requirement
* Ensure and maintain internal and external change control process of device
* Prepare FMEA master plan
* Establish a robust process to manage enquiry and device complaints management system including to reach 3rd parties
* Establish a documented process to evaluate risks and mitigation plans prior to launch a device product. Ensure there is a process to manage and follow up corrective actions as part of complains management.
* Will be current of new device regulations and will build relationship in support of Regulatory advocacy.

Qualifications

Education Requirements:

BA / BS Degree (Engineering, Biological Sciences, Chemistry, Life Science/Science)

Preferred Education Requirements:

MS / MBA / PhD degree

Required Qualifications:

At least 8 years of QA experience with a minimum of 5 years recent experience with delivery device development and approval

Knowledgeable and track record of QA methodologies, tools and processes

Experience with development / approval of biologic injectable delivery devices

Ability to travel up to 35% of the time

Preferred Qualifications:

Lean Six Sigma Certification

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # QUA002619.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Qual Assurance & Ops Generic

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Director-Quality-Assurance-Drug-Delivery-Devices-Job-PA-19486/1483108/148310814831082012-06-15Merck/MSDQual Assurance & Ops Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The individual will work with teams consisting of statisticians and engineers supporting small molecule development, manufacturing, packaging, laboratory, supply, and stability. Areas of expertise include, but are not limited to, design of experiments (DOE), linear models, statistical process control (SPC), and exploratory data analysis (EDA). As required, the incumbent will also evaluate data for submission to regulatory agencies and pharmacopoeia. The incumbent may also serve on various company task forces and outside industry groups as appropriate. The individual should be able to work effectively with multiple technical disciplines. Knowledge of pharmaceutical manufacturing is a plus.

* Collects, organizes and summarizes data for statistical projects. Performs basic statistical analyses such as ANOVA models, process capability and control, linear regression, ANCOVA for stability studies. Generates a wide variety of statistical graphics adapted to the need of the statistical project.
* Applies basic and advanced statistical techniques and graphics and recognizes the need for more sophisticated methods.
* Develops or adapts sophisticated techniques to meet the needs of specific projects.
* Mentors junior staff members in the application of basic and advanced statistical methods and graphics. Prepares and conducts seminars throughout MMD to familiarize scientists and management personnel in the understanding of statistical techniques and methods.
* Proposes design of experiments and analysis plans through consultation with MMD personnel and teams.
* Contributes to the generation of objectives and hypotheses to be evaluated via statistical studies.
* Independently prepares oral and written reports to effectively communicate statistical study designs and the interpretation of statistical analyses.
* Reviews literature and attends appropriate seminars and classes in order to develop and maintain the necessary skill levels.
* Contributes talks to statistical meetings.
* Stays abreast of the advances made in statistics as well as the field of computer applications, and brings the relevant advances into group practices.
* Participates as a full member on internal and external teams providing statistical expertise.
* Evaluates the impact of new regulatory proposals to Merck operations.

Qualifications

Education:

* Masters in Statistics with a minimum of 10 years experience

or

* PhD with a minimum of 5 years experience

Required:

* The scope of technical skills expected is broad, including design of experiments, linear and nonlinear models, and univariate/multivariate statistical process control.
* Outstanding statistical computing skills with substantial experience in at least two of the following statistical software packages: SAS, S‑Plus/R, JMP, Minitab.
* Superior oral and written communication skills to convey statistical concepts and analyses to non-statisticians.
* Requires demonstrated resourcefulness and the ability to develop and implement innovative and new concepts/ideas.
* Demonstrated ability for managing and initiating change.
* Requires demonstrated leadership, ability to manage multiple projects/tasks simultaneously with competing priorities.
* Requires established ability to lead cross-functional teams effectively, motivate people, delegate appropriately and resolve conflicts.

Preferred:

* Knowledge of pharmaceutical manufacturing
* Undergraduate degree in chemistry, engineering, or related technical field.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition WQUA002899.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-AS1

Job
: Quantitative Sciences Generic

Primary Location: US-PA-West Point
Other Locations: US-NJ-Summit
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Scientific-Fellow-%28Manufacturing-Statistician-Small-Molecules%29-Job-PA-19486/1866485/186648518664852012-06-15Merck/MSDQuantitative Sciences Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The RNA Therapeutics - Biology Co-op will work closely in a team environment at our West Point, PA site with Merck scientists in the exciting new discipline of RNAi therapeutics. Merck is committed to developing RNAi therapy for treatment of diseases with unmet needs.

The responsibilities of this position include:

* Characterizing potential targeted delivery reagents
* RNA candidates through novel assays, elucidating pathway mechanisms, analyzing crucial disease - related RNA/proteins
* Data analysis
* Utilizing basic statistical and programming skills to support research projects, including data management and maintenance of informatics tools and workflows.

This is a paid 6 months co-operative assignment. Housing or housing subsidy is not available as part of this program and if required by the student must be funded 100% by the student.

Qualifications

Education:

* Pursuing Bachelor's degree in biochemistry, biological sciences, biomedical engineering or a related field.

Required:

* Available for full-time employment for 6 months with a targeted start date in September 2012
* Currently enrolled in an academic program and will be returning to school following this assignment
* Solid problem-solving skills and attention to detail and to quality control required
* General computer knowledge, good communication required
* Some positions may require work with in vivo models and/or cell culture
* Basic statistical skills
* Basic programming skills

Preferred:

* Some basic laboratory skills preferred.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #RNA000175.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-PA-West Point

Job Type
: Co/Op
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/West-Point-RNA-Therapeutics-Biology-%28Co-op%29-Job-PA-19486/1883038/188303818830382012-06-15Merck/MSDCo/Opfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Currently, we are sourcing candidates for full time Union positions for Biotechnician-Level 1 for the Merck Manufacturing Division at our West Point, PA site.

* Openings may be for 1st, 2nd or 3rd shift positions which may include working on weekends.
* Training for this position may last up to 7 months.

Position Overview:

Following the appropriate SOPs, MPDs and other pertinent documentation, the incumbent will be responsible for performing all functions required to produce vaccines. Essential functions of this position include, but are not limited to the following:

* Maintains production records, physical inventory and accounting reports, instructs and directs assigned personnel; maintains in-process checks and assists in developmental work pertaining to production methods when required.
* Documents all work according to proper cGMP documentation practices and performs review of manufacturing documentation.
* Performs all work duties via automated systems or manual operations in compliance with safe operating procedures, company and government regulations, and good manufacturing practices.
* Process monitoring documentation and process review will be completed as required to ensure that only the highest quality product is released.
* Cleans, assembles, operates, disassembles, maintains, trouble shoots and initiates corrective actions as required to meet production schedules.
* Trains personnel on approved processes and procedures.
* Dispose of Process waste material as per departmental SOP and regulatory guidelines.

Qualifications

Education:

* Must have a minimum of a Bachelor's degree in one of the following: Biology, Chemistry, Biochemistry, Microbiology, Molecular Biology, Chemical Engineering, Biochemical Engineering or other relevant Life Science/Engineering program.

Required:

* No relocation or work authorization sponsorship will be offered for these positions.
* Candidates must pass a computer-based Skills Assessment
* Positions require aseptic gowning during performance of job duties.
* Must successfully demonstrate and maintain proficiency in aseptic techniques and aseptic gowning by passing monitoring testing.No relocation or work authorization sponsorship will be offered for these positions.
* Must continue to progress towards attaining a Level 2 position by completing training on required skills.
* Must be able to lift up to 50 lbs.
* Must obtain all required titers, including but not limited to Mumps, Measles, Rubella, Varicella and Hepatitis A prior to start date.

Preferred:

* Previous vaccine manufacturing experience
* Previous laboratory or manufacturing operations experience requiring aseptic or sterile technique
* One year or more experience working in pharmaceutical, chemical, and/or biological manufacturing
* One year or more experience working under cGMP regulations

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # USW000928.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: USW, LOCAL 2-86

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Biotechnician-Level-1-%28continuous-recr_%29-Job-PA-19486/1733749/173374917337492012-06-15Merck/MSDUSW, LOCAL 2-86full-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the direct supervision of the Customer Service Area Team Lead, Global Logistics serves as Order Fulfillment and Customer Service Agent for customers and Merck personnel in support of clinical drug supply orders and distribution, invoicing and shipment delivery. Responsible for the preparation of documentation, order entry, shipment tracking, and acknowledgement related to clinical shipments. Individual processes clinical orders and addresses customer inquiring to support on-time delivery for world-wide distribution of the clinical studies

* Ensures the preparation of all documentation related to shipments including: proformas, any local documents and invoices within select timelines to allow clinical studies to start on time.
* This will include but not be limited to a) receiving order; b) arranging order acceptance; c) input order into system; d) ensuring accuracy of order in system; e) acknowledging that order has been placed; and f) tracking shipments for performance metrics.
* Role includes problem solving and delegating daily tasks within the customer service area to include shipping arrangements, timely shipment and customer inquiries.
* Liaison role with Supervisor, Team lead, CDPMs, Supply Planners, Lead Clinical Packaging Technicians and Packaging Operations in support of MRL's Global Clinical Supply Operations to provide information.
* Interacts and builds relationships with key stakeholders
* Communicates any changes to order status to all appropriate individuals/ customers along the supply chain.
* Responsible and accountable for accuracy in invoicing (proforma/ pre-invoicing) and assures all required documentation is generated and accompanies each domestic or international shipment.
* Maintains knowledge of current procedures and business issues so as to facility effective and practical solutions to all customer orders, complaints and inquiries.
* Responsible for inputting and maintaining metrics to report monitor and improve customer service.
* Responsible for follow-through with customer's complaints,
* Identifies and support the implementation of business process changes which are consistent with departmental and/or Merck continues improvement initiatives.
* Supports the review and creation of departmental SOPs.
* This position reports to Team Lead, Clinical Logistics Operations (NA), Global Logistics

Qualifications

Education:

Required: High School Diploma or equivalent. Bachelor's degree may be accepted in lieu of some work related experience.

Experience:

Required:

* 1-2 years of clinical supplies experience; in lieu of clinical supplies experience, 1-2 years pharmaceutical customer service / order fulfillment
* Must possess strong interpersonal and communication skills (both written and verbal) as well as a demonstrated ability to anticipate and solve problems
* Must be able to manage multiple priorities simultaneously
* Excellent performance in the areas of attention to detail, accuracy, organization and follow-up required
* Must demonstrate exceptional judgment and a genuine willingness/ desire to develop successful business relationships with customers
* General knowledge of logistics activities and policies
* Practical experience in customer service, warehousing, distribution or related activities.

Preferred:

* Export documentation, commercial invoice preparation experience
* Experience with computer systems/ databases are also desirable.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition TRA000602.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-PA-West Point

Job Type
: Full Time
Employee Status: Regular

Travel
: No
Number of Openings: 1

Relocation Provided
: None]]>http://jobs.merck.com/job/West-Point-Transportation-Specialist-Job-PA-19486/1868787/186878718687872012-06-15Merck/MSDFull Timefull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview

The incumbent will lead or participate with the team in the preparation of new filing applications and maintenance of chemical and pharmaceutical manufacturing and control (CMC) documentation for worldwide registration. The position will require continual correspondence with regulatory agencies and other Merck scientists to support either new or in-line product filings worldwide.

Additional responsibilities are as follows:

* Maintain working knowledge of current governmental and worldwide requirements for initial registration, re-registration and post-approval changes. Assure that filed information on the current manufacturing and testing procedures is kept updated for each product using appropriate departmental systems.

Commercialization/Early Development

* Lead/prepare/review the chemistry, manufacturing, and controls information for Investigational New Drug applications (IND, CSA, IMPD) and worldwide marketing of pharmaceutical products (NDA, WMA, CTD).
* Provide scientific and regulatory guidance throughout product development to assure that the information available will meet regulatory requirements.
* May serve as CMC representative on IDST.
* Participate in strategy discussions pre and post filing within Merck.
* Lead/prepare/review responses to agency questions.

Supply

* Lead/prepare/review the chemistry, manufacturing, and controls information for worldwide marketing of pharmaceutical products (NDA, WMA, CTD) to include annual reports, registration renewals, supplements, variations and responses.
* Participate in strategy discussions for filing post approval changes, responding to agency or subsidiary questions.
* Maintain and resolve Product Board and Issues Board.
* Track approvals of post-approval changes. Conduct follow-up.

General CMC Responsibilities

* Adhere to requirements for use of new and existing CMC systems (PCR, ACR, CoreWMA, PMD, ORION, WMCS, IST).
* Support staffing needs, training, promote growth through new opportunities and understanding of each person's EDP (managers only).
* Identify and promote best practices within CMC.
* Support filing and maintenance of pharmacopeial monographs for drug substances and drug products.
* Continually gain knowledge of current government regulations and worldwide requirements for initial registration, re-registration and post-approval changes.
* Demonstrate leadership in departmental improvement activities such as system modifications, maintenance of standard operating procedures, internal guidelines, etc.
* Provide effective supervision (if applicable) by reviewing documents as necessary to ensure the quality, accuracy and timeliness.
* Work one on one with direct reports (if applicable), initiating any necessary meetings to resolve issues.
* Notify Team Lead or Lead Scientist of significant issues.

Qualifications

Education:

* B.S. degree in pharmacy, biopharmaceutics, analytical chemistry, organic chemistry, chemical engineering, or a related discipline .

Required:

* 5 years relevant pharmaceutical experience
* Industrial experience in chemical/pharmaceutical research or manufacturing including processing and/or analytical testing.
* Strong oral and written communication skills.
* Working knowledge of WORD, EXCEL, POWERPOINT and Documentum.
* Demonstrated knowledge of regulations related to CMC.
* Developing leadership skills.
* Innovative, flexible and collaborative.
* Effective problem solving and decision making skills.
* Manage projects to achieve high productivity, prioritizes, manages effective meetings.

Preferred:

* Experience/knowledge of sterile products and prior CMC related experience

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # REG000949.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Regulatory Affairs Generic

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-CMC-Regulatory-Scientist-Job-PA-19486/1866478/186647818664782012-06-15Merck/MSDRegulatory Affairs Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the supervision of a Senior Engineer or Manager, is responsible to provide day-to-day equipment and facility engineering support for assigned area including vaccine bulk manufacturing, and/or associated facility/utilities mechanical support. Assigned tasks include support and monitoring of equipmentperformance and maintenance, propose & develop equipment and facility improvements and troubleshoot process equipment to ensure reliable, compliant and efficient operations. Actively ensures compliance to current Good Manufacturing Practices, Safety, and Environmental regulations while achieving operating cost goals.

* Reports to and receives supervision from a Senior Engineer or Manager. On routine process operations, is guided by standard operating procedures.
* Provides shop floor day-to-day equipment / instrumentation / robotic & utilities engineering support to manufacturing operations.
* Ensures adequate spare parts inventory, optimizes & coordinates scheduling of preventative, predictive & corrective maintenance to improve equipment reliability.
* Interacts with hourly, salaried and contract employees in routine matters, troubleshooting equipment and automation systems.
* Provides supervisory coverage when required. Assists in the training of hourly employees. Promotes open communications and team work.
* Maintains a high level of technical knowledge and may coordinate safety, current Good Manufacturing Practices, and environmental compliance programs.
* Actively supports productivity improvement program and resolution of deviation events. Participates in root cause investigations, evaluates, develops and improves business processes and develops technical rationale for system improvements.
* Develops Qualification, SOP and Preventative Maintenance documentation and provides reports, data and information to support on-going operations.
* Executes projects from concept to qualification, which may involve facilities, utilities, equipment, automation, or process related upgrades based on project requirements and site procedures.
* Summarizes project progress, delays, or improvement opportunities. Frequently communicates with immediate supervisor about status of projects or assignments.
* Develops strong relationships with site operations to ensure consensus on operational and regulatory compliance issues.
* Supports regulatory agency inspections.

Qualifications

Education:

* B.S. or M.S. in Engineering, Science or equivalent industry experience.

Required:

* Minimum 3 years of cGMP, technical/mechanical services experience.

Preferred:

* Good interpersonal skills including flexibility and ability to work in a team environment.
* Good analytical abilities, organizational skills.
* Good written and verbal communication skills.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAI000259.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Maintenance/Utilities

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Manufacturing-EngineerScientist-Job-PA-19486/1885951/188595118859512012-06-15Merck/MSDMaintenance/Utilitiesfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This is an excellent opportunity for a highly motivated individual to join the Pharmaceutical Sciences and Clinical Supply organization in Merck Research Laboratories (MRL). The successful candidate will join the Formulation and Basic Pharmaceutical Sciences Department and will be primarily responsible for development of robust drug product compositions, processes and primary packaging to support Merck's pipeline. Specifically, the candidate will:

Description of Duties

* Use innovative approaches to design robust formulations and manufacturing processes for oral solid dosage forms.
* Actively participate on formulation development teams and interface with other functional areas to drive project milestones.
* Originate research ideas and design, execute & interpret complex laboratory experiments with broad priorities set by supervisor.
* Use statistical experimental design & data analysis and draft technical reports, regulatory submissions and patent applications.
* Lead and/or serve as strong contributor to new technology development activities including but not limited to solubility enhancement, taste masking, rapid release and controlled release.
* The candidate should have strong communication skills, good interpersonal skills, ability to multi-task and a strong desire to learn and contribute.

Qualifications

Education:

* B.S. with greater than 6 years of industrial experience

* M.S. with greater than 4 years of industrial experience

* PhD in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, Bioengineering, or other relevant discipline.

Required:

* Strong team player with excellent communication and collaboration skills.
* Highly flexible and adaptable.
* Able to work independently and effectively manage projects.
* Able to effectively represent functional area on cross-functional teams, and also lead small to medium sized teams within functional area.

Preferred:

* Prior experience in solid dosage form design and development and associated dosage form manufacturing technologies.
* Prior experience in solid dispersion technologies (extrusion, spray drying).
* Prior experience in process development, scale-up, and technology transfer.

Exemplary candidates with commensurate experience in the food, consumer products, or polymer processing industries will be considered.
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PHA001073.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-MG1

Job
: Pharma Process Development

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Active Pharmaceutical Ingredients]]>http://jobs.merck.com/job/West-Point-Senior-Research-Engineer-Job-PA-19486/1858710/185871018587102012-06-15Merck/MSDPharma Process Developmentfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Essential functions include, but are not limited to: support Security, West Point Monitoring System (WPMS), and Fire System operations at the West Point site and its satellites. Provides assessment of, and response to, potential threats indicated by security alarms and closed circuit TV (CCTV) systems. Monitors utility, security, and fire protection systems remotely, and dispatches alarms to appropriate personnel. Supports the department during emergency response. Calls for appropriate internal or external ambulance, fire department, or law enforcement assistance, as necessary. This is a multi-tasking position.

* Reports to Lead Supervisor, Operations.
* Operates the department monitoring systems for Security, Utilities, and Fire protection. Acknowledges and dispatches out-of-normal conditions to appropriate personnel to ensure the situation has been remediated and/corrected.
* Provides emergency dispatch for medical, fire, or security-related incidents on plant site during 24 by 7 operations.
* Develops and maintains comprehensive knowledge of West Point facilities, operations, and personnel. Utilizes available resources to ensure continuous smooth operation of the site. Documents emergencies as required, and engages internal or external emergency services personnel as appropriate. Notifies Plant Supervision of all relevant site problems or concerns, documents significant shift activities and work order information.
* Prepares accurate and timely shift reports and records of shift activities. Executes all required training in a timely manner.
* Ensures continuous operations of all card access, monitoring, and communications systems. Generates reports to document shift activities. Troubleshoots system problems. Maintains large-scale video recording system to assure proper records are created and available for review or as legal evidence.
* Upon proper authorization, makes temporary adjustments to card access/alarm system time schedules and access levels to provide for exceptions to normal operations. Assures prompt return to normal operations.
* Develops, maintains, and follows intrusion Alarm Response and/or GEMS plans as required.
* Follows Site Good Manufacturing Practices or Good Laboratory Practices as required. Develops proficiency in all department Standard Operating Procedures or Departmental Procedures as required.
* Assists/coordinates mechanics during WPMS PM's issues. PM listings as required PM records, including resolution of instrumentation problems.
* Coordinates the activities of electricians, instrument technicians and scheduled contractors when working on the Security WPMS, and fire systems.
* Fully functional in all aspects of the job duties as listed above. Capable of execution of all job responsibilities with limited direction from Supervisor.

This position requires shift work, including nights, weekends and holidays with staggered days. Flexibility with work schedule required.

Qualifications

Education:

* BS degree in Engineering highly preferred

Required:

* Formal training in power system, computer system operations, dispatching and utility resource conservation desirable.
* Minimum one year in design and operation of industrial utility systems and control with a good understanding of computer systems desirable.
* General industrial power plant experience and site utilities experience desirable.
* Ability to work in a group setting with strong organization, follow-up, and multi-tasking skills. Must be detail-oriented and exhibit excellent communications skills, both written and verbal.
* Ability to work shift work, including nights, weekends and holidays with staggered days.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # SEC000112.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Security Generic

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 2

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/West-Point-Command-Center-Operator-Job-PA-19486/1885948/188594818859482012-06-15Merck/MSDSecurity Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Description:

Under the supervision of a Senior Engineer or Manager, is responsible for assisting in demonstrating process improvements, monitoring process performance, and troubleshooting. Provides day-to-day technical support for assigned area which may include vaccine bulk manufacturing, filling, lyophilization, packaging, and/or mechanical support. Actively ensures quality, safety, environmental, and operating cost goals are achieved. Completes projects and prepares reports while adhering to Good Manufacturing Practices, safety, and environmental regulations.

* Reports to and receives supervision from a Senior Engineer or Manager. On routine process operations, is guided by standard procedures. Confers with immediate supervisor in resolving atypical events.
* Provides supervisory coverage when required. Assist in the training of hourly employees. Promotes open communications and team work in work area.
* Maintain systems to monitor process performance. Assist in troubleshooting process control difficulties related to safety, quality, environmental compliance, and cost control.
* Carries out projects that may involve facilities, equipment, or process based on specific guidance from supervisor. Actively supports productivity improvement program and resolution of atypical events.
* Maintain a high level of knowledge and may coordinate safety, Good Manufacturing Practices, and environmental compliance programs. Assist in schedule of audits for the department.
* Summarizes project progress, delays, or additional opportunities in reports. Frequently communicates with immediate supervisor about status of projects or assignments.

Qualifications

Education Minimum Requirement:

* BS or BA degree in Science, Engineering, or Business or equivalent experience

Required Experience and Skills:

* Minimum 2 years experience in a manufacturing or process support role, OR
* Associates Degree in a Science, Engineering, or related field with minimum 7 years engineering/maintenance experience
* Working knowledge of cGMPs and of regulatory requirements as they apply to the vaccine/pharmaceutical industry
* Experience in equipment management, troubleshooting and/or maintenance

Desired Experience and Skills:

* Strong communication (written/verbal), and multi-tasking abilities
* Experience in prioritizing conflicting responsibilities in a manufacturing environment
* Plant maintenance, instrumentation, project engineering and/or operations experience
* Experience interfacing with Computer Maintenance Management Systems (CMMS)
* Experience in GMP/regulated manufacturing environment

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition MAI000263.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Maintenance/Utilities

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 2nd

Hazardous Materials
: NO]]>http://jobs.merck.com/job/West-Point-Manufacturing-Engineer-Scientist-Job-PA-19486/1895227/189522718952272012-06-15Merck/MSDMaintenance/Utilitiesfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Supplier Development & Performance Management (SD&PM) Technology Process Engineer will work with the SD&PM Team as the primary technical interface with SD&PM suppliers of components and materials to MMD sites and this SD&PM Team includes dedicated SD&PM Technology, SD&PM Quality, and SD&PM Procurement personnel. This position will partner with site / divisional Quality, Procurement, Technical, and Operations groups that have business with our SD&PM suppliers and be responsible for component/material specifications, atypical resolution (either internally with our use of SD&PM components/materials or externally with the manufactures of same), change control, component/material optimization, and technical due diligence assessments for prospective suppliers. The SD&PM Technology Process Engineer will perform these tasks with the assistance of distributed resources within GSTC as needed.

The SD&PM Technology Process Engineer will be the point person in the areas of:

* Technology Collaboration including developing an understanding of and optimization of our component/materials usage
* Documentation including development of formal purchase specifications for SD&PM managed components/materials
* Coordination, communication, up-skilling (e.g. six sigma, etc.), and oversight on general technical matters pertaining to SD&PM suppliers
* Responsibility for the technical aspects of fact finding around major component/material based issues
* Coordination and evaluation of supplier driven change control notifications and MMD site initiated changes impacting SD&PM Suppliers
* Lead deviation investigations at SD&PM Suppliers on behalf of the MMD sites, obtain the root cause, and implement corrective actions (as needed)
* Execution of prequalification testing program for major components/materials, including fit for use testing, piloting work, or other characterization studies to assess suitability for use
* Establishment of a calibrated technical oversight approach for SD&PM suppliers based on the criticality of the component/material, supplier capability, and historical experience
* Establishment of clear expectations, measures and periodic monitoring of quality performance associated with SD&PM suppliers
* Provides technical consultation and review on commercial agreements
* Participate in technical due diligence assessments in concert with other functions of the SD&PM organization
* Partner with SD&PM personnel in Procurement and Quality to manage suppliers of components/materials
* Participate in Periodic Business and Relationship Review Meetings with SD&PM Managed Suppliers

Qualifications

Minimum Education Requirement:

* Minimum BS in engineering, materials science, or equivalent scientific field

Required Experience and Skills:

* Minimum of 5 years technical experience in these areas:
* Demonstrated technical skills in the areas of chemical, pharmaceutical and/or vaccine manufacturing and packaging
* Demonstrated leadership skills including professional and interpersonal communication skills
* Ability to development and maintain commercial relationships external to Merck is key
* Ability to work in a matrix organization to leverage expertise from other functions and departments within Merck

* Travel will be associated with this position on an as-needed basis and is estimated at 15 to 25% of the time.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CHE003363.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Chemical Engineering

Primary Location: US-PA-West Point
Other Locations: US-NJ-Summit, US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-SD&PM-Technology-Process-Engineer-Job-PA-19486/1835826/183582618358262012-06-15Merck/MSDChemical Engineeringfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


We currently have an exciting opportunity to join our Analytical Sciences Organization located at our West Point, PA facility. We're looking for a motivated, scientific leader who is interested in applying innovative analytical characterization technologies to drive pharmaceutical drug product development.

In this role, you would be developing and utilizing characterization techniques to support product formulation of developmental Merck products. You will have the opportunity to:

* Utilize your skills and expertise to serve as a departmental expert and scientific resource for challenging technical problems.
* Develop and utilize characterization techniques to support product formulation activities for a growing array of early development drug candidates in novel formulation vehicles.
* Develop chemical and physico-chemical assays to characterize small molecules, peptides, and functional excipients in formulated products.
* Evaluate and utilize new enabling analytical technologies in support of process and product characterization for state of the art drug product delivery technology, including conventional solid oral dosage forms, amorphous dispersions, and parenteral formulations.
* Assess the chemical and physical stability of active pharmaceutical ingredients and the excipients involved in drug delivery.
* Work within cross functional scientific teams to collaborate in the development, characterization, and release of new formulations.
* Support multiple projects.
* Interact with other technical, regulatory, research and manufacturing groups.
* Develop your career through learning & expanding your knowledge base.

Qualifications

Education:

* PhD

Required:

* Minimum 5 years industrial experience
* 4 years experience in pharmaceutical drug product development

Preferred:

* Experience in a Pharmaceutical Analytical Science Organization
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # PRE000307.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Preclinical Dev Generic

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Standard Analytical Laboratory Chemicals]]>http://jobs.merck.com/job/West-Point-Research-Fellow-Job-PA-19486/1866476/186647618664762012-06-15Merck/MSDPreclinical Dev Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the supervision of the Maintenance Supervisor and direction of the maintenance team leader and working from blueprints, drawings, sketches, or other instructions, the pipefitter/plumber installs, lays out, bends, cuts, threads and joins pipe and fittings that will withstand steam, gas, hydraulic, vacuum, water or air pressure, or process materials. Also Installs and maintains drainage, waste, and vent systems.

Additional responsibilities include, and not limited to the following:

* Handles and installs pipes of various materials such as: stainless steel, glass, iron, steel, aluminum, synthetic materials, copper, etc., and the necessary fittings, valves, specialties, etc.
* Cuts access holes to install pipe through floors and walls, using suitable tools.
* Fabricates and fits pipe hangers and supports to walls and ceilings, etc. Acid cleans coils, equipment, and pressure vessels as instructed.
* Visually inspects pressure and vacuum gauges and recommends repair work if necessary.
* Maintains restroom facilities including handicapped fixtures with appurtenances and washroom fixtures in t-class operational condition.
* Installs and maintains insulation for all pipelines except refrigerant lines.
* Installs temporary insulation on all repairs and extensions to refrigerant lines.
* Installs, inspects, maintains, repairs or replaces pipes, pipelines, filters, steam traps, strainers, valves, etc.
* Install and replaces safety valves, relief valves, rupture discs, pressure regulators, conservation vents, flame arrestors, etc.
* Tests equipment and piping for pressure and leaks.
* Attend and actively participates in HAZOPS, waste walkthroughs, kaizen events, or any other operations, lean six-sigma, quality, safety or environmental training/initiatives as required.
* Prepares and assists technicians, supervisors and planners in preparing labor and material estimates.
* Assists supervision with the assigning, scheduling and prioritization of work order requests using maintenance management systems.
* Makes recommendations and prepares orders for spare parts, additional stock room items, tools, etc.
* Consults with Supervision and other mechanics on problem resolution/troubleshooting.
* Keeps Supervision informed of problem issues.

Qualifications

Education:

* High School Diploma or GED required
* Completion of a formal pipefitter plumber apprentice program that is approved by the United States Department of Labor or equivalent. AND/OR is a graduate of a recognized pipefitter plumber trade school with subjects that include blueprint reading, plumbing, and various industrial piping systems (steam, gas, air, potable water, fire protection, process materials, etc.)

Required:

* Three (3) years of recent full time experience as a journeyman pipefitter/plumber. Experience must include installing and repairing a broad range of industrial piping systems (steam, gas, air, potable water, fire protection, process materials, etc.), AND/OR the completion of four years of on-the-job training as part of a formal pipefitter plumber apprentice program that is approved by the United States Department of Labor.
* Ability to read blueprints, drawings, sketches, etc. Some heavy lifting, heat & cold, use of solvents, subject to immunizations, dirt and dust, safety shoes & glasses, respirators, works in trenches, works from ladders and scaffold. May be required to carry a pager or a radio.
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition USW001105.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: USW, LOCAL 2-86

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Mech_-Techn_-PipefitterPlumber-Job-PA-19486/1874866/187486618748662012-06-15Merck/MSDUSW, LOCAL 2-86full-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the guidance of Manufacturing Engineers, the Viral Vaccine Engineering Co-op will support the on-going operation of Vaccine Operations facilities and equipment as a member of the Viral Vaccine Engineering Services department (VVES).

This position is responsible for but not limited to:

* Provide daily equipment trouble shooting, technical, and mechanical support to the daily operations of bulk biological manufacturing departments. Facilities will be in regular operation or will be in start-up mode.
* Interact with other production support groups (technology, automation, maintenance, quality) and capital project teams while completing assignments.
* Provide progress updates to mentor summarizing the status of the assignments that are underway.
* Work with assigned mentor to develop personal and professional skills.

Note that this is a paid co-operative assignment, whereby a weekly stipend will be provided.

Housing subsidy is not available as part of this program and if required by the student must be funded 100% by the student.

Qualifications

Education:

* Candidate must be pursuing BS degree in Chemical, Mechanical, or related Engineering discipline, with a focus on manufacturing process or related field.

Required:

* Candidate must be available for full time employment for a period of 6 months targeted to begin in March 2012.
* Currently enrolled in an academic program and returning to school following this assignment.
* U.S. citizen and permanent residents required.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers (University Opportunities) to create a profile and your resume for requisition #ADM004915.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-PA-West Point

Job Type
: Co/Op
Employee Status: Regular
Number of Openings: 2

Relocation Provided
: None]]>http://jobs.merck.com/job/West-Point-Viral-Vaccine-Engineering-Services-MMD-Co-op-%28West-Point%2C-PA%29-Job-PA-19486/1729517/172951717295172012-06-15Merck/MSDCo/Opfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview

Under the direction of a Manager or Director, the Senior Regulatory Coordinator is responsible for implementing CMC regulatory strategies for Merck's vaccine product franchise in accordance with domestic and international regulations and guidances, and is responsible for the preparation and submission of CMC sections for new vaccine products.

Primary responsibilities include, but are not limited to:

Project Responsibilities:

* Works to compile data and information in support of new and in-line vaccine product license/registration worldwide.
* Prepares license supplements to existing vaccine product license applications (BLAs) or marketing authorization applications (MAAs) worldwide.
* Authors Annual Reports for licensed vaccine products.

Technical Competence:

* Demonstrates an understanding of regulatory affairs and applies this understanding to the benefit of the company to ensure the continued market supply of Merck vaccines worldwide.

Quality Responsibilities:

* Working understanding of the domestic and international regulations that govern the licensure of vaccines and provides Regulatory input and support during time of governmental inspections of the site.

This position is in the HPV/ Alum franchise.

Qualifications

Education:

* B.S. in a biological science or a related field.

Preferred:

* M.S. in a biological science or a related field. Preferred fields of study include Microbiology, Virology, Molecular Biology, or Biochemistry.

Required:

* At least three (3) years of relevant experience, including biological/pharmaceutical research; manufacturing, testing, or licensure of biological products; or related fields.
* Demonstrated sound understanding of related fields (e.g., manufacturing, analytical, quality assurance) and the ability to be creative and imaginative in the approach to new and diverse problem solving.
* Proven experience in critically reviewing detailed scientific information and assessing whether technical arguments are presented clearly and conclusions are adequately supported by data.
* Demonstrated superior oral and written communication skills in multicultural settings and ability to communicate complex issues in a succinct and logical manner. Strong listening skills.
* Demonstrated flexibility in responding to changing priorities or dealing with unexpected events.
* Demonstrated effective leadership, communication, interpersonal and negotiating skills.
* Demonstrated ability to generate innovative solutions to complex regulatory problems and effectively work with and communicate to key stakeholders.

Preferred:

* Understanding of recombinant vaccine manufacture and/or analytical testing.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition REG000959.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Regulatory Affairs Generic

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Senior-Regulatory-Coordinator-Job-PA-19486/1871148/187114818711482012-06-15Merck/MSDRegulatory Affairs Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview:

Under the direction of the Manager, Global Trade Compliance COE, responsible for providing analytical support to Global Trade Compliance COE to include HTS Classification determinations ,Global Trade Compliance database and SAP/GTS system support, project management in support of trade compliance programs globally. Additionally ensures adherence to policies and procedures while continually striving to improve trade compliance level.

Primary responsibilities to include: Primary activities include, but are not limited to:

* Assist in the development, implementation and review of policies and procedures to ensure a strong global trade compliance management system.
* Assist in the development and update of trade compliance training materials and provide training to involved Employees with the best possible training methods.
* Provide assistance on valuation, assists, royalty, and reconciliation.
* Provide assistance with Country of Origin and Trade Preference Programs.
* Assigns Tariff classifications and other trade determinations for imports.
* Advise management of regulatory changes and additions that may impact the business.
* Provide timely support for site trade compliance activities.
* Propose ways to utilize the trade laws and regulations to get the most benefit for the company.
* Continuously improve company trade compliance level.

Qualifications

Education:

Required:

* Bachelors Degree

Preferred:

* Advanced degree

Experience:

Required:

* Minimum 4 years functional expertise with international trade or equivalent
* Strong project management and process improvement skills
* Demonstrated analytical and problem solving skills

Preferred:

* Trade related certificate
* Licensed Customs Broker
* Strong leadership and teamwork skills, collaboration, and facilitation skills
* Advanced Computer / Technical skills to include SAP

*LI-AS2

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition MAN001730.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Manuf./Operations Generic

Primary Location: US-PA-West Point
Other Locations: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Logistics-Analyst-Trade-Job-PA-19486/1885945/188594518859452012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The successful candidate will be responsible for developing and applying in vitro, ex vivo, and in vivo models for evaluations of alternative drug delivery for development compounds and life cycle management candidates in dynamic drug development teams. Primary responsibilities include designing and conducting in vitro and in vivo experiments, performing permeation and pharmacokinetic analysis, and writing study reports. Extensive interactions with other functional groups engaged in preclinical and clinical drug development will be required. Strong communication skills, great interpersonal skills and a motivation to work in a team environment are critical.

Qualifications

Education:

* B.S. or M.S. degree with at least 5 years industrial experience in drug delivery
* Ph. D. degree in Pharmaceutics, Pharmaceutical Science or related field with hands-on experience in evaluation of alternative delivery of pharmaceutical formulations using in vivo and in vitro models.

Required:

* Required hands-on experience includes the assessment of drug delivery systems via at least two distinctive routes of administration among the following delivery systems (but not limited to) - buccal, sublingual, intranasal, pulmonary, and oral administrations.
* Experience in handling and working with various preclinical in vivo and tissue models.
* Course work including pharmaceutics, advanced drug delivery, and pharmacokinetics.

Preferred:

* Knowledge or experience in using in silico model for guiding drug delivery will be a plus.
* Strong knowledge in pharmaceutical formulations is highly desirable.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # RES001301.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-MG1

Job
: Research Pharmacy

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Senior-Research-Pharmacist-Job-PA-19486/1799252/179925217992522012-06-15Merck/MSDResearch Pharmacyfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Supplier Development & Performance Management (SD&PM)

Overview / Basic Functions & Responsibilities:

Responsible for serving as the primary point of contact with Suppliers for MMD sites within the region. Responds to requests from SD&PM-Core and other MMD representatives outside of the region to manage Suppliers within the region.

Responsible for implementing procedures and best practices supporting Merck's Supplier Development & Performance Management program, under the direction of the SD&PM Relationship Manager. The incumbent will exercise leadership in monitoring and maintaining Supplier compliance with worldwide regulatory requirements, current Good Manufacturing Practices (cGMPs), MMD Quality Manual, and pertinent legal and / or business contract requirements. Key responsibilities include leading Supplier Deviation investigations, evaluation and execution of Supplier Change Management, upskilling Suppliers, and interfacing with MMD sites associated with Supplier issues within the region. The incumbent will assist the SD&PM Relationship Manager in calibrated Quality oversight and interfacing with Procurement and Technology colleagues.

The incumbent will work with an assigned SD&PM Relationship Manager for personnel-related requirements and workload balancing as well as a functional SD&PM Relationship Manager in a matrix organization for functional guidance.

The incumbent will possess Analytical, Scientific, Technical, Manufacturing, and / or Quality experiences in order to effectively administer and control Quality and Technical programs and projects needed to manage Suppliers, under the direction of the SD&PM Relationship Manager.

Primary Roles include, but are not limited to:

* Travels up to 50% of the time, to and from Supplier sites and MMD sites within the region.
* Serves as the primary point of contact to Suppliers in the region.
* Responsible for coordination, oversight and communication on matters related to the cGMP status with the Suppliers. Must understand worldwide regulatory requirements and current Good Manufacturing Practices associated with materials supply.
* Acts as a liaison between Suppliers and internal Merck site personnel.
* Travels to and from Suppliers' locations to resolve Manufacturing, Quality, Technical and supply issues as well as facilitating overall Quality improvements to proactively prevent Supplier issues.
* Provides support to the Suppliers to facilitate, qualify, and / or validate materials for new product introductions.
* Provides compliance input and support for implementation of analytical methodology and process development initiatives.
* Coordinates and evaluates Supplier-initiated or Merck-initiated Change Control associated with materials supply.
* Coordinates, communicates and oversees general technical matters pertaining to Suppliers, including understanding and optimizing component / material usage and upskilling Suppliers to provide improved materials and services.
* Partners with SD&PM Quality, Procurement and Technology colleagues to provide efficient and effective solutions and Corrective Actions / Preventative Actions (CAPAs) to Supplier and / or site issue resolution, including Deviation Management, response to Supplier audit issues and customer complaints.
* Provides technical consultation, review and execution of Quality Agreements, Change Control Agreements and Supply Agreements.
* Tracks and monitors Supplier operational and quality performance. Escalates issues to the SD&PM Relationship Manager, SD&PM Technology Managers, and to site personnel.
* Assists in development and delivery of Supplier metrics and scorecards.
* Participates in periodic Business and Relationship review meetings with Suppliers

Qualifications

Education:

* BS/BA degree in Engineering, Science or Business

Required:

* Minimum 5 years experience in Quality, Technical, Manufacturing Operations, or related Business Operations working with products or processes.

Preferred:

* Demonstrated Quality, Technical and / or Manufacturing experience in the areas of chemical, pharmaceutical and / or vaccine manufacturing or packaging.
* Six Sigma Black Belt, Green Belt or Yellow Belt certification
* Experience conducting technical investigations
* Ability to develop and / or improve commercial relationships
* Knowledge of cGMPs, technical writing, data management collection and analysis
* Facilitates business negotiations in a professional manner

Works independently with all levels of the organization, and has demonstrated the following skills:

* Rapid / Disciplined decisions
* Acts with courage and candor
* Drives results
* Escalation of issues / concerns to management, as appropriate
* Ability to Prioritize, Align and Simplify

*LI-AS2

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition QUA002868.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Qual Assurce - 3rd Party Manuf

Primary Location: US-PA-West Point
Other Locations: US-NJ-Rahway, US-NJ-Kenilworth, US-NJ-Summit, US-PA-Danville
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 6

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-SD&PM-Field-Generalist-Job-PA-19486/1809483/180948318094832012-06-15Merck/MSDQual Assurce - 3rd Party Manuffull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


We currently have an exciting opportunity for an experienced engineer or scientist to support the life cycle management of Merck's vaccine portfolio. The position is solid line to Vaccine Manufacturing Science and Commercialization (VMSC) and dotted line to Sterile Liquid Commercialization (SLC). The role will primarily focus on the formulation and filling processes associated with the drug product. Key responsibilities may include process enhancements, development of new images and product value extensions, and new technology development. This is a unique opportunity to make a significant impact to life saving vaccines.

The specific activities associated with this position may include:

* Facilitate strategic discussions with project teams, contributing to assessment of life cycle management opportunities for vaccines
* Lead drug product working groups responsible for project implementation
* Apply drug product understanding and manufacturing expertise to develop robust and scalable manufacturing processes
* Enable process risk assessments to guide and prioritize development work
* Design and plan process development studies for sterile solutions, suspensions, and/or lyophilized products
* Manage the execution of development studies, including the potential for providing guidance and supervision of laboratory personnel
* Analyze and document experimental results and make recommendations for path forward, communicating key findings to both project teams and area management
* Lead the preparation of materials for clinical trials and/or stability studies by collaborating with a network of pilot plants and launch facilities
* Manage the technology transfer of processes into commercial supply sites, enabling the execution of validation lots and contribute to regulatory filing documentation
* Evaluate and demonstrate the feasibility of new technologies and the potential application to vaccine products

Qualifications

Education:
* Required: BS in Chemical Engineering, Materials Engineering/Science, Pharmaceutics or related field
* Preferred: MS or PhD Degree in Chemical Engineering, Materials Engineering/Science, Pharmaceutics or related field

Required:

* Minimum 6-8 years post-bachelors degree experience in manufacturing, process development, or a related field
* Previous experience working with sterile drug products with a pharmaceutical or biotechnology company

Preferred:

* Ph.D. degree + 2 years of industrial experience focused on formulation development
* Experience with aseptic techniques and manufacture of sterile products
* Experience with viral vaccines
* Knowledge of cGMPs and experience working in a GMP environment

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition CHE003484.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Chemical Engineering

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Senior-Development-Engineer-Job-PA-19486/1868793/186879318687932012-06-15Merck/MSDChemical Engineeringfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Department of In Vivo Pharmacology at Merck Research Laboratories (MRL) located in West Point, PA is offering a co-op position. West Point In Vivo Pharmacology focuses on Discovery & Preclinical Sciences research projects and diagnostic support for various groups at MRL. The support is provided for both small targeted studies and larger studies with localization/expression of genes and proteins as endpoints. This co-op will provide anatomy and histopathology experience in the diverse research projects that will include necropsy techniques, tissue collection and handling, immunohistochemistry, tissue staining, paraffin embedding of tissue, microtomy (tissue sectioning), histopathology and image analysis.

We are seeking candidates with a strong interest in neuroscience research, excellent communication skills and able to work in a team environment.

Candidates must be willing to work a 4-6 month assignment in the West Point, PA area.

Qualifications

Required:

* Must be pursuing a Master's or Bachelor's degree in a Biological or Chemical Science, Neuroscience or Pharmaceutical Sciences degree with one year remaining post internship.
* Applicants must have completed basic laboratory courses and have research experience related to biological sciences.
* Applicants must be available for full-time employment for 4-6 months

Preferred:

* Applicants should be competent with basic laboratory skills (e.g. pipetting, tissue sectioning, and safety procedures.)
* Applicants should be familiar with scientific record-keeping and image analysis.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #PHA001047.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-PA-West Point

Job Type
: Co/Op
Employee Status: Regular

Travel
: No
Number of Openings: 1

Relocation Provided
: None]]>http://jobs.merck.com/job/West-Point-In-Vivo-Pharmacology-Research-Co-Op-2012-BS-or-MS-Job-PA-19486/1729544/172954417295442012-06-15Merck/MSDCo/Opfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Vaccines are a key component of Merck's product portfolio. Vaccines Research (our department) is responsible for the identification and development of novel vaccine candidates that meet Merck's mission to address unmet medical needs. Vaccines Research works closely with colleagues in Process Development and Manufacturing during Vaccine development.

The candidate will be working in a team-setting with colleagues from mutliple disciplines. The candidate will gain experience in multiple Molecular Biology methodologies and in microbiological techniques. The candidate will be constructing phage display libraries used in the identification of reagent antibodies supporting multiple vaccine programs. These reagent antibodies are viewed as critical reagents needed to support programs from early stage research through late stage and clinical development as well as post-product approval. The responsibility of this position is the construction of a phage display library from human B-cells for use in antibody discovery efforts within Vaccines Research. The position requires working with human blood and blood products.

Qualifications

Required:

* Must be a second or third year student working toward a Bachelor in biology, biochemistry or molecular biology
* Must have laboratory experience with DNA and RNA purification, PCR, gene cloning, vector construction, ELISA and bacterial culture & cloning
* Must be able to work independently
* Must be able to work full time during the 4-6 month co-op at Merck's West Point, PA facility (paid relocation or housing unavailble)

Preferred:

* Phage display and Fab expression

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #BIO003437.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-PA-West Point

Job Type
: Co/Op
Employee Status: Regular

Travel
: No
Number of Openings: 1

Relocation Provided
: None]]>http://jobs.merck.com/job/West-Point-Vaccine-Research%2C-Molecular-Biology-BS-Co-Op-Job-PA-19486/1729514/172951417295142012-06-15Merck/MSDCo/Opfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Currently, we are sourcing candidates for Sterile & Packaging Operators - Level 2 for the Merck Manufacturing Division at our West Point, PA site.

Openings may be for 1st, 2nd or 3rd shift positions and may include working on weekends.

* Some positions require aseptic gowning during performance of job duties.
* Incumbents will be required to obtain all required titers, including but not limited to Mumps, Measles, Rubella, Varicella and Hepatitis A.

Position Overview:

Under the direction of management, the incumbent performs a wide variety of tasks and operations in GMP, aseptic and controlled environments to support and execute production. Duties include but are not limited to:

* Performs line/process changeover procedures as well as general cleaning and disinfecting duties in work areas.
* Sets up, operates and troubleshoots packaging equipment including making minor repairs as necessary.
* Interfaces with departmental computer systems/databases including PCL Entries, start/end batches and timely accurate SAP transactions as necessary.
* Cleans and ships material to off-site vendor for refurbishment
* Performs in-process testing/monitoring via paper or electronic systems (dose/seal checks, leak checks, broken glass checks, standards/challenges, reconstitution, control boards/charts, etc.)
* Sets up and operates steam and dry heat sterilizers including computer interface operations.
* Assembles equipment and performs washing and cleaning of components and equipment.
* Prepares and operates lyophilization cabinets including computer interface operations, manual cleaning, loading and unloading.
* Completes all required log sheets, batch records, (including but not limited to 2nd Person reviews, sampling and accountability calculations, ) training rosters and additional documentation as required and adherence to Right First Time (RHT) accountability.
* Performs disinfection of items entering the aseptic core and other areas.
* Operates equipment associated with, but not limited to: washing, autoclaving, loading, filling, tray loading, capping and inspection.
* Monitors equipment, components, and flow of materials to ensure quality.
* Runs equipment for various size containers, stoppers, caps and other packaging components as required. Makes minor adjustments to equipment to clear jams as necessary, and communicates issues or problems to technicians or supervisors.
* Coordinates activities required to manage inventory of supplies, components and equipment to meet production schedules. Ensures materials are organized, stored, segregated and staged for production operations.
* Performs sampling as required.
* Adheres to Current Good Manufacturing Practices.
* Empties wastebaskets, transports waste materials and properly tags waste.
* Replaces lights and light covers.
* Mops, dusts, polishes, details, sprays, wipes and vacuums floors, ceilings, walls, machinery, windows, and laminar flow hood curtains, etc.
* Prepares, removes and properly labels cleaning solutions and cleaning equipment.
* Attends training sessions, as required, to maintain skills/knowledge of operations.

Qualifications

Education:

* Must have a minimum of a High School Diploma or equivalent.

Required:

* The incumbent may be required to lift up to 50 pounds, periodically work on ladders and handle trash, perform disinfection, etc.
* Exposure to high and low temperatures and extensive standing are required with this role.
* Employees that are required to work in an aseptic processing area must successfully demonstrate and maintain proficiency in aseptic gowning by passing monitoring tests.
* No relocation or work authorization sponsorship will be offered for these positions.
* All qualified candidates must pass a computer-based Skills Assessment
* .

Preferred:

* Previous aseptic gowning experience
* 12 months or more experience working in a manufacturing and/or packaging environment
* Experience working in a cGMP, clean room, and/or aseptic environment
* Experience operating automated washers/sterilization equipment
* Experience operating manual, automatic and semi-automatic packaging equipment
* Experience with lyophilization cabinet operations
* Experience with steam sterilization equipment, thaw baths, and other equipment associated with packaging.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # USW001018. Open to U.S. Residents & Citizens only.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Former Military, Transitioning Service Members, National Guard & Reserves - We value your past and present service.

Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: USW, LOCAL 2-86

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/West-Point-Sterile-&-Packaging-Operator-Level-2-%28continuous-recruitment%29-Job-PA-19486/1781701/178170117817012012-06-15Merck/MSDUSW, LOCAL 2-86full-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Description:

* Serve as a consultant and advocate of statistics to technical specialists and managers in Merck's biological and vaccine laboratories and stability groups.
* Key member of teams supporting all large molecule bioassay and stability issues from late-stage development to supply including support for critical reagents (e.g. qualification, trending).
* Provide technical leadership in tasks that include design of experiments, analysis of data, statistical process control, simulation, design of sampling plans, and problem solving.
* Evaluate data for submissions and responses to regulatory agencies and pharmacopoeia.

Qualifications

Education Minimum Requirement:

* M.S. in Statistics (or equivalent), with 0-5 years of experience.

Required Experience and Skills:

* Coursework/experience should include DOE, Mixed Models, Nonlinear Regression and Generalized linear models.
* Demonstrated teamwork skills and leadership ability.
* Excellent statistical computing skills in packages such as SAS, S-Plus/R, JMP and Minitab.
* Effective oral and written communication skills to communicate statistical concepts and analyses to non-statisticians.

Desired Experience and Skills:

* Additional experience in Biology, Engineering, Chemistry and Six Sigma is considered a plus.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition QUA002925.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-AS1

Job
: Quantitative Sciences Generic

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Project-Statistician-Job-PA-19486/1871154/187115418711542012-06-15Merck/MSDQuantitative Sciences Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The co-op assignment will be located in the Merck Manufacturing Division's (MMD) Packaging Technology department. MMD Packaging Technology is Merck's central packaging group that has worldwide responsibility of all packaging related activities. These include packaging development, packaging equipment, distribution testing, thermal testing, packaging documentation and operational excellence activities. The selected candidate will have the opportunity to gain experience in a wide variety of areas within pharmaceutical packaging.

These areas include, but are not limited to:

* Packaging development (pharmaceutical and sterile), packaging equipment, packaging operations, distribution testing, thermal packaging, radio frequency identification (RFID) / mass serialization and packaging related documentation.
* These activities will also provide the intern with exposure of working with other departments, cross function teams, and with suppliers.
* Note that this is a paid co-operative assignment whereby a weekly stipend will be provided.

This position is based in West Point, PA.

This is a full-time co-op position anticipated to start is June 2012. The position will be from June - December 2012. Housing subsidy is not available as part of this program and if required by the student must be funded 100% by the student.

Qualifications

Education:

* This position requires applicants to be currently pursuing a degree in Packaging Science, Packaging Engineering, Mechanical Engineering, or a related discipline.
* Grade Point Average (GPA) of at least 3.0 or higher is preferred.

Required:

* Ideal candidate will possess strong project management, problem solving, organizational and communicational skills.
* Successful candidate will possess the ability to quickly gain working knowledge on unfamiliar computer software that supports packaging equipment.
* Candidate must be available for full time employment (40 hours per week) for a period of 6 months beginning in June 2012.
* Applicants must be currently enrolled in an academic program and returning to school following this assignment.
* U.S. citizen and permanent residents required

Preferred:

* Technical writing skills and experience with SolidWorks / AutoCAD is preferred.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ADM004961.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-PA-West Point

Job Type
: Co/Op
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Packaging-Technology-Co-op-%28West-Point%2C-PA%29-Job-PA-19486/1891869/189186918918692012-06-15Merck/MSDCo/Opfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This is a paid 6 months co-operative assignment. Housing or housing subsidy is not available as part of this program and if required by the student must be funded 100% by the student.

The selected candidate will be a member of the Global Facilities Management team in West Point, PA and will report into the lead superintendent and/or manager and be responsible for the following activities:

* Implementing plant safety practices and procedures
* Assisting in system/equipment startups. Research and develop startup procedures/check lists for engineering review. Coordinate startup implementation/testing activities.
* Evaluate area requirements and plans for associated capital/expense improvements. Perform administrative duties such as job audits, computer system audits and safety/housekeeping inspections.
* Keep abreast of new developments in area of responsibility, and recommends changes to improve service, operation, reliability, efficiency, and state-of-the-art applications. Maintains personal familiarity and expertise concerning equipment and systems, and conducts frequent inspections to insure proper maintenance and operation.
* Maintaining an effective organization via appropriate communication and planning

Qualifications

Education:

* Pursuing a Bachelor's degree in Administration or Engineering.

Required:

* Good communication skills both oral and written.
* Good communication computer skills.
* Ability to work independently as well as in a group environment.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAI000264.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-PA-West Point

Job Type
: Co/Op
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Engineering-Coop-Job-PA-19486/1889121/188912118891212012-06-15Merck/MSDCo/Opfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck's Biological Sterile Validation (BSV) department, located in West Point, PA, is currently seeking a Staff Engineer/Scientist. BSV serves as a center of excellence for process/equipment validation supporting the manufacture of vaccine and sterile pharmaceutical products manufactured at Merck's West Point site.

The basic function of this position is to serve as a project lead to design and implement varied technical projects requiring knowledge of engineering and/ or the biological/ physical sciences. Job focus is on project life cycle of initiating, planning, design, execution, and closeout of cleaning validation, sterilization validation, filter validation, container closure integrity, controlled temperature units, and process validation activities, and may include relevant lab work.

Position Expectations

* Apply sound scientific principles, theories, concepts, and techniques in validation processes.
* The incumbent is expected to collect and interpret information and conceive, develop and implement solutions to projects of a more general scope.
* Able to collaborate across multiple departments, prioritize tasks to meet project demands, and possess project leadership/management experience which preferably includes supervisory experience managing contract personnel.
* While the ability to work independently is desirable, routine guidance and direction will be employed by the supervisor to review soundness of technical judgment and the status/schedule of the candidate's work.
* Able to author technical documents (validation protocols, final reports etc) and communicate intent and results in a clear and concise manner.

Qualifications

Education:

* Required: B.S. in Engineering or Biological Sciences or equivalent industry experience
* Preferred: M.S. in Engineering or Biological Sciences or equivalent industry experience

Required:

* Minimum of (3) years relevant work experience required; at least
* Minimum of (2) years of work experience specifically in the field of validation
* Demonstrated project management, leadership, and teamwork skills
* Excellent analytical abilities
* Established written and verbal communication skills

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # CHE003477.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-AW1

Job
: Chemical Engineering

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Staff-Engineer-Job-PA-19486/1840115/184011518401152012-06-15Merck/MSDChemical Engineeringfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The External Manufacturing - Formulation & Packaging Sourcing Manager is responsible for overall category management for one or more categories on a global scale, either directly (for Global and International spend categories) or indirectly through collaboration with regional sourcing professionals (for Regional and Local spend). Leads the Global Category Management team to define optimal LRIG and develop and implement sourcing strategy. Responsible to establish and lead cross-functional teams of stakeholders through the Sourcing Management Process for Global and International categories and to provide strategy oversight for Local and Regional categories to deliver breakthrough results, including significant cost reduction targets. Responsible for identifying and managing profit plan savings targets for global categories.

* Category Scope - Direct responsibility for a portfolio of categories and supplier relationships that are Global or International in nature. Indirectly responsible for Local and Regional categories. In collaboration with stakeholders and Regional procurement professionals, creates and implements 1-3-5 year strategic sourcing strategies.
* Global Category Management: Leads Global Category Management teams to develop and implement strategic source plans for one or more categories of spend.
* Sourcing Management - Uses the Sourcing Management Process to manage assurance of supply, quality, service, cost, innovation and regulatory compliance within Global or International category of spend, resulting in breakthrough strategies which optimize value and ensure appropriate risk management. Understands the Sourcing Management Process and how to apply required tools in the creation and implementation of source plans.
* Proactive Cost Management: Achieves cost control, cost reduction, and cost containment targets, and adds value to area of expenditure through a strong total cost orientation.
* Market Knowledge and Insight: Uses thorough market knowledge and data analysis to gain critical insights that drive the selection of Sourcing Strategies and continuous improvement activities.
* Supplier Management and Conditioning: Responsible for building relationships with Global, International and Enterprise suppliers and managing supplier performance against business requirements using proven processes; ensures adequate inclusion of diversity suppliers in RFPs and contracts as applicable. Supports major Regional supplier relationships
* Stakeholder Management and Business Sponsorship: Ensures appropriate stakeholders are identified and managed through stakeholder matrix. Engages assigned stakeholders and partners with them to define and meet or exceed business requirements and identify and manage profit plan savings targets. Understands strategic business requirements at 1-3-5 year horizon.
* Contract Negotiation and Management: Once strategy is approved, personally leads the sourcing including RFX, RFP, negotiations and contracting for Global and International categories to put in place the right suppliers. Negotiates at tactical and strategic levels to develop local, regional, global company contracts.

Qualifications

Education:

Required:

* BS Degree in Business, Finance, Engineering, Science or related field

Preferred:

* MBA or advanced degree and/or relevant certification

Experience:

Required:

* 3 to 5 years experience in strategic sourcing or related role, including Contract Manufacturing of Pharmaceutical, Biological, or Consumer Care products.
* Knowledge of Procurement related business processes, including commercial negotiations and contracting

Preferred:

* Experience in international business desirable
* Demonstrates Leadership Standards at the Manager or Manager of Manager level, with particular strengths in Championing Change, Communicate Candidly, Build Talent, and Achieves Results.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # TEC000498.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-PA-West Point
Other Locations: US-NJ-Whitehouse Station

Job Type
: Full Time
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 3]]>http://jobs.merck.com/job/West-Point-Sourcing-Manager-Job-PA-19486/1893495/189349518934952012-06-15Merck/MSDFull Timefull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Research Associate in the Applied Mathematics and Modeling group, within Informatics IT, develops mathematical models and computational solutions using optimization, simulation, pattern recognition, discrete algorithms, knowledge representation, data mining, automated induction and inference, decision analysis, and related techniques. Project areas include vaccine and biologics design, toxicity profiling, experimental design and analysis, disease and biochemical kinetics/systems biology modeling. Work is objective-related and requires the efforts of a skilled scientist.

Qualifications

Education Minimum Requirement:

* Must currently possess a PhD or expect to earn a PhD within the next 12 months OR must have a Master's Degree with at least 5 years of research experience and 2 first-author publications.
* A degree in one of the following fields: computer science, computational biology, statistics, or another computational area with an emphasis on the use of machine learning and informatics to solving problems in biology or chemistry. The position requires advanced and thorough scientific knowledge related to the above-mentioned areas of expertise.

Required Experience and Skills:

* The position requires advanced and thorough scientific knowledge related to the above-mentioned areas of expertise.
* Must have the ability to plan, recommend and complete research programs of major divisional importance
* The incumbent must be capable of motivating and training junior scientists and offering counsel to peers within the Division
* Experience in several and extensive knowledge in one or more of the following areas is Required: optimization, discrete and numerical algorithms, machine learning and automated pattern recognition, signal and/or image processing, computational biology, mathematical analysis and modeling, probability, stochastic processes, stochastic optimization, scientific software engineering, parallel algorithms, complexity theory, or knowledge representation
* Mature communication and interpersonal skills are required
* Plans and schedules daily computing, research and reporting activities in order to meet established timetables and objectives
* Develops the technical expertise that enables proprietary positions to be established. Participates in strategic research planning at the department level
* Enhances individual and corporate reputation through one or more of the following activities: Preparing and publishing or presenting technical papers to internal and external audiences
* Prepares basic patent applications in support of patent coverage of divisional research efforts.

Preferred Experience and Skills:

* Advanced, thorough scientific understanding of one or more of: cell biology, vaccine and antibody discovery, genetics, biochemistry
* A strong publication record as part of a research team
* Post-graduate research experience or some combination of directly relevant R&D work and training, especially if relevant to solving problems in the pharmaceutical, biotechnology, or biomedical industries.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BUS000436.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-PD1

Job
: Business Analysis

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Research-Associate%2C-Vaccines-&-Biologics-Design-Applied-Mathematics-&-Modeling-Job-PA-19486/1577193/157719315771932012-06-15Merck/MSDBusiness Analysisfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


This high impact role in Merck Manufacturing assures that products manufactured comply with cGMPs, operating procedures, and other applicable regulations. This position is 3rd Shift.

Responsibilities include and are not limited to the following:

* Supervise the direct processing of materials and the associated hourly workforce to ensure attainment of business results.
* Effectively collaborate with and manage a work team with specific responsibility for motivating others, ensuring performance, schedule execution, task coordination, equipment and area preparation and effective administration of personnel policies and procedures.
* Ability to manage conflict; affect resolution to technical and personnel challenges is key; openness to change; and the ability to affect positive change.

Because our business is dynamic and advances in science and technology require new methods of production we are looking for individuals who can do the following:

* Collaborate with team members in the identification and implementation of continuous improvement initiatives and action plans.
* Support activities in the areas of cost containment, efficiency, productivity, energy conservation, waste minimization, operational excellence and lean practices
* Independently coordinate and complete optimization activities, in a multi-shift, shared ownership environment
* Utilizes lean principles and six sigma methodology to solve problems, and develops these problem solving skills in work teams.
* Facilitate implementation of corrective actions to correct past performance
* Proactively identify safety and quality-related trends, and be responsible for initiating actions to prevent issues from reoccurring.
* Recognizes and investigates opportunities for financial savings
* Understands lean principles and applies these concepts to all aspects of the production environment.
* Excellent verbal and written communication skills
* Due to the high impact nature of this role it is essential that the incumbent demonstrate integrity, credibility and flexibility in their daily performance so as to motivate others to do the same.

In this role you will assure compliance with safety and environmental practices, cGMPs and SOPs in the work area.

* Participate in external and internal audits and inspections.
* Initiate the investigation when a quality or safety event occurs during the shift.
* Work with members from Quality and Technical Operations to properly handle unplanned events.
* Ensure corrective actions are implemented.
* Ensure personnel under his/her supervision are properly trained in cGMPs, procedures, good documentation practices and regulatory matters.
* Participate in design and implementation of training and development programs
* Perform performance management and disciplinary process.
* Ensure materials receiving and verification in the work area, equipment cleaning, set-up and area cleaning and verification are completed according to procedures.
* Assure that materials are properly handled and equipment is properly operated according to SOPs, guidelines, and regulations.
* Maintain control of processes and product quality by ensuring compliance with cGMPs, safety and environmental regulations.
* Monitor the manufacturing processes during the shift.

Under the general direction of an IPT Leader, Manager, or Director, incumbent is responsible for:

* Leading, coaching and mentoring new and junior supervisors.
* Will also take part in enterprise wide projects working closely with the Director / Sr. Director on Quality, GMP, Regulatory and Technical related items.
* Participates and/or leads cross-functional teams and interdepartmental teams focusing on investigation or continuous improvements.
* At times, acts as the shift-wide lead supervisor.
* Providing guidance and supervision to hourly employees in completing process, production, maintenance, or production support activities.
* Responsible for motivation, training, interviewing, hiring, and problem resolution for subordinates.
* Ensure the area adheres to Good Manufacturing Practices, approved process steps, SOPs, quality procedures, safety, and environmental standards while operating within the profit plan.

Please note this position is 3rd shift 11:15pm - 9:00am Sun-Thurs or Mon-Fri.

Qualifications

Education Minimum Requirement:

* High School Diploma or GED

Education (preferred):

* B.S. with emphasis in Engineering

Required Skills and Experience:

* Miniumum of 6 months experience in responsible line or staff position related to pharmaceutical production or 2 years supervisory experience.
* Willingness to work off-shift or weekends
* Computer literacy in MS Office, Word, Outlook, Excel

Preferred:

* cGMP experience in a sterile, bulk or finished pharmaceutical environment.
* Supervisory experience in a heavily regulated industry (ex. FDA, Military, Nuclear, Petro-Chemical)
* Manufacturing plant experience in operational capacity
* Experience working within a Union environment
* Experience with working in SAP or other Enterprise software
* Technical writing experience related to investigations in to manufacturing process variation

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAN001359.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Manuf./Operations Generic

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 3rd]]>http://jobs.merck.com/job/West-Point-Manufacturing-Supervisor-Job-PA-19486/1670756/167075616707562012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Responsible for implementing Quality Assurance policies, procedures and guidelines supporting Merck's Suppliers, under the direction of, or on behalf of, the Director, Supplier Development & Performance Management. The incumbent will exercise a leadership role in monitoring and maintaining the Supplier's compliance with world-wide regulatory requirements, current Good Manufacturing Practices and other pertinent legal and business requirements. Key responsibilities include developing Quality standards, AQLs, Quality Agreements, MMD Procedures, Quality Bulletins, Supplier Quality system remediation including calibrated quality oversight, interfacing with Procurement and Science & Technology counterparts in Supplier Development & Performance Management and managing the Supplier Development & Performance Management Field Generalist staff.

Possesses unique combination of analytical/scientific/Quality skills as well as excellent managerial skills in order to effectively manage and control all activities necessary to support a Supplier Development & Performance Management - Quality program governing Suppliers in conjunction with and under the direction of the Director, Supplier Development & Performance Management.

* Along with Supplier Development & Performance Management counterparts in Procurement and Science & Technology, serves as the primary point of contact to the Suppliers and MMD sites. Responsible for coordination, oversight, and communication on matters related to the GMP status with the Suppliers. Must be conversant with all regulations and compendia (domestic and foreign) governing the Supplier's operations.
* Acts as a liaison of contact between Suppliers and internal Merck site personnel.
* Tracks and monitors Supplier operational and quality performance. Escalates Supplier issues to the Director, Supplier Development & Performance Management.
* Assures that the Supplier Development & Performance Management organization operates within established policies/procedures of the Division and Corporation and complies with all applicable governmental regulations.
* Manages activities associated with the Supplier Development & Performance Management Field Generalists (M06).
* Assures the development and maintenance of a Quality Agreements, specifications, standards and AQLs with Suppliers. Provides input into the development of Supplier contractual agreements.
* Works directly with senior management at the Suppliers to resolve quality and supply issues as well as providing overall quality improvements.
* Executes a program of calibrated Quality oversight based on the component/raw material risk profile, capabilities, and quality/compliance performance of the Suppliers.
* Responsible for Quality Assurance and control functions to include direct support to Suppliers, coordination and oversight for component and/or raw material testing for qualification purposes.
* Serves on behalf of the MMD sites, provides assistance to Suppliers for Deviation investigations and Change Control management.
* Responsible for maintenance and oversight of ongoing performance management to include regulatory inspection support and monitoring, internal complaint management, internal customer feedback coordination, and review of annual product reviews.
* Reviews audit outcomes pertaining to Suppliers and ensures appropriate and timely corrective actions.
* Monitors efforts to improve the Suppliers' quality and reliability through ongoing oversight, upskilling, and formal communication programs and forums.
* Provides support to the Suppliers to facilitate and validate new product introductions. Provides compliance input and support, as appropriate for implementation of analytical methodology and process development initiatives.
* May act as or support the regulatory compliance liaison on Merck's behalf to interface with Regulatory Agencies relating to Suppliers.
* Provides support and develops presentations for site Quality Council and Supplier Development & Performance Management leadership meetings. Provides oversight for presentation content / issuance of minutes.
* Leads coordination of significant investigations including Fact Findings and regulatory communications.
* Participates in external benchmarking and internal voice of customer analyses for best practices management.
* Authors technical documents such as Policies, Procedures, Guidelines.
* Assists in the development and delivery of Supplier metrics.
* Partners with Supplier Development & Performance Management Procurement and Science & Technology colleagues to provide efficient and effective solutions to Suppliers' and / or MMD sites' problems associated with material supply.

Qualifications

Education:

* Required: BS/BA degree in Engineering, Science, or Business.

Required:

* Minimum 6 years experience in commercial, business, quality, technical or manufacturing operations functions
* Ability to work independently with all levels of the organization
* Demonstrated interpersonal and communication skills.
* Demonstrated networking and relationship building skills.

Preferred:

* cGMPs, technical writing skills, data management, collection and analysis.

*LI-AS2

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition QUA002889.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Qual Assurce - 3rd Party Manuf

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-SD&PM-Supplier-Relationship-Manager-Job-PA-19486/1830553/183055318305532012-06-15Merck/MSDQual Assurce - 3rd Party Manuffull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under the general direction of an Area Head, Manager or Director, is responsible for providing guidance and supervision to hourly employees in completing process, production, maintenance, or production support activities. Responsible for motivation, training, interviewing, hiring, and problem resolution for subordinates. Uses teamwork and good communications to administer personnel policies and the local agreement. Ensures the area adheres to Good Manufacturing Practices, approved process steps, Standard Operating Procedures, quality procedures, safety, and environmental standards while operating within the profit plan.

Qualifications

Education:

Bachelor's degree in science or engineering, OR equivalent work experience.

Required:

At least one year of prior manufacturing support experience.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAN001742.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Manuf./Operations Generic

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 3rd]]>http://jobs.merck.com/job/West-Point-Manufacturing-Supervisor-Job-PA-19486/1885946/188594618859462012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The function of this position is to assure that products manufactured within the Integrated Process Team (IPT) comply with cGMPs, operating procedures, and other applicable regulations. The responsible person will manage the direct processing of materials and supervise the associated hourly workforce within the integrated process team. The position has specific responsibility for motivating the workforce, work performance, scheduling, task coordination, equipment and area preparation, complying with MPD requirements, and administration of personnel policies and procedures.

Ensure materials receiving and verification in the work area, equipment cleaning and set-up, and area cleaning and verification are completed according to procedures. Assure that materials are properly handled and equipment is properly operated according to SOPs, guidelines, and regulations. Maintain control of processes and product quality by developing appropriate procedures and ensuring compliance with cGMPs, safety and environmental regulations. Monitor the manufacturing processes during the shift.

Enforce the compliance with safety and environmental practices, cGMPs and OSHA regulations in work area. Participate in external and internal audits and inspections. Initiate the investigation when a quality or safety event occurs during the shift. Work with IPT members from Quality and Technical Operations to properly handle unplanned events. Ensure that corrective actions are implemented.

Ensure that personnel under his/her supervision are properly trained in cGMPs, procedures, good documentation practices and regulatory matters. Monitor personnel practices to ensure compliance with SOPs, practices and regulations. Participate in design and implementation of training and development programs. Supervise and motivate hourly employees. Perform performance management and disciplinary process.

Collaborate with IPT members in the identification and implementation of continuous improvement initiatives and action plans. Support activities in the areas of cost containment, efficiency, productivity, energy conservation, waste minimization, operational excellence and lean practices.

This is a night shift position 7pm to 7am (5 days on and 5 day off and then 2 days on and 2 days off).

Qualifications

Education:

* HS Diploma
* Bachelor's degree preferred

Required:

* Minimum of 6 months experience in responsible line or staff position related to pharmaceutical production or 2 years supervisory experience or 1 to 2 years experience as an Associate Supervisor or Associate Engineer/Scientist.
* Working knowledge of manufacturing processes
* Ability to focus on and obtain business results
* Ability to effectively collaborate with and manage a work team
* Ability to enact conflict resolution
* Ability to effectively respond to change
* Excellent analytical and organizational skills
* Excellent oral and written communication skills
* Leadership and interpersonal skills to motivate direct reports and peers toward the achievement of production goals
* High personal integrity, credibility and energy
* Flexibility to perform related tasks to support the business

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # MAN001406.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Manuf./Operations Generic

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 2

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/West-Point-Manufacturing-Supervisor-Job-PA-19486/1717352/171735217173522012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


We currently have an exciting opportunity for a Senior Research Biochemical Engineer to join our team within Vaccine Manufacturing Sciences and Commercialization (VMSC), Merck Manufacturing Division (MMD), in the Viral Vaccines Process Development department.

The qualified individual will be responsible for leading upstream process development campaigns supporting the development of robust and scalable bulk processes for the production of live virus vaccines. The ideal candidate will have significant experience and demonstrated technical proficiency with mammalian cell culture and/or bioreactor process development for industrial applications. The candidate will have considerable knowledge of mammalian cell culture and media development which they will be able to independently and proactively apply to the design and execution of process development experimentation, methods development and process improvement. Late stage process development, serum free media development, process scale-up, technology transfer, and process validation experience is desirable.

The successful candidate will have the opportunity to:

* Apply their enthusiasm for the scientific process to design, carry out and/or supervise studies related to the scale-up and demonstration of upstream cell culture processes.
* Design, supervise, and execute experiments at laboratory and pilot scale with particular emphasis on ensuring scalability.
* Utilize multivariate statistical methods to design efficient, iterative approaches in order to minimize time required to achieve key process development milestones.

The candidate must be able to work efficiently in a high paced environment, collaborate well with others, and have excellent interpersonal skills. Periodic off-shift or weekend coverage will be required. In addition, the candidate will meet the following expectations:

* Employ strong verbal and written communication skills, including the skill for listening to others.
* Lead effectively within functional area and within a multidisciplinary team.
* Develop and demonstrate strong project management skills
* Keep abreast of innovative and novel scientific developments in the vaccine industry by presenting at meetings, attending scientific seminars, and maintaining awareness of the scientific literature.
* Scientific supervision and mentoring of associate staff.

Qualifications

Education:

* Required: Master's degree in field of study in Applied Cell Biology/Biochemistry, Chemical or Biochemical Engineering
* Preferred: Ph.D. Degree

Required:

* Minimum (8) years of work related experience
* Demonstrated ability to drive an independent research project by conducting clear hypothesis-driven experiments, generating solid conclusions, and communicating results in peer-reviewed, published literature.
* Extensive cell culture experience (deep knowledge of cell biology, physiology, molecular biology etc)

Preferred

* Strong virology knowledge/experience
* Prior experience with live viral vaccine processes in a GMP environment
* Prior experience and/or demonstrated knowledge of process technology transfer and associated regulatory milestones

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003581.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-PA-West Point

Job Type
: Full Time
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Senior-Development-Engineer-Job-PA-19486/1842906/184290618429062012-06-15Merck/MSDFull Timefull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Quality Specialist provides direct Quality support to a production area as part of a Quality IPT (Integrated Production Team) operating model. The Quality Specialist, with guidance from the IPT Quality Lead or Focus Factory Quality Lead, ensures product / process quality and performs activities to facilitate the release of product to the marketplace and ensures proper control of material through maintenance of the quarantine system. The Quality Specialist performs 100% process document / log book audits for accuracy and completeness and works closely with the assigned Focus Factory in a team environment to ensure timely review and documentation is done right first time. He or she provides Generalist Quality support directly to the production floor, to include oversight for adherence to cGMPs, right-first-time completion of production GMP documentation, and effective investigation of deviations. Additionally, the Quality Specialist performs routine GMP walk through inspections of the shop floor within the assigned Focus Factory to ensure compliance with cGMPs and regulatory requirements.

The Quality Specialist will become knowledgeable in Federal and other regulatory agency requirements and cGMPs to assure that all areas in compliance, and will train on and gain competency in activities to facilitate release of product for assigned Focus Factory. Job functions are performed primarily on the production shop floor and in a team environment. Specific responsibilities include but are not limited to the following:

· Performs 100% audit of process documents / log books to ensure completeness and accuracy for assigned Focus Factory. Maintains any tracking databases and logs associated with this review.

o Provides coaching and mentoring of manufacturing supervisors and operators completing documentation.

o Coordinates with Production to discuss, resolve, and eliminate documentation observations.

· Performs GMP walk through inspections of assigned departments within Focus Factory to ensure compliance with cGMPs and regulatory requirements.

· Ensures proper identification of release status and control of materials through maintenance of quarantines in the IMPACT system and through physical tagging of material as required.

· Performs Quality review / approval of new and updated SOPs and CJAs.

· Assists with training of incoming personnel and ensures compliance with departmental procedures.

· Actively participates in the Tier process and uses this forum to escalate concerns and best practices.

· Collaborates with IPT members in the identification and implementation of continuous improvement initiatives and action plans.

· Collaborates with IPT members to investigate deviations on production floor during shift.

· Works with necessary groups within the Focus Factory to resolve outstanding issues with process documents / log books, GMP walk through inspection observations and quarantine, management.

· Prioritizes review of process documents / log books in order to maximize cycle-time efficiency.

· Performs IMPACT transactions required to document Batch Record review.

· Reviews Emergency Stamps / hand Stamps entered into OPG and batch record.

· Performs Quality review of new and updated Site Master Formulas.

Note: Off shift times may include conventional 2nd shift M-F 4:00 to midnight, conventional 3rd shift midnight to 8AM and a 12 hour backshift 6PM to 6AM

Qualifications

Education:

· Bachelor's degree required. Technical emphasis in an appropriate scientific or engineering field preferred; candidates with majors in other fields will be considered if accompanied by significant relevant experience.

Required:

· At least one year of relevant post-degree work experience in a laboratory, manufacturing, or quality position.

· Evidence of leadership skills coupled with good oral and written communication skills, i.e. effective presentation of concepts and ideas, as well as interpersonal and conflict resolution skills.

· Attention to detail, flexibility and an awareness of production and attendant quality control problems.

· Basic understanding of cGMPs and of regulatory requirements as they apply to the pharmaceutical field or a related area.

· Must be able to work any shift with the possibility of a rotating schedule and/or including weekends.

Preferred:

· Familiarity with vaccine and/or pharmaceutical processing.

· Familiarity with manufacturing batch records is a key skill necessary for success in this position; prior batch record experience is a strong plus.

· Experience in quality assurance audits or inspection of vaccine or pharmaceutical manufacturing areas is a strong plus.

· Aseptic gowning may be required.

Note: Titers may be required.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition REL000265.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-BR1

Job
: Release Control

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/West-Point-Quality-Assurance-Specialist-Job-PA-19486/1853552/185355218535522012-06-15Merck/MSDRelease Controlfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview:

This position is in the Formulation and Filling Franchise, which supports the final formulation and filling of all biological products at all facilities (West Point, Haarlem, Durham, Carlow, Mirabel and External Manufacturing).

Position Description:

* Utilize information from MRL/MMD scientists and MMD production and quality personnel, prepares chemistry, manufacturing and controls (CMC) sections for new biological products, license supplements to existing biological product license applications (BLAs) or marketing authorization applications (MAAs) for US, Europe and the rest-of-world (ROW).
* Under direction of a Manager or Director, is responsible for implementing CMC regulatory strategies for Merck's biological product franchise in accordance with domestic and international regulations.
* Works independently to compile data and information in support of new and in-line biological product licenses/registrations worldwide. Reviews proposed changes in the manufacturing, testing or packaging of a biological product and provides recommendations regarding the potential regulatory impact on product registration. Coordinates and prepares the post-approval documentation (Annual Reports, license renewals, etc) for tal to the appropriate agency to assure compliance with existing registrations.

Qualifications

Education Requirements:

* Minimum of B.S.

Preferred Education:

* M.S. or Ph.D.

Required Experience and Skills:

* Minimum 5 years of experience in biological/pharmaceutical research or manufacturing to include activities directly related to manufacturing, testing, or licensure of biological products.
* Demonstrated effective leadership, communication, interpersonal and negotiating skills.
* Knowledge of regulatory aspects of in-line and new biological products required;
* Sound demonstrated understanding of related fields (e.g., analytical, quality assurance).
* Ability to be creative and imaginative in the approach to new and diverse problem solving.
* Generates innovative solutions to complex regulatory problems.
* Effectively works with and communicates to key stakeholders.
* Meticulous attention to detail.
* Able to critically review detailed scientific information and assess whether technical arguments are presented clearly and conclusions are adequately supported by data.
* Sets clear priorities in support of departmental objectives.
* Able to perform multiple, simultaneous projects and manage projects to aggressive timelines.
* Able to assess project risks and, where appropriate, recommend contingency plans and strategies to mitigate risk.
* Exhibits strong oral and written communication skills in multicultural settings. Able to communicate complex issues in a succinct and logical manner. Strong listening skills.
* Possesses strong working knowledge of business systems and compliance requirements related to the manufacture of biologics.
* Demonstrates flexibility in responding to changing priorities or dealing with expected events.

Preferred:

* Knowledge as applied to vaccines preferred
* Demonstrated technical expertise in formulation, filling, and lyophilization desired.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and submit your resume for requisition REG000957.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Regulatory Affairs Generic

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Sr-Regulatory-Coordinator-Job-PA-19486/1871149/187114918711492012-06-15Merck/MSDRegulatory Affairs Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Currently, we are sourcing candidates for full time union positions for Sterile & Packaging Operators for the Merck Manufacturing Division at our West Point, PA site.

Openings may be for 1st, 2nd or 3rd shift positions which may include working on weekends.

* Some positions require aseptic gowning during performance of job duties.
* Incumbents will be required to obtain all required titers, including but not limited to Mumps, Measles, Rubella, Varicella and Hepatitis A.

Position Overview:

Under the direction of management, the incumbent performs a wide variety of tasks and operations in GMP, aseptic and controlled environments to support and execute production. Duties include but are not limited to:

* Performs line/process changeover procedures as well as general cleaning and disinfecting duties in work areas.
* Cleans and ships material to off-site vendor for refurbishment
* Mops, dusts, polishes, details, sprays, wipes and vacuums floors, ceilings, walls, machinery, windows, and laminar flow hood curtains, etc.
* Empties wastebaskets, transports waste materials and properly tags waste.
* Replaces lights and light covers.
* Prepares, removes and properly labels cleaning solutions and cleaning equipment.
* Completes cleaning related logbooks and documentation.
* Performs disinfection of items entering the aseptic core and other areas.
* Completes log sheets, batch records, training rosters, and other documentation.
* Operates equipment associated with, but not limited to: washing, autoclaving, loading, filling, trayloading, capping and inspection.
* Makes minor adjustments to equipment to clear jams as necessary, communicates issues or problems to technicians or supervisors.
* Monitors equipment, components, and flow of materials to ensure quality.
* Performs sampling as required.
* Interfaces with departmental computer systems as necessary and ensures transactions are processed in a timely and accurate manner.
* Adheres to Current Good Manufacturing Practices.
* Attends training sessions, as required, to maintain skills/knowledge of operations.

Qualifications

Education:

* Must have a minimum of a High School Diploma or a G.E.D.

Required:

* The incumbent may be required to lift up to 50 pounds, periodically work on ladders and handle trash, perform disinfection, etc.
* Sterile & Packaging Operator - Level 1 that are required to work in an aseptic processing area must successfully demonstrate and maintain proficiency in aseptic gowning by passing monitoring tests.
* No relocation or work authorization sponsorship will be offered for these positions.
* All qualified candidates must pass a computer-based Skills Assessment

Preferred:

* 6 months or more experience working in a manufacturing and/or packaging environment
* Experience working in a cGMP, clean room, and/or aseptic environment
* Experience operating automated washers/sterilization equipment

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # USW001016.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: USW, LOCAL 2-86

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Sterile-&-Packaging-Operator-Level-1-%28continuous-recruitment%29-Job-PA-19486/1780439/178043917804392012-06-15Merck/MSDUSW, LOCAL 2-86full-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Position Overview - Roles & Responsibilities

* Under the general direction of an Area Head or Manager, the incumbent is responsible for providing guidance and supervision to hourly employees in completing process, production, maintenance, or production support activities. Responsible for motivation, training, and problem resolution for subordinates.
* Uses team work and good communications to administer personnel policies and the local agreement.
* Ensure the area adheres to Good Manufacturing Practices, approved process steps, SOPs, quality procedures, safety, and environmental standards while operating within the profit plan.

The function of this position is to assure that products manufactured within the integrated process team (IPT) comply with cGMPs, operating procedures, and other applicable regulations. The responsible person will manage the direct processing of materials and supervise the associated hourly workforce within the IPT. The position has specific responsibility for motivating the workforce, work performance, scheduling, task coordination, equipment and area preparation, and administration of personnel policies and procedures.

* Maintain control of processes and product quality by developing appropriate procedures and ensuring compliance with cGMPs, safety and environmental regulations.
* Monitor the manufacturing processes during the shift.
* Participate in internal sub-teams focused on process improvements by using lean methodology.
* Work with IPT members from Quality and Technical Operations to properly handle unplanned events and ensure that corrective actions are implemented.
* Ensure that personnel under his/her supervision are properly trained in cGMPs, procedures, good documentation practices and regulatory matters.
* Monitor personnel practices to ensure compliance with SOPs, practices and regulations.
* Participate in design and implementation of training and development programs.
* Supervise and motivate hourly employees.
* Collaborate with IPT members in the identification and implementation of continuous improvement initiatives and action plans.
* Support activities in the areas of cost reduction, efficiency, productivity, operational excellence and lean practices.

8 or 12 hours rotating shifts - ie. 6 AM - 6 PM / 6PM - 6AM

Qualifications

Education:

* Required: HS Diploma
* Preferred: B.S. or B.A. degree in Science, Engineering, Business or equivalent.

Required:

* Ability to focus on and obtain results.
* Ability to effectively collaborate with and manage a work team.
* Ability to enact conflict resolution.
* Ability to effectively respond to change.
* Excellent analytical and organizational skills.
* Leadership and interpersonal skills to motivate direct reports and peers toward the achievement of production goals.
* High personal integrity, credibility and energy.
* Flexibility to perform related tasks to support the business.

Preferred:

* Experience in responsible line or staff support position related to manufacturing.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition MAN001697.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

*LI-SS2

Job
: Manuf./Operations Generic

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 2

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/West-Point-Associate-Manufacturing-Facilitator-Job-PA-19486/1824602/182460218246022012-06-15Merck/MSDManuf./Operations Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Quality Specialist provides direct Quality support to a production area as part of a Quality IPT (Integrated Production Team) operating model.

The Quality Specialist, with guidance from the IPT Quality Lead or Focus Factory Quality Lead, ensures product / process quality and performs activities to facilitate the release of product to the marketplace and ensures proper control of material through maintenance of the quarantine system.

The Quality Specialist performs 100% process document / log book audits for accuracy and completeness and works closely with the assigned Focus Factory in a team environment to ensure timely review and documentation is done right first time.

He or she provides Generalist Quality support directly to the production floor, to include oversight for adherence to cGMPs, right-first-time completion of production GMP documentation, and effective investigation of deviations.

Additionally, the Quality Specialist performs routine GMP walk through inspections of the shop floor within the assigned Focus Factory to ensure compliance with cGMPs and regulatory requirements.

The Quality Specialist will become knowledgeable in Federal and other regulatory agency requirements and cGMPs to assure that all areas in compliance, and will train on and gain competency in activities to facilitate release of product for assigned Focus Factory.

Job functions are performed primarily on the production shop floor and in a team environment. Specific responsibilities include but are not limited to the following:

¨ Performs 100% audit of process documents / log books to ensure completeness and accuracy for assigned Focus Factory. Maintains any tracking databases and logs associated with this review.

¨ Provides coaching and mentoring of manufacturing supervisors and operators completing documentation.

¨ Coordinates with Production to discuss, resolve, and eliminate documentation observations.

· Performs GMP walk through inspections of assigned departments within Focus Factory to ensure compliance with cGMPs and regulatory requirements.

· Ensures proper identification of release status and control of materials through maintenance of quarantines in the IMPACT system and through physical tagging of material as required.

· Performs Quality review / approval of new and updated SOPs and CJAs.

· Assists with training of incoming personnel and ensures compliance with departmental procedures.

· Actively participates in the Tier process and uses this forum to escalate concerns and best practices.

· Collaborates with IPT members in the identification and implementation of continuous improvement initiatives and action plans.

· Collaborates with IPT members to investigate deviations on production floor during shift.

· Works with necessary groups within the Focus Factory to resolve outstanding issues with process documents / log books, GMP walk through inspection observations and quarantine, management.

· Prioritizes review of process documents / log books in order to maximize cycle-time efficiency.

Note: This shift would be a 12 hour day shift work day currently from 7AM to 7PM (days would be WHF).

Qualifications

Education:

· Bachelor's degree required. Technical emphasis in an appropriate engineering field preferred; candidates with majors in other fields will be considered if accompanied by significant relevant experience.

Required:

· At least two (2) years of relevant post-degree work experience in a manufacturing, or quality position.

· Evidence of leadership skills coupled with good oral and written communication skills, i.e. effective presentation of concepts and ideas, as well as interpersonal and conflict resolution skills.

· Attention to detail, flexibility and an awareness of production and attendant quality control problems.

· Basic understanding of cGMPs and of regulatory requirements as they apply to the pharmaceutical field or a related area.

· Must be able to work any shift with the possibility of a rotating schedule and/or including weekends.

Preferred:

· Familiarity with vaccine and/or pharmaceutical processing.

· Familiarity with steam sterilization technology, dry heat sterilization equipment and/or cleaning equipment./

· Experience in quality assurance audits or inspection of vaccine or pharmaceutical manufacturing areas is a strong plus.

· Aseptic gowning may be required.

Note: Titers required.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # QUA002900.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Quality Operations

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/West-Point-Quality-Specialist-Job-PA-19486/1883044/188304418830442012-06-15Merck/MSDQuality Operationsfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Summer Internship in the In Vivo Pharmacology Department in West Point, PA provides an opportunity to perform experiments using preclinical species to evaluate in vitro/in vivo efficacy of compounds. The team is responsible for establishing assays and models for diseases such as diabetes and osteoporosis to characterize lead compounds. The team collaborates with other groups within MRL to efficiently execute on program needs and integrates and communicates activities of the group with other functions including Disease Area Biology Program Teams, Chemistry Team, Imaging Team, and Laboratory Animal Resources groups.

The primary responsibilities of the intern in this team include:

* Perform experimental bench work to implement routine in vitro / in vivo assays for functional muscle testing as well as gene silencing using short interfering RNA sequences.
* Enter data and analysis into appropriate notebook
* Work collaboratively within team/department
* Provide an appropriate level of communication with supervisor regarding agreed upon responsibility for data qualification
* Ensure appropriate animal care and use, following institutional care and "3R" (reduce, reuse, refine) principles
* Understand and follow regulations to assure and promote a safe work environment

Qualifications

Required:

* Must be pursuing a Bachelor or Master's degree in a Biological Science field (primarily Physiology, Kinesiology, Biology)
* Must have at minimum one year remaining before graduation
* Basic physiology knowledge
* Ability to utilize pharmacological, physiological, and/or surgical techniques
* Accurately and clearly record data/experiments
* Effective oral and written communication skills
* Good working knowledge of Microsoft Excel, Word, Power Point

Preferred:

* Working in a regulated environment (e.g. familiar with personal protective equipment, chemical hazard regulations)
* A theoretical background in kinesiology, bone biology, or short interfering RNA biology

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #PHA001048.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-PA-West Point

Job Type
: Intern
Employee Status: Regular

Travel
: No
Number of Openings: 1

Relocation Provided
: Domestic (within country)]]>http://jobs.merck.com/job/West-Point-Disease-Research-%28In-VivoIn-Vitro%29-Internship-2012-Job-PA-19486/1729545/172954517295452012-06-15Merck/MSDInternfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The team member within the Department of Neurosymptomatic Disorders will be a member of a team of scientists that uses in vitro and in vivo pharmacological approaches in preclinical discovery and development of drug candidates for the treatment of Alzheimer's disease and other neurodegenerative disorders.

The responsibilities of the team member include:

* Conducting experiments to support preclinical drug discovery efforts at different stages of development including target identification and validation, lead identification and lead optimization.
* Designing and executing preclinical research studies to support the clinical development of small molecule candidates
* Generating and integrating data from in vitro and in vivo experiments towards the discovery and validation of target engagement, pharmacodynamic, efficacy and safety biomarkers of drug candidates.
* Collaborating with members from several functional areas including In Vitro Pharmacology, In Vivo pharmacology, Medicinal Chemistry, Basic Pharmaceutical Sciences, Safety Assessment, and Exploratory and Translational Sciences.
* Working with external academic, biotech, and contract research organizations.
* Monitoring the external research environment and help to establish collaborations that are aligned with the Neuroscience franchise strategy.
* Managing internal and external resources to accomplish scientific goals in a rigorous and cost effective manner.

Additional responsibilities of the team member include:

* oversight of summarization and consolidation of experimental data;
* ensuring that study objectives and results are communicated in a concise and clear manner to the appropriate teams and committees;
* managing the design of research protocols and execution of experimental studies using standard and innovative scientific approaches and techniques;
* may represent franchise biology on cross-functional project teams;
* monitors external trends and developments;
* works with and communicates with all levels of individuals within the DPS functional and Neuroscience franchise discovery groups;
* may have scientific management responsibilities of other scientists within the group.

Qualifications

Education:

* PhD in Neuroscience or related areas (example: Pharmacology, Cell and Molecular Biology, Biochemistry, etc)

Required:

* Experience in discovery of drug candidates in preclinical stage and/or at least 3 years of post-doctoral training in related area
* Expert knowledge of biological principles, concepts and theories
* Demonstrated ability to develop practical research strategies and to translate strategy into experiments
* Demonstrated ability to thrive in a team environment
* Ability to communicate clearly and candidly
* Demonstrable leadership skills
* Proven ability to create and work within high performance teams in a matrix organization

Preferred:

* Subject matter expertise in the biology and pathophysiology associated with Alzheimer's disease
* Subject matter expertise in preclinical research approaches related to Alzheimer's disease models and/or lipid metabolism.
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # BIO003586.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Biology-Discovery

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Radioactive material, human and non-human primate samples]]>http://jobs.merck.com/job/West-Point-Neuroscience-Biology-Team-Member-Job-PA-19486/1862509/186250918625092012-06-15Merck/MSDBiology-Discoveryfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Currently, we are sourcing candidates for Sterile & Packaging Operations Technician - Level 1 for the Merck Manufacturing Division at our West Point, PA site. Under the direction of a supervisor, the incumbent will be responsible for the essential functions of the position.

Duties include, but are not limited to:

* Perform a wide variety of tasks and operations in GMP, aseptic and controlled environments that are required to support and execute production. This includes formulating bulk product and culture media, performing cleaning and sterilization of equipment, setting-up and operating filling equipment, staging and loading components and bulks, setting-up and operating inspection equipment, setting-up and operating the nitrogen tunnels for freezing, completing lyo cabinet operations, staging and loading packaging components, setting-up and operating packaging equipment, and completing associated batch record and log-book documentation.
* Operate and maintain assigned equipment in SPO by performing mechanical, electronic, electrical, and pneumatic/hydraulic troubleshooting and repairs.
* Complete preventative maintenance and repairs as assigned for the equipment and facilities within Sterile and Packaging Operations.
* Perform cleaning and housekeeping requirements as assigned in the areas.
* Perform all duties of other classifications in Sterile and Packaging Operations as assigned by supervision.
* Perform in a leadership role to coordinate and execute line/equipment set-up, start-up, and on-going operations on a daily basis.
* Provide real-time status of the operation of a line or individual piece of equipment and guides the activities of other classifications assigned to a specific operation or production activity to ensure effective operation of the equipment and completion of scheduled activities.
* Responsible for completing documentation as assigned by supervision to monitor the performance of equipment and line operations; and participates in team meetings to focus on increased performance and safety of the equipment in each operating area

PLEASE NOTE:

* This is a Union position in a manufacturing environment.
* The hourly rate for this position is $22.31
* Openings may be for 1st, 2nd or 3rd shift, which may include working on weekends.
* Some positions require aseptic gowning during performance of job duties
* No relocation or work authorization sponsorship will be offered for these positions.

Qualifications

Required Education:

* High School Diploma or Equivalent.

72 hours - Packaging Machine Electricity/Electronics I

72 hours - Packaging Machine Electricity/Electronics II

72 hours - Packaging Mechanics I

72 hours - Packaging Mechanics II

OR, the equivalent accredited courses consisting of ALL of the following:

144 hours - Electricity/Electronics

144 hours - Machine Trades

Required Experience:

In addition to the educational requirements listed above, candidates must have a minimum of three (3) years recent (within the last seven years) experience after completion of required coursework, in the set-up, repair & operation of complex mechanical equipment used in washing, filling, conveying, sealing or inspection of products/containers. It also must include equipment set-up, changeover, mechanical repairs, disassembly and repair, and preventative maintenance.

Required Assessment:

* Candidates must pass a computer-based Skills Assessment
* Candidates must pass the Merck Manufacturing Division's (MMD) "Standard Timing Model" as well as the MMD Electrical standard training module for consideration.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # USW000867. Open to U.S. Residents & Citizens Only.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: USW, LOCAL 2-86

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Sterile-&-Packaging-Ops-Technician-Level-1%28continuous-recruitment%29-Job-PA-19486/1324108/132410813241082012-06-15Merck/MSDUSW, LOCAL 2-86full-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Future Talent Program features paid internships targeted to start in June 2012 for 10 - 12 weeks and will include one or more projects. Housing is available for those interns meeting the housing distance guideline. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals.

The successful candidate will be responsible for assisting with the implementation of all necessary federal, state and local government regulations pertaining to employee safety and environmental protection at the West Point site. This position will work directly with a number of Safety and Environment Engineers on the following activities:

* Completion of hazard assessments, industrial hygiene monitoring, incident investigations, respirator fit testing, training, environmental regulatory analysis, environmental reports and permit applications.
* Provides support to client groups in completing injury/illness analysis, training, self assessments and addressing specific Environmental, Health and Safety (EHS) concerns as they are raised.

Location: West Point, PA

Qualifications

Education:

* Working towards completion of BS, MS or PhD degree with a concentration in Safety or Environmental related technical discipline

Requirements:

* Available for 10 week internship beginning June 2012
* Strong personal character and ethics
* Superior communication and interpersonal skills
* Excellent academic achievement, analytical ability
* Good team player and ability to work independently
* U.S. citizen or lawful permanent resident of U.S.

Preferred:

* Previous EH&S experience via internship

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ENV000195

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-PA-West Point

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Environmental%2C-Health-and-Safety-Internship-2012-Job-PA-19486/1729505/172950517295052012-06-15Merck/MSDInternfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Future Talent Program features paid internships targeted to start in June 2012 for 10 -12 weeks and will include one or more projects. Housing is available for those interns meeting the housing distance guideline. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals.

The ideal candidate will work with a member of the Center on a project related to Merck's chemical, pharmaceutical or vaccine manufacturing. The project will involve researching possible statistical approaches, implementing the most effective approach using the appropriate software package and reporting the results. The candidate will also have the opportunity to work with staff members on ongoing consulting projects. This will provide the opportunity to experience how statistics is used in real world situations.

LOCATIONS: West Point, PA - Summit, NJ - Whitehouse Station, NJ

Qualifications

Education:

* Working toward Masters or Ph.D. in Statistics Program (or equivalent such as Industrial Engineering with a statistics focus).

Requirements:

* Available for 10 week internship beginning June 2012
* Coursework should include 1-2 semesters of graduate level statistical theory and methods
* Course work in Regression, ANOVA and design of experiments (DOE) is beneficial.
* Teamwork skills.
* Statistical computing skills in at least one package such as SAS, S-Plus/R, JMP or Minitab.Excellent oral and written communication skills
* U.S. citizen or lawful permanent resident of U.S
* Titers may be required for this position

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #ADM004816.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-PA-West Point
Other Locations: US-NJ-Whitehouse Station, US-NJ-Summit

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1

Relocation Provided
: None]]>http://jobs.merck.com/job/West-Point-MMD-Statistics-Intern-2012-Job-PA-19486/1729520/172952017295202012-06-15Merck/MSDInternfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Future Talent Program features paid internships targeted to start in June 2012 for 10 - 12 weeks and will include one or more projects. Housing is available for those interns meeting the housing distance guideline. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals.

We are seeking an intern to join the Global Human Health (GHH) IT Global Solutions Delivery organization. The Global Solutions Delivery organization provides capabilities to support Merck's commercial operations world-wide.

The selected candidate will be responsible for one or more of the following activities:

* Business analysis
* Technical analysis
* Process definition
* Process management and testing

The selected candidate will likely gain hands-on experience with salesforce.com and/or Oracle's Siebel CRM platform.

Qualifications

Education:

* Second (2nd) Year Bachelor's Program

Required:

* Available full-time from June 2012 through August 2012

Preferred:

* Strong communication and teamwork skills
* Strong technical analysis skills
* Ability to learn complex, new business processes and technologies
* Experience with System Life-Cycle methodologies
* Completed at least two years in a field of study that combines information technology and general business skills

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # ADM005014.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations

.

Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Primary Location: US-PA-West Point

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Intern-Technical-Analyst-Anthony-Posca-Job-PA-19486/1862952/186295218629522012-06-15Merck/MSDInternfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under direction from a Manager/Director, the QS/Compendial Staff Scientist is responsible for: providing functional support for activities such as: new products, in-line products, packaging, outsourcing, divestitures, analytical compliance, Quality Standards, compendial monitoring and compliance, SLC, Quality Assurance, etc.; providing customer support to MMD manufacturing sites and laboratories, other Quality and Regulatory functional groups, Analytical Development, MRL, Technical Operations, Joint Ventures, etc.; performing the appropriate document review and support activities associated with their position and ensuring their work is in compliance with all regulatory expectations. The incumbent is also responsible for the application of and conformance to current Good Manufacturing Practices (cGMP). Primary responsibilities include, but are not limited to:

* Providing internal/external support as part of Merck's official review and response to compendial proposals/issues and may represent Merck at external pharmaceutical/excipient trade organizations to influence the compendia.
* Authoring and issuing clearly written Quality Standard documents and/or new/revised compendial monographs in accordance with established divisional and departmental procedures for both biological and pharmaceutical materials.
* Providing support to the MMD Quality Standard/Compendial customers.
* Performing the evaluation, disposition and implementation of Quality Standard changes/modifications in accordance with the Analytical Change Control (ACR) process.
* Providing Quality Standard/compendial support and coordination for new product introductions and registrations, and may participate in new product teams and activities associated with the Developmental Quality Standards.
* Participating in activities and providing appropriate support to Merck Business partners in accordance to the approved supply agreements/contracts.

Qualifications

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

Education Minimum Requirement:

* BS/MS in Chemistry/Biology or related science in a relevant discipline

Required Experience and Skills

* BS with minimum of 2 years experience OR MS with no minimum experience.
* Strong technical knowledge and high level of technical performance.
* Established laboratory experience, knowledge of laboratory operations and analytical instrumentation and/or technical experience and knowledge and general knowledge of the major pharmacopoeia.
* Superior written and oral communications skills, advanced problem solving and proficient decision making skills.
* Proficient computer skills.

Preferred Experience and Skills

* Ability to work in teams, manage multiple projects/tasks simultaneously with competing priorities, provide customer support, and manage time and personal effort.
* Ability to think originally and imaginatively in developing creative ideas.
* Possess the skills to persuade and motivate others.

merck.com/careers to create a profile and your resume for requisition REG000963.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Regulatory Affairs Generic

Primary Location: US-PA-West Point
Other Locations: US-NJ-Summit
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-QS-Scientist-Job-PA-19486/1895229/189522918952292012-06-15Merck/MSDRegulatory Affairs Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Pain & Migraine is a key research area within Merck Research Laboratories (MRL) located in West Point, PA. The department focuses on both discovery of novel therapeutics and the identification/validation of novel pain and migraine targets.

We are seeking an intern to support early compound discovery and disease target localization in the central nervous system. The successful applicant will participate in localization of small molecule binding sites using a diverse set of molecular and biochemical approaches to elucidate the underlying pathophysiology of the disease. Other responsibilities may include the preparation of technical reports, presentations, and external publications (as appropriate).

The ideal individual will be highly motivated, creative, and well-organized. In addition he/she will possess excellent communication skills and work in a team environment. The intern will gain pharmaceutical research experience not only within the Pain & Migraine department, but will have the opportunity to interface with other divisions within discovery biology.

This is a 9-11 week, paid internship beginning in June 2012. Housing will be provided to those who meet distance requirement.

Qualifications

Required:

* Currently pursuing MS or PhD in a Biological Sciences field
* Must be able to complete a 9-11 week internship beginning June 2012 at Merck's facility in West Point, PA
* Candidate will have demonstrated good laboratory skills

Preferred:

* Basic immunohistochemistry skills and research experience

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #BIO003468.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-PA-West Point

Job Type
: Intern
Employee Status: Regular

Travel
: No
Number of Openings: 1

Relocation Provided
: Domestic (within country)]]>http://jobs.merck.com/job/West-Point-Pain-&-Migraine-Research-Internship-2012-Job-PA-19486/1729506/172950617295062012-06-15Merck/MSDInternfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Under direction from a Manager or Director, the Document Specialist is responsible for general administrative work and for work in various systems for Merck's vaccine product franchise in accordance with department procedures and direction from management, Primary responsibilities include, but are not limited to:

Project Responsibilities:

· Prepares incoming agency correspondence for posting to edossier - Merck's official regulatory submission repository. Follows procedures to understand the nature of the submission and ensures it is posted correctly.

· Serves as a coordinator of information for the department (managing regulatory commitments and closeouts database, planned regulatory submissions database, training database, etc.).

· Uses various databases/systems to compile changes for inclusion in each product's annual report, under the guidance of team scientists. Systems include Trackwise, QSIS, Core WMA, etc.

· Creates new change entries in the registration information system (Orion or other) under the direction of team scientists.

· Serves as a Trackwise GCM Coordinator to assign change requests to scientists, to populate various fields in Trackwise, and to ensures CR closeout according to established timelines.

· Collects data from Core WMA, Trackwise, and Orion, to confirm that regulatory closeout can occur for change requests. Prepares and sends regulatory closeout memos to the change control unit.

· Formats cover letters and completes FDA forms for US regulatory submissions. Works with the Sr. Director to collect signatures as needed.

· Mentors newly hired staff, dependent upon experience level

· Completes general administrative tasks such as scheduling meetings, helping with expense reports, filing, copying, etc.

Technical Competence:

· Good oral and written communication skills.

· Flexible, collaborative, and good people-skills.

· Advanced knowledge of WORD. Experience working in Merck systems.

· Superior attentiveness to detail.

· Ability to prioritize tasks to meet deadlines and work with team when help is needed.

· Ability to identify problems and work with team to formulate a potential course of action.

Quality Responsibilities:

· Demonstrates awareness of the compliance nature of regulatory activities.

This position is in Vaccine CMC which supports regulatory work for change control and licensing for all vaccine manufacturing sites.

Please note, relocation assistance is not provided for this position.

Qualifications

Required:

* High school diploma
* At least two (2) years of relevant experience i.e. as an administrative assistant and in using GMP system(s).
* Demonstrated oral and written communication skills with the ability to communicate issues in a succinct and logical manner. Strong listening skills.
* Demonstrated flexibility in responding to changing priorities or dealing with unexpected events.
* Demonstrated interpersonal and negotiating skills to work effectively with and communicate with key partners one-on-one or in a team setting.

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition # REG000961.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: Regulatory Affairs Generic

Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Document-Specialist-Job-PA-19486/1885953/188595318859532012-06-15Merck/MSDRegulatory Affairs Genericfull-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Currently, we are sourcing candidates for Pharmaceutical Technician - Level 1 positions for the Merck Manufacturing Division at our West Point, PA site. Under the direction of a supervisor, the incumbent will be responsible for the essential functions of the position.

Duties include, but are not limited to:

Operates automated and non-automated equipment, including processing and non-processing equipment. Performs material handling duties and cleaning of equipment in process areas involved in the receipt, arrangement, issue, classification, and storage of incoming and outgoing materials.

Responsibilities include setup, operation, teardown and cleaning of all equipment directly associated with, and in support of, pharmaceutical manufacturing and packing processes.

The Pharmaceutical Technician-Level 1 documents all work on Manufacturing Process Descriptions or on departmental forms. Complies with Manufacturing Process Descriptions (MPDs), Standard Operating Procedures (SOPs), Material Safety Data Sheets (MSDS), environmental regulations, and all aspects of current Good Manufacturing Practices (cGMPs) in order to ensure that products and services are of the highest quality.

Note:

* Must successfully complete the Pharmaceutical Operations mathematics, reading and accountability modules upon placement.
* Must successfully complete all departmental training modules and TQM requirements as part of ongoing training.
* Must successfully complete all material handling training/verification as part of ongoing training.
* Must successfully complete Logistics/Supply Chain development training as part of ongoing training.

Please note, this is a Union position in a manufacturing environment.

The hourly rate for this position is $19.87/hr.

Openings may be for 2nd, or 3rd shift positions which may include working on weekends.

Candidates must be flexible to work any available shift/day offered.

No relocation or work authorization assistance is offered for this position.

This position may require heavy lifting (with assistance) of up to 100 lbs.

In the performance of work, there may be exposure to solvents, heat and humidity.

Qualifications

Required Education:

* High School Diploma or equivalent (GED)

Required Assessment:

* Candidates must pass a computer-based Skills Assessment
* Candidates must pass the Merck Manufacturing Division's (MMD) "Standard Timing Model"

Required Experience:

* Must have 3 of last 5 years experience working in a skilled job requiring mechanical or electrical aptitude.

Preferred:

* Familiarity with Microsoft applications
* Familiarity with computer touch screens relating to manufacturing processes

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #USW001029.

Open to U.S. Residents & Citizens only.



Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Search Firm Representatives

Please Read Carefully:

Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

Job
: USW, LOCAL 2-86

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/West-Point-Pharmaceutical-Tech-Level-1-%28Continuous-Recruitment%29-Job-PA-19486/1804838/180483818048382012-06-15Merck/MSDUSW, LOCAL 2-86full-timeUSDstarting0BSWest Point, PA, US
Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


The Future Talent Program features paid internships targeted to start in June 2012 for 9 to 11 weeks and will include one or more projects. These opportunities can provide you with great development and a chance to see if we are the right company for your long-term goals.

This position will be working in Shared Business Services (SBS) America's Procure to Pay organization in Charlotte, NC.

This position will include working in a team environment on a special project. The primary focus will be the identification of improvement areas by analyzing process exceptions. The deliverable will be a report which details the exceptions or defects within the process and recommendations for changes from a systems or process perspective.

The individual in this position will be responsible for but not limited to:

* Collect relevant data, interview individuals within and outside of Merck to gauge their knowledge of the process and system to begin to narrow the root cause behind the defects.
* Work with system and process flow diagrams.
* Diagram recommendations and articulate in a clear and concise manner the problem, root cause and recommendation to eliminate defects from recurring.

Qualifications

Education:

* Pursuing a Bachelors degree

Required:

* Ability to work full-time beginning in June, 2012 for a period of 9 to 11 weeks
* Analytical skills
* Communication skills
* Presentation experience

Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

merck.com/careers to create a profile and your resume for requisition #IT 000328.

Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.


Primary Location: US-NC-Charlotte

Job Type
: Intern
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Charlotte-Intern-Procure-to-Pay-Job-NC-28201/1868796/186879618687962012-06-15Merck/MSDInternfull-timeUSDstarting0BSCharlotte, NC, US