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Description

The NPI Engineer will be the technical lead for new product introduction and tech transfer in a formulation/fill production facility.

This role sets the strategy for process development, scale up activities associated with the technology transfer of multiple products.

Key Responsabilities

1. Will lead Design of Experiments and complex technical investigations associated with the introduction of new products and commercial products.

2. Network within the internal and the external technical communities to bring best practices to Carlow and share best practices with the wider MSD/Merck organisation.

3. Mentor other Engineers and Scientists in the Tech Ops organization to increase its capability in the area of technology transfer and process support.

4. Co-ordination of process development activities on the manufacturing floor, the technology operations laboratory and at other MSD sites associated with specific tech transfers.

5. Collaborate with product owners, process subject matter experts, operations, quality, validation etc. to introduce robust processes to the Carlow site.

6. Work collaboratively to drive a safe and compliant culture in Carlow.
May be required to perform other duties as assigned.

Qualifications

· Bachelors Degree or higher preferred; ideally in a Science or Engineering discipline.

· 6-8 years experience in a process engineering role in a pharma environment; preferably in the biopharm industry.

· Proven track record of accomplishment in the area of tech transfer/process development/process scale up.

· Excellent protocol and report writing skills.
Strong communication skills both verbally as well as written.

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/New-Product-Introduction-Engineer-Job/1510512/151051215105122012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
Description

MSD is seeking an individual to manage a portfolio of capital projects at the Carlow site. Reporting to the Global Engineering Services Regional Director the incumbent will manage projects which typically range up to 1 million Euros with an estimated annual value of 10 million Euros. Project types include process improvements, infrastructure upgrades, regulatory upgrades, and equipment replacements implemented within operating facilities. The incumbent may also potentially manage some projects at other Ireland sites.

Major/Key Accountabilities:

· Work with manufacturing plant management teams to identify and initiate projects

· Develop Capital Expenditure Authorization documents to include cost estimates and project justification.

· Develop project plans and successfully execute them according to established schedule, cost and performance standards.

· Directly manage/co-ordinate a team of site-based AE/CM resources to ensure safe and effective project implementation

· Track and report progress as required against project deliverables

· Interface with Site Operations, Quality, and Maintenance to coordinate project activities

· Ensure strict adherence to Site Change Control procedures as well as project specific plans and procedures.

Qualifications

Qualifications:

· Must have as a minimum a 3rd level Degree in Engineering.

Skills and Knowledge:

· A minimum of eight years project experience, preferably in Pharmaceutical Industry in a project engineering type role.

· Strong interpersonal skills and an understanding of the customer/client relationship involved in project engineering

· Excellent communication /presentation skills

· Familiar with engineer project management methods and tools such as MS Project

· Solid technical skills including an ability to review detailed engineering documents

· Basic financial management skills with a focus on capital expenditure. Must have ability to work within budgets.

· Experience in preparing requests for bid and administering environmental, design and construction contracts.

· Understands the typical project life cycle from concept through to qualification and has proven experience in this area.

· Superior organizational and planning skills.

· Capable of managing and prioritizing multiple projects

· Have proven knowledge, appreciation and proven experience of working in strongly regulated GMP environment.

· Experience in lean six sigma and root cause analysis techniques would be and advantage

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Senior-Project-Engineer-Job/1437635/143763514376352012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
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

Primary Location: IE-L*-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/1510510/151051015105102012-03-04Merck/MSDfull-timeUSDstarting0BSDublin, 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.

Primary Location: IE-L*-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/1538425/153842515384252012-03-04Merck/MSDfull-timeUSDstarting0BSCarlow, L*, IE
Description

Under the direction of the Regional Quality Director (AH - International Vaccines & FMD), the Project Manager (Blackbelt) will: 1) operate as an internal consultant for Site Quality Heads and their teams to develop plans and execute performance improvement activities particularly with regard to roll out of Lean Lab across all (28) AH sites; 2) develop Lean management and people development processes and plans; 3) manage processes and projects to realize intended business benefit; 4) utilize various Lean and six sigma tools and techniques to analyze and improve business processes; 5) provide teaching and coaching to effectively transfer Lean skills into the organization.

The Lean lab Project 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 relevant IT systems.

- Apply scientific problem solving (PDCA), standardized work, and six sigma to solve process and system (full value stream) problems.

- Facilitate Kaizen workshops.

- Effectively manage and monitor project progress using self determined metrics and relevant project management tools

-Coach and develop E2E managers and supervisors to apply Lean management principles and develop their direct reports or teams in problem solving and standardized work.

- Develop and manage continuous improvement processes (Visual Work Place, Lean Experts Selection & Development Process, etc..)

- Apply behavior coaching techniques to influence decision making and to guide continuous improvement activities.

Qualifications

Qualified candidates must have a bachelor's degree in a related field as well as hands-on experience with application of most of the following Lean and Six Sigma tools and techniques: Standardized Work, Scientific Problem Solving, value stream mapping, SMED, mistake proofing, 5S-Visual Factory, DMAIC.

Must also have the ability to apply Lean Sigma skills to both operatonal and transactional processes and have extensive experience with MSA (measurement system analysis) and gauge RnR

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.

Desired: Extensive Lean application experience, Six Sigma black belt certification; excellent skills using IT applications to organize and analyze data (MS-Access, MS-Excel, Minitab).

Experience in operations management, QC, or related disciplines preferred.

Experience within pharmaceutical industry preferred.

Primary Location: IE-L*-Dublin
Other Locations: Spain
Employee Status: Regular
Number of Openings: 1

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Black-Belt-Manager-Job-L/1385044/138504413850442012-03-04Merck/MSDfull-timeUSDstarting0BSDublin, 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.


Responsibilities include participating in all elements of the marketing mix including marketing plan development, advertising and promotion planning, marketing research and consumer insights, new product development, market and competitive analysis, sales forecasting, budget and financial management, and manufacturing and operations interface. Once acclimated to the position, the candidate will assume sole ownership of several areas of the marketing mix under the supervision of a Product Manager or Senior Product Manager within the Marketing department of the Suncare, Footcare, GI or Respiratory strategic business units. Major brands include Claritin, MiraLax, Coppertone, Dr. Scholl's, Tinactin, Lotrimin, Afrin, and Coricidin.

* With support from others, conduct strategic market analysis to help improve strategic decisions about products.
* Solicit, gather and undertake database analysis, segmentation, and forecasting with direction
* Analyze market trends, sales potential and prepare forecasts for use in planning control
* Develop sales forecasting and inventory flow models and manage brand budgets
* Help establish key issues, strategies tactics, action plans, market growth strategies, and profits for key products
* Help develop brand strategy and engage in life-cycle planning
* Support Product Mangers in implementing product plans enable the deliver of brand value
* Work closely with sales and field personnel to meet their needs, communicate strategy, and service their issues.
* Develop materials
* Conduct pricing analysis
* Manage project budgets
* Work under general supervision
* Look for ways to use best practices and seek others to learn from.

This is a paid internship targeted to start in June 2012 for 10 weeks, whereby a weekly stipend will be provided. Subsidized housing is available for interns living more than 50 miles from the site of their internship.

Summer Interns will be responsible for 1 larger "strategic" project, which will be the basis for their end of summer presentation. Additionally, they will work on a broad range of other projects that will immerse them into the typical APM role

Qualifications

* MBA (1 year of Business School to be eligible for Summer Internship)
* 3+ 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 # MAR004076.

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


Primary Location: United States
Employee Status: Regular
Number of Openings: 3

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Consumer-Marketing-Summer-Intern-Job/1455394/145539414553942012-03-04Merck/MSDfull-timeUSDstarting0BSUnited States
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.

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Record-to-Report-Finance-Analyst-Job/1366985/136698513669852012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
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 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

Qualifications:

Education:

* Bachelors Degree required.
* Business Level fluency (oral and written) in French or Dutch 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.

Primary Location: IE-L*-Dublin
Employee Status: Regular
Number of Openings: 3

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Dutch-or-French-Collections-Analyst-Job-L/855119/8551198551192012-03-04Merck/MSDfull-timeUSDstarting0BSDublin, IE
Beschreibung

Die Veterinaria AG als Schweizer Niederlassung von MSD Animal Health ist ein führendes veterinärmedizinisches Unternehmen. Wir stellen die Tiergesundheit und die veterinärmedizinische Ethik in den Mittelpunkt unseres Handelns.

Zur Verstärkung unseres motivierten und dynamischen Management Teams suchen wir per sofort oder nach Vereinbarung für die Business Unit Nutztiere einen/eine kommunikative/n, kundenorientierte/n und engagierte/n

Leiter/Leiterin Geschäftsbereich Nutztiere

Nach Ihrem abgeschlossenen Studium der Veterinärmedizin, Pharmazie, Naturwissenschaften oder Agronomie konnten Sie sich einige Jahre Erfahrungen in der veterinär- oder pharmazeutischen Industrie oder Agrarwirtschaft aneignen. Nun möchten Sie Ihre Führungserfahrung, Ihre sehr guten fachlichen Kenntnisse, Ihr Marketingflair sowie Ihr unternehmerisches Denken unter Beweis stellen.

In Ihrer Funktion sind Sie für den Erfolg des Geschäftbereiches Nutztiere als grösste Business Unit verantwortlich. In dieser Funktion erstellen und überwachen Sie das Verkaufs- und Marketingbudget. Sie sind verantwortlich für das das Definieren der Marketingstrategien in enger Zusammenarbeit mit Ihrem Team, setzen diese praktisch um und motivieren und coachen Ihr Verkaufsteam. Ihre kommunikative, kundenorientierte und überzeugende Art erlaubt Ihnen die Pflege vielfältiger Kontakte mit Meinungsbildnern und Produzentenorganisationen sowie wichtigen Kunden in der tierärztlichen Praxis und an Universitäten. Sie haben Freude an einer interdisziplinären Tätigkeit in einem nationalen und internationalen Umfeld.

Qualifikationen

Nebst obgenannten Qualifikationen verfügen Sie über gute Sprachkenntnisse in D/E/F. Ihre sehr gute Sozialkompetenz ermöglicht Ihnen Ihr Team zu motivieren und weiterzuentwickeln.

Bei uns erwarten Sie selbständige und abwechslungsreiche Aufgaben, gute Weiterbildungs-möglichkeiten, fortschrittliche Anstellungsbedingungen und gute Sozialleistungen. Selbstverständlich werden Sie sorgfältig in das Fachgebiet eingearbeitet.

Sind Sie interessiert an dieser vielseitigen Aufgabe mit Entwicklungsmöglichkeiten? Dann freuen wir uns auf Ihre vollständigen Bewerbungsunterlagen.

Veterinaria AG, Personalabteilung, Frau Pascale Jenzer, Churerstrasse 158, 8808 Pfäffikon/SZ, pascale.jenzer@merck.com

Primärer Standort: CH-Schwyz

Mitarbeiterstatus: Permanent

Reisebereitschaft:: Ja, 25 % der Zeit

Anzahl offener Stellen: 1]]>http://jobs.merck.com/job/Schwyz-LeiterLeiterin-Gesch%C3%A4ftsbereich-Nutztiere-Job/1553320/155332015533202012-03-04Merck/MSDfull-timeUSDstarting0BSSchwyz, CH
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.

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/ItalianGerman-Order-to-Cash-Finance-Analyst-Job/1366982/136698213669822012-03-04Merck/MSDfull-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

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Process-Engineer-%28Inspection-Systems%29-Job/1405510/140551014055102012-03-04Merck/MSDfull-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.


A Senior Laboratory Technician is responsible for critical laboratory procedures and duties in the production of veterinary products. Technicians may work a variety of technical equipment while completing cell culture processes throughout the manufacturing process. At all times technicians must follow Good Manufacturing Practices and Standard Operating Procedures and adhere to all safety and company policies, perform duties assigned by department supervision.

Some of the duties may include, but are not limited to:

* Perform procedures including aseptic work, media preparation, antigen inoculation and harvest, tissue culture preparation and harvest, filling vaccines, etc.
* Assist in formulations and calculations
* Maintain accurate and reliable record keeping including charts, log books, and all pertinent documentation
* Communicate any unusual and/or non-routine occurrences when performing tasks
* Cleaning work areas, prepare, clean and sterilize glassware and equipment for use
* Equipment setup and operation
* Train and mentor other technicians in manufacturing

This is a Monday-Friday 1st shift position

Qualifications

Education Minimum Requirement:

* High School diploma/ GED with a minimum of 3 years laboratory or related laboratory experience, OR Associates degree with a minimum of 2 years laboratory or related laboratory experience OR Bachelors degree in Biology, Biological Sciences or related Life sciences discipline

Required Experience and Skills:

* Applicant must be able to work a flexible schedule to meet the demands of the manufacturing process
* Must have the ability to read, write and understand technical information and to effectively communicate information to colleagues are various levels

Preferred

* Training in Aseptic Clean room Behaviors
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 # TEC000437.

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-DE-Millsboro
Employee Status: Regular
Number of Openings: 4]]>http://jobs.merck.com/job/Millsboro-Lab-Tech-II-Production-Job-DE-19966/1703554/170355417035542012-03-04Merck/MSDfull-timeUSDstarting0BSMillsboro, DE, 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 train and supervise a team of animal husbandry technicians and must have expertise in caring for a variety of species including, but not limited to dogs, cats, poultry, large animals (horse) and fish.
* The candidate must work closely with the Supervisor of Animal Use to coordinate day-to-day activities.
* The candidate will manage the daily operations of two facilities which includes, not only maintaining animal housing in good repair, but also includes, and is not limited to, procurement of animals and supplies, maintaining fleet vehicles and monitoring incineration activities.
* The candidate will serve as the project leader for all capital projects at the animal facilities.
* The candidate must have the ability to work across functional teams such as engineering and maintenance, as well as quality control and manufacturing and external contractors.
* This site is a regulated site and subject to audits by Federal, State and corporate agencies for which the candidate serves as the departmental lead.
* The candidate must have excellent communication skills and be proficient in Microsoft Office applications.

Qualifications

Education Minimum Requirement:

* High School diploma with 10 years' of relevant experience or Bachelor degree in a related field with 5 years industry experience (each with a minimum of 5 years in an animal facility).

Required Experience and Skills:

* Minimum of 3 years supervisory experience working in an animal facility.
* Advanced knowledge of facility management is required.

Preferred:

* AALAS certification at Laboratory Animal Technologist, (LATG) level OR equivalent advanced knowledge of animal husbandry, health and welfare for the specific species at the facility.
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 # ANI000119.

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-DE-Millsboro
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Infectious organisms, chemical disinfectants]]>http://jobs.merck.com/job/Millsboro-Sr-Animal-Care-Supervisor-Job-DE-19966/1694176/169417616941762012-03-04Merck/MSDfull-timeUSDstarting0BSMillsboro, DE, 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 seeking a highly motivated individual with a broad background and skill set to support the production process at our Millsboro Manufacturing Facilities within our Engineering and Maintenance department. We are seeking a self-motivated, independent engineer with strong analytical and problem solving skills to provide engineering support for our plant facilities, process equipment and systems. The successful candidate will have an attention to detail, be quality and customer focused, and have excellent written and oral communication skills. Other responsibilities include project management of internal facility capital projects.

As part of a plant team the project engineer will provide direct process validation support for projects related to the manufacture of vaccine products. Must embrace and help to establish an empowered team culture, including significant interaction with manufacturing, quality, and automation groups. Also responsible for analytical and engineering studies associated with the development of new components, products, processes, systems, and facilities. Your responsbilities include but are not limited to:

* Provides technical support to Production and other site departments as needed for troubleshooting, repairs and process optimization.
* Manages internal plant capital projects as assigned, including scope development, estimating, budget, scheduling, change control and project management of design, construction, commissioning and validation support.
* Manages contractors as required, including construction trades, calibration and maintenance.
* Develops and maintains Maintenance SOP's, including preventive maintenance and calibration.
* Maintains facility design and engineering documentation including proper change management techniques.
* The individual will develop and implement various validation protocols and technical projects requiring knowledge of validation, engineering, and/or the physical sciences.
* Responsible for maintaining the ongoing validation effort.
* Provides basic technical support to research and staff groups on matters relating to the validation of equipment and processes for the manufacturing operations.
* Conducts validation studies to assist in engineering activities associated with process optimization and improvement of process quality while mindful of company and regulatory requirements.
* The incumbent is expected to collect and interpret information, develop and implement solutions to a range of projects and support activities.
* Development, execution, and closeout of initial validation with periodic assessments/continuing validation for cleaning, sanitization/sterilization, filtration and manufacturing process validations.
* cGMP Compliance activities to maintain an acceptable compliance posture with respect to validation and manufacturing activities.
* Assists in the Shakedown and Operation Qualification phases of the capital project in aseptic processing areas where needed, to include media preparation, vaccine filling, lyophilization, and capping/inspection unit operations. Subsequently assists in the execution of Performance Qualification for these same areas, to include media challenge, engineering runs, and process validation lots of vaccine product.
* Provides leadership for troubleshooting and efficiently resolving manufacturing problems. Effectively develops and implements corrective actions to unplanned (atypical) manufacturing events to ensure a consistent and reliable supply of vaccine products.
* Upon receipt of assignment, works semi-independently in the coordination and execution of assigned projects. Maintains active dialogue with project team members and keeps management well informed of project progress.
* Reviews literature and attends training sessions in order to develop and maintain a high level of expertise in validation technology and related science fields. Applies this knowledge in the development of validation procedures and protocol in support of validation projects.
* Supports all quality and safety initiatives.
* Helps to foster empowered teams to achieve site mission, vision and goals through: Efficient and safe operation of process systems, compliance with current Good Manufacturing Practices and production of product that is safe and efficacious.

Qualifications

Minimum Education Requirement:

* Bachelor's degree in Electrical, Mechanical or Chemical Engineering. Advanced degree and/or professional license preferred.

Required Skills and Experience:

* Minimum 5 years of technical and/or project management experience
* Experience with GMP or VMD/USDA in a regulated industry.
* Minimum 2 years of experience in production or validation in a regulated environment
* Experience with building or production utilities systems
* Proficient in MS Office applications including MS Project.
* Demonstrated written and verbal communication skills.
* Demonstrated interpersonal skills with an ability to work in a team environment.
* Must be flexible to support critical issues on a 24/7 basis as needed.
* Gown aseptically for work in Clean Room environments.
* Work around laboratories, manufacturing and equipment areas, noisy environments and climb ladders.

Desired Skills and Experience:

* Experience with equipment and process validation of aseptic processes in prep/fill/finish operations in the biotechnology industry
* Aseptic and Biotech manufacturing experience.
* Autocad.

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 # ENG002322.

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-DE-Millsboro
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Millsboro-Project-Engineer-Process-and-Validation-Job-DE-19966/1689817/168981716898172012-03-04Merck/MSDfull-timeUSDstarting0BSMillsboro, DE, 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.




Manages the development and implementation of selected promotional programs based on product-specific marketing strategies for assigned products. Prepares, s and handles promotional materials according to the approved current procedure. Fulfills all required duties for processing, including filing and reconciliation for sponsoring, sales related events and other implementation activities. Achieves results by performing the following duties, ensuring and enforcing compliance with company policies and procedures, Ethical Business Practices, and applicable regulations. Provides guidance to marketing/sales colleagues on procedures to be followed depending on the type of activity to be carried.

MAJOR ACTIVITIES AND RESPONSABILITIES:

* Coordinates the development and implementation of disease awareness, promotional materials, programs, and other product support activities to ensure availability and distribution of educational and promotional materials, when appropriate, according to marketing plans.
* Submits and ensures Medical-Legal approval of assigned product / disease awareness materials and plans for CARD.
* Identifies and ensures required approvals of field educational / disease awareness / promotional materials, branded and unbranded Direct to Consumer (DTC) campaigns (where applicable) to be used in support of product action marketing plans implementation.
* Actively participates in the development of the Integrated Marketing Plan and supports implementation of product action plans with Business Managers, Customer Focus Team, ACMs, Communications and Sales Force.
* Event coordination and execution.
* Interacts and collaborates closely with Communications, Medical, ACMs and Compliance.
* Orders and coordinates distribution of educational awareness / promotional materials to field employees in alignment with product action plans.
* Orders, coordinates and conducts regular monitoring of samples in its assigned business unit, carefully monitoring alignment with compliance and ensuring a transparent system control for audits.
* Coordinates the execution of product integrated campaigns, particularly Rep facilitated meetings and sponsorships.
* Participates as active member of cross functional teams, such as product core teams, to provide input and advice regarding promotional aspects.
* For central filing purposes, ensures proper submission by the responsible party of all documentation related to sponsorships and Rep facilitated meetings prior to performing the final financial reconciliation.
* Performs reconciliation of actual expenses vs budget and ensures timely approval of overruns beyond "tolerated" levels by the corresponding head, as defined by the SOP, within one month of receipt of relevant documentation by the involved parties.
* Performs reconciliation of samples for its assigned product portfolio
* Centralizes all final documentation related to each event, ensuring its "closing." Communicates closing of the event to the applicant area.
* Participates as active member of MSD CARD Compliance Committee.
* Provides guidance to marketing/sales colleagues on procedures to be followed depending on the type of activity to be carried out.
* Performs other duties as required to support the achievement of business goals.

Qualifications

Education:

College degree, preferably in pharmacy, medicine, business administration or marketing.

Languages:

English and Spanish languages.

Work Experience:

Three or more years of experience within the pharmaceutical industry environment, including but not limited to sales field experience of pharmaceutical products.

Required knowledge:

MS Office (Word, Excel and Power Point).

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Technical Competencies:

* Analytical Skills
* Problem Solving
* Strategic Thinking
* Planning and Organizational Skills (Project management)
* Change Management
* Reasoning Ability
* Detail orientation for filing, reconciliation and supportive on Compliance and Merck's Ethical Business Practices
* Basic Financial skills
* Mathematical 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.

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

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/Panam%C3%A1-Integrated-Marketing-Coordinator-Job/1689819/168981916898192012-03-04Merck/MSDfull-timeUSDstarting0BSPanamá, Panamá, PA
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

Primary Location: IN-AP-Hyderabad
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Hyderabad-Territory-Business-Manager-Hyderabad-%28Neuro%29-Job-AP/1672542/167254216725422012-03-04Merck/MSDfull-timeUSDstarting0BSHyderabad, AP, IN
Description

Primary scientific face of MSD for SLs/OLs

• Spearhead implementation of research activities: directed towards enhancing research capabilities, generation of clinical/epidemiological evidences, Merck Investigator Studies Program (MISP) etc

• Spearhead implementation of educational activities: directed towards dissemination of evidence based clinical guidelines and best practices, establishing local academic networks, enhancing translation of guidelines in to practice and improving overall treatment patterns

Primary scientific resource for the sales team

• Training on therapy area, disease and products at induction and on ongoing basis

• Responding to all relevant scientific clinical queries raised by HCPs

• Speaker briefing and conduct of scientific meetings planned by sales & marketing team

• Scientific, non-promotional resource for implementation of other marketing campaigns of marketed products

• Reporting of adverse events related to MSD products

• Compliance advisor for sales and marketing activities and for promotional practices

Conflict of interest management

• To ensure scientific sanctity of all promotional and non-promotional activities being conducted by or on behalf of MSD

• To carefully avoid any inadvertent linkage of educational or research activities with commercial returns

Self development

• To update self on scientific developments in the respective therapy areas, not only to ensure professional development but also to ensure proper execution of responsibilities mentioned above

• To work on special project(s) of the department, including those related pipeline products, allocated primarily with the objective of job enrichment and career growth

• To acquire skills and strengths required to realize carrier development plans

Qualifications

• Medical Graduate having a MCI recognized degree

• Candidates with post graduate degree/diploma would be given preference

Primary Location: IN-KA-Bangalore
Employee Status: Regular

Travel
: Yes, 75% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Bangalore-Medical-Specialist-Chennai-Job-KA/1670751/167075116707512012-03-04Merck/MSDfull-timeUSDstarting0BSBangalore, KA, 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 sales territory manager will be responsible for but not limited to:

* The sales and technical support for Merck Animal Health's aquaculture products.
* This field sales position will be responsible for sales to commercial feed mills and aquaculture operations throughout the United States, primarily in the Mississippi Delta and Pacific Northwest.
* Additional responsibilities include field technical support and training to feed mills and distributor sales representatives as well as to conduct and/or assist in market support trials.

Qualifications

Minimum Education Required:

* Bachelor's Degree in Animal Science, Fisheries Biology, Marine Science or Aquaculture.

Required Experience and Skills:

* Must have at least 2 or more years of successful business to business sales and/or aquaculture experience.
* Excellent communication skills
* Must be proficient in Microsoft Excel, Word, Power Point and Outlook.

Desired Experience and Skills:

* Animal health products and/or agricultural background/experience.
* Field or research experience in aquaculture or fisheries 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 # DIR003530.

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-Mississippi
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Sales-Territory-Manager-Aquaculture-Animal-Health-Products-Job/1484866/148486614848662012-03-04Merck/MSDfull-timeUSDstarting0BSUS-Mississippi
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.

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/LSS-Engineer-Tech-Transfer-Job/1487041/148704114870412012-03-04Merck/MSDfull-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.


Responsibilities include but are not limited to:

* Conduct formulation development studies for oral dosage products.
* Includes pre-formulation studies covering literature and patent review, characterization of drug substance and excipients.
* Prepares laboratory batches of product for analytical method development and validation, formula optimization and developmental stability evaluation.
* Collaborates with respective Groups in R&D in scale-up studies, defining raw material and product specifications, manufacture of clinical supplies and writing CMC sections for IND's and NDA's.

Qualifications

Education Requirement:

* Bachelors Degree required (preferably in pharmacy, chemistry or chemical engineering)
* Advanced degree (MS or PhD) preferred

Required:

* Minimum 3 years of work experience required
* Formulation development of pharmaceutical products

Preferred:

* Broad based experience in oral dosage form formulation development, including immediate and controlled release products, emphasis on solid dose form development.

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 # CHE003207.

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-TN-Memphis
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Memphis-Senior-Scientist-Job-TN-37501/1445426/144542614454262012-03-04Merck/MSDfull-timeUSDstarting0BSMemphis, TN, 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

Primary Location: IN-DL-Delhi City
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Delhi-City-Territory-Business-Manager-Delhi-%28Critical-Care%29-Job-DL/1689821/168982116898212012-03-04Merck/MSDfull-timeUSDstarting0BSDelhi City, DL, IN
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

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/1567420/156742015674202012-03-04Merck/MSDfull-timeUSDstarting0BSMumbai, MH, 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.


Responsible for the design, development and implementation of short- and long-term solutions to information technology needs through new and existing applications, systems architecture, network systems and applications infrastructure. Often involved in modifying or adapting existing designs. Reviews IT requirements and business processes; codes, tests, debugs and implements software solutions. Roles are often project based, delivering IT change within the business. Responsible for providing management of the IT infrastructure within an organization. This infrastructure includes the physical network (e.g., WAN/LAN, servers, terminals) as well as server applications and software (e.g., PeopleSoft, Oracle). Responsible for the configuration, maintenance and installation of server applications and hardware.

Additional input on the local work:

Essential Duties and Responsibilities

The IT Systems Analyst supports the users of company's information technology systems. Responsibilities of this position include, but are not limited to:

* Responds to user problems for both software and hardware applications.
* Maintain all networks, including Internet interfaces.
* Ensure regulatory compliance (Sarbanes - Oxley, FDA Part 11 as needed, etc…)
* Assist with hardware/software purchasing and inventory.
* Network/hardware installations, troubleshooting and repair; data backup and archiving.
* Installs software upgrades when required.
* Manage/ensure software licensing; network security in compliance with company standards.
* Laboratory computer system installation and maintenance.
* May provide systems analysis and participate in making recommendations on potential hardware and software purchases and upgrades.
* Printer/copier/scanner/fax purchasing and maintenance.
* Propose and implement system enhancements (software and hardware updates) that will improve the performance and reliability of existing systems.
* Manage telecommunications - wired and wireless including telephone switch and voicemail maintenance.
* With assistance of Director, Business Operations, negotiate and manage vendor support contracts

Qualifications

Minimum Education Requirement:

* Bachelors degree preffered, but not required.

Minimum Required Experience and Skills:

* Minimum of 2 years related experience.

* Strong hardware and software troubleshooting skills, and a strong working knowledge of PC operating systems.

* Experience with MS Server 2003 and MS Exchange 2003 including Active Directory and Group Policy

* Ability and motivation to learn new technologies quickly and with minimal oversight

* Excellent communication skills and the ability to interact professionally with a diverse group of users

* Must have excellent listening, reasoning and problem-solving abilities

* Experience in higher-level computer languages is required.

* Experience with Cisco router, firewall, antivirus, Citrix Metaframe and SQL

* Must have a strong sense of urgency and the ability to prioritize work using good judgment when confronted with crisis or emergency situations

* Must be able to maintain professional demeanor when in stressful situations and when troubleshooting or reacting to user problems and questions

Working Conditions/Environment:

Most work is carried out in an office setting. Moderate lifting (10-50 pounds) and repetitive activities may be required. While performing the duties of this job, the employee is frequently required to sit; stand; walk; reach with hands and arms; climb or balance; stoop.

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 000293.

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-CO-Boulder
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Boulder-IT-Services-Analyst-%28Boulder%2C-CO%29-Job-CO-80301/1703558/170355817035582012-03-04Merck/MSDfull-timeUSDstarting0BSBoulder, CO, 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

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

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Material-Handler-Job/963989/9639899639892012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
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 Group Support functions we are currently looking to fill the position for an

Accounting Manager

Main tasks:

- Responsibility for the regular subsidiary accounting including the related close activities (Swiss & US GAAP).

- Leading a team of 2 accountants.

- Coordination of tax and VAT issues and requests with external tax advisors and tax authorities.

- Coordination function with internal and external audit teams and ensures that audit findings are taken into account and corrected if required.

- Taking charge of all financial reporting tasks.

- Book close activities at month, quarter and year-end.

- Documentation of internal controls and SOX reporting.

- Responsibility for all Swiss authority reporting.

- Strong collaboration with various departments within the subsidiary and also with corporate functions.

- Design and documentation of procedures surrounding all accounting reconciliation and controls.

- Evaluation of the business impact of accounting issues and elaboration of recommendations to management regarding the accounting treatment of items.

- Exploring potential opportunities for continuous process improvements within the function

- Project Management: eg Legal Entity Integration support post merger, Financial System Integration;

- Collaborate with finance and system experts to ensure correct accounting set up.

Qualifications

Qualifications:

- Bachelor degree in Business Administration and/or Swiss Certified Accounting Degree (Eidg. Dipl Buchhalter or similar)

- CPA desired

- At least 5 years experience in Accounting or in a similar position.

- First experiences in leading a team.

- Strong communication skills as well as knowledge of financial accounting tools (e.g. AS 400/SAP).

- Flexible and multi-tasking person who prioritizes effectively and is skilled at conflict resolution

- Copes well with stressful situations demonstrating high degree of resilience

- Ability to work independently but also in a team.

- Strong analytical skills and has sound knowledge of US + Swiss GAAP, VAT,income tax law, tax processing and reporting standards.

- Fluent (oral and written) in English and German and have basic knowledge of French.

Are you interested in this challenging role? Then please apply online.

Primary Location: CH-Lucerne
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Accounting-Manager-Job/1669057/166905716690572012-03-04Merck/MSDfull-timeUSDstarting0BSCH-Lucerne
Description

To develop business plans for the key accounts that integrate the brand's strategies objectives, and tactics with the general objectives for MCC. Based on a complete marketing analysis and clear vision of the Consumer Unit's business and focused on the maximizing resources and achieving the sales goals. Plan and participate in high impact meetings with clients to come up with future commercial strategies that align with MCC's sales objectives

Qualifications

Profesional degree with more than 3 years experience in leading key accounts in the Consumer Industry. Experience in channel partners (Retail) is required.

Primary Location: CO-Distrito Capital de Bogotá-Bogotá
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Bogot%C3%A1-Key-Account-Manager-Job/1705728/170572817057282012-03-04Merck/MSDfull-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.


:

* 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.

Primary Location: GT-Guatemala-Guatemala
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Guatemala-Clinical-Project-Manager-Job/1694175/169417516941752012-03-04Merck/MSDfull-timeUSDstarting0BSGuatemala, Guatemala, GT
Description

The Recruiting & Staffing Regional Coordinator will be a member of the EMEAC Recruiting & Staffing team. This important role will provide support and assistance to the Recruitment Consultants across the EMEAC region. This support will allow the Recruitment Consultants to be as efficient as possible, but just as importantly allow MSD to provide a candidate experience that is responsive and consistent. The Coordinators will also allow Recruiting and Staffing to track, measure and report on the service we are delivering to the business.

The coordinators will be responsible for:

* Posting requisitions as directed by the Recruitment Consultants to internal and external job boards, networks and other potential candidate sources
* Ensuring filled or closed posting are removed in a timely fashion from all recruiting mediums
* Updating the applicant tracking System (Taleo) so that the data held is up to date, has no duplicate candidates, etc
* Recording the sourcing costs for each placed candidate
* Candidate and Hiring manager communication: sending status updates, requesting further details, etc
* Creating and maintaining a library within Taleo to support hiring managers in the future
* Run standard reports from Taleo and recognise opportunities to develop further automated reports to help support business decision making
* Supporting Hiring Managers without Taleo access by sending short listed candidate CVs as directed by Recruitment Consultants
* Work with SBS and HR colleagues to improve process flow within the complete recruitment process through to "Day 1"

Once experienced and established in this role. Other responsibilities are likely to develop, such as:

* Pre-screening candidates against clearly identified requirements, education, licenses held, etc
* Initial LinkedIn name and profile (long list) generation

Qualifications

ý Bachelors degree

ý Recruitment or other complex administration experience

ý Experience of applicant tracking systems - preferably Taleo

ý Ability to work effectively with many different cultures and styles

ý Excellent attention to detail

ý Languages Fluent English required, another European language/s a benefit

ý Good verbal and written communication skills

ý Proven ability to handle multiple priorities and deliver quality work on time

ý High energy individual who has a positive, enthusiastic, flexible and pragmatic approach

ý A mindset of looking for opportunities and areas where processes can be improved

ý Motivated by providing excellent service

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Recruitment-Coordinator-Job-L/1577191/157719115771912012-03-04Merck/MSDfull-timeUSDstarting0BSDublin, IE
Description

MSD in Lucerne/Switzerland is a Swiss subsidiary of the successful global pharmaceutical ompany 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 finance department in Lucerne and are therefore recruiting for a position as

General Accountant

and Responsibilities:

* Co-ordinates the monthly, quarterly and yearly closing.
* Ensures timely and accurate booking and justification of monthly accruals and prepaid amounts.
* Monitors certain entries into Holding company's books in order to ensure that these are all accurate, timely and correct.
* Performs expense account reviews and analysis by cost center and by fin reporting.
* Performs the monthly closing by using company financial systems JD Edwards/SAP and COMET and tool to report financials to US/Whitehouse.
* Ensures that balance sheet accounts are reconciled. Collects account reconciliations from various support groups (SBS, Treasury etc).
* Provides data for completing timely preparation of the monthly VAT reporting, ad-hoc mandatory reporting and internal tax reporting (iTax) and the annual Corporate Tax declaration.
* Monitors Fixed Asset Management: creating item numbers, booking of invoices, approval of JDE receiving, monitoring depreciation calculations.
* Prepares and s to the external auditors the financial information distributed to the Worker's Council.
* Monitors the intercompany invoicing process (payables and receivables) for MSD International GmbH
* Provides information to the internal and external auditors during their visits.
* Prepares and monitors the annual Statutory reporting for the Holding companies and any other statutory/annual statistics reports.
* Monitors the intercompany invoicing process (payables and receivables) for MSD International GmbH, processes the intercompany reporting (FIN 7 / 7C) on a monthly basis.
* Provides information to the internal and external auditors during their visits.
* Prepares and monitors the annual Statutory reporting for MSD International GmbH and any other statutory/annual statistics reports.
* Monitor Access Security: Periodically review the access of all menus, define employee profiles and how to align with roles defined in the system, review the user list of system access and document all access right changes made in the system
* Participates in Transformation Initiative projects on preparation for SAP/COMET blueprint, in view of a common SAP implementation: gathering of data, workflow of processes, master data maintenance and clean-up, preparation of regional/HQ Accounting, participates in Shared Business Services project, process reengineering

Qualifications

* Degree and experience in Swiss and US GAAP
* English and German fluent
* Experience in Accounting required (min. 2 years)
* Strong problem identification & analysis skills.
* Strong communication skills.
* Good interpersonal and leadership skills.
* Ability to think broadly while handling the details as required.
* Strong MS Office knowledge.
* Srong accounting system knowledge (AS400, SAP, or other)
* Tkes initiative, is dynamic.
* Strong customer / client focus.
*
Primary Location: CH-Lucerne
Employee Status: Regular

Travel
: No
Number of Openings: 2

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/General-Accountant-Job/1292064/129206412920642012-03-04Merck/MSDfull-timeUSDstarting0BSCH-Lucerne
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 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 with currently 700 employees.

We are in the process of extending the regional headquarter for our Supply Chain Operations Group based in Lucerne.

We want to add talent in the following position as soon as possible:

SUPPLY OPERATIONS SPECIALIST

Core Responsibilities:

* Supply Planning (SAP-APO) of assigned APIs, bulk and finished drug products.
* Develop production and purchase requirements (make to order and make to stock environment)
for manufacturing plants and suppliers
* Process purchase orders in SAP and ensure plan execution.
* Ensure timely supply of products within a complex network of international manufacturing sites and distribution centers.
* Planning tolling operations and supply from assigned manufacturing sites and vendors
* Reconciliation of SAP system transactions, management of safety stocks and development of replenishment plans.
* Analyze sales demand and purchase requirements from markets
* Participation in process improvement projects, new product launches and implementation
of sourcing strategies.
* Rough Cut Capacity Planning (RCCP)
* Communication to all stakeholder groups

Qualifications

* Hands on Supply Planning experience
* University studies in Supply Chain or related discipline
* Knowledge of Supply Chain Operations and Management
* SAP - APO knowledge
* MS Office experience (proficient excel user)
* Strong English communication skills written and verbally

If you are interested in this career step and want to become part of the development of our company
please contact us by sending your informative CV in English.

Primary Location: CH-Lucerne
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Supply-Chain-Operations-Specialist-Job/1546078/154607815460782012-03-04Merck/MSDfull-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 Specialty Representative - HCV is a key member of the HCV Specialty Team and plays a critical role in supporting Merck's customer centric business model. He/she is responsible for working with the HCV 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 Phoenix North and North County Arizona

The ideal location to reside is within the territory.

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 required

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
* HCV 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 # DIR003813.

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-AZ-Phoenix
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Phoenix-Specialty-Representative-HCV-%28Phoenix-North%2C-AZ%29-Job-AZ-85001/1642242/164224216422422012-03-04Merck/MSDfull-timeUSDstarting0BSPhoenix, AZ, 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 seeking a qualified undergraduate student for a summer internship to join a talented multidisciplinary team focusing on optimizing properties of biotherapeutics. This position is within the Protein Purification group at GlycoFi Inc., part of Merck Research Laboratories, located at Lebanon, New Hampshire. In this lab based role, you will help support the development of protein purification of therapeutic proteins. Strong background in biochemistry and knowledge of protein purification is preferable. You will apply a variety of analytical and biophysical characterization techniques such as chromatography, SDS-PAGE, western blot analysis, protein concentration determination and many of the principles you have learned in the classroom on a pharmaceutical research project. You will also have the opportunity to interact with scientists in other functions of the company and learn and demonstrate Merck's leadership behaviors. In addition to research, responsibilities include learning standard operating procedures (SOP) and safety procedures, writing technical reports and presenting technical data. Effective oral and written communication skills are essential.

This is a 9-11 week internship based in Lebanon, NH and beginning in June 2012.

Qualifications

Required:

* Must be currently enrolled in an undergraduate program in: Chemistry, Chemical Engineering, Biochemistry, Pharmaceutical Science, or related discipline.
* Must be available for a period of 9-11 weeks, beginning in June 2012.

Preferred:

* GPA of 3.0 or higher

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 #BIO003438.

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


Primary Location: US-NH-Lebanon
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Lebanon-Protein-Purification-Intern-Job-NH-03756/1700165/170016517001652012-03-04Merck/MSDfull-timeUSDstarting0BSLebanon, NH, 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 for this position this position include:

* Responsibility for Respiratory Claims Guidance Franchise functions operating within a Consumer Division
* Provide leadership from Claims Guidance Center of Excellence and interface with Franchise Leadership team & Medical Affairs for Global, Regional and Local Brand support as needed
* Recommends and proposed disruptive new claims for mainly Allergy & Congestion/Cough Cold categories and potential means for substantiation

Qualifications

Education:

* Required: Bachelor's degree
* Preferred: PhD

Required:

* Minimum 5 years of work experience
* Deep medical knowledge in related respiratory field and literature
* Expertise in clinical research and statistics interpretation
* Strong leadership, communication and negotiation skills
* Critically must understand flexibility around advertising for Consumer products
* Influencing skills

Preferred:

* Knowledge of GCP regulations and drug and/or device development process

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 # CLI002558.

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-TN-Memphis
Other Locations: US-NJ-Summit
Employee Status: Regular

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

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Memphis-Respiratory-Global-Claims-Strategy-Champ-Job-TN-37501/1568999/156899915689992012-03-04Merck/MSDfull-timeUSDstarting0BSMemphis, TN, 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.

Primary Location: IE-L*-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/1531832/153183215318322012-03-04Merck/MSDfull-timeUSDstarting0BSCarlow, L*, IE
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

Primary Location: IE-L*-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/1689825/168982516898252012-03-04Merck/MSDfull-timeUSDstarting0BSDublin, IE
Description

Responsible for all aspects of production scheduling and Direct material procurement to support customer requirements, while managing inventory/capacity constraints utilizing SAP tools and providing input into the site capacity planning model.. Ensure that objectives are effectively achieved, consistent with Merck's requirements to ensure compliance, safety and reliable supply to our customers.

The incumbent is also responsible for the Management of all transactional procurement and sales order processing of Direct Materials for the site to ensure continuous supply of materials, components and miscellaneous supplies, using and supporting continuous improvement methodologies to eliminate waste in the supply, logistics, production and planning processes.

Qualifications

* Bachelors Degree or higher preferred; ideally in a Science, Engineering or other Technical discipline
* Relevant SAP 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
* Lean Six Sigma Methodology experience desired
* Customer service
* Self motivated
* Flexible approach

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/MES-Process-Steward-Job/1703532/170353217035322012-03-04Merck/MSDfull-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.


The selected individual will sell Merck Animal Health products to animal care facilities, SPCA's, and shelter accounts in the Virginia and Washington DC area, to meet or exceed sales objectives while projecting a professional image.

* Plans sales calls, selects products and programs that meet customer needs.
* Educates customers about the benefits and value of Merck Animal Health products and services; conducts presentations to customers.
* Manages accounts within the assigned territory.
* Ensures clear, concise and timely communication.
* Maintains accurate records and account profiles.
* Primary contacts are with the Regional Manager, other representatives in the region, customers within the territory, distributor representatives and extend beyond territories.
* Identifies problems and develops solutions.
* Will be expected to have significant impact on territory performance. May impact regional business performance.

Qualifications

Education Minimum Requirement:

* Bachelor's Degree

Required Experience and Skills:

* Minimum 2 years sales experience.

Desired Experience and Skills:

* Excellent interpersonal, communication and presentation skills are required for this quality driven position.
* Experience selling animal healthcare products and services through veterinary and/or shelter channel is preferred.
* Knowledge of biological products and the ability to engage in dialogue with medical professionals is a plus.
* Understanding & past experience with distribution.
* Candidate will need to be flexible and have the ability to adapt to a changing 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 # DIR003705.

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-Virginia
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Sr-Territory-Rep-Virginia-Territory-Job/1567415/156741515674152012-03-04Merck/MSDfull-timeUSDstarting0BSUS-Virginia
Description

The Process Engineering Lead is responsible for leading and co-ordinating the activities of a number of Process Engineers engaged in Tech Transfer / Process Development and other process engineering activities.

Key Responsabilities

1. Establish systems and practices to monitor and improve formulation / fill processes within the Carlow facility.

2. Collaborate with multiple partners (e.g. project managers, donor sites, operations and validation) in achieving excellence in tech transfer and process support.

3. Sponsor and Foster lean six sigma and standard work within the Process Team (e.g. Structured Root Cause Analysis, Statistical Process Control, Data driven decision making).

4. Coach and Mentor Process Team to develop their technical skills and product knowledge and to realise their full potential.

5. Support Operational readiness activities and facility license readiness.

6. Leadership activities including selection, development, coaching and day to day management. Ensure that the team receives appropriate resources and programmes to develop technical and other skills, to complete their jobs whilst stimulating personal growth and development in line with role. Develops and maintains training programmes.

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

May be required to perform other duties as assigned.

Qualifications

· Bachelors Degree or higher preferred; ideally in a Science or Engineering discipline.

· 6-8 years experience in a process engineering role in a pharma environment; preferably in the biopharm industry.

· Proven track record of excellent people management and coaching skills.

· Strong communication and collaboration skills.

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Process-Engineering-Lead-Job/1510511/151051115105112012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
Description

Primary scientific face of MSD for SLs/OLs

• Spearhead implementation of research activities: directed towards enhancing research capabilities, generation of clinical/epidemiological evidences, Merck Investigator Studies Program (MISP) etc

• Spearhead implementation of educational activities: directed towards dissemination of evidence based clinical guidelines and best practices, establishing local academic networks, enhancing translation of guidelines in to practice and improving overall treatment patterns

Primary scientific resource for the sales team

• Training on therapy area, disease and products at induction and on ongoing basis

• Responding to all relevant scientific clinical queries raised by HCPs

• Speaker briefing and conduct of scientific meetings planned by sales & marketing team

• Scientific, non-promotional resource for implementation of other marketing campaigns of marketed products

• Reporting of adverse events related to MSD products

• Compliance advisor for sales and marketing activities and for promotional practices

Conflict of interest management

• To ensure scientific sanctity of all promotional and non-promotional activities being conducted by or on behalf of MSD

• To carefully avoid any inadvertent linkage of educational or research activities with commercial returns

Self development

• To update self on scientific developments in the respective therapy areas, not only to ensure professional development but also to ensure proper execution of responsibilities mentioned above

• To work on special project(s) of the department, including those related pipeline products, allocated primarily with the objective of job enrichment and career growth

• To acquire skills and strengths required to realize carrier development plans

Qualifications

• Medical Graduate having a MCI recognized degree

• Candidates with post graduate degree/diploma would be given preference

Primary Location: IN-KA-Bangalore
Employee Status: Regular

Travel
: Yes, 75% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Bangalore-Medical-Specialist-Hyderabad-Job-KA/1682097/168209716820972012-03-04Merck/MSDfull-timeUSDstarting0BSBangalore, KA, IN
Description

Primary scientific face of MSD for SLs/OLs

• Spearhead implementation of research activities: directed towards enhancing research capabilities, generation of clinical/epidemiological evidences, Merck Investigator Studies Program (MISP) etc

• Spearhead implementation of educational activities: directed towards dissemination of evidence based clinical guidelines and best practices, establishing local academic networks, enhancing translation of guidelines in to practice and improving overall treatment patterns

Primary scientific resource for the sales team

• Training on therapy area, disease and products at induction and on ongoing basis

• Responding to all relevant scientific clinical queries raised by HCPs

• Speaker briefing and conduct of scientific meetings planned by sales & marketing team

• Scientific, non-promotional resource for implementation of other marketing campaigns of marketed products

• Reporting of adverse events related to MSD products

• Compliance advisor for sales and marketing activities and for promotional practices

Conflict of interest management

• To ensure scientific sanctity of all promotional and non-promotional activities being conducted by or on behalf of MSD

• To carefully avoid any inadvertent linkage of educational or research activities with commercial returns

Self development

• To update self on scientific developments in the respective therapy areas, not only to ensure professional development but also to ensure proper execution of responsibilities mentioned above

• To work on special project(s) of the department, including those related pipeline products, allocated primarily with the objective of job enrichment and career growth

• To acquire skills and strengths required to realize carrier development plans

Qualifications

• Medical Graduate having a MCI recognized degree

• Candidates with post graduate degree/diploma would be given preference

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

Travel
: Yes, 75% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Mumbai-Medical-Specialist-Mumbai-Job-MH/1682102/168210216821022012-03-04Merck/MSDfull-timeUSDstarting0BSMumbai, MH, IN
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 Switzerland Human Health organization, based in Lucerne we are currently looking to fill the position of:

Policy & Communications Director

The position of Public Policy & Communications Director reports directly into the Managing Director of Switzerland. Responsibilities include the following:

* Partner with the Managing Director and the management team to formulate and implement a Policy & Communications strategic plan that supports our business and healthcare environment and enhances MSD's image as a global healthcare leader.
Key stakeholders include healthcare providers, patients, government authorities, media outlets, patient advocacy groups, academic institutions, and non-profit organizations.
* Recognize, initiate, and manage opportunities to partner with key stakeholders to advance mutual interests in helping identify solutions for current and upcoming healthcare challenges.
* Represent MSD externally, acting as a spokesperson / thought leader on issues impacting the company, including participation in industry associations and working groups.
* Monitor external environment and regularly update the management team on key issues significant to our business.
* Prioritize key therapeutic areas in which to focus advocacy efforts, in conjunction with the management team.
* Acts as MSD Switzerland's expert in initiating media messages or responding to media inquiries.
* Support MSD business leaders in Switzerland increase their effectiveness as company spokespersons and thought leaders.
* Partner with MSD departments to support internal communication needs.
* Effectively manage, develop and coach a team of four direct reports

Qualifications

* University degree
* Several years of related experience in communications or public relations.
* Excellent network of opinion leaders, media, advocacy groups and decision makers within the healthcare industry
* German and English fluency, both excellent written and verbal communications skills. French language skills desired.

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

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Policy-&-Communications-Director-Job/1646166/164616616461662012-03-04Merck/MSDfull-timeUSDstarting0BSCH-Lucerne
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 Kriens and are therefore recruiting a Financial Planning & Analysis Analyst for our Emerging Markets Region.

The role of Emerging Markets "Financial Planning & Analysis (FP&A)" Analyst is dedicated to compile and analyze financial results, forecast and plan of the EM geographies (China, Brazil, EEMEA, LA, AP).

Primary activities/responsibilities:

• Provide Financial Planning & Analysis support and manage compilation of accurate and timely financial submissions, including forecast, budget and 5 year plan.

• Perform detailed and accurate tracking of actual performance vs. plan and forecasts, and latest projections/estimates

• Support the preparation of regional reviews/presentations and special projects

• Support standardization of reporting and processes for EM and have active involvement in helping drive continuous improvement

• Collaborate with regional (Finance Teams in each geography) and global finance teams

Qualifications

• Bachelors or Master Degree, preferably in Accounting or Economics

• Significant experience working in a Finance department supporting the Business

• Excellent analytical skills.

• Strong technical skills (Excel, BPC, Merck Systems)

• Ability to work in virtual teams.

• Need to be pro-active, open minded & flexible due to regional nature of the position and exposure to various cultures.

Desired skills:

• Postgraduate qualification

• CPA or CFA

Are you interested to join this fast growing region? Then please apply online.

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

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/EM-Financial-Planning-&-Analysis-Analyst-Job/1643324/164332416433242012-03-04Merck/MSDfull-timeUSDstarting0BSCH-Lucerne
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 local Supply Chain Group and are currently recruiting the position as

Global Chemical Planning Manager

Role Description:

* Oversees site chemical planning for selected site(s) in selected region(s).
* Conducts chemical production planning to support customer demand for tactical through strategic/LROP timeframe.
* Conducts on going chemical inventory coverage and risk assessments/management as part of supply assurance.
* Performs short through long term demand management reviews/validations for chemical sites.
* Provides inventory EA and active inventory management at item level of detail on a monthly basis.
* Actively manage chemical sites' inventory/production volumes to meet and improve on divisional goals.
* Interfaces with selected chemical sites in setting/changing production volumes.
* Key point of contact for various customers/support functions (ie: Product Leaders, External Manufacturing, Procurement, Product Source Management, Business Affairs, etc.) for chemical planning needs for selected site(s).
* Team member on relevant source change, Network, and Global Supply teams.
* Lead profit plan related activities for selected chemical sites.
* Lead ad-hoc projects in line with Global Supply Chain Management needs.

Qualifications

* BS or advanced Degree in Engineering or other equivalent technical background required
* 5-10 year experience in chemical manufacturing operations, planning or other functional areas, preferably within Merck.
* SAP experience preferred.
* Green Belt, Black Belt, CSCP, CPIM certification(s) preferred.
* Must be able to manage multiple priorities.
* Understanding of financial, planning information systems (SAP, Data3), and MRP II practices/principles are a plus.
* Detail oriented with strong analytical, computer, interpersonal and communication skills, and a demonstrated ability to anticipate and solve problems.
* Demonstrated effective leadership and proactive approach to business issues.
* Ability and willingness to search out for and implement/realize/own business improvements.
* Flexibility necessary to deal with global nature of position.
* Effective interpersonal skills in working with remote teams and strong people management skills.
* Strong ability to lead during times of uncertainty and ability to enable transformational organizational goals.
* Must demonstrate exceptional judgment and a genuine willingness and desire to develop successful business relationships with partners/customers.

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

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Global-Chemical-Planning-Manager-Job/1659999/165999916599992012-03-04Merck/MSDfull-timeUSDstarting0BSCH-Lucerne
Description

Based in the EMEA Shared Business Service (SBS) 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 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 Analyst is responsible for supporting and performing business analysis and reporting, spanning operational reporting through advanced analytics projects. In this role, you will also be involved with model development to support Shared Business Services (SBS) globally.

This position supports Power Users within Shared Business Services and defines requirements and develops/implements plans to deliver on those requirements. You will also work with SBS workstreams and Power Users to provide knowledge transfer on existing data and analytic capabilities as well as to define and document requirements regarding gaps to enable prioritization of new demand.

Primary Activities

* Providing support to stakeholders regarding ad hoc requests for data and analysis from multiple systems across SBS.
* Participating in projects related to data integration globally.
* Supporting and participating in analytic projects that will include data mining, modeling and results presentation.
* Assisting in the development and ongoing maintenance of the SBS Analytics Inventory.
* Building strong collaborative relationships and establish credibility with key stakeholders.
* Working with business users to gather specifications for data and report requirements.
* Identifying data sources to extract business information for reporting purposes.
* Analyzing available data, identify and recommend best sources for building reports.
* Developing dashboard reports from relational database.
* Identifying best practices to communicate metrics through dashboard, and recommending enhancements.
* Assisting business users with self-service report development, including training support.
* Providing ongoing analysis of internal business data to include monthly reporting and ad-hoc analyses so that key internal clients are provided with critical information and analytics.

Qualifications

Bachelor's Degree or equivalent and at least 2 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:

§ 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.

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Reporting-&-Analytics-Analyst-Job-L/1566043/156604315660432012-03-04Merck/MSDfull-timeUSDstarting0BSDublin, 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

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-%28Neuro%29-Job-MH/1554253/155425315542532012-03-04Merck/MSDfull-timeUSDstarting0BSMumbai, MH, IN
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.

Primary Location: IE-L*-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/1510514/151051415105142012-03-04Merck/MSDfull-timeUSDstarting0BSDublin, IE
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.
Must have experience in sterile/vaccine operations.

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/1703538/170353817035382012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
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.

Dans ce rôle, vous superviserez tous les aspects relatifs aux opérations d'emballage dans le but de rencontrer les objectifs de production tout en respectant les règlements et procédures gouvernementales et les bonnes pratiques d'efficacité.

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.

Exigences

* Baccalauréat en science ou Baccalauréat en cours (une expérience considérée comme équivalente pourrait être acceptée);
* Expérience en supervision d'une équipe d'emballage, de préférence dans l'industrie pharmaceutique ou cosmétique;
* Connaissances approfondies des règles des BPF;
* Habileté à résoudre des problèmes;
* Orienté vers les résultats;
* Excellent français et anglais fonctionnel;
* Bonne connaissance des outils Microsoft;
* Excellentes aptitudes pour les relations interpersonnelles;
* Connaissances des principes de production à valeur ajoutée.

Localisation principale: CA-QC-Montreal (Pointe-Claire)

Statut de l'employé: Permanent

Nombre de postes vacants: 1]]>http://jobs.merck.com/job/Claire%29-Superviseur%2C-Production%2C-d%C3%A9partement-de-l%E2%80%99emballage-COL-%28Quart-de-soir%29-Job/1705732/170573217057322012-03-04Merck/MSDfull-timeUSDstarting0BSMontreal, QC, CA
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 Ophthalmology Specialty Team and plays a critical role in supporting Merck's customer centric business model. He/she is responsible for working with the Ophthalmology 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 position covers Dallas, Texas proper, east to Tyler and Longview, north to Plano, McKinney and Denison, and as far west as Denton

No regular overnight travel is required. 60% of business is in Central Dallas; 15-20% is in Tyler and Longview so the ideal place of residence for this role is Central Dallas, TX.

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
* Ophthalmology and/or Glaucoma 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 # DIR003999.

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-TX-Dallas
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Dallas-Specialty-Representative-Ophthalmology-%28Dallas%2C-TX%29-Job-TX-75201/1705724/170572417057242012-03-04Merck/MSDfull-timeUSDstarting0BSDallas, TX, 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 in the process of extending the regional headquarter for our Supply Chain Operations Group based in Lucerne.

We want to add talent in the following position as soon as possible:

SUPPLY CHAIN INFORMATION SPECIALIST

Core Responsibilities:

50 - 60 % of time

- Generate KPI's

- Support operational teams through reporting and analysis

40 - 50 % of time

- Generate and maintain supply and demand information data to support Customers and Supply Operations activities

- Coding processes, distribution and maintenance of master data information to internal and external customers

- Maintain and monitor planning hierarchies in SAP and perform planning runs in SAP

- Analysis of supply chain information and development of special reports

- Communication with customers and suppliers to ensure data accuracy and appropriate set-ups

Qualifications

Required skills:

- Bachelor of Science - preferably Supply Chain or related discipline

- Very Strong analytical skills

- Strong Excel user skills

- Fluency in English written and verbally

- Knowledge of Supply Chain Management and/or manufacturing processes is preferred

- SAP experience is preferred

Are you interested in this position? Then please apply online for this role.

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

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Supply-Chain-Information-Specialist-Job/1643325/164332516433252012-03-04Merck/MSDfull-timeUSDstarting0BSCH-Lucerne
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

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/production-lead-technican-Job/1703543/170354317035432012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
Description

Nos encontramos en búsqueda de profesionales egresados en Administración, Marketing, Ingeniería Industrial o carreras afines para ocupar la posición de Representante de Ventas.

Entre sus principales funciones destacan los siguientes:

El cumplimiento de los objetivos de venta

Conocimiento del mercado y de la competencia

Organización de actividades de capacitación para los médicos

Desarrollo e implementación de planes de acción dirigidos a los clientes.

Qualifications

El perfil del puesto señala un Profesional con:

Experiencia mínima de 2 años en una posición similar.

Conocimiento de computación a nivel usuario

Conocimiento de procesos de venta en la industria farmacéutica

Orientación al cliente

Orientación a resultados

Comunicación transparente y directa

Iniciativa y dinamismo

Trabajo en equipo

Alta capacidad de autogestión.

Primary Location: PE-Lima-Lima
Employee Status: Regular
Number of Openings: 9]]>http://jobs.merck.com/job/Lima-Representante-de-Ventas-Job/1606557/160655716065572012-03-04Merck/MSDfull-timeUSDstarting0BSLima, Lima, PE
Description

To guarantee through his/her team, an adequate management of inventory, profitability and market share growth. To identify, create and take advantage of new business opportunities that are aligned with market strategies. To guarantee adequate planning, execution and monitoring of the business plan.

Qualifications

Professional degree with experience of more than 4 years in sales force leadership in the consumer Industry. Knowledge or experience in channel partners (distributors and consumers) is required.

Primary Location: CO-Distrito Capital de Bogotá-Bogotá
Employee Status: Regular

Travel
: Yes, 75% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Bogot%C3%A1-Regional-Leader-MCC-Job/1705729/170572917057292012-03-04Merck/MSDfull-timeUSDstarting0BSBogotá, Distrito Capital de Bogotá, CO
Description

Merck is in the process of establishing regional finance, meetings, travel, customer support and HR shared services organizations as part of a company wide initiative to establish shared services across the EMEA region. Key to the delivery model of shared services is the standardization of business processes and consolidation of the delivery of certain services within regional shared service centers and with external suppliers. Such initiatives drive the need for strong change management and communications programs within Merck as well as ongoing measurement, assessment and improvement of the customer service performance of the shared services function.

Manager - Customer Relations and Communications Manager

Key Responsibilities include:

Communications and Customer Relations

* Leads the development of the overall SBS regional communication strategy, schedule, and ensures that all forms of communication are effective - including written and oral, email and formal presentations.
* Facilitates regular communication planning reviews with SBS EMEA Leadership Team: maps interdependencies, scope, objectives, legal / HR / regulatory requirements, resource requirements, logistics.
* Ensures timely, accurate, and quality information reaches the functions employees, the wider organization, and our suppliers, customers, and partners effectively.
* Enables efficient customer/client feedback gathering, measurement of all aspects of our customer experience, from oral and written surveys, to ad hoc feedback and partner assessments
* As a service organization, the manager will lead ongoing efforts to improve the quality of our service delivery from a customer perspective. This includes ensuring appropriate and timely follow-up on queries, proactive engineering of contact center services, and instilling excellence in the regional customer-service mindset.

* Channel and Content Management for SBS Communications / Information
* Manages communications channels to ensure relevant stakeholder and internal communications including internal newsletters, business updates, program updates, service level and operational performance updates
* Ensures external and internal distribution of corporate and financial news releases through the designated news wire (e.g. Business Wire), the Internet (e.g. Merck.com newsroom) and employee news outlets (e.g. Sync).
* Works with SBS groups to enable the effective distribution and targeting of content within the region
* Other including project management , people management, change management, people development

Qualifications

* 5-7 years of experience in Communications and Customer Relations
* Project Management experience
* Leadership skills are required, along with excellent written, communication, and presentation skills.
* Knowledge of the pharmaceutical industry
* Knowledge of change management processes information systems and business processes is highly desirable.
* Strong ability to coordinate action across multiple geographies including external customers, suppliers and partners
* Six Sigma Knowledge is preferred
* Fluency in two or more major European languages preferred

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Dublin-Customer-Relations-Manager-Job-L/1606558/160655816065582012-03-04Merck/MSDfull-timeUSDstarting0BSDublin, 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 Analytical Specialist will carry out independent technical projects in the laboratory as part of the department's program to continuously improve operations. Major responsibilities for the role include, but are not limited to......

* Method Development - Taking methods, validating them and developing modifications to ensure their applicability for QC use.
* Automation Development - Working with lab personnel and vendors to design, develop, install, and validate new automated analytical instruments.
* New Instrumentation Evaluation - Working with lab personnel and vendors to make assessments of sophisticated, modern analytical instruments.
* Computerization Projects - Working with IT and QC personnel on new computerized systems.
* Technical recommendations to management on equipment and methods.
* Direct and Indirect supervisory activities including backup for laboratory personnel, training of analysts, monitoring of training progress and coaching of analysts.
* High priority product release testing including troubleshooting on release materials, testing of critical batches in emergencies, etc.
* Determine technical pathways on suitability of test methods, feasibility of automation of test methods, technical evaluation of equipment/vendors, analytical troubleshooting.
* Contribute in the areas of personnel development through evaluation of training needs of analysts and training programs.
* Communication with production to troubleshoot and identify technical problems, and subsequent support for identifying solutions.
* Consultations with vendors of scientific instruments, reagent suppliers, automation consulting companies, etc.

Qualifications

Education:

Bachelor's degree in science or engineering.

Required:

At least 5 years of related work experience, or 3 years of work experience with a Master's degree in science or engineering.

Full knowledge of QC testing activities and testign equipment.

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 # QUA002779.

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-FL-Miami Lakes
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Miami-Lakes-Analytical-Specialist-M-O-Job-FL-33014/1700167/170016717001672012-03-04Merck/MSDfull-timeUSDstarting0BSMiami Lakes, FL, 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 Chemist will be responsible for testing components, raw and in-process materials used in the manufacturing process at the Miami Lakes facility as well as finished products. Will perform testing in accordance with USP, regulatory requirements and established standard procedures involving instrumentation and quantitative analysis. Additional responsibilities include, but are not limited to......

* Perform routine analysis of finished products including dissolutions.
* Perform routine analysis on raw and in-process materials.
* Perform routine analysis on stability and accelerated stability formulations.
* Perform environmental analysis and waste/rinse water testing using the GC, HPLC and/or atomic absorption.
* Also other work related duties as assigned.

Qualifications

Education:

Bachelor's degree in Chemistry, or an Associate's degree in Chemistry with at least 3 years of prior related work experience.

Required:

* Knowledge of HPLC, UV, AA, and/or TLC principles.
* Strong computer usage 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 # QUA002721.

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-FL-Miami Lakes
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Miami-Lakes-CHEMIST-ASSOC-Q-C-M-O-Job-FL-33014/1672545/167254516725452012-03-04Merck/MSDfull-timeUSDstarting0BSMiami Lakes, FL, 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 Regional Medical Director (RMD) is a product and disease expert who engages in discussions with healthcare professionals (HCPs) to help them to achieve positive health outcomes for their patients. The RMD provides HCPs accurate information about Merck products and clinical science in a balanced and credible manner consistent with the regulatory environment and Merck's ethical standards. The RMD seeks ways to collaborate with HCPs and Healthcare Organizations to improve patient outcomes.

The RMD has a broad understanding of basic and clinical science in the therapeutic areas related to Merck franchises, including quality management and the business environment of medicine. He/She is a resource to MM&P Account Executives and to Directors of Commercial Operations and their teams. The RMD develops and maintains relationships with health care providers and provides clinical and scientific support to key decision makers in managed care organizations and state Medicaid agencies

This is a home based position responsible for clients/customers within the defined territory. Travel is estimated at approximately 40%.

Qualifications

Education Minimum Requirement:

* MD or DO

Required:

* MD or DO, and US residency/fellowship trained
* ABIM or equivalent ABMS Member Board certification in primary care/internal medicine/family practice field
* Active US licensure to practice medicine
* Minimum of 4 years active practice experience in the United States

Preferred:

* Subspecialty certification (ABMS Member Board) and/or experience in the areas of cardiology/cardiovascular disease, infectious disease or respiratory disease
* Experience in a medical business-related role (i.e. pharmaceuticals, managed care, practice management, clinical research organizations, consulting, diagnostics and devices)
* Active role in a scientific, medical or teaching institution.
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 # SCI003991.

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-Maryland
Other Locations: US-Rhode Island, US-Delaware, US-District of Columbia, US-Connecticut, US-Pennsylvania, US-Maine, US-Vermont, US-Massachusetts, US-New York, US-Virginia, US-New Jersey, US-New Hampshire
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Regional-Medical-Director-NE-Region-Job/1672548/167254816725482012-03-04Merck/MSDfull-timeUSDstarting0BSUS-Maryland
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.

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/QC-Lead-Technician-Job/1703551/170355117035512012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
Description

Primary scientific face of MSD for SLs/OLs

• Spearhead implementation of research activities: directed towards enhancing research capabilities, generation of clinical/epidemiological evidences, Merck Investigator Studies Program (MISP) etc

• Spearhead implementation of educational activities: directed towards dissemination of evidence based clinical guidelines and best practices, establishing local academic networks, enhancing translation of guidelines in to practice and improving overall treatment patterns

Primary scientific resource for the sales team

• Training on therapy area, disease and products at induction and on ongoing basis

• Responding to all relevant scientific clinical queries raised by HCPs

• Speaker briefing and conduct of scientific meetings planned by sales & marketing team

• Scientific, non-promotional resource for implementation of other marketing campaigns of marketed products

• Reporting of adverse events related to MSD products

• Compliance advisor for sales and marketing activities and for promotional practices

Conflict of interest management

• To ensure scientific sanctity of all promotional and non-promotional activities being conducted by or on behalf of MSD

• To carefully avoid any inadvertent linkage of educational or research activities with commercial returns

Self development

• To update self on scientific developments in the respective therapy areas, not only to ensure professional development but also to ensure proper execution of responsibilities mentioned above

• To work on special project(s) of the department, including those related pipeline products, allocated primarily with the objective of job enrichment and career growth

• To acquire skills and strengths required to realize carrier development plans

Qualifications

• Medical Graduate having a MCI recognized degree

• Candidates with post graduate degree/diploma would be given preference

Primary Location: IN-WB-Kolkata
Employee Status: Regular

Travel
: Yes, 75% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Kolkata-Medical-Specialist-Kolkata-Job-WB/1672535/167253516725352012-03-04Merck/MSDfull-timeUSDstarting0BSKolkata, WB, IN
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

Primary Location: IN-AP-Hyderabad
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 2]]>http://jobs.merck.com/job/Hyderabad-Territory-Business-Manager-Hyderabad-%28Musculo%29-Job-AP/1672541/167254116725412012-03-04Merck/MSDfull-timeUSDstarting0BSHyderabad, AP, 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.


At Merck & Co., Inc Manufacturing facility in Elkton, Virginia, we currently have an Industrial Utilities and Building Automation Engineer position available 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 basic function of this position is to assist in the planning, design, continuous improvement, reliability, troubleshooting and administration of utilities systems at the site with guidance and direction from the supervisor.

Utility systems include the generation and distribution of the following: steam, electricity, compressed air, water, glycol, brine and nitrogen. Other systems include cold storage, refrigeration and HVAC. The administration of the site's building and utility automation systems is a key responsibility.

Primary Activities

Responsible for by assignment:

· Assisting in new system implementation.

· Assisting in maintaining compliance with cGMP, environmental and safety requirements.

· Performing routine monitoring, data acquisition, and user administration.

· Providing training for operators, mechanics and staff.

· Maintaining and establishing standard operating procedures.

· Assist with scheduling and coordinating large maintenance jobs.

Qualifications

Skills

· Bachelor of Science degree in an appropriate engineering/scientific field

· Minimum of 1 year experience in an Industrial, Commerical or similiar setting supporting large scale Utilitiy Processes

· Internship or Co-op in a Manufacturing facility

· Demonstrated skills to include analytical skills,written and verbal communication skills and teamwork skills.

Preferred

· Knowledge and application of cGMP principles, theories, and concepts.

· Bachelor of Science degree in Mechanical or Electrical Engineering

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 # ENG002328.

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: United States
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Industrial-Utility-Systems-and-Building-Automation-Engineer-Job/1689818/168981816898182012-03-04Merck/MSDfull-timeUSDstarting0BSUnited States
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

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Systems-Engineer-Job/1703536/170353617035362012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
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

Primary Location: IN-OR-Bhubaneshwar
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Bhubaneshwar-Territory-Business-Manager-Bhubaneshwar-%28Critical-Care%29-Job-OR/1689823/168982316898232012-03-04Merck/MSDfull-timeUSDstarting0BSBhubaneshwar, OR, IN
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

Primary Location: IE-L*-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/1705735/170573517057352012-03-04Merck/MSDfull-timeUSDstarting0BSCarlow, L*, 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 Engineering and Maintenance Manager will be responsible for facilitating the manufacturing operations of the Miami Lakes facility. Major responsibilities include, but are not limited to.....

Project Management

* Manages a number of large projects or a single project of major scope.
* Assembles and leads cross functional teams and contractors.
* Uses knowledge and experience to select the appropriate solutions for projects from multiple options.
* Proactively monitors project progress and performance and reporting to management
* Consults with team, business owner, and contractors for the identification and resolution of potential project scheduling delays, scope changes, and/or scope discrepancies.
* Ensures compliance with all SHE, Quality and Business Policies within the design and execution of projects.

Operations and Production Support

* Directs/supports operations in running plants and/or utilities.
* May direct and supervise colleagues and contractors.
* Leads the planning and directs the execution of complex engineering and site improvement studies.
* Provides technical expertise in the investigation of complex technical problems, and develops innovative solutions using current and new technologies or approaches.
* Directs the development of complex technical procedures and documentation to meet operational and regulatory requirements.
* Leads the planning, justification, design, installation, commissioning and validation efforts for large new facility, equipment and/or technology projects.
* Executes major capital projects and ensures scope, timeline, cost perameters, and quality are achieved.
* Reviews and modifies recommendations for annual operating budget and expense control planning.
* Directs various risk analysis scenarios for management's review and decision making.
* Directs/undertakes the development of best engineering/business practices and standards.

Maintenance

* Ensures the management of project schedule, costs and quality utilizing proper controls.
* Manages the development of capital plan requirements due to known vulnerabilities within the facility.
* Considers/collects feedback from various project team members to assess design solutions.
* Encourages/supports/champions operational design enhancements to increase efficiencies.
* Serves as an expert in evaluating new or existing site standards.
* Provides technical expertise and engineering consultation on operational issues; retains ownership of previously delivered projects.
* Participates in Energy purchases for the facility.
* Evaluates new technologies and manages their implementation.
* Tracks and completes all compliance related requirements.
* May conduct/coordinate training.

Qualifications

Education:

Bachelor's degree in science, engineering, or business.

Required:

* At least 5 years of work experience in the pharmaceutical industry
* At least 5 years of prior management experience.

Desired:

* Six Sigma certification (Black Belt preferred)
* Strong aptitude and knowledge of Continuous Improvement Process techniques

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 # MAI000238.

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-FL-Miami Lakes
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Miami-Lakes-Engineering-&-Maintenance-Manager-Job-FL-33014/1669046/166904616690462012-03-04Merck/MSDfull-timeUSDstarting0BSMiami Lakes, FL, 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 Finance Intern will provide various financial analyses in a corporate function or in support of one of Merck's operating divisions. Depending on the position, this could include evaluating and analyzing potential business acquisitions and divestitures, product licensing proposals, joint ventures, and major capital investments; developing and implementing the Company's capital structure policy; managing foreign currency exposure and hedging strategies; arranging financing and managing investments for Merck and its worldwide subsidiaries; consulting with the Company's operating areas and providing advice on controlling risk, improving businesses processes, and incorporating best practices; analyzing divisional strategic investments and on-going business alternatives; forecasting, reporting, and analyzing divisional operating results.

Internships may be located in Whitehouse Station NJ, Upper Gwynedd PA, Rahway, NJ, Kenilworth, NJ

This is a paid internship targeted to start in June 2012 for 10 weeks, whereby a weekly stipend will be provided. Subsidized housing is available for interns living more than 50 miles from the site of their internship.

Qualifications

Required:

* First year MBA student with a concentration in Finance
* Demonstrated academic excellence
* Analytical ability and leadership capability
* Be eligible to work in the US on a permanent basis (US citizen or Permanent Resident) without sponsorship

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 # FIN000676.

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


Primary Location: US-NJ-Whitehouse Station
Other Locations: US-NJ-Rahway, US-NJ-Kenilworth, US-PA-Upper Gwynedd, US-PA-West Point, US-NJ-Summit
Employee Status: Regular
Number of Openings: 5

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Whitehouse-Station-Senior-Financial-Analyst-Intern-Job-NJ-08889/1455405/145540514554052012-03-04Merck/MSDfull-timeUSDstarting0BSWhitehouse Station, NJ, 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 finance department in Lucerne and are therefore recruiting for a position as

Tax Accountant

The position holder will be accountable for various tax reporting & compliance processes.

and Responsibilities:

· Corporate income taxes: tax calculations & accounting for US GAAP reporting, Swiss statutory reporting and Swiss tax purposes for MSDIG and opportunity to extend to other MSD Swiss Holding companies in the future.

· VAT: preparation, filing and reconciliation of VAT returns for the Swiss VAT-Group

· Withholding taxes: working towards standardized withholding tax filing process for all Swiss Holding

· Calculates and takes ownership of the corporate income tax position of MSDIG including reconciliations between US Gaap & Swiss statutory reporting and from Swiss statutory reporting to tax in an accurate, timely and correct manner.

· Co-ordinates the monthly, quarterly and yearly closing of the corporate income tax position for MSDIG

· Ensures correct, accurate and timely booking of all corporate income tax entries and correct and timely payment of corporate income tax assessments.

· Calculates and takes ownership of the VAT positions for the Swiss VAT-group including reconciliations between P&L and VAT returns in an accurate, timely and correct manner.

· Ensures correct, accurate and timely filing and payments of all VAT returns and correct, accurate and timely booking of associated tax entries.

· Calculates and takes ownership of the withholding tax positions of all Swiss Holding companies in an accurate, timely and correct manner.

· Ensures correct, accurate and timely filing and payments of all Withholding tax returns and correct, accurate and timely booking of associated tax entries.

· Provides accurate financial information upon (internal) requests from the US, from Auditors, Tax Authorities and from the Finance Manager

Qualifications

· A degree in Accounting or Tax or similar education (KV) and adequate business experience (min. 3-5 years).

· Preferably knowledge and experience in tax reporting (specifically VAT reporting).

· Strong communication skills.

· Ability to think broadly while handling the details as required.

· Ability to think in processes and focused at continuous process improvement

· Preferably strong MS Office knowledge.

· Takes initiative, is dynamic.

· Fluent in German and English.

· Strong customer / client focus

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

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Tax-Accountant-Job/1650157/165015716501572012-03-04Merck/MSDfull-timeUSDstarting0BSCH-Lucerne
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

Primary Location: IN-DL-Gurgaon
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Gurgaon-Territory-Business-Manager-Gurgoan-%28Critical-Care%29-Job-DL/1672536/167253616725362012-03-04Merck/MSDfull-timeUSDstarting0BSGurgaon, DL, IN
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

Primary Location: IN-WB-Kolkata
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Kolkata-Territory-Business-Manager-Kolkata-%28Musculo%29-Job-WB/1672543/167254316725432012-03-04Merck/MSDfull-timeUSDstarting0BSKolkata, WB, IN
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

Primary Location: IN-DL-Delhi City
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Delhi-City-Territory-Business-Manager-Delhi-%28HIV%29-Job-DL/1672544/167254416725442012-03-04Merck/MSDfull-timeUSDstarting0BSDelhi City, DL, IN
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

Primary Location: IN-TN-Chennai
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Chennai-Territory-Business-Manager-Chennai-%28Critical-Care%29-Job-TN/1682095/168209516820952012-03-04Merck/MSDfull-timeUSDstarting0BSChennai, TN, IN
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

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Planner-Buyer-Job/1703534/170353417035342012-03-04Merck/MSDfull-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.


The US Regulatory Policy (USRP) staff is responsible for developing Merck's regulatory policy for the US and forwarding Merck's position with industry thought leaders and US regulators. The Associate Director is responsible for two major functions:

* Proactively monitors emerging scientific trends/strategies, both internally and externally, to shape and influence changes in the US regulatory environment. Under the supervision of the Head, USRP, the incumbent will represent Merck in assigned areas on industry committees and maintain productive relationships with industry staff and US regulators to ensure productive Agency interactions.
* Plans and manages USRP interactions with MRL regulatory management and liaison staff for submission of product applications and other related interactions with FDA.

· Monitors emerging regulatory policy issues in assigned areas, including issues arising from FDA or other regulatory authorities, Congress, within the pharmaceutical industry or elsewhere, and identifies those issues likely to impact Merck's regulatory strategy or product portfolio. In consultation with USRP Head, coordinates and leads internal teams to address regulatory policy issues.

· Coordinates with appropriate internal staff to develop Merck responses to FDA draft regulations, guidances and policies and plans and manages interactions and communications with FDA on regulatory policy matters.

· Participates in regulatory project team meetings and rehearsals for FDA meetings to learn about product matters likely to surface which may require involvement/action of the USRP staff.

· Manages on-site (at FDA) activities for key milestone meetings (e.g., pre-submission, end-of-Phase II, Advisory Committees) as assigned for selected projects and/or during absences of the Head, USRP.

· Maintains liaison with outside scientific and professional organizations to represent MRL on product and regulatory policy matters under the supervision of the Head, USRP.

· Participates in industry and professional meetings to maintain competency on regulatory policy issues.

Qualifications

EDUCATION:

* Bachelor of Science is required, preferably in science, health care, public health or health policy or BS in any field accompanied by a post-graduate degree in science, health care, public health, health policy, or law

Required:

* At least 5 years experience with FDA or other health authority, either directly (working within a health authority) or indirectly (closely interacting with health authority)
* A minimum of 2 years experience in pharmaceutical regulatory policy.
* Strong interpersonal and communication skills with ability to demonstrate analytic thinking
* Ability to work in cross-functional team environment

Preferred:

* Master's degree or PhD in science, health care, public health, health policy, or law

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 # REG000889.

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-DC-Washington
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/Washington-Director%2C-US-Regulatory-Policy-Job-DC/1682098/168209816820982012-03-04Merck/MSDfull-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.


merck.com/careers to create a profile and your resume for requisition # MAT000154.



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


SUPPLY & COMMERCIALIZATION MASTER SCHEDULER

LOCATION: LAS PIEDRAS

Develops, administers and controls the Master manufacturing / packaging for Supply and Commercialization plan, which satisfies Merck Las Piedras Operations objectives of customer service, inventory levels (financial & physical), manufacturing efficiencies and material utilization. Guarantees plan execution through monitoring and constant communication with the manufacturing process, customer requirements and inventory changes. Responsible for the Sales, Inventory, Operations and Planning process including forecasting, capacity planning, inventory projections and development of production estimates.

Qualifications

EDUCATION AND Experience:

Bachelor Degree in Industrial Engineering or Business Administration with concentration in Materials Management, Accounting and/or Management.

Five or more years experience in pharmaceutical industry working in all phases of planning, scheduling, inventory control and analysis.

At least 3 years experience with PRISM.

Experience or Exposure to Commercialization Operations is required.

Experience with SAP Operations System is a plus.

Strong computer knowledge (Microsoft Office).

Excellent communication skills (oral and written) in English and Spanish.

Knowledge of GMP's,.

Knowledge of MPR II, Inventory Control, Purchasing and Organizational Development.

APIC's certified preferred.

Experience with manufacturing of Solids, Tablets and Capsules or related manufacturing processes.

Experience with purchasing of direct materials is a plus.

Excellent interpersonal, analytical and customer relationship skills.

Highly developed negotiating techniques.

Primary Location: Puerto Rico
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Supply-&-Comm_-Master-Scheduler-Job/1703549/170354917035492012-03-04Merck/MSDfull-timeUSDstarting0BSPuerto Rico
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

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

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Pune-Territory-Business-Manager-Pune-%28Neuro%29-Job-MH/1689822/168982216898222012-03-04Merck/MSDfull-timeUSDstarting0BSPune, MH, IN
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

Primary Location: IN-TN-Chennai
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Chennai-Territory-Business-Manager-Chennai-%28Musculo%29-Job-TN/1669050/166905016690502012-03-04Merck/MSDfull-timeUSDstarting0BSChennai, TN, IN
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.

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 4]]>http://jobs.merck.com/job/Production-operator-Job/947331/9473319473312012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
Description

Responsible for the creation, qualification, data analysis, data accuracy and change control for SAP Master Data, including but not limited to all objects, views and fields within the function. Working independently, he/she will use SAP knowledge, business processes knowledge and SOP's to correctly maintain master data. He/She will communicate and interact with other Operational and Information Stewards to resolve issues regarding master data.

He/ she will be responsible for SOPs, maintaining process documentation/maps, metrics, planning, training and change management in regards to SAP. Ensure that objectives are effectively achieved, consistent with Merck's requirements to ensure compliance, safety and reliable supply to our customers.

Qualifications

* Bachelors Degree or higher preferred; ideally in a Science, Engineering or other Technical discipline
* SAP Master Data management knowledge and experience essential
* Broad understanding and knowledge of applicable business processes.
* Relevant experience and a particular skill set in their area of expertise that adds value to the business; ideally in a manufacturing, preferably GMP setting
* 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
* 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
* Knowledge of Six Sigma preferred
* Customer service
* Self motivated
* Flexible approach

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/SAP-Information-Steward-Job/1703535/170353517035352012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
Description

* Work with the maintenance team to ensure that Planned Maintenance and Calibration program are complete to the schedule.
* 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;
* Participates in internal and external audits and inspections;
* 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 or equivalent required in Engineering, Science or related discipline.
* 5 + years of related work experience in a GMP manufacturing environment.
* 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

* ~

Primary Location: IE-L*-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/1703555/170355517035552012-03-04Merck/MSDfull-timeUSDstarting0BSCarlow, L*, 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 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.

Primary Location: US-NJ-Whitehouse Station
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Internal-Auditor-Job-NJ-08889/1211082/121108212110822012-03-04Merck/MSDfull-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 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

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-08889/924196/9241969241962012-03-04Merck/MSDfull-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 managing and overseeing Merck's North American Foreign Trade Zone (FTZ) duty management program and Global Export Compliance Program. Provides FTZ & Export regulatory support as required. Develops and maintains market-wide FTZ & Export compliance procedures and webpage content. Assists with the development and upgrade of FTZ & Export management training materials and facilitates training. Ensures site compliance with all FTZ & Export policies, procedures, and guidelines. Provides export ECCN classifications and determines whether export license are required. Applies for export license when it is required. Interfaces with internal customers, external vendors and service providers as well as government agencies.

Primary activities include, but are not limited to:

1. Provides technical expertise to FTZ subzones regarding the admission, entry, zone to zone transfer, export and destruction of the FTZ materials;
2. Provides support for FTZ subzone inventory control & Export operations;
3. Assists in developing procedures and guidelines in regard to FTZ subzone operations, FTZ compliance control & Export compliance control;
4. Development and update of FTZ & Export training materials and the Global Logistics FTZ/Export webpage;
5. Performs on site or net meeting FTZ/Export compliance trainings;
6. Assists in the assessment and analysis of FTZ/Export compliance risks and proposes action items for corrective actions;
7. Reviews FTZ subzones' Annual Board Reports and CBP Reconciliation Reports and ensures timely submission to the regulatory agencies;
8. Identifies FTZ opportunities for the smooth transportation of material in and out of FTZ subzones and utilizes the FTZ for duty avoidance;
9. Represents the company in NAFTZ/AAEI and other trade organizations;
10. Classifies items for Export Classification Control Number (ECCN), determines licensing requirements, applies for export licenses where applicable, establishes master data in Integration Point (FTZ software provider) and GTS systems;
11. Serves as the company's AES and SNAP-R Administrator, issues metrics for continuous improvement

Qualifications

Required:

* Minimum of a Bachelors Degree is required.
* Minimum of 5 years of Supply Chain, Manufacturing or related experience
* FTZ/ECCN classification working experience (Foreign Trade Zone/Export Classification Control Number).

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 # CLI002569.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Senior-Trade-Compliance-Analyst-Job-NJ-08889/1650162/165016216501622012-03-04Merck/MSDfull-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 and supervision of the Director of Accounting Standards and Procedures, this position is responsible for technical accounting matters for the Corporation; being up to date on all principles and concepts and the rules and regulations of professional and regulatory agencies such as the Financial Accounting Standards Board, American Institute of Certified Public Accountants and the Securities and Exchange Commission.

* Monitors, reviews and interprets impact on the Company of new accounting/reporting regulations or proposals promulgated by various professional and regulatory agencies including the Financial Accounting Standards Board (FASB), The Emerging Issues Task Force (EITF), the American Institute of Certified Public Accounts (AICPA), the Securities Exchange Commission (SEC) and the International Accounting Standards Board (IASC).
* Develops responses to FASB, EITF, AICPA, SEC and IASC on their proposals for comment.
* Establishes, maintains and documents the Company's standard accounting practices and procedures as required in order to maintain a controlled system of accounting and reporting on a world-wide basis within Company policies.
* Provides support and services to all operating and corporate divisions regarding accounting and reporting issues, including divestitures, acquisitions, joint ventures, restructuring, etc. Responsible for external accounting issues relating to these transactions.
* Develops procedures and recommends changes in method or practices when required to assure compliance with professional and regulatory bodies.
* Prepares financial verbiage for the Annual Report, 10-K and 10-Q's. This includes working with the Manager of External Reporting on sections of management Discussion and Analysis as well as all required disclosures in the financial statements and footnotes.

Qualifications

EDUCATION:

* BS/BA degree in Accounting required.

Required:

* A minimum of 5 years of demonstrated experience in an accounting and/or financial reporting related role.

* Must be able to cope with changing priorities and work under the pressure of rigid time schedules

Preferred:

* Experience working in a public accounting firm.
* CPA

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 # ACC002216.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Manager-Accounting-Standards-Job-NJ-08889/969176/9691769691762012-03-04Merck/MSDfull-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 primary responsibility of this position will be to manage the operational performance for MMD's (Merck Manufacturing Division) and MRL's (Merck Research Labs) imports. Ensure compliance with all US Customs, FDA, DEA, and any other regulatory bodies concerning the import of finished goods, raw materials, clinical supplies, etc. Drive compliance into other organizations to ensure compliance is embedded in the process. Trains staff to be compliant with SBPs as directed by GTCA.

Manages a staff of 15+ people. Builds a cohesive team.

Primary activities include, but are not limited to:

* Managing daily import activities
* Drive operational efficiencies within team
* Monitors performance of 3rd party customs brokers
* Seeks opportunities for continuous improvement

Qualifications

Required:

* Minimum of a Bachelors degree is required.
* Minimum of 5 years of operations experience with global teams and supporting global manufacturing environment. Should understand costs and improvement opportunities for global logistics and the impact across other functional areas. Ability to function in a regulatory role and business role simultaneously.
* Minimum of 5 years experience with import and export operations; knowledge of US Customs/FDA/DEA procedures.
* Strong project management and leadership skills, able to shift roles as required by the group dynamic (e.g. contributor, facilitator).
* Track record of driving process improvement with quantified results, demonstrated change management skills, and be at ease in fast-changing environments.
* Must possess the ability to work cross-functionally. Strong command of language and communication skills is required. Must be able to interact, influence and lead at all levels of the organization.

Preferred:

* Experience with customs tariff and classification procedures for imported and exported materials is preferred. Knowledge of healthcare products and their regulatory requirements (UL, FDA, ISO and others) is a plus.
* Team building experience is a plus.
* Experience in highly regulated industries preferred, such as Education, Healthcare, Government Contracting, Food and Drug, Insurance or Financial Services.

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 # IMP000131.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-North-America-ImportExport-Manager-Job-NJ-08889/1655966/165596616559662012-03-04Merck/MSDfull-timeUSDstarting0BSWhitehouse Station, NJ, US
Description

• Serve as truly strategic partner to Franchises and Regions in brands management through the commercial lifecycle.

• Provide medical and scientific contribution to the achievement of MSD Vision and Mission.

• Be recognized as the scientific leader of MSD internally and externally.

• Provide focused Medical Affairs leadership for commercialized brands.

• Engage in medical dialogue that supports key Merck products as Brands Of Choice.

• Represent the medical community inside the company.

• Be the medical interface for local customers and provide response and solutions to HCPs and patients.

• Excellence in Execution to support Franchise Medical strategy

• Boundary-less partnership across Merck medical community

• Simplifies coordination of complex, multi-party, in-market medical affairs activity.

• Be a model of MSD leadership principles and compliance behavior.

• Promote and ensure alignment with corporate policies, procedures and quality standards.

Qualifications

Medical doctor with experience (at least 1 year). Internist or pulmonologist are required, with experience in Pharmaceutical companies (desired). Desired comprehension of pharmaceutical product markets. Fluent in english is required.

Primary Location: CO-Distrito Capital de Bogotá-Bogotá
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Bogot%C3%A1-Medical-Affairs-Manager-Job/1655962/165596216559622012-03-04Merck/MSDfull-timeUSDstarting0BSBogotá, Distrito Capital de Bogotá, CO
Description

Overview:
Experienced communications executive required to execute internal and external communications strategies for MSD in CARD.

Provides direct communications support and counsel to Managing Director at MSD CARD and other senior regional executives (as requested).

Provides counsel to CARD organization on local communications activities to ensure alignment with Latin America Region business objectives and Global Communications objectives.

Duties, Responsibilities, Activities:
Oversees development and coordination of internal and external communication strategies supporting the objectives of the MSD Managing Director.

Ensures country alignment with Latin America Region and Global Communications strategies for reputation management, employee communications, product communications and media relations.

Counsels MSD Managing Director on communications strategies to improve understanding and support for the company and its business objectives.

Functional:

* Attends and participates in marketing team meetings as needed
* Participates in remote and in person communications team meetings
* Drives the establishment of processes to further advance efficacy and efficiency
* Represents function in different task forces on an as needed basis

Setting and executing strategy: Under the supervision of the Managing Director, MSD CARD, and LA Region communications lead, works closely with local CARD teams to set internal and external communications strategies and ensure local alignment with LA Region and Global Communications strategies.

Decision making: Responsible for day-to-day decisions guiding communications within the CARD. Accountable to the Managing Director, MSD CARD, and LA Region communications director for strategic communications issues impacting the business. Partners with CARD business to ensure that all organizations under the MSD umbrella are aligned (if applicable) and support for all critical business issues impacting the CARD.

Problem solving: Communicating consistently and seamlessly across the CARD to ensure that all employees understand corporate goals and strategy as well as LA Region objectives. Enhancing visibility and reputation for MSD in CARD. Ensures adherence to standard Global Communications practices for media relations, employee communications, reputation management and issues management communications. Effectively navigates across multiple divisions and functions within the CARD to optimize communications effectiveness for all parts of the business. Work with PR agencies at an as needed basis.

Influence/liaison: The individual occupying this position will guide the execution of all ongoing communications within the CARD and will have ongoing interaction with the Managing Director, MSD CARD business units, LA Region executives and LA Region communications director, as well as Global Communications leaders.

Qualifications

* Required: Bachelor's Degree in communications/journalism/business
* Minimum experience required/Preferred: 8-10 years
* Background in pharma, consumer goods. Experience in highly regulated industry is preferred.
* Languages: Spanish (native), English
* Strong written and verbal communications skills. Understands and effectively communicates across business units and divisions
* Demonstrates good understanding of the business and regulatory environment in which MSD competes and communicates.
* Demonstrates initiative, strategic thinking and creative problem solving in response to the communications challenges and opportunities faced by the company within CARD.
* Effectively coaches, counsels and builds teams with MSD CARD team.
* Embodies the Merck Leadership Standards as ambassador, mentor, colleague and senior level communications counselor.
* Embodies the MSD Leadership Standards as ambassador, colleague and communications counselor.
* Excellent knowledge/understanding of CARD Healthcare Authorities, good contacts in this field
* Excellent knowledge/understanding of media in CARD/ good journalist contacts

Primary Location: PA-Panamá-Panamá
Other Locations: HN-Francisco Morazán-Tegucigalpa, GT-Guatemala-Guatemala, NI-Managua, CR-San José-San José, HN-Cortés-San Pedro Sula, SV-San Salvador-San Salvador, DO-Santiago-Santiago, DO-Santo Domingo-Santo Domingo
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Panam%C3%A1-Country-Communications-Lead-MSD-Central-America-and-Dominican-Republic-Job/1659998/165999816599982012-03-04Merck/MSDfull-timeUSDstarting0BSPanamá, Panamá, PA
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.


In this role, you supervise all pharmaceutical packaging operations in order to meet Production Plan in accordance with government regulations and procedures and the best practices relating to efficiency.

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.

Qualifications

* Bachelor in Science or in progress (An equivalent working experience could be considered)
* Relevant experience in supervision of a Packaging team, preferably in the Pharmaceutical, Cosmetics industry;
* In-depth knowledge of GMP Regulations;
* Ability to solve problems;
* Result-oriented;
* Excellent French and sufficient knowledge of English language;
* Familiar with Microsoft tools;
* Excellent interpersonal skills;
* Knowledge of the best practices, i.e: Value Added production.

Primary Location: CA-QC-Montreal (Pointe-Claire)
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Claire%29-Supervisor-Production-Evening-shift-Job/1708750/170875017087502012-03-04Merck/MSDfull-timeUSDstarting0BSMontreal, QC, CA
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:

Maintenance Process / Engineer

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

* 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;
* Participates in internal and external audits and inspections;
* 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.

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.
* Experience of six sigma and lean methology.
* Applicant should have previously demonstrated strong team and communication skills, flexibility, motivation, ability to project amange, 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

* B.S. /B.A. degree required (science, engineering or other technical field preferred) OR minimum, Associate Degree with 10 years related technical industry experience required.

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Process-Maintenance-Engineer-Job/965303/9653039653032012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
Description

Under the direction of a Principal Engineer and Process Director, the Process Engineer is responsible for the planning, design, and implementation of vaccine, biologics, and sterile process projects.

The Process Engineer participates in and provides process leadership to project implementation activities including early pre-charter activities, conceptual scope development, detailed design, peer reviews, estimating, equipment procurement / fabrication / installation, commissioning and qualification, and close-out with varying degrees of responsibility.

The Process Engineer collaborates with other Integrated Project Team (IPT) members, plant operations personnel, and outside contractors and is able to coordinate the work of vendors in the preparation of project related deliverables.

The Process Engineer also undertakes studies, applies Lean Six Sigma (LSS) methods and capital effectiveness, and provides consulting to ongoing projects and existing business operations.

The Process Engineer exhibits sound leadership, interpersonal and communication skills, and is expected to develop and maintain technical knowledge in process engineering with a particular focus in vaccine, biologics, and sterile processing.

Primary Activities

Responsible, under the direction of the European Process Lead for Vaccines, Biologics, and Sterile Projects and the Process Engineering Director, for executing capital projects supporting Vaccine, Biologics, and Sterile Manufacturing business areas. Responsible for development of project scope, including project definition/scope generation, process design, facility layout, equipment selection, vendor interaction, technology transfer, facility start-up, process demonstrations and qualification. The individual will lead technical evaluations, interdisciplinary discussions, and be expected to independently plan and implement recommendations.

Successful performance requires technical knowledge in process systems and facilities as well as strong project management stills.

* Prepares and executes user requirements specifications, equipment specifications, equipment selection, vendor management, HAZOPs, factory acceptance testing, equipment shakedown, and supports equipment start-up.
* Supports installation qualification (IQ), operational qualification (OQ) and supports tech transfer to operations.
* Works with other technical functions, including Operations, Quality, Validation, and Technical Operations, to ensure successful project execution and technology transfer of new and in-line products. Provides technical support and guidance to support business goals through the application of appropriate technologies and facility design.
* Responsible for analytical and engineering studies associated with the development of new products, processes, systems and facilities.
* Maintains knowledge of current internal practices and industry trends and may participate in professional/technical organizations. Executes projects in alignment with Lean Six Sigma design.
* Participates in the development and review of engineering guidelines, safety/environmental policies, process descriptions and change requests.

The individual will work in a department within Global Engineering Services that supports vaccine, biologics, and sterile process related projects throughout the European and Asia-Pacific regions.

While the role will be based at the Carlow, Ireland site, significant travel, ( ~ 50 % of the time), to MSD sites in Europe as well as possible travel to Emerging Markets sites in Turkey and Russia is anticipated.

Qualifications

Skills/Requirements

* B.S. or higher degree in Engineering. B.S./M.S. in Chemical, Biochemical or Mechanical Engineering preferred.
* Minimum 5 years post-B.S. experience in related technical positions in Engineering, Operations/Manufacturing, or Research.
* Excellent analytical abilities, a solid base in engineering fundamentals, strong technical skills, competent leadership and teamwork skills.
* Accomplished verbal and written communication skills.
* Experience with capital project execution, equipment/vendor interaction, and exposure to biologics processes.

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Process-Engineer-%28Global-Engineering-Services%29-Job/1505470/150547015054702012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
Description

Technology Transfer Lead

MSD Ireland (Carlow)

Role

· Process equipment and technology selection

· Develop and/or review Process description and process flow diagram with originating site/team part of process gap analysis for receiving site facility assessments

· Definition and transfer of process

· Process parameter definition and alongside process scientists

· Definition, planning and completion with TT team of supporting studies such as water runs, process scale-up, engineering runs and process validation

· TT Execution in Vaccine/biologics environment

· Project planning, schedule development and definition for technology transfer

· Management of global virtual cross-functional teams within a large multi-national organisation

· Overview and awareness of all site activities to enable TT

· Management of knowledge transfer to receiving site

· Demonstrable team building and management skills

· Excellent analytical and decision making skills
· Knowledge and understanding of European and US regulations and standards affecting Clinical Investigation

Qualifications

Qualifications/Experience

· Minimum of BSc in Science/Chemistry/Engineering

· Minimum 3-5 Years Experience in Technology Transfer Activities including water runs, process scale-up, engineering runs and process validation

· Tech transfer, capital project support, and start-up experience of multiple projects and product from early stage development to commercial scale

· Experience in equipment and technology design, selection, testing and procurement.

· Current knowledge of GMP regulatory requirements

· Project Management skills

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Technology-Transfer-%28TT%29-Lead-ScientistEngineer-Job/1094575/109457510945752012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
Description

To reach Sales/Invoicing monthly goals with adequate inventory management and profitability, through out a sucesfull execution of a Trade and Marketing Business Plan. To guarantee visits to the most potencial clients, to present the current and new products with the right message. Try to close business deals while focused on achieving or exceeding Sales/Invoicing goals and to maximize their products market share.

Qualifications

Profesional degree with experience of more than 4 years in sales work in the consumer industry. Experience in chanel partners (distributors) is required.

Primary Location: CO-Antioquia-Medellín
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Medell%C3%ADn-Sales-Representative-Consumer-Job/1705730/170573017057302012-03-04Merck/MSDfull-timeUSDstarting0BSMedellín, Antioquia, 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.

Primary Location: IE-L*-Dublin
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Dublin-Real-Estate-Regional-Portfolio-Manager-Job-L/1354335/135433513543352012-03-04Merck/MSDfull-timeUSDstarting0BSDublin, 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.




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.

Primary Location: CO-Distrito Capital de Bogotá-Bogotá
Employee Status: Temporary
Number of Openings: 7]]>http://jobs.merck.com/job/Bogot%C3%A1-Associate-Data-Coordinator-Pharmacovigilance-Job/1691724/169172416917242012-03-04Merck/MSDfull-timeUSDstarting0BSBogotá, Distrito Capital de Bogotá, CO
Description

Member of the Quality Team to review core site Automation Compliance aspects of CGMP for operational areas of Vaccine Sterile and Pharmaceutical Operations including site facilities, utilities, manufacturing, packaging, labeling, and laboratories. Support and perform core activities associated with Automation that may include Qualification of Automation Systems, System Life Cycle Management, Business Systems Ownership, and Compliance Oversight. Responsible for compliance review, assessments, and conformance to Merck Manufacturing Standards, MMD Quality Policies/Guidance for Automation System Life Cycle, and site procedures in accordance with government regulations as related to the qualification, maintenance, auditing, and retirement of automated systems.

Primary Activities:

· Reports to Director of Quality Operations. Upon receipt of assignment, works on the coordination and execution of multiple independent projects.

· Provides guidance and technical skill knowledge to site to MSD employees and contingent workforce relating to scientific area and/or automation SLC and computer validation concepts. Guidance is consistent with department, company, regulatory policies and practices.

· Maintains and supports proactive communications regarding automation related activities to ensure conformance and maintain related work schedules.

· Facilitates and/or provides guided training and internal consulting services incorporating current industry practices and governmental regulations pertinent to automation qualification, compliance oversight, quality systems business ownership, and SLC.

· Performs effective document review to support Automation Compliance activities.

· Performs compliance oversight assessments and support regulatory inspections related to automation.

· Performs Quality System ownership functions including, SLC requirements and procedures/training.

· Supports development of procedures and processes to support strategic automation initiatives, projects, and compliance oversight initiatives.

· Maintains project tracking systems and associated systems that support SLC automation efforts, Quality Systems, and Compliance Systems.

· Has dotted line reporting to Manager Automation Compliance (CoE) to ensure network alignment.

Qualifications

Education: BSc experience in science or a pharmaceutical related technical discipline. Automation experience a plus.

Skills:

° Project management and organizational experience

° Working knowledge of automation engineering, computer systems and/or computer system validation, various SLC methodologies, applicable predicate rules (21CFR 210,211, 21 CFR Part 820, 21 CFR Part 11 and industry related automation standards).

° Knowledge of cGMPs, API, pharmaceutical and/or biological manufacturing, Quality/regulatory trends related to automation

° Knowledge of Eudralex Annex 11 Regulations for Computerised Systems

° Strong interpersonal/communication skills to ensure team negotiation and remediation activities are business and compliance based.
Ability to work with teams and escalate issues to Management in a proactive manner.

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Carlow-Automation-Compliance-Specialist-Job-L/1415923/141592314159232012-03-04Merck/MSDfull-timeUSDstarting0BSCarlow, L*, 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.


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.

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-08889/1658097/165809716580972012-03-04Merck/MSDfull-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 000269). 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, US-NJ-Union, US-NC-Charlotte
Employee Status: Regular
Number of Openings: 4

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Whitehouse-Station-Global-Services-Associate-Analyst-Job-NJ-08889/1689830/168983016898302012-03-04Merck/MSDfull-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.

The Future Talent Program features paid internships targeted to start in June 2012 for 9 - 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 on can be in one of the following areas:

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.

Merck Sigma

Merck Sigma works on a diverse portfolio of projects that range from large-scale, global, cross-divisional/functional projects, to high-impact transformational initiatives, to strategic process improvement projects. Merck Sigma staff members have challenging and exciting roles on these high profile projects with regular interaction and exposure to senior leaders and management.

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, West Point, PA; Elkton, VA; Durham, NC; Rahway, NJ; Summit, NJ, Union, NJ, Charlotte, NC, Upper Gwynedd, PA, Cokesbury, NJ, Boston, MA.

Qualifications

Required:

* Currently enrolled in a (BS/BA, MS, MBA, 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 be able to work for a period of 9-12 weeks, beginning June 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 000250). 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.


Primary Location: US-NJ-Whitehouse Station
Other Locations: US-NJ-Rahway, US-PA-Upper Gwynedd, US-NJ-Lebanon, US-PA-West Point, US-VA-Elkton, US-NJ-Union, US-NC-Durham, US-NJ-Summit, US-NC-Charlotte, US-MA-Boston
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Global-Services-Intern-2012-Job-NJ-08889/1464581/146458114645812012-03-04Merck/MSDfull-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:

Reporting to the Head of Global Media Relations, the Director of Research & Innovation

Media Relations will work with colleagues in Merck Research Laboratories and Global Human Health to develop and implement strategies to differentiate Merck's licensing and R&D functions from the company's competitors. The Director will handle day-to-day activities associated with top-tier media including reporter inquiries, relationship building with key journalists, managing inquiries concerning scientific research and working with divisional colleagues to ensure consistent delivery of succinct and focused messages. The Director will be a company spokesperson for R&D and Business Development inquiries.

In this role the Director, Media Relations will:

· Compose and edit news releases and develop briefing documents to inform colleagues and gain agreement on key messages.

· Provide media relations support including arranging media interviews to research executives at scientific meetings and company R&D events.

· Implement new strategies to ensure communications are in concert with rapidly changing technologies, including social media and other web-based technologies.

· Work closely with corporate, divisional and local site representatives to ensure broad understanding of external scientific and business development communications strategies.

Qualifications

Education:

* Bachelor's degree in Communications, Journalism or Public Relations
* A graduate degree in a life science discipline is preferable

Required Experience/Skills:

* A minimum of five to seven years media relations or communications experience
* Solid knowledge of the pharmaceutical industry including the science of drug discovery and development
* Sound judgment and ability to work with multiple clients both internally and externally
* Proven writing, editing and verbal communications skills
* Ability to manage multiple projects and meet fast deadlines, while working with multiple stakeholders
* Ability to succeed in a fast-paced, high-visibility environment
* In-depth knowledge of biomedical science and the drug discovery and development process
* Established relationships with key healthcare reporters
* Proven ability to manage and develop junior staff

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 # MED000598.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Director-MRL-Media-Relations-Job-NJ-08889/1650164/165016416501642012-03-04Merck/MSDfull-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 Import Specialist will be responsible for the providing broker clearance instructions and required documentation for individual import shipments arriving for delivery in the US. Obtain compliant valuations, HTS codes, FDA product codes, country of origin and other trade determinations from a center of excellence, then ensure these are evident within required documentation. Interface directly with the Customs Broker to import entries, resolve issues or provide additional information as required. Adheres to company policies and procedures. Ensures compliance with governmental regulations. Executes routine functions with minimal guidance. Provides customer service in support of product quality and supply chain principles. Maintain relationships with the Import/Export contacts at local and worldwide locations to identify and collaborate on root cause and corrective actions for issues affecting international shipments. Provide back up for colleagues within the team.

Interface directly with the requestors/stakeholders (internally and externally) to provide pre-shipment requirements which facilitate import clearance with US Customs and OGA (Other Government Agencies). Apply regulatory and departmental changes to align with import compliance and operational effectiveness. Support Global Trade Compliance strategic initiatives. Develop and maintain relationships with the other trade compliance team within the global organization. Support internal self audits and metrics programs. Supports functional management and associated projects through data compilation and coordination.

1. Provides technical expertise to shippers regarding the trade compliance requirements for US import shipments of supplies, capital equipment, MRL samples, marketing and training materials, supply chain and commercialization materials to support evolving and ongoing business for the Company.
2. Maintains current knowledge of government regulations on trade compliance matters. Provides expertise in trade compliance with respect to shipping materials via all modes of transportation.
3. Reviews broker entries to ensure accuracy of information submitted to regulatory agencies.
4. Monitors and expedites critical inbound shipments. Provides imternal/external stakeholders with delivery and shipment status updates as needed.
5. Escalates and supports resolution of import shipments that are held by US Customs, FDA, USDA and other government agencies to facilitate trade compliance and uninterrupted commerce for the Company.
6. Maintains a central log of data elements for import entries and supports monthly metrics to measure supplier performance and global trade compliance.

Qualifications

Required:

* Bachelor's Degree is required
* Minimum 3 years of import trade compliance experience
* Knowledge of US trade regulations, and regulatory awareness (Pharmaceuticals, FDA, USDA focus)
* Knowledge of research and development and supply chain interdependencies

Preferred:

* Experience in the pharmaceutical or chemical 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 submit your resume for requisition # IMP000127.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Import-Specialist-Job-NJ-08889/1528627/152862715286272012-03-04Merck/MSDfull-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 audits within established deadlines, and in accordance with departmental standards. As determined by audit scope, the incumbent reviews and assesses financial controls/procedures and ensures compliance with key policies and procedures. The incumbent is expected to provide leadership by managing complex, large or sensitive audit engagements with limited management supervision. On occasion, the incumbent may be requested to participate in special assignments, where special circumstances and sensitive situations exist which usually require quick response and a high degree of adaptability.

The incumbent's primary role will be to manage and perform varied and complex audits with limited management supervision. The incumbent is responsible for the overall preparation and quality of workpapers as defined in Corporate Audit's Policies and Procedures.

Assist the Client Audit Director . The primary role will be to lead 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 its efforts to become a "world class" audit organization. The incumbent will accomplish this by completing tasks efficiently and according to established milestones, encouraging positive team interactions and providing periodic 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. The incumbent should provide technical guidance and consultation on computer security and control issues to the client and Corporate Audit staff, as well as coach, mentor and train new members of the department.

Qualifications

Education Requirement:

* BS/BA required preferably in Accounting or Finance.

Required:

* Knowledge of audit methodology and internal controls.
* A minimum of 5 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 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 # FIN000480.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Audit-Manager-Job-NJ-08889/1025365/102536510253652012-03-04Merck/MSDfull-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 Customer Service Process Leader will have global responsibility to design and manage the all customer service processes for Merck, including ordered management, billing and receivables, and customer returns. He/she will be responsible for the overall process performance across the company. Specific responsibilities include:

* Design and improve planning and logistics processes. Define global standards
* Collaborate with other process leaders to define and improve cross functional processes - examples are pricing processes, distribution and logistics, etc.
* Define KPI and process health metrics, implement and define and execute approaches for improvement. Co-own performance with line/business leaders
* Support the SAP implementations; prioritize blueprint enhancements

Qualifications

Education Minimum Requirement:

* Bachelor's degree required
* Master's degree preferred

Required Experience and Skills:

* 10+ years experience in customer service processes
* Process knowledge in multiple customer service areas
* Strong influence and conflict resolution skills
* "Lean" mindset
* Ability to develop people
* Track record of delivering results
* Demonstrated ability to navigate and collaborate across organizational boundaries (removes roadblocks and barriers)
* Experience working across geographies
* Ability to manage complexity and ambiguity; business and financial acumen; working knowledge of multiple areas of the supply chain
* Approximately 20-25% international travel required

Preferred:

* Working knowledge of COMET (SAP) solution 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 # BUS000448.

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
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Customer-Service-Process-Leader-Job-NJ-08889/1669059/166905916690592012-03-04Merck/MSDfull-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.

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-Senior-Internal-Auditor-IT-Job-NJ-08889/1655963/165596316559632012-03-04Merck/MSDfull-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 Regional Strategy Manager is responsible for but not limited to the following:

* Partners with regional clients to ensure a strategic contact center model is implemented in accordance with business objectives utilizing Merck/MSD capabilities and industry best practices.
* Provides in-region support, oversight and subject matter expertise (SME) for execution of strategic contact center goals and objectives.
* Works with the Leader of International Strategy and other regional strategy and capabilities managers to create a comprehensive strategic plan that balances local business needs with global objectives. Collaborates with local management to identify priorities and ensure that regional and global strategies are aligned.
* Partners with regional clients to achieve their business objectives by developing and leveraging Merck/MSD capabilities and industry best practices.
* Shares best practices for contracting, vendor oversight, and partner management, including performance scorecards, communication plans and key performance indicators.
* Provides input and acts as a SME during quarterly business reviews and makes process improvement recommendations.
* Acts as a point of escalation for local contact center management as well as vendor partners.
* Ensures successful adoption and implementation of best practices, metrics, and reporting, while identifying opportunities for case studies that promote these successes, while sharing information across markets and regions.
* Promotes the use of global tools (Global Team Site) to access a repository of best practices and supports collaboration among clients.
* Provides dashboard reporting to global leaders to track contact center performance.
* Monitors regional competitive landscape and shares case studies that support strategic decision making at the local, regional and global levels.
* Supports the international leader of strategic planning to ensure that global strategies are aligned with regional and local business objectives, and provides input into short and long term objectives.

There will be 40% travel for this position.

Qualifications

Education:

* Bachelor's degree required
* Masters degree preferred

Required:

* A minimum of 3 years experience in a contact center or customer care operation

* A minimum of 3 years in a marketing, franchise or strategy development role

* Strong interpersonal
* Ability to lead through influence
* Effective verbal and written communication skills
* Strong presentation and project management skills
* Technical aptitude
* Ability to translate strategy into execution
* Strong change management skills

Preferred:

* Work experience in multiple countries

* Experience and/or understanding of different contact center technologies such as Adobe Connect Pro, WebEx for remote agent capabilities
* Sigma belt or PMI 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 # CUS000735.

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-Upper Gwynedd
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Regional-Strategy-Manager-Job-NJ-08889/1568986/156898615689862012-03-04Merck/MSDfull-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.


Performs functions within the Global Closing Sales & Inventory (GCSI) group regarding sales, inventory and product cost data, analysis and reporting in support of the monthly accounting close and management reporting cycles.

* Participates in monthly sales and inventory consolidated close which includes: working with associates in the field to ensure that the data submissions meet quality and schedule requirements for internal and external reporting purposes.
* Analyzes consolidated costs and intercompany profit differences.
* Addresses entity/divisional customer questions and requests on a variety of data and system issues.
* Provide ad-hoc support of business development projects.
* Post WFRS Adjustments and CAM entries requested by DFS.
* Work with Information Technology Group to enhance all computer systems and financial processes related to the collection, processing and reporting of the data

Qualifications

Education:

* BS/BA required preferably in Accounting or Finance

Required:

* A minimum of 2 years of demonstrated experience in an accounting or finance related role.
* Demonstrated experience with MS Excel , specifically with the use of Pivot Tables.

Preferred:

* MBA or CPA

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 # FIN000712.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Whitehouse-Station-Financial-Analyst-Job-NJ-08889/1708749/170874917087492012-03-04Merck/MSDfull-timeUSDstarting0BSWhitehouse Station, NJ, US
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

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Production-Technician-Job/1155628/115562811556282012-03-04Merck/MSDfull-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

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/QA-Specialist-Job/1157466/115746611574662012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
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.

Primary Location: Ireland
Employee Status: Regular
Number of Openings: 2

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Order-to-Cash-Finance-Analyst-Job/1366986/136698613669862012-03-04Merck/MSDfull-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.


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 (BS/BA, MS, MBA, 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 000249). 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.


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, US-NJ-Union, US-NC-Charlotte
Employee Status: Regular
Number of Openings: 18

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Whitehouse-Station-Global-Services-Associate-Job-NJ-08889/1473790/147379014737902012-03-04Merck/MSDfull-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.


Responsibilities include but are not limited to:

* Responsible for the development and leadership of multiple Cattle Parasitology US R&D Projects leading to licensure of new or improved products
* Responsible for the scientific leadership of projects providing guidance, data analysis, planning and interpreting results
* Provide in-depth knowledge and advice to research staff and management in the science of Cattle Parasitology
* Key interface with Discovery and Technology in the planning and delivery of products and new technologies transferring from D&T into R&D, as needed
* Manage the intellectual property (patents/product information) to meet corporate guidelines
* This position will require strong knowledge of General Parasitology and basic knowledge of Molecular Parasitology and parasite antigen expression, in addition to the general Qualifications. Experience in Bovine product development will be highly desirable.

Qualifications

Education Minimum Requirement:

* M.S. degree

Preferred Education:

* Ph.D. degree

Required Skills and Experience:

* Minimum 7 years vaccine development industry experience with MS - or - 3 years vaccine development industry experience with PhD.

*
Successful experience in training and supervising Lab Technicians (M.S.- or B.S.-degreed individuals)

*
Ability to manage Lab Technicians and Research Associates. Must have aptitude to provide leadership for his/her research teams and manage team's personnel issues.

*
Good project management skills. Must have aptitude to manage technical and logistical aspects of assigned research projects.

*
Must have aptitude to provide interdepartmental leadership in product development and licensing; chair interdepartmental team meetings.

*
Good problem-solving and decision-making skills.

*
Good knowledge of production processes.

*
In-depth knowledge of government regulations required for product licensure.

*
Computer literacy as appropriate for the position.

*
Strong oral and written communication skills.

*
Experience in working with cattle/animals in vaccine development research.

*
Must be able to work effectively with upper management and properly carry intra- or inter departmental 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 # BIO003367.

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-KS-DeSoto
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/DeSoto-Assoc-Principle-Scientist-Parasitology-Cattle-DeSoto%2C-KS-Job-KS-66018/1464578/146457814645782012-03-04Merck/MSDfull-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.


The Sr. QC Lab Technician is responsible for performing and evaluating mid-level laboratory and support procedures for the testing of veterinary biologicals according to strict government and company imposed guidelines. The major activities and responsibilities include but are not limited to:

* Perform routine quality control procedures with an emphasis on safety and potency testing. This requires an understanding of the principles underlying the testing procedures used in the area of assignment.
* Maintain inventories of critical reagents required for testing.
* Enter test results in the appropriate tracking system.
* Report all unusual, non-routine occurrences when performing tasks to QC Supervisor. This includes completing the necessary documentation.
* Participate in the creation/revision of SOPs for testing performed in the area(s) of assignment.
* With limited guidance, troubleshoot testing methods.
* Complete extra duties including general animal husbandry, as assigned.

Qualifications

Education Minimum Requirement:

* Associate degree in a related field with 2 or more years experience or a Bachelor's degree in a related field or a non-related Bachelor degree with some relevant experience

Required Experience and Skills:

* Familiarity with and ability to perform basic laboratory techniques and procedures required.
* Ability to work independently with minimal supervision.
* Ability to follow oral and written instructions.
* Good mathematic and writing skills.
* Good time management skills with an ability to be flexible with respect to changing priorities.
* Ability to work on a team with people from both inside Quality Control as well as Production and Research.
* Experience with Microsoft Office software products.

Desired Experience and Skills:

* Experience with SAP
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 # QUA002748.

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-KS-DeSoto
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/DeSoto-Sr_-QC-Lab-Tech-Job-KS-66018/1660003/166000316600032012-03-04Merck/MSDfull-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:

* Ensures that all biological starting materials, containers, and printed labeling/packaging materials meet company specifications for identity and quality.
* Provides timely review and release of these materials to ensure the integrity of the production schedule.

Qualifications

Education Minimum Requirement:

* Minimum associate degree with 2 years relevant training and experience. Bachelors degree preferred.

Required Experience and Skills:

* General knowledge in the areas of biology and chemistry.
* General computer skills
* A high level of organization, tact and patience.
* Ability to work independently and also be a team worker.
* Ability to handle large amounts of detail work and work on several projects at one time.
* Good written and oral communication skills.
* Ability to lift and move material, i.e., lifting up to 50 lbs., manually and through the use of dollies/hand trucks.

Preferred

* Understanding of regulated packaging
* Experience with Sharepoint, Microsoft 7 and Office 2010 (Word, Excel)

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 # QUA002760.

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-KS-DeSoto
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/DeSoto-QC-Materials-Inspector-Job-KS-66018/1703550/170355017035502012-03-04Merck/MSDfull-timeUSDstarting0BSDeSoto, KS, 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 local organization in Lucerne and are therefore recruiting for a new position as

Swiss Entity Controller (Director Level)

Summary:

· Responsible and accountable for all the US GAAP and Statutory financial results of all hub entities (+30 entities) in Switzerland.

· Complete and all Accounting and Tax forms as required by USGAAP and Swiss standards

· Provide analysis to the business on all accounts

· Execute all Legal Entity integration steps and record in the Company's books

· Main contact to tax authorities, outside accounting firms, pension fund representatives and any other authorities requiring access to Swiss books

· Execute on internal controls as instructed by local Internal Control procedures

Job Description and Responsibilities

· Maintain appropriate records of Company's accounts based on US and Local accounting standards

· Specifically focus on local statutory accounts and ensure external auditors are comfortable by the level of management and controls exercised in Switzerland

· Take over responsibility for all Managed and Controlled entities including these based in Ireland, Bermuda and US

· Provide evidence of good accounting record keeping to auditors and authorities

· Complete all VAT, Withholding tax, Stamp duty tax and any other tax forms as required

· Provide support to the business by providing analysis on all accounts as required including on a historical and a prospective view.

· Provide monthly analysis and monthly reconciliations of all critical accounts

· Provide support to SBS and ensure smooth hand off of transactions between Finance and SBS. Facilitate execution of the new Finance model

· Prepare any other analysis as required by the Swiss Council or any other internal governance structure

· Prepare analysis and present any supporting evidence of financial transactions to tax authorities

· Maintain a system in place to ensure all transactions are supported by agreements, contracts, approvals and bonafide documentation

· Follow evolution of tax and accounting legislation and make proposal to adjust reporting and structure accordingly

· Fluent in using the COMET system for all entities

· Participate in all accounting projects within the boundaries of legislation

· Manage a team of approximately 15 people of which approximately 5 direct reports. Regularly make recommendations to adapt the structure, hire and retain the best talents

Qualifications

· Accounting diploma equivalent Swiss and US CPA

· English and German fluent

· Several years' experience in Accounting

· Leadership Experience

· Tax expertise

· Strong Communicator (ability to explain complex situations)

· Excellent ethics and behaviors

· Fully autonomous

· Proactive

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

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Swiss-Entity-Controller-Job/1650158/165015816501582012-03-04Merck/MSDfull-timeUSDstarting0BSCH-Lucerne
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.

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Maintenance-Technician-Job/1703556/170355617035562012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
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

Primary Location: Peru
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/Sales-Representative-Job/1679789/167978916797892012-03-04Merck/MSDfull-timeUSDstarting0BSPeru
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.

The Marketing Communications Manager is part of the Global Customer Support (GCS) group in the Europe/Canada Commercial Operations Team (ECOT) and part of the new regional Europe/Canada Marketing organization.

Key Responsibilities will be:

· Development of customized materials for assigned franchise according to identified customer needs and strategic brand priorities by ensuring medical accuracy

· Close collaboration with countries and Regional Marketing Leaders to ensure alignment with global and regional strategies, utilization of relevant brand and customer tactics

· Integration of materials or programs in the product portfolio approach to take into account each customer segment and local implementation for meaningful customer execution

The Marketing Communications Manager will:

· Develop integrated portfolio marketing solutions and services for specific customers or franchise/disease areas

· Support Regional Marketing Leaders (RML) in positioning franchises for a specific customer segment (portfolio approach, marketing solutions, selling schemes)

· Collaborate closely with Global Marketing Communications teams and Regional Marketing Leaders (RML) in transforming brand strategies into integrated portfolio campaigns

· Work closely with country stakeholders to understand their market and customer needs and to determine similarities & differences across Mid Europe markets

· Work as a country partner in order to propose solutions and give guidance by supporting local implementation

· Drive cross-functional collaboration within the ECOT (MCM, L&D, GMRA, etc.) to provide comprehensive and aligned customer solutions

· Collaborate closely with Regional Portfolio Team (RPT) and country stakeholders to ensure flawless execution around customer strategy

Qualifications

Required:

Experience

* Minimum: University degree from accredited university
* Minimum: 5 years experience in Pharmaceutical Marketing

Skills/Capabilities

Marketing Experience

* Experience with new launches and management of product life cycle
* Financial and Budget management experience
* Ability to create integrated Marketing Campaigns
* Business acumen (e.g., knowledgeable in policies, practices, trends, technology, and information affecting Merck's business)

Strategic Planning / Analytical Skills

* Ability to interpret data sources and translate into strategic plans
* Ability to plan and develop marketing strategies for different customer segments
* Ability to prioritize country needs vs. global strategy and make resource allocation decisions

Project Management

* Ability to lead a project, delegate tasks and ensure proper implementation
* Excellent prioritization and time management skills
* Ability to multitask and see projects through to the end

Customer Understanding/Interaction

* Knowledge of different specific attitudes/behaviors of multiple customers segment
* Ability to understand/analyze customer behaviors (from various sources: market research, field, country feedback, scientific leader interaction)
* Experience with varieties of selling techniques and first-hand customer interactions

Communication Skills

* Open, transparent and candid communication
* Excellent command of both written and spoken English
* Able to manage multiple ongoing communication channels with stakeholders

Interpersonal Skills

* Team player, ability to collaborate with different personalities
* Flexibility to adapt easily to changing situations
* Active listening skills
* Problem solving skills
* Optimistic, motivated and passionate
* Open to feedback & learning

Leadership / Change Management

* Courage to take risks or challenge the status quo
* Ability to influence and persuade at different levels of the organization
* Capability to energize and motivate teams
* Entrepreneurship / Innovative Thinking
* Work with country, regional and global marketing teams to shape customer/franchise strategies and programs

Primary Location: CH-Lucerne
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/Marketing-Communications-Manager-Mid-Europe-Job/1538424/153842415384242012-03-04Merck/MSDfull-timeUSDstarting0BSCH-Lucerne
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 local organization in Lucerne and are therefore recruiting for a new position as

Financial Services Manager

Summary:

* Ensure the efficient and timely controlling, recording and processing of all incoming and outgoing financial data of MSD International GmbH reporting accurately to Headquarter in accordance with US GAAP.
* Prepare consolidated US GAAP accounts, bridge for CH GAAP within local requirements and timely MSD International GmbH statutory accounts.
* Maintain internal control of MSD International GmbH according to Swiss and group requirements.
* Manage all financial services matters for MSD International GmbH in accordance with company policies and procedures, and the applicable laws and regulations.

Job Description and Responsibilities

* Ensures that the financial, tax and statutory obligations of the companies are complied with.
* Ensures that the financial procedures are adequate to achieve satisfactory internal controls.
* Controls the application of all company policies and procedures, as well as, the compliance with and maintenance of the Grants of Authority delegation system.
* Ensure that all financial activities of the subsidiary not covered by specific procedures are in accordance with the normal conduct of the business.
* Ensures Internal and External Auditors recommendations are implemented.
* Maintain internal external contacts at an appropriate level, to ensure the optimization of tax expenses in strict compliance with existing regulations.
* Ensures that the financial statements represent fairly the company situation and controls the security and the accuracy of this information by periodically reviewing all accounts (B/S analysis each quarter with corrective actions implemented before next quarterly analysis - monthly for sensitive B/S accounts i.e. banks, accruals, payroll, fixed assets and depreciation, employees and vendors)
* Ensures that all financial information is made available to management on a timely and need -to- know basis.
* Analyses financial data and proposes corrective actions to management.
* Maintain financial set-up in according with company MCCOA and JDE system requirements
* Ensure integrity reports and suspected duplicate payment reports is analyze monthly and any issue resolved
* Is responsible to control the accurate and timely processing of suppliers invoices, employee expense reports and other disbursements.
* Is responsible for verifying the appropriateness of the expenses and their proper approval prior payment.
* Is responsible for verifying that payroll related data is properly authorized, computed and recorded.
* Ensures that the financial staff is adequately trained, supported on controls and co-ordinates the work within the accounting team.
* Ensures proper functioning and increasing, efficiency of all existing and new applications and systems used in the areas of Finance and other users of JDE.
* Develop, control and maintain accounting systems, to ensure up-to-date financial system in accordance with corporate and local management's requirements.
* Assists the Swiss Hub Finance in the development and the implementation of major new projects.

Qualifications

* Bachelor Degree in Accounting as a minimum
* US and CH GAAP, Swiss Tax and Internal Control expertise.
* Strong computer skills (Financial Systems: SAP & JD Edwards) and MS Pack (Excel, Word, Powerpoint).
* German and English languages.
* Collaborative team player, inter -relation skills.
* Natural Leadership or good people management skills.

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

External Job Board Posting
: Switzerland - Jobs.ch]]>http://jobs.merck.com/job/Accounting-Manager-Job/1650163/165016316501632012-03-04Merck/MSDfull-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 is a field based technical services position within the US dairy cattle business unit and is to be located in the western United States. Ideally this candidate will be located in California near the dairy industry. A bilingual English/Spanish speaking candidate is preferred. This position will require approximately 50% or more travel. The position encompasses numerous duties including and not limited to:

* Technical representation of products and services offered by the company. This representation will be to both internal and external customers and will include sales force training as well as guidance on implementation for external customers.
* Planning and performance of post-approval trials.
* Working with marketing on key business initiatives.
* Working with customers on product questions and adverse events. This position requires an individual who is a self starter and is comfortable in an independent work environment. This candidate must be competent in their public presentation skills and the use of Microsoft office including word, power point and excel.

Qualifications

Education:

* DVM

Required:

* Minimum 5 year clinical practice experience as a practicing dairy veterinarian.

* Working knowledge and experience with required dairy practice skills including management of reproduction, mastitis, and general health programs as wells as protocol development and implementation.

* Additional requirements include good presentation skills, a high level of competence with Dairy Record Keeping systems, proficiency in Microsoft office including Word, PowerPoint and Excel

Desired

* Spanish fluency

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 # TEC000406.

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-California
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Technical-Services-Manager-Western-US-Job/1550476/155047615504762012-03-04Merck/MSDfull-timeUSDstarting0BSUS-California
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.

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Business-Financial-Analyst-Job/1606560/160656016065602012-03-04Merck/MSDfull-timeUSDstarting0BSIreland
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

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

External Job Board Posting
: Ireland - IrishJobs.ie]]>http://jobs.merck.com/job/Report-Process-Steward-Job/1703533/170353317035332012-03-04Merck/MSDfull-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.


Responsibilities include but are not limited to:

* Conduct and use strategic market analysis to precipitate and improve strategic decisions about products. Provide in-depth market, industry, and competitive analysis and positing. Analyze market trends, sales potentials, and expenses, and prepare simple, short-term forecasts for existing products for use in planning and control. Analyze market potential for the product and prepare revenue forecasts for review. Interpret sales forecasting and inventory flow models. Identify and monitor customer requirements and satisfaction. Establish key issues, elements of strategies, tactics, action plans, investment to impact the market share, market growth strategies, and profits for key products. Develop brand strategy and engage in life-cycle planning. Develop SWOT analysis for competitors and business problems.
* Interpret sales forecasting and inventory flow models. Draw implications from consumer insight analyses. Identify and monitor customer requirements and satisfaction. Probe for underlying themes and product implications from data. Direct and guide brand strategy and engage in life-cycle planning.
* Develop overall promotional and media activities to deliver brand objectives. Determine best promotional communications plan to deliver brand objectives designed to differentiate products, maintain leadership position, and increase awareness. Work with Production Management team responsible for product to ensure consistent product messaging. Gain legal, regulatory approval of all materials. Execute the brand strategy through implementation of tactics. Develop promotional materials in time for each cycle.
* Work under general supervision. Identify and use best practices and seeks out others to learn from.

Qualifications

Education Minimum Requirement:

* Bachelor degree

Required Experience and Skills:

* Minimum of eight (8) years experience in Marketing and Sales and/or Animal Health Operations is required, broad and in-depth knowledge of the market, products, and competitive environment.
* A thorough understanding of US Swine market
* Strong ability to work cross functionally with all business units, regulatory, legal, R&D, manufacturing, and with Global Marketing colleagues.
* Computer competency is required. (The individual must demonstrate competency with applications, including but not limited to, Microsoft Office products and Customer Relationship Management (CRM) applications.)

Desired Experience and Skills:

* Prior experience in swine sales

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 # MAR004105.

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-KS-DeSoto
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/DeSoto-Sr-Product-Manager-Job-KS-66018/1517898/151789815178982012-03-04Merck/MSDfull-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.


The Sr. QC Lab Technician is responsible for performing and evaluating mid-level laboratory and support procedures for the testing of veterinary biologicals according to strict government and company imposed guidelines. Responsibilities include, but not limited to;

* Perform routine quality control procedures. This requires an understanding of the principles underlying the test procedures used in the area of assignment.
* Tracking and maintenance of the Quality Control Special Test Request (STR) database.
* Receipt storage, and distribution of test samples, USDA submission samples, USDA retention samples, Merck retention samples, and stability samples.
* Preparation of media, general laboratory reagents and solutions, sterilization of labware, and decontamination of waste material.
* Complete additional duties as assigned.

Qualifications

Education Minimum Requirement:

* Bachelors degree in a related field with no experience, or a non-related Bachelor degree with some relevant experience, or an Associate degree in a related field with 2 or more years of experience.

Required Experience and Skills:

* Familiarity with basic laboratory techniques and procedures required.
* Ability to follow oral and written instructions.

Desired Experience and Skills:

* Ability to work independently with minimal supervision.
* Ability to work and contribute in a team environment.
* Good mathematics and writing 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 # QUA002757.

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-KS-DeSoto
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/DeSoto-Sr_-QC-Laboratory-Technician-Job-KS-66018/1679791/167979116797912012-03-04Merck/MSDfull-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.


The incumbent should perform laboratory work under limited supervision necessary to help complete a project. Must keep thorough notebooks to the standard required by GLP. Must have assay development and troubleshooting skills. Employee must have proven ability to write protocols and reports for specific experiments. Employee must have familiarity of production processes for outline preparation.

General microbiology laboratory duties that may include, but are not limited to:

* Preparation of cell/organism growth media and cell cultivation and growth of viruses for various reasons (e.g. optimize yields, seeds, challenge material)
* Perform assays to enumerate antibodies, organisms, etc. and develop and/or fine-tune laboratory assays
* Run laboratory equipment (e.g. bioreactors, ELISA, incubators, centrifuges, filtration, liquid nitrogen tanks, electrophoresis, chromatography, densitometry, etc) and prepare reagents and solutions as well as maintain inventories of supplies.
* Prepare and log samples (e.g. organisms, sera) for storage and prepare samples for analysis. Also be able to carry routine laboratory chores, including the cleaning of laboratory equipment and laboratory in general.

The incumbent should participate in interdepartmental activities such as assisting with technology transfer and scale up of technologies. Assist supervisor with project planning and protocol/report and outline preparation. Assist with or conduct parts of animal studies such as inoculations, challenges, sample collections, observations, including protocol preparation and scheduling. Recordkeeping such as logging results on bench records and/or in laboratory notebooks Miscellaneous - keep current on literature that relates to projects.

Qualifications

Minimum Education Requirement:

* B.S. degree in microbiology/virology and one year experience in molecular microbiology work, experience as a technician in viral vaccine development work that will allow the candidate to perform complex tasks (development activities and more involved interdepartmental activities) preferred.

Skills and Experience Required:

* Other degrees will be considered on a case-by-case basis, and may require additional laboratory experience
* Ability to use skills and experience to conduct important facets of projects with minimal supervision (e.g. assay development, report preparation, animal studies). Must have proven ability to work under limited supervision on projects. Excellent time management and problem solving skill.
* Ability to assist supervisor in planning and monitoring activities of Laboratory Technicians and may be responsible for leading technic
* Computer literate (Word/Excel/Windows) and strong oral and written communication skills.
* Experience in working with animals in vaccine development research will be 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 # BIO003408.

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-KS-DeSoto
Employee Status: Regular
Number of Openings: 3]]>http://jobs.merck.com/job/DeSoto-Assistant-Scientist-Bio-Rsch-Job-KS-66018/1560771/156077115607712012-03-04Merck/MSDfull-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.


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

Responsibilities will include 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

Minimum Education Required:

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

Required Experience and Skills:

* Minimum 10 years swine 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 # BIO003378.

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-KS-DeSoto
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/DeSoto-Head%2C-Swine-Healthcare-Products-Research-Job-KS-66018/1466969/146696914669692012-03-04Merck/MSDfull-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:

* Maintain, inspect and repair filling and packaging equipment and facilities in the Production Facility, with minimal supervision required in accordance with Good Manufacturing Practices.
* Good working knowledge and trouble shooting ability of automation equipment.
* Handle generated waste in accordance with facility procedures and government regulations.
* Be responsible for their safety and the safety of others in the workplace

Qualifications

Education Minimum Requirement:

* High School Diploma or equivalent with technical or trade school training

Required Experience and Skills:

* Minimum 5 years experience with filling / packaging systems.
* Must be able to follow detailed instructions associated with the operation and maintenance of production equipment.
* Must be able to work independently with minimal direct supervision.
* Able to fabricate parts and components for equipment modifications / improvements.
* Ability to repair and install pumps, gear drives, mixers, production equipment, and perform preventative maintenance to same as required

Desired Experience and Skills:

* Certification and/or specific training related to filling / packaging equipment, engineering or technical experience a real 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 # FAC000305.

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-KS-DeSoto
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/DeSoto-Maintenance-Mechanic-Job-KS-66018/1567427/156742715674272012-03-04Merck/MSDfull-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.


Position Overview

The incumbent will clean, sanitize and assemble various pieces of equipment which will require confine space entry into manufacturing tanks for cleaning and inspection. Must be able to obtain forklift licensing and pass physical requirements to wear respirators and lift up to 50 lbs.

Additional responsibilities are as follows:

* Accurately compound bulk materials in accordance with approved SOPs and pharmaceutical GMPs.
* Must operate processing equipment which includes the following: steam jacketed mixing vessels, process pumps, various types of mixers, transfer systems, process flow meters and valves.
* Read and interpret scales, load cells, gauges; translate formula instructions into equipment operation.
* Provide feedback on bills of material, labor routings, and demonstrated capacity issues to Manufacturing Management to collaborate as owners of accountable for achieving, maintaining, and continuous improvement of labor routing 95 - 100% metric performance and bill of material 98-100% metric performance.

Please note: Position will be 2nd or 3rd shift. Must be willing to work off shift. Position requires frequent overtime during seasonal peaks.

Qualifications

Educational requirements:

* High School Graduate or Equivalent.

Preferred:

* Technical degree, college degree or chemistry background.

Required skills and Experience:

* Ability to read, write and perform intermediate level math.
* Communicate clearly with individuals and teams, interpret and follow SOPs, batch formula instructions and follow pharmaceutical GMPs.
* Must be able to lift up to 50 lbs and demonstrate hands-on mechanical ability.
* Must pass GMP assessment.

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 # PRO009234.

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-TN-Cleveland
Employee Status: Regular
Number of Openings: 3]]>http://jobs.merck.com/job/Cleveland-Compounder-Job-TN-37311/1650161/165016116501612012-03-04Merck/MSDfull-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 Lab Technician is responsible for conducting microbiological tests on raw material components, product intermediates, finished products, purified water, and environmental sites according to established testing procedures. This position is also responsible for the preparation, tracking and documentation of all bacteriological media. Additional responsibilities include: routine equipment calibrations, lab glassware cleaning, operation of the steam sterilizers, and operation and maintenance of basic ancillary lab equipment. Major responsibilities include, but are not limited to......

* Compendial testing of manufactured products, raw materials and Purified Water, post-market stability testing.
* Preparation of microbiological media.
* Glassware cleaning, general lab cleaning.
* Perform environmental monitoring tests.
* Support laboratory equipment calibration and qualification program.
* Other duties as assigned.

Qualifications

Education:

Associates Degree in a scientific field with courses in Microbiology and Biological Science

Desired:

Prior experience working in a laboratory environment.

cGMP knowledge

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 # LAB000182.

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-TN-Cleveland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Cleveland-Lab-Technician-Job-TN-37311/1691715/169171516917152012-03-04Merck/MSDfull-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.


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.

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-37311/1473786/147378614737862012-03-04Merck/MSDfull-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.


Position Overview:

Accurately compounds bulk materials in accordance with approved SOPs and pharmaceutical GMPs. Must operate processing equipment which includes the following: steam jacketed mixing vessels, process pumps, various types of mixers, transfer systems, process flow meters and valves. Read and interpret scales, load cells, gauges; translate formula instructions into equipment operation. Clean, sanitize and assemble various pieces of equipment which will require confine space entry into manufacturing tanks for cleaning and inspection. Must be able to obtain forklift licensing and pass physical requirements to wear respirators and lift up to 50lbs.

Responsible to provide feedback on bills of material, labor routings, and demonstrated capacity issues to Manufacturing Management to collaborate as owners and accountable for achieving, maintaining, and continuous improvement of labor routing 95 - 100% metric performance and bill of material 98-100% metric performance.

Qualifications

Education Minimum Requirements:

* High School or Equivalent
* Technical degree, college degree or chemistry background would be a plus.

Required:

* Ability to read, write and perform intermediate level math
* Communicate clearly with individuals and teams
* Interpret and follow SOPs
* Batch formula instructions and follow pharmaceutical GMPs.
* Must be able to lift up to 50lbs
* Demonstratable hands-on mechanical ability.
* Must pass GMP assessment.
* Position requires frequent overtime during seasonal peaks.

Primary Location: US-TN-Cleveland
Employee Status: Regular
Number of Openings: 4

Shift (if applicable)
: 2nd]]>http://jobs.merck.com/job/Cleveland-Associate-Compounder-Job-TN-37311/1468463/146846314684632012-03-04Merck/MSDfull-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 Site Sourcing Representative (SSR) is an essential resource responsible for a spectrum of support activities, including stakeholder support, contract execution and management, and supplier management. Assists Site Sourcing Managers in stakeholder support, contract execution and management, and supplier management. Represents supply sector(s) locally, understanding supply strategies and agreements and describing the benefits to their site and Merck overall. Conducts research and analysis in support of local sourcing plans. Implements regional, int'l and global sourcing initiatives locally and participates on local sourcing teams focused on improvements in AQSCI. Identifies and documents all cost reduction and profit plan improvements. Conducts RFPs, RFQs and quotation analysis as well as negotiations as required. Operates with a Grant of Authority of up to $25,000 for individual transactions in accordance with GP Policy.

Primary activities include, but are not limited to......

Sourcing - Understands the supplier/site strategy developed by the Supply Sectors and executes action plans to achieve the sourcing team's objectives. Participates in Site Sourcing strategies and local program implementation. Liaise with the Supply Sectors to ensure site spend is managed in line with agreed to sourcing strategy. Assists in evaluating potential suppliers on site specific issues. Is familiar with the various suppliers and product lines available in stakeholder areas. Assists in analyzing customer's business and evaluates potential savings through supplier consolidation. Creates and executes RFI's, RFP's and FRS's; wherever possible using e-RFX

Transactional Process - Within assigned stakeholder and supply sector area, responsible for processing purchase orders, change orders and contracts in accordance with grants of authority guidelines. Ensures that purchase agreements are in compliance with master agreements and preferred suppliers. Resolves discrepancies through interaction with PtP Service Center, Receiving and Stakeholders. Expedites critical and strategic deliveries.

Contract Negotiation and Management - Leads and participates in negotiation sessions with suppliers. Prepares, implements and audits compliance with appropriate contract. Resolves issues regarding supplier delivery of assurance, quality and service, documents agreed resolution.

Supplier Management and Performance Tracking - Monitors, reports and seeks to continuously improve supplier performance. Acts as a primary point of contact for supplier interactions and assists in supplier's performance assessments. Maintains a working knowledge of supplier's organization, product lines, contractual agreements and transportation terms. Compiles information to be incorporated in Supplier's Scorecard. Assists Sourcing Managers in analyzing departmental spends with certain suppliers and recommends consolidation or redirection to preferred suppliers. Conducts periodic supplier surveys/evaluations/visits and provides feedback to sourcing managers.

Analysis - Conducts data analysis at the local level on suppliers, supply market, cost and price of goods and services that are supplied to Merck using available data.

Continuous Improvement - Keeps abreast of current procurement general knowledge, procedures, and business issues in order to facilitate effective and practical solutions to client requests, concerns, and inquiries. Continuously learns new areas of the global procurement supply sectors, its business practices, and issues in order to provide superior support to stakeholders. Administers and conducts customer service surveys to key stakeholders (managers and planners to validate their needs. Assists in providing feedback to the sourcing managers regarding the integration of preferred supplier alliances including the effectiveness of the stakeholder/supplier interface, problem resolution and optimization. Makes recommendations as to how to improve the existing environment.

System Support - Assists in systems training for stakeholders. Assists in the maintenance of catalog items, specifically electronic catalogs. Ensure agreements are in the document management system.

Please note : There is no re-location assistance offered for this position.

Qualifications

Education:

Associate's Degree in business, finance, engineering, or related field of study.

Required:

At least 2 years of work experience in commercial, business, operations function required or experience in non-procurement role.

Proficient in the use of personal computers and business software.

Excellent oral/written communications.

Desired:

Knowledge of Procurement related business 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 # PUR000172.

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-TN-Cleveland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Cleveland-Site-Sourcing-Rep-Job-TN-37311/1553319/155331915533192012-03-04Merck/MSDfull-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.


Position Overview:

Provide direct technical support and work in conjunction with Packaging Mechanics, Packaging Supervisors, and Packaging Engineering personnel to resolve day to day issues. Duties include troubleshooting and training personal on specialized areas of packaging equipment and devices. Perform other duties as assigned.

Additional responsibilities are as follows:

* Provide direct technical support and work closely with Packaging Mechanics, Packaging Supervisors and Packaging Engineering personnel to resolve day to day issues as required.
* Develop and train Packaging Mechanics on specialized areas of packaging equipment and devices.
* Interface with equipment manufacturers and vendors to resolve packaging issues.
* Evaluate packaging line efficiencies and provide process improvement recommendations and implementation.
* Support new equipment installations, engineering studies and validation activities.
* Work from CAD drawings, prints, schematics, sketches or verbal instructions.
* Maintain work area and equipment in a safe, efficient and clean operating condition. Strictly adhere to all safety rules and regulations.
* Report to supervisor any equipment in need of repair or any unsafe situation or condition.
* Operate efficiently, all hand/power tools, test instruments and equipment normally used by this trade and maintain/return in good condition.
* Recommend and requisition critical spare parts to be kept in inventory to minimize downtime.
* Provide full arrangement of tools that are required to perform tasks.
* Adequately perform all required job functions.

Please note: Flexibility to work varied shifts and support a 3 shift operation as needed.

Qualifications

Educational requirements:

* Engineering degree or related technical school degree.

Required skills and Experience:

* Minimum of 10 years experience in a cGMP packaging environment.
* Experience with machine vision, barcode systems and related equipment. Ability to understand electrical schematics and troubleshoot electrical related issues.
* Experience with PLC's and ladder logic including troubleshooting, basic programming and installation.
* Thorough knowledge of the various types of electrical motors and controls.
* Obtain passing score on Workkeys electrical aptitude test.
* Ability to lift, bend, and move in such a way as to perform job tasks in a safe and approved manner.
* Operate required hand/power tools, test instrumentation and equipment required by this trade in a safe and approved manner.
* Ability to work in varied environmental conditions based on job being performed.
* Good verbal and written communication skills.
* Possess skills necessary to communicate using tools in Microsoft Office Suite.

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 # PRO009038.

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-TN-Cleveland
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Cleveland-Packaging-Maintenance-Technician-Job-TN-37311/1510513/151051315105132012-03-04Merck/MSDfull-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 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.

Position Overview

The incumbent in this position will be responsible for the following:

* Maintain, troubleshoot and repair manufacturing equipment through set-up, changeover, production and preventive maintenance.
* Provide technical training/guidance to shift mechanics.
* Facilitate the preventive maintenance program for all manufacturing equipment to ensure operational effectiveness.
* Provide technical leadership to the maintenance team on a daily basis addressing site wide mechanical issues.
* Evaluate current processes and make necessary recommendations to optimize manufacturing operations.
* Provide technical assistance to the engineering group in the procurement and implementation of automated process systems.

Please note: This position will be either first, second or third shift.

Qualifications

Educational requirements:

* High School Diploma

Preferred Education Requiremet:

* Associate Degree in a technical field

Required skills and Experience:

* Fifteen years manufacturing experience plus 8 job related courses or 20 years manufacturing experience.
* Excellent ability to trouble shoot equipment site wide including electrical components using an electrical meter.
* Ability to follow all required SOP's and cGMP's.
* Strong working knowledge of a maintenance tracking system.
* Proficient in PLC applications, electrical systems and Mechanical Processes.
* Ability to read wiring and pneumatic schematics and basic ladder logic diagrams.
* Must maintain a sense of urgency with the ability to make sound judgment and logical decisions.
* Demonstrate a willingness to enhance skill level through in-house and external pursuits.
* Ability to work when and where business demands require.

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 # TEC000306.

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

Primary Location: US-TN-Cleveland
Employee Status: Regular
Number of Openings: 6

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/Cleveland-Mechanic-I-Job-TN-37311/1392585/139258513925852012-03-04Merck/MSDfull-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 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.

Position Overview

This high impact role in Merck Manufacturing assures that products manufactured comply with cGMPs, operating procedures, and other applicable regulations.

Responsibilities are as follows:

* Supervise the direct processing of materials and the associated 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 and effect resolution to technical and personnel challenges is key as is openness to change and the ability to effect 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.
* 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.
* Assure compliance with safety and environmental practices, cGMPs and SOPs in the work area.
* 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 that corrective actions are implemented.
* Ensure that personnel under his/her supervision are properly trained in cGMPs, procedures, good documentation practices and regulatory matters.
* 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.

PLEASE NOTE: This position will train on 1st shift but will eventually move to either a 1st (day), 2nd (evening) or 3rd (night) shift

Qualifications

Educational requirements:

* Bachelor's Degree.

Preferred:

* Master's Degree in Science or Engineering.

Required Skills / Experience:

* Excellent written and oral communication skills.
* Excellent interpersonal skills.
* Proven project management experience.
* Ability to lead teams.
* Willingness to work off-shift (evening / night).

Preferred Skills / Experience:

* Strong regulatory background in GMP compliance.
* Working knowledge of SAP.
* Previous experience in Consumer Products or Pharmaceutical environment.
* Previous leadership 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 # PRO008839.

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

Primary Location: US-TN-Cleveland
Employee Status: Regular

Travel
: No
Number of Openings: 5

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/Cleveland-Production-Supervisor-Job-TN-37311/1394457/139445713944572012-03-04Merck/MSDfull-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 Scientist 1 position works under the direction of a Supervisor in the Validation / Stability group. This position will perform analytical testing for pharmaceutical and cosmetic formulations and assist in designing, conducting, analyzing and reporting the results of laboratory experiments supporting validation and stability studies.

Major Activities and Responsibilities:

* Finished product testing to support informal and premarket stability testing
* Perform verification and validation testing
* Peer review of GMP data for accuracy, completeness and conformance
* Troubleshooting problems that arise during routine testing
* Maintenance activities, laboratory maintenance, SOP updates
* Additional assignments related to maintaining laboratory operations will be assigned on an as-needed basis. They may include preparing standard operating procedures as well as participating on safety or audit teams.

Qualifications

Education:

* Required: Bachelor's Degree (preferably in Chemistry)

Required:

* Minimum 3 years work experience in pharmaceutical finished product testing.
* Proficiency in the use of Word and Excel, as well as strong technical skills
* Thorough practical and theoretical knowledge of analytical chemistry and experience working with a variety of techniques (HPLC, GC, AA, IR, and UV-Vis).
* Maintain accurate and detailed records in accordance with GMP documentation.
* Participate as a team member as well as independently demonstrate strong ethical and scientific behaviors
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 # CHE003360.

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-TN-Memphis
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Laboratory Chemicals]]>http://jobs.merck.com/job/Memphis-Scientist-1-Chem-Research-Job-TN-37501/1670752/167075216707522012-03-04Merck/MSDfull-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.

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-37501/1522574/152257415225742012-03-04Merck/MSDfull-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.


This Planning position is responsible for all forecasting activities associated with Merck Consumer Care (MCC) customers for all strategic business units (i.e.: Skincare, Footcare, Gastro Intestinal and Upper Respiratory). The Forecast Analyst creates and maintains forecast models for their customers, incorporating business intelligence and forecast information gathered from Sales, Marketing, Finance, retailer replenishment analysts, and other sources (i.e.: IRI or other syndicated consumer data). This position is the talent pool for the Demand Manager, Customer Supply Chain Analyst/Manager and SBU MRP backfills within the Supply Chain organization.

The Senior Customer Forecast Analyst is the integration point into the Sales organization. Basic forecast modeling is the responsibility of this position. This position leads the dialogue each month for their respective customers with CBM's, CFM's and Channel Leads during the forecast collaboration process with sales.

This position is also responsible for customer collaborations (CPFR). The Forecast Analyst frequently communicates with the customer's replenishment and forecasting groups.

Major Activities and Responsibilities:

* Develop demand forecasts (operational forecasts) at multiple levels of aggregation for multiple time horizons as part of a demand planning function.
* Review historical sales trends, research demand drivers, prepare forecast data, develop statistical forecast models, and evaluate forecast results.
* Coordinate cross-functional research activities to reconcile significant variances and refine the forecast model to reflect updated sales and market assumptions.
* Interact with sales, marketing, and customer finance to understand demand forecast drivers.
* Utilize a collaborative and consensus approach by working with Sales, Marketing and Finance to obtain and ensure that current and accurate information is used for demand forecasts.
* Use and maintain SAP/APO Demand Planning software as the primary forecasting system tool.
* Leads CPFR discussions.
* Provide input to the Supply Planning organization in developing inventory strategies on existing items, new products, and product phase-outs.
* Closely coordinate and communicate customer action plans with supply planning
* Create statistical forecasts:
* Gather, analyze and validate data
* Execute statistical modeling software
* Review resulting statistical forecast model
* Apply error analysis techniques to improve forecasting
* Summarize/aggregate statistical forecasts
* Review sales plans , customer finance EA and demand drivers:
* Present, solicit, and assess feedback on the various forecasts from Sales and finance
* Recommend adjustments for operational forecasts
* Review promotional plans with Sales
* Collaborate with key MCC customers.
* Develop CPFR analysis for review with customer Forecast/Replenishment group.
* Lead CPFR collaboration meetings.
* Achieve consensus for operational demand forecasts by facilitating a collaborative planning process with Sales and Finance personnel
* Prepare relevant material to facilitate research and discussion
* Provide input to volume planning.
* Facilitate and manage demand planning/customer meetings
* Achieve consensus
* Maintain demand planning system:
* Enter and modify data
* Monitor trends in forecast accuracy
* Identify relevant market-related data
* Prepare and maintain relevant reports pertaining to demand planning process
* A customer demand forecast which incorporates current and accurate market information that allows Merck Consumer Care to correctly predict customer demand and provide its supply chain with the appropriate information to plan how to meet that customer demand.
* Improved relationships among Planners, Sales, Marketing and Finance, which will lead to effective knowledge sharing and an optimal consensus forecast to better guide Merck Consumer Care.
* Refined systems and methods to continually improve forecasts so that Merck Consumer Care can better anticipate customer needs.

Qualifications

Education:

* Required: Bachelor's degree
* Preferred: MBA

Required:

* Minimum (3) years of work experience.
* Demonstrated proficiency in statistics, forecasting and forecasting methods with an understanding of their financial and operational impacts.
* Experience with Windows, Microsoft Office and forecasting software.
* Strong analytical, organizational, decision making, and presentation skills.
* Strong interpersonal skills are also essential to effectively interact with all customers, teams and levels of business affecting the forecast process.

Preferred:

* Previous work experience in packaged goods/consumer products industry
* APICS certification
* Knowledge of SAP/APO, Manugistics, and/or JDA related to demand planning
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 # SUP000322.

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-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-Senior-Customer-Forecast-Analyst-Job-TN-37501/1689826/168982616898262012-03-04Merck/MSDfull-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 incumbent is responsible for statistical planning and data analysis of clinical 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, MRL scientists, and Regulatory staffs in designing and analyzing clinical trials and providing the statistical support for clinical drug projects.

* Reports to Manager/Associate Director/Director, Biostatistics and Research Decisions Sciences (BARDS).
* Provides biostatistical support for a drug/vaccine project under the supervision of management. This includes the following activities:
* Is involved in early development planning to ensure that study designs are consistent with clinical program objectives and meet worldwide regulatory and marketing needs.
* Independently identifies and anticipates technical or other potential problems arising in the design, conduct, and analysis of clinical or pre-clinical trials, and pursues solutions.
* Develops individual protocols and data analysis plans, or collaborates with nonclinical scientists. Independently determines appropriate statistical methodology for data analysis.
* Participates in Worksheet development, database (collector and view) design meetings to ensure that the data evaluated are free of bias, contain maximum information (minimum variance) and satisfy the analysis requirements.
* Writes programs to retrieve data and perform statistical analyses and organizes the programming activities to ensure that all programs meet analysis requirements, internal SOP's, validation, and external regulatory requirements.
* Evaluates appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology.
* Analyzes data and interprets results from experiments to meet objectives of the study protocol. Independently applies and implements basic and complex techniques to these analyses.
* Prepares oral and written reports to effectively communicate results of clinical trials to the project team, Merck Management, regulatory agencies, or individual investigators.
* Provides responses to queries relating to study design, analysis, and interpretation posed by the medical monitors, regulatory agencies, or investigators.
* Is responsible for ensuring the accuracy of Statistical Review Aids ted to regulatory agencies.
* Participates in discussions with corresponding technical personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.

* Collaborates in publication of research results in areas of applications.
* Conducts research on statistical methodology, pursues solutions to various technical problems, adapts known methods and develops new ones.
* Maintains technical skills and increases own knowledge of new methods or areas of applications by reading journals and attending professional society meetings. Presents own research at meetings and seminars. Communicates with statisticians outside Merck concerning technical problems.
* Participates in department activities including recruiting and training other statisticians, providing statistical training for non-statistical groups, department research effort, and other committee works, etc., as needed.

Qualifications

Education Minimum Requirement:

* Ph.D. or M.S. in statistics or biostatistics

Required Experience and Skills:

* Ph.D. with 0 years or M.S. with at least 3 years relevant experience
* Strong technical skills and interest in applications to clinical research
* Strong interpersonal skills, as well as the ability to function in a team environment

Preferred:

* Experience with statistical software such as SAS, R, and/or 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 submit your resume for requisition # BIO003428.

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
Other Locations: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Upper-Gwynedd-Biometrician-Job-PA-19436/1658089/165808916580892012-03-04Merck/MSDfull-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.

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-19436/1660008/166000816600082012-03-04Merck/MSDfull-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 Regulatory Liaison is responsible for developing the global regulatory strategy for assigned Biologics early development projects with the objective to guide pre-clinical and early clinical development through proof of concept studies.

In this position your responsibilities include but are not limited to:

* Independently manage regulatory activities for early development of biologic products; functioning as the single, accountable, global regulatory point of contact on those projects.
* Provides expertise as worldwide regulatory representative to Product Development teams
* Independently interacts with the Worldwide Regulatory Agencies and/or subsidiaries with regard to global regulatory strategy/registration requirements with one or more Merck investigational Biologics products.
* Responsible for preparation, regulatory review and final approval of all submissions and associated documentation.
* Responsible for follow-up contact with regulatory agencies and/or subsidiaries for assigned projects.

Qualifications

Education Minimum Requirement:

* Bachelor's degree with at least 10 years experience in regulatory affairs or a related discipline
* Master's degree with at least 8 years experience
* PhD in a biological science, chemistry or related field with at least 5 years experience
* MD with at least 5 years experience

Required Experience and Skills:

* Regulatory experience with biologics development especially with early development projects
* Good organizational, communication, interpersonal and negotiating skills are required
* Has experience with conducting agency meetings with health authorities
* Has ted US IND, Clinical study applications
* General competency with drug development
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 # REG000828.

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
Other Locations: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Upper-Gwynedd-Director%2C-Early-Biologics-Job-PA-19436/1425107/142510714251072012-03-04Merck/MSDfull-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 Biometrician will be responsible for statistical aspects for clinical trials involving all phases of clinical development (phases I, II, III and post-marketing) at Merck Research Laboratories. Work closely with Clinical, Regulatory, Data Management, Programming staffs in MRL and/or CROs for designing, monitoring and analyzing clinical trials and coordinating statistical related activities. Requires knowledge of statistical methodology and experimental design to ensure sound scientific principles and statistical methods are applied.

Primary Activities:

* Provides biostatistical support for a vaccine/drug project under the supervision of management. This includes the following activities:
* Is involved in early development planning to ensure that study designs are consistent with clinical program objectives and meet worldwide regulatory and marketing needs.
* Independently identifies and anticipates technical or other potential problems arising in the design, conduct, and analysis of clinical or pre-clinical trials, and pursues solutions.
* Develops individual protocols and data analysis plans, or collaborates with nonclinical scientists. Independently determines appropriate statistical methodology for data analysis.
* Participates in Worksheet development, database (collector and view) design meetings to ensure that the data evaluated are free of bias, contain maximum information (minimum variance) and satisfy the analysis requirements.
* Writes programs to retrieve data and perform statistical analyses and organizes the programming activities to ensure that all programs meet analysis requirements, internal SOP's, validation, and external regulatory requirements.
* Evaluates appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology.
* Analyzes data and interprets results from experiments to meet objectives of the study protocol. Independently applies and implements basic and complex techniques to these analyses.
* Prepares oral and written reports to effectively communicate results of clinical trials or non-clinical experiments to the project team, Merck Management, regulatory agencies, or individual investigators.
* Provides responses to queries relating to study design, analysis, and interpretation posed by the medical monitors, regulatory agencies, or investigators.
* Is responsible for ensuring the accuracy of Statistical Review Aids ted to regulatory agencies.
* Participates in discussions with corresponding technical personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.

* Collaborates in publication of research results in areas of applications.
* Conducts research on statistical methodology, pursues solutions to various technical problems, adapts known methods and develops new ones.
* Maintains technical skills and increases own knowledge of new methods or areas of applications by reading journals and attending professional society meetings. Presents own research at meetings and seminars. Communicates with statisticians outside Merck concerning technical problems.
* Participates in department activities including recruiting and training other statisticians, providing statistical training for non-statistical groups, department research effort, and other committee works, etc., as needed.

Qualifications

Education Minimum Requirement:

* Ph.D or M.S in statistics or biostatistics or related field

Required Experience and Skills:

* P.D. or M.S with minimum 3 years relevant work experience

Preferred:

* Theoretical and applied course work in statistics or biostatistics
* Effective communication skills
* Statistical software (SAS, R and/or S+)
* Strong interest in statistical applications
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 # BIO003430.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Upper-Gwynedd-Biometrician-Biostatistics-Job-PA-19436/1672540/167254016725402012-03-04Merck/MSDfull-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 incumbent is responsible for statistical planning and data analysis of modeling & simulation (M&S) related project and early stage clinical trials. This position requires a solid knowledge of statistical methodology and strong knowledge in computing software. The knowledge must be sufficient to ensure that sound scientific principles and statistical methods are applied M&S projects and clinical trials in support of decision making and worldwide regulatory submissions. This position involves interaction with Medical, Data Coordination, MRL scientists, and Regulatory staffs in developing PK/PD models and analyzing clinical trials and providing the M&S and statistical support for clinical projects.

Primary Activities:

* Reports to Manager/Associate Director, Biostatistics and Research Decision Sciences (BARDS).
* Provides M&S and biostatistical support for a drug project under the supervision of management. This includes the following activities:
* Develop population PK and PK/PD models with M&S scientists across multi function areas for protocol designs and developments.
* Integrate data from pre-clinical and clinical studies to assist the project team in key decision making such as "Go/Go No" and dose selections for Phase I and II studies.
* Is involved in early development planning to ensure that study designs are consistent with clinical program objectives and meet worldwide regulatory and marketing needs.
* Independently identifies and anticipates technical or other potential problems arising in the design, conduct, and analysis of clinical or pre-clinical trials, and pursues solutions.
* Writes programs to retrieve data and perform M&S and statistical analyses and organizes the programming activities to ensure that all programs meet analysis requirements, internal SOP's, validation, and external regulatory requirements.
* Evaluates appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology.
* Construct PK/PD models, analyzes data and interprets results from experiments to meet objectives of the study protocol. Independently applies and implements basic and complex techniques to these analyses.
* Prepares oral and written reports to effectively communicate results of clinical trials or non-clinical experiments to the project team, Merck Management, regulatory agencies, or individual investigators.
* Provides responses to queries relating to study design, analysis, and interpretation posed by the medical monitors, regulatory agencies, or investigators.
* Participates in discussions with corresponding technical personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.

* Collaborates in publication of research results in areas of applications.
* Conducts research on statistical methodology, pursues solutions to various technical problems, adapts known methods and develops new ones.
* Maintains technical skills and increases own knowledge of new methods or areas of applications by reading journals and attending professional society meetings.
* Presents own research at meetings and seminars.
* Communicates with modeler ad statisticians outside Merck concerning technical problems.
* Participates in department activities including recruiting and training other statisticians, providing statistical training for non-statistical groups, department research effort, and other committee works, etc., as needed.

Qualifications

Education Minimum Requirement:

* Master in Biostatistics or Statistics or related areas required
* PhD preferred

Required Experience and Skills:

* PhD with 3 years related experience or Masters degree with 6 years related experience
* Strong technical skills and interest in applications to clinical research and M&S
* Strong interpersonal skills, as well as the ability to function in a team environment

Preferred:

* Experience in clinical research and/or basic science would be a plus
* Deep understanding of non-linear mixed effect 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 # BIO003444.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Upper-Gwynedd-Sr-Biometrician-Biostatistics-Job-PA-19436/1682100/168210016821002012-03-04Merck/MSDfull-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.


Note: This position can be located in Kenilworth, NJ or Upper Gwynedd, PA.

Responsibilities include and not limited to the following:

* Responsible for clinical research protocol development and medical/scientific oversight of clinical trials (Phases 2-4) involving experimental or marketed drugs in the hepatology (clinical research group).
* Participates in all phases of clinical development process for Merck Research Laboratories sponsored studies including study design, medical monitoring and medical/scientific interpretation of study analyses for both efficacy and safety, participation in non study safety reports and authors scientific and regulatory documents.
* Expected to be able to apply an in-depth understanding of the disease under study and provide input to the development and implementation of short and long-term objectives of the hepatology clinical research group.
* Provide internal scientific leadership for cross functional areas supporting clinical development and external leadership through interaction with study investigators.

Qualifications

Education:

* MD from a recognized school of medicine, preferably training in Gastroenterology (Hepatology) or Infectious Diseases

Required:

* Gastroenterology (Hepatology) and / or Infectious Disease background; and/or experience in development of drugs for Hepatitis C
* Excellent communication and writing skills.
* Demonstrated ability to work as part of a high performing team.
* Travel - up to 30%

Preferred:

* Demonstrated leadership skills with ability to work in a high performance teams and/or matrix organization.
* Prior pharmaceutical industry experience in a similar clinical research 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 # CLI002614.

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-Kenilworth
Other Locations: US-PA-Upper Gwynedd
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Kenilworth-Associate-DirectorDirector%2CClinical-Research-Hepatology-Job-NJ-07033/1694174/169417416941742012-03-04Merck/MSDfull-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.

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-07033/1401645/140164514016452012-03-04Merck/MSDfull-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/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.
* 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 twenty percent of the time of order to visit clinical investigators in regard to potential or active clinical research projects

Qualifications

Education:

* MD
* MD/PhD

Required:

* Prior industry or academic experience;
* Must have strong communication (verbal and written), interpersonal, and analytic skills

Preferred:

* Board certification or eligibility is preferred
* Training in rheumatology, gastroenterology, dermatology, allergy or related immunology subspecialty
* Research background in the design and implementation of clinical studies and familiarity with biostatistics
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 # CLI002511.

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-Kenilworth
Employee Status: Regular
Number of Openings: 2

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Kenilworth-Associate-Director%2C-Clinical-Research-Immunology-Job-NJ-07033/1475851/147585114758512012-03-04Merck/MSDfull-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.


This Trial Manager position will support the Respiratory & Immunology Therapeutic Areas within the Global Trial Management group. This position is accountable for the operational planning and execution of Clinical Trial Teams from planning phase of a trial through Clinical Study Report; management and oversight of the Clinical Trial Team and the accountability of the delivery of key milestones for the clinical trial. Primary responsibilities include, but are not limited to:

* Accountable for comprehensive operational planning and execution of Clinical Trials. Leads the Clinical Trial Team (CTT) or Outsourced Trial Team (OTT) and manages trial level timelines with proactive completion of activities. Proactively communicates shifts in timelines and creates/implements contingency plans. Escalates issues to Clinical Program Operational Team (CPOT) and Program Manager. Presents at Clinical Trial Allocation Committee (CTAC) and Inv meetings.
* Leads and collaborates with others to prepare specs for Requests for Outsourcing, Information and Proposals. Drives vendor selection. Primary contact with vendors, reviews/confirms vendor financial commitments are met. If leading an outsourced study allocation of time will increase to 50% or more time spent.
* Oversees study tracking and communication, including internal and external communications. Primary point of contact for communications with vendors, trial team, and country Project Managers (PMs). Works closely with Global Trial Optimization (GTO) for protocol feasibility and retention. Coordinates recruitment materials and provides in life enrollment oversight for trials
* Manages and oversees the completion of country feasibility, protocol feasibility, investigator meetings and timeline generation for protocols. Oversees country/site selection and milestone tracking at trial-level. Facilitates the development of protocol level budgets and manages trial-level budget to plan.

Qualifications

Education Minimum Requirement:

* Bachelor's Degree (Life Science or BSN degree preferred)

Required Experience and Skills:

* 6+ years with a minimum of 5 years in Pharmaceutical clinical research
* Demonstrated knowledge and experience with leading teams.
* Excellent project management, collaboration and problem-solving skills.

Preferred:

* Demonstrated project management skills and proven ability to lead teams and individuals.
* Effective communication (both oral and written) and analytical skills.
* Must be able to collaborate cross-functionally to resolve issues.
* Understanding of functional area responsibilities associated with the clinical development process.
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 # CLI002538.

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-Kenilworth
Employee Status: Regular

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

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Kenilworth-Trial-Manager-Job-NJ-07033/1689829/168982916898292012-03-04Merck/MSDfull-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.

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

Travel
: Yes, 20% of the time
Number of Openings: 3

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Kenilworth-Assoc_Dir_Director-Clinical-Research-Oncology-Job-NJ-07033/1511374/151137415113742012-03-04Merck/MSDfull-timeUSDstarting0BSKenilworth, 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

Primary Location: IN-WB-Kolkata
Employee Status: Regular

Travel
: Yes, 100% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Kolkata-Territory-Business-Manager-Kolkata-%28Critical-Care%29-Job-WB/1672534/167253416725342012-03-04Merck/MSDfull-timeUSDstarting0BSKolkata, WB, 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.


Under the general direction of the Clinical R&D Head, Cardiovascular Disease, Diabetes, Metabolism, Endocrinology and Neurology, 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 diabetes and endocrinology and will include the development of new products (particularly fixed dose combinations, new delivery forms, and novel formulations) as well as expansion of existing products into the emerging markets.

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 works with them to access subject matter expertise;
* Maintains close working contacts with the Marketing colleagues and supports them with competitive issues and marketing strategies;

Location: Merck facilities in Rahway NJ, Kenilworth, NJ or Upper Gwynedd, PA.

Qualifications

Education Requirements:

* MD

Required:

* Some research experience, in either clinical or basic science
* Willingness to spend up to 20% of time traveling
* Interest in expanding skills beyond clinical research to include business development and strategy

Preferred:

* At least 3 or more years experience working as a trial physician in clinical research in industry or academia
* Postgraduate training and board certification in internal medicine
* Board certification in endocrinology or extensive clinical experience
* 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 # CLI002577.

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

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

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Rahway-Director-Emerging-Markets-Clinical-Research-Job-NJ-07065/1603921/160392116039212012-03-04Merck/MSDfull-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 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.

Primary Location: US-PA-Upper Gwynedd
Other Locations: US-NJ-Kenilworth, 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-19436/1596741/159674115967412012-03-04Merck/MSDfull-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, Cardiovascular Disease, Diabetes, Metabolism, Endocrinology and Neurology, 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 women's health but will include work in diabetes, endocrinology, and neurology. Work will focus on the development of new products (particularly fixed dose combinations, new delivery forms, and novel formulations) as well as expansion of existing products into the emerging markets.

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 works with them to access subject matter expertise;
* Maintains close working contacts with the Marketing colleagues and supports them with competitive issues and marketing strategies;

Location: Merck facilities in Rahway NJ, Kenilworth, NJ or Upper Gwynedd, PA.

Qualifications

Education Requirements:

* MD

Required:

* Some research experience, in either clinical or basic science
* At least 3 years direct patient care experience
* Willingness to spend up to 20% of time traveling
* Interest in expanding skills beyond clinical research to include business development and strategy

Preferred:

* 3 or more years experience working as a trial physician in clinical research in industry or academia
* Board certification or eligibility in obstetrics/gynecology or extensive clinical experience
* Experience with international studies and filings especially in EM countries
* Experience in managing outsourced clinical trial in collaboration with CROs
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 # CLI002608.

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
Other Locations: US-NJ-Kenilworth, 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-Research-Emerging-Markets-Womens-Health-Job-PA-19436/1672547/167254716725472012-03-04Merck/MSDfull-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 Human Resources Business Partner acts as a partner to business management formulating HR plans. He/she develops and implements a variety of programs, including recruitment, learning and development, performance management, compensation and benefits, equity and diversity, etc., within a business line/unit.

Primary responsibilities of the business partner include but are not limited to:

* Provide Human Resources support to several groups within the Global Support Functions (GSF) departments/organizations.
* Partners with leaders to support business results by maximizing performance management, competencies, talent and leadership.
* Coach Leadership Teams to successfully manage all annual people management processes (performance management, talent management, compensation planning, etc.).
* Coach Leaders and Managers to improve leader effectiveness and teamwork.
* Execute change initiatives based on local client needs (retention, deployment, compensation, organizational design, etc.).

Qualifications

Education:

* Bachelor's degree required

Required

* A minimum of 7 years demonstrated HR experience in related fields ( eg: HR BP , Compensation, Benefits, Employee Relations)
* Ability to build relationships and influence clients.
* Ability to work independently
* Knowledge of employment legal practices/policies.
* Ability to work effectively in a matrix organization.
* Excellent communications skills

Preferred:

* HR Business Partner/Generalist experience
* Advanced degree
* Center of Excellence (CoE) 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 # HR 000276.

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
Other Locations: US-PA-West Point, US-NJ-Whitehouse Station
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Upper-Gwynedd-Human-Resources-Business-Partner-Global-Support-Functions-Job-PA-19436/1682107/168210716821072012-03-04Merck/MSDfull-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 Marketing: Successful marketers at Merck reflect the company's commitment to patients as well as strengths in leadership, teamwork, communication, innovation, strategic thinking, problem solving, qualitative and quantitative analytic skills.

Merck's Marketing Management Associate Program (Internship): Over approximately ten weeks, MBA interns in Merck Marketing work closely with experienced marketers on projects addressing current business needs with the opportunity to make significant impact. MBA interns typically focus on one substantial, pre-determined project over the course of the summer. MBA interns in Marketing gain exposure to a range of functional areas within Merck to gain a comprehensive understanding of the company and industry. MBA interns may have the opportunity to focus on key marketing skills depending on specific project needs, including

* Brand Strategy Development
* Physician and Consumer Promotion
* Pre-launch Pricing Analysis
* Market Research

At the end of the summer, MBA interns will make a final presentation based on the results of their summer assignments to members of their marketing team and Merck Marketing senior leadership.

The MBA internship program features an Executive Speaker Series, in which interns regularly meet as a group with leaders from across the organization. Merck also provides interns with opportunities throughout the summer to meet and learn from employees throughout the organization, and social functions to facilitate interaction with other summer interns and Merck employees. Interns are also provided with resources and information to make the most of their time outside of work in the Philadelphia and New Jersey area. The MBA intern program at Merck Marketing has traditionally been a strong source for full-time candidates.

The Merck Marketing organization seek MBA Candidates with a commitment to improving health care, a passion for making a difference in patient lives, and desire for long-term contribution to Merck's mission and growth.

This is a paid internship targeted to start in June 2012 for 10 weeks, whereby a weekly stipend will be provided. Subsidized housing is available for interns living more than 50 miles from the site of their internship.

Qualifications

QUALIFICATIONS

· Analytic skills (qualitative and quantitative), strategic thinking and problem-solving

· Superior communication, presentation and interpersonal skills

· Strong capacity for leadership and cross-functional teamwork in a diverse work environment

· Ability to take initiative, responsibility, and demonstrate results-oriented project management

· Aptitude for innovation and creativity

· Demonstrate a high degree of ethics and values

· 3 or more years of full-time work experience in the pharmaceutical, healthcare or related industry preferred

Requirements:

· Have completed one year of their MBA program at the time of the internship with a concentration in Marketing

· Be eligible to work in the US on a permanent basis (US citizen or Permanent Resident) without sponsorship

· Have a minimum of 2 years 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 DIR003409.

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


Primary Location: US-PA-Upper Gwynedd
Other Locations: US-NJ-Whitehouse Station
Employee Status: Regular
Number of Openings: 3

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Upper-Gwynedd-2012-MMA-Summer-Intern-Job-PA-19436/1455395/145539514553952012-03-04Merck/MSDfull-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 principal pharmacoepidemiology 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 to coordinate activities and studies in epidemiologic research programs.

* Special knowledge of Pharmacoepidemiologic methods
* Experience with use of large, automated databases for general epidemiology and drug safety analyses
* Adept/fluent with biostatistic analyses of epidemiologic data
* 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 Minimum Requirement:

* Doctoral degree in Epidemiology or closely related topic

Required Experience and Skills:

* 4 years post PhD database analysis experience in pharmacoepidemiology in academic, industry, or government setting
* Extensive knowledge of biostatistics and epidemiologic methods and basis knowledge of statistical programming and drug development science and processes.
* Must have strong communication (written and orah) and academic or practical experience in experimental design.
* Familiar with the basic computer systems and more than one computer language or software package used to process epidemiologic data.
* Knowledge of all aspects of epidemiology research with designing, implementing, analyzing and interpreting epidemiology studies and/or outcomes research studies.
* Must have knowledge of health care databases used in pharmacoepidemology.

Preferred:

* Experience as a leader of teams, collaborative research experience and industry experience.
* Prior training and experience in pharmacoepidemiology and drug/vaccine safety 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 # EPI000196.

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
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Upper-Gwynedd-Senior-Epidemiologist-Job-PA-19436/1666993/166699316669932012-03-04Merck/MSDfull-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 leadership of the Executive Director, Shared Business Services-Americas Region, responsibilities include but are not limited to:

* Enhances existing change management plans and creates new plans to meet the needs of the SBS leadership team and to meet SBS business obligations.
* Influences SBS leaders and SBS initiative sponsors on the application of change management practices and tools to achieve initiative realization.
* Develops change management plans, strategies and realization indicators to support SBS's short term and long term objectives. Ensures that change management messages are considered and integrated into all communications. Performs change management risk assessments and ensures risk mitigation plans are included into overall initiative plans.
* Provides performance coaching, feedback, development and guidance to site managers, team leaders, and colleagues.
* Identifies key elements of risk and develops mitigation plans.
* Development of SBS employee competency matrix and career pathing framework.
* Establishment of Alternate Dispute Resolution (ADR) and Employee Feedback mechanisms.
* Development and communication of work environment metrics including supervisor effectiveness dashboards and 360 degree feedback tool.
* Member of Regional Shared Services Leadership team
* Partners extensively with leadership on developing a high performance and inclusive culture and work environment.

Qualifications

Required:
* Minimum of 7 years relevant work experience with a proven ability to provide excellent customer service in a large scale corporate setting.
* Must be articulate and able to communicate and address issues around service to a broad range client community.
* High personal integrity, credibility, and energy.
* Demonstrated knowledge and application of change management tools and practices.
* Strong presentation skills with ability to influence senior audiences.

Preferred:

* Bachelor's or Master's Degree preferred
* Experience operating in a Sigma Shared Services or HR delivery function.
* Sigma Green or Black 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 # PRO008978.

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-NC-Charlotte
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Charlotte-Shared-Services-Project-Manager-Job-NC-28201/1512539/151253915125392012-03-04Merck/MSDfull-timeUSDstarting0BSCharlotte, 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 Payroll Analyst is responsible for timely and accurate processing, audit and related processes of Payroll and Time, including special projects and quarter and year end audits. Performs troubleshooting and analysis & research related to payroll processing and operations. Will be directly responsible for a selected set of activities as directed by the Payroll Shared Business Services Manager or Team Lead.

Qualifications

Education:

* Bachelor's Degree preferred

Required:

* Three or more years PeopleSoft payroll processing and/or operations experience in multi-state complex corporate environment or other relevant work experience (e.g., Human Resources, Finance).
* Proficiency in MS Office.

Desired:

* CPP or FPC certification,

* Previous work experience with ADPeTime and iPay

* Previous work experience collaborating with HR/Benefits in a shared services 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 # PAY000134.

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-NC-Charlotte
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 2]]>http://jobs.merck.com/job/Charlotte-Payroll-Analyst-Job-NC-28201/1691720/169172016917202012-03-04Merck/MSDfull-timeUSDstarting0BSCharlotte, 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 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 Amityville, NY and surrounding geography.

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 # DIR003931.

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-New York
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/New-York-City-Specialty-Representative-Neuropsychiatry-%28Amityville%29-Job-NY-10001/1698521/169852116985212012-03-04Merck/MSDfull-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.


Responsibilities include but are not limited to:

* In charge of maintaining a 153K square foot facility.
* Includes 20K sq. feet office space and balance is Warehouse/DC space.
* Responsible to maintain, repair all facets of the building, including but not limited to Conveyors, Controls, HVAC, Minor Electrical, Generators, Lighting, Grounds/Parking Lot, Misc Maintenance items.
* Candidate will work with multiple departments, heavy interactions with different department managers/colleagues.
* Direct Janitorial Operations.
* Strong safety culture, position is a base member of the safety committee.
* Ability to multi-task, set priorities.
* Maintenance tasks and preventive maintenance are loaded and directed by MAXAMO scheduling tool.
* In charge of maintaining and order parts.
* Eligible for overtime

Qualifications

Education Minimum Requirement:

* High School Diploma or equivalent

Required Experience and Skills:

* Minimum 6 years experience in Maintenance and Repair
* HVAC, Conveyor Controls, Minor Electrical, Diesel Generator Management, Microsoft email, excel.
* On line training tools.
* Excellent Customer service skills.
* Ability to work with deadlines.
* Schooling to improve skill set will be required.

Desired Experience and Skills:

* Certifications IVAC, Plumbing, Electrical, HazMat

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 # TEC000407.

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-NE-Omaha
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Omaha-Sr-Maintenance-Mechanic-Job-NE-68046/1543933/154393315439332012-03-04Merck/MSDfull-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.


The Record to Report (RtR) group within Shared Business Services Americas Commercial Services seeks a qualified individual for a position as Record to Report Service Specialist in our Charlotte, NC facility. Responsibilities include, but are not limited to:

The RtR (Record to Report) General Ledger Service Specialist provides general ledger support and analysis inclusive of period end financial close responsibilities for the USA, Mexico and Puerto Rico local markets. The Specialist will work closely with Local Market Finance colleagues in order to ensure that the accounting records (i) accurately reflect the country's transactional reality and (ii) comply with local statutory and tax requirements.

* Maintaining an accurate and current accounting ledger which accurately reflects the country's transactional reality through timely posting of all required items.
* Ensuring that all transactions are correctly reflected in the ledger on a country basis.
* Producing accurate and timely period reporting that complies with Corporate and country requirements.
* Responsible for monthly Account Reconciliation processes on a timely basis and applying all required controls
* Actively identifies opportunities for streamlining and rendering service delivery more efficiently, and participates in special projects to support RtR Shared Services.
* Will work closely with other team members to effectively manage workload and gain exposure to multiple finance and business disciplines within Merck.

Qualifications

Education:

* Bachelors Degree with a major in Finance / Accounting is preferred

Required:

* Minimum of 7 years of relevant work experience in the accounting department of a multinational company including demonstrated experience in dealing with ex-US accounting
* Demonstrated track record of working with non-US cultures
* Must be comfortable in an environment of changing technologies and processes, and demonstrate flexibility in adjusting to new ways of working
* Must be able to work in a fast-paced, dynamic environment, under pressure, and with a high degree of professionalism
* 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
* Effective team player with collaborative focus
* Experience in dealing with internal and external auditors (in a SOX environment)

Desired:

* Experience with SAP
* Experience in a finance/accounting shared services environment
* Experience with non-US GAAP environments

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 # FIN000773.

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-NC-Charlotte
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 4]]>http://jobs.merck.com/job/Charlotte-RtR-Service-Specialist-Job-NC-28201/1705725/170572517057252012-03-04Merck/MSDfull-timeUSDstarting0BSCharlotte, 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. Financial Analyst position for the Global Hospital and Neuroscience & Ophthalmics (N&O) franchises will provide financial support to the franchise teams. Financial support will include forecasting and modeling work, support during the financial planning processes (periodic Forecasts, annual Budget, and 5 Year Plan), and routine performance reporting for the global franchise businesses. Specific responsibilities include:

* Creating/maintaining global late stage and LCM forecast models for given products, aligning with regions and supporting pipeline valuations, prioritization and stage and other reviews.
* Reviewing in-line and early stage forecasts with marketing for given products and supporting pipeline valuation and other reviews.
* Assessing business options, including pricing options, and analyzing potential return on investment for given projects/programs.
* Coordinating with FE&A and validating forecasts for certain new business development initiatives.
* Managing financial aspects of certain new or existing business development activities for the franchises.
* Assisting with planning and reporting for the franchises, including developing appropriate review processes and interaction with the regions.
* Tracking, analyzing and reporting on drivers of product performance and profitability for given brands/regions.

Position will require utilization of forecasting methodologies and application of best practices: statistical trending, analogy research and analysis, and market research analysis. Position will also require use of financial systems including BPC and WFRS. Individual will work closely with groups across the company, including Marketing, Market Research, Manufacturing and other Finance functions. Individual will report to Franchise Finance Lead - Hospital and N&O.

Qualifications

Education:

* Bachelor's Degree

Required:

* 2 years of finance related experience
* Strong Microsoft Office and computer skills.
* Strong analytical skills and ability to learn new techniques.
* Proven ability to work independently.
* Excellent interpersonal and communication skills across all levels of the company.

Preferred:

* MBA preferred
* BPC, WFRS (financial systems)
* Prior experience with sales forecasting or financial modeling.

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 # FIN000749.

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
Other Locations: US-NJ-Whitehouse Station
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/Upper-Gwynedd-Sr_-Financial-Analyst-Job-PA-19436/1691713/169171316917132012-03-04Merck/MSDfull-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.

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-19436/1431789/143178914317892012-03-04Merck/MSDfull-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 Biometrician will be responsible for statistical aspects for clinical trials involving all phases of clinical development (phases I, II, III and post-marketing) at Merck Research Laboratories (MRL). Work closely with Clinical, Regulatory, Data Management, Programming staffs in MRL and/or CROs for designing, monitoring and analyzing clinical trials and coordinating statistical related activities. Requires knowledge of statistical methodology and experimental design to ensure sound scientific principles and statistical methods are applied.

Primary Activities

1. Provides biostatistical support for a vaccine/drug project under the supervision of management. This includes the following activities:

i) Is involved in early development planning to ensure that study designs are consistent with clinical program objectives and meet worldwide regulatory and marketing needs.

ii) Independently identifies and anticipates technical or other potential problems arising in the design, conduct, and analysis of clinical or pre-clinical trials, and pursues solutions.

iii) Develops individual protocols and data analysis plans, or collaborates with nonclinical scientists. Independently determines appropriate statistical methodology for data analysis.

iv) Participates in Worksheet development, database (collector and view) design meetings to ensure that the data evaluated are free of bias, contain maximum information (minimum variance) and satisfy the analysis requirements.

v) Writes programs to retrieve data and perform statistical analyses and organizes the programming activities to ensure that all programs meet analysis requirements, internal SOP's, validation, and external regulatory requirements.

vi) Evaluates appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology.

vii) Analyzes data and interprets results from experiments to meet objectives of the study protocol. Independently applies and implements basic and complex techniques to these analyses.

Viii) Prepares oral and written reports to effectively communicate results of clinical trials or non-clinical experiments to the project team, Merck Management, regulatory agencies, or individual investigators.

ix). Provides responses to queries relating to study design, analysis, and interpretation posed by the medical monitors, regulatory agencies, or investigators.

x). Is responsible for ensuring the accuracy of Statistical Review Aids ted to regulatory agencies.

xi). Participates in discussions with corresponding technical personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.

2. Collaborates in publication of research results in areas of applications.

3. Conducts research on statistical methodology, pursues solutions to various technical problems, adapts known methods and develops new ones.

4. Maintains technical skills and increases own knowledge of new methods or areas of applications by reading journals and attending professional society meetings. Presents own research at meetings and seminars. Communicates with statisticians outside Merck concerning technical problems.

5. Participates in department activities including recruiting and training other statisticians, providing statistical training for non-statistical groups, department research effort, and other committee works, etc., as needed.

Qualifications

Education Minimum Requirement:

* PhD or M.S in statistics or biostatistics or related field

Required Experience and Skills:

* Ph.D, or M.S with minimum 5 years relevant work experiece

Preferred:

* Theoretical and applied course work in statistics or biostatistics
* Effective communication skills
* Statistical software (SAS, R and/or S+)
* Strong interest in statistical applications

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 # BIO003427.

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
Other Locations: US-NJ-Rahway
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Upper-Gwynedd-Biometrician-Job-PA-19436/1653012/165301216530122012-03-04Merck/MSDfull-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 direction of the Head of Clinical Pharmacology, Emerging Markets, the incumbent will:

* Be responsible for assisting in the development and/or execution of the Clinical Pharmacology strategy, primarily for programs emanating from specific formulation hub(s), in support of local marketing applications in specific geography/ies.
* Be responsible for helping to build capabilities and associated processes in support of the Clinical Pharmacology operating model that defines Headquarters - Emerging Markets country interactions.
* Ultimately work as an extended member of the Clinical Research & Development team in Emerging Markets, providing support with regard to design and execution of early clinical development strategy.
* Be responsible for assisting in authorship of documents which may include initial clinical plans, product development clinical plans, Clinical Pharmacology Phase 1 study protocols, etc.
* Function independently to ensure local support of Clinical Pharmacology program studies both respect to their timely and safe execution.
* Interact closely with internal and external clinical study support staff and scientists (which could include the headquarters team - clinical, regulatory affairs, global clinical trials operations - as well as similar staff in local subsidiaries and contract research organizations, as necessary).
* Provide Clinical Pharmacology support for programs through the local marketing application filing, potentially to include supportive registration documents and presentations.
* Be responsible for supporting clear, timely communication and interpretation of Clinical Pharmacology results for internal stakeholders.

Qualifications

Education Minimum Requirement:

* M.Sc. ≥15 years pharmaceutical/biotechnology/generic industry experience
* Ph.D. or Pharm.D. ≥6 years pharmaceutical/biotechnology/generic industry experience
* MD or MD/PhD > 3 years pharmaceutical/biotechnology/generic industry experience

Required Experience and Skills:

* Demonstrated record of scientific scholarship and achievement.
* Proven track record as a clinical monitor of clinical studies, with some of this experience gained across multiple markets.
* Demonstrated record of successful conduct of Clinical Pharmacology studies, particularly pharmacokinetic studies (e.g., bioavailability, bioequivalence and drug-drug interaction studies), with at least some of this experience gained in the generic drug industry.
* Strong interpersonal skills and the demonstrated ability to work remotely as a valued contributor in a virtual team environment are both essential.

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 # CLI002574.

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
Other Locations: US-NJ-Kenilworth, US-NJ-Rahway
Employee Status: Regular

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

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Upper-Gwynedd-Director%2C-Clinical-Pharmacology-Emerging-Markets-Job-PA-19436/1666999/166699916669992012-03-04Merck/MSDfull-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 incumbent is responsible for statistical planning and data analysis of clinical 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 Research Laboratories scientists, and Regulatory staffs in designing and analyzing clinical trials and providing the statistical support for clinical drug projects.

* Reports to Manager/Associate Director/Director, Biostatistics and Research Decisions Sciences (BARDS).
* Provides biostatistical support for a drug/vaccine project under the supervision of management. This includes the following activities:
* Is involved in early development planning to ensure that study designs are consistent with clinical program objectives and meet worldwide regulatory and marketing needs.
* Independently identifies and anticipates technical or other potential problems arising in the design, conduct, and analysis of clinical trials, and pursues solutions.
* Develops individual protocols and data analysis plans and independently determines appropriate statistical methodology for data analysis.
* Participates in Worksheet development, database (collector and view) design meetings to ensure that the data evaluated are free of bias, contain maximum information (minimum variance) and satisfy the analysis requirements.
* Writes programs to retrieve data and perform statistical analyses and organizes the programming activities to ensure that all programs meet analysis requirements, internal SOPs, validation, and external regulatory requirements.
* Evaluates appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology.
* Analyzes data and interprets results from experiments to meet objectives of the study protocol. Independently applies and implements basic and complex techniques to these analyses.
* Prepares oral and written reports to effectively communicate results of clinical trials to the project team, Merck Management, regulatory agencies, or individual investigators.
* Provides responses to queries relating to study design, analysis, and interpretation posed by the medical monitors, regulatory agencies, or investigators.
* Is responsible for ensuring the accuracy of Statistical Review Aids ted to regulatory agencies.
* Participates in discussions with corresponding technical personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.

* Collaborates in publication of research results in areas of applications.
* Conducts research on statistical methodology, pursues solutions to various technical problems, adapts known methods and develops new ones.
* Maintains technical skills and increases own knowledge of new methods or areas of applications by reading journals and attending professional society meetings.
* Presents own research at meetings and seminars.
* Communicates with statisticians outside Merck concerning technical problems.
* Participates in department activities including recruiting and training other statisticians, providing statistical training for non-statistical groups, department research effort, and other committee works, etc., as needed.

Qualifications

Education Minimum Requirement:

* Ph.D. or M.S. in statistics or biostatistics or related field

Required Experience and Skills:

* Ph.D. with 0 years
* M.S. with at least 3 years relevant work experience

Preferred:

* Theoretical and applied course work in statistics or biostatistics
* Effective communication skills
* Statistical software (SAS, R and/or S+)
* Strong interest in statistical applications
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 # BIO003458.

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
Other Locations: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Upper-Gwynedd-Biometrician-Biostatistics-Job-PA-19436/1708745/170874517087452012-03-04Merck/MSDfull-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 Basic Pharmaceutical Science (BPS) group in NJ is seeking applicants for a Ph.D. scientist position. BPS is a multidisciplinary research group that provides drug delivery, solid state and solution chemistry tools in Discovery and early Development. The successful candidate will have key responsibilities including characterization of potential pre-clinical drug candidates' physicochemical properties and the identification of suitable oral and parenteral preclinical formulations for early pharmacology and toxicology studies. The candidate will also plan and execute studies for elucidating API chemical degradation pathways and phase optimization. The candidate will closely interact with Discovery, Safety Assessment, Process Research, Analytical Research and Drug Metabolism and Pharmacokinetics, as well as other members of Pharmaceutical Sciences

Qualifications

Education Minimum Requirement:

* Ph.D. degree in in pharmaceutical sciences, chemistry, or a related discipline

Required Experience and Skills:

* At least 3 years of experience in industry within preformulation, analytical chemistry or formulation development.
* Excellent verbal and written communication skills
* Demonstrated creativity
* Strong leadership/interpersonal skills,
* Ability to work in a team environment with cross-functional interactions are essential.

Preferred:

* Experience with enabled formulations, solid state characterization, polymorphism, and solution chemistry is desirable.
* Candidates with experience in analytical techniques (e.g., X-Ray diffraction, differential scanning calorimetry (DSC), and high pressure liquid chromatography (HPLC)) and/or drug delivery (e.g., controlled release, transdermal) 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 # PRE000275.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Potent compounds]]>http://jobs.merck.com/job/Rahway-Research-Fellow-Job-NJ-07065/1670755/167075516707552012-03-04Merck/MSDfull-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 Analytical Chemistry department of Merck Research Laboratories has a Senior Research Chemist position available to be located in the Rahway, New Jersey research facility. The Senior Research Chemist is a laboratory-based scientific role in a fast-paced, multidisciplinary team environment. The role is tasked with solving high complexity analytical problems related to development of active pharmaceutical ingredients (APIs). The successful candidate must have demonstrated successful application of state-of-the-art analytical techniques to solve chemistry problems, including chiral / achiral separations (HPLC / SFC/ GC / CE / IC), MS, NMR, and other spectroscopy techniques (UV-vis / IR / Fluorescence / Raman). Experience in high throughput analysis and data processing, automation for analysis, and new analytical technology evaluation and development is a plus. Applicants must have effective organizational, multi-tasking, oral / written communications skills, and demonstrate potential for continued scientific development and growth as a scientific leader. Minimum educational requirements include a Ph.D. degree in analytical chemistry or a closely-related field, with 0-5 years suggested experience and clear evidence of strong past academic achievement.

Qualifications

Education Minimum Requirement:

* Ph.D.

Required Experience and Skills:

* HPLC/UHPLC, GC, chiral analysis, LC-MS, spectroscopy

Preferred:

* SFC, CE, NMR, microfluidics, high throughput analysis and data processing, automation for analysis, and new analytical technology evaluation and development

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 # PHA001041.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Senior-Research-Chemist-Job-NJ-07065/1596744/159674415967442012-03-04Merck/MSDfull-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 is currently seeking a qualified organic synthetic chemist within Process Chemistry Department located at our Rahway, NJ site. The successful candidate will be joining a group of innovative chemists to work in the RNAi Therapeutics area, and will be responsible for the design and synthesis of compounds to support on-going programs. A Ph.D. in organic synthetic chemistry is required. Demonstrated ability in innovative problem solving in synthesis as well as timely execution of complex syntheses is required. Expertise with analytical instrumentation is preferred. The candidate must have a proven track record of successful research. Strong written and oral communication skills, flexibility and the ability to adapt to a fast-paced research environment are required.

Responsibilities will include:

* Collaborate with medicinal chemists on various programs
* Identify and solve critical chemistry challenges
* Impact chemistry aspects of RNAi therapeutics programs
* Execute efficiently and deliver in a timely fashion

Qualifications

Education Minimum Requirement:

* PhD in organic chemistry

Required Experience and Skills:

* Expertise in organic synthesis
* Demonstrated creativity and innovation in problem solving
* Productivity and efficiency working in the lab
* Proven track record of successful research in academia or industry
* Strong written and oral communication skills

Preferred:

* Highly motivated individual
* Demonstrated ability to take research projects to the next level
* Flexibility and agility to learn and research in areas of chemistry beyond traditional small molecules
* Experience with process development
* Expertise with analytical instrumentation
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 # CHE003344.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: general chemicals]]>http://jobs.merck.com/job/Rahway-Sr-Research-Chemist-Job-NJ-07065/1642243/164224316422432012-03-04Merck/MSDfull-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.

Primary Location: US-NJ-Rahway
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-07065/1708752/170875217087522012-03-04Merck/MSDfull-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 Department of Process Chemistry in Merck Research Labs located in Rahway, NJ is seeking undergraduate summer interns. The interns will function as a fully-integrated member of a project chemistry team. In addition to the discovery and development of synthetic routes to potential drug candidates, the Merck Process Chemistry department is engaged in bio- and chemocatalysis screening and development, laboratory automation, preparative-scale chromatography, analytical research, and the synthesis of single and double strand siRNA drug candidates. Day-to-day research will focus on using techniques in organic chemistry to understand and solve key synthetic challenges of potential drug candidates.

The intern will also attend departmental and team meetings to provide a wider perspective on the drug development process in the pharmaceutical industry. The intern is responsible for accurate electronic notebook recording, reaction set-up techniques, use of vacuum evaporation devices, thin-layer chromatography, flash chromatography, basic workup procedures, basic NMR interpretation, basic MS interpretation, and safe lab practices. Intern will have the opportunity to gain further knowledge and skill sets via refinement of organic chemistry skills, introduction to new spectroscopic and purification techniques, exposure to problems in process research, and perspective on the practical aspects of drug development.

This 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, if candidate is selected for an interview, applicant must be prepared to letters of recommendation and a brief research statement and a copy of transcript.

Qualifications

Required:

* Pursuing Bachelor's degree in chemistry or related field
* Applicants must be currently enrolled in an academic program at the time of the application
* Applicants must be available for full-time employment for 9-11 weeks during the months of June - August 2012.

Preferred:

* Basic laboratory skills and research experience preferred, such as: electronic notebook recording, reaction set-up techniques, use of vacuum evaporation devices, purification techniques such as thin-layer chromatography, flash chromatography, HPLC, recrystallization, and distillation, basic workup procedures, basic NMR interpretation, basic MS interpretation, and safe lab 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 submit your resume for requisition #PRE000269.

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


Primary Location: US-NJ-Rahway
Employee Status: Regular
Number of Openings: 6]]>http://jobs.merck.com/job/Rahway-Process-Chemistry-Intern-Job-NJ-07065/1670754/167075416707542012-03-04Merck/MSDfull-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.


Chemical and Biochemical 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:

Chemical Process Development & Commercialization (Rahway, NJ) and Pharmaceutical Commercialization Technology (West Point, PA; Summit, NJ) perform process development and demonstration for new chemical and pharmaceutical processes;

Technology Rotation Program (multiple sites) is a 3 year rotational program allowing employees to experience one chemical, one biological and one pharmaceutical assignment over their first three years in the company.

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.

LOCATIONS INCLUDE: Rahway, NJ; West Point, PA; Summit, NJ

Qualifications

* PhD in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), or related field
* Strong personal character and ethics
* Superior Communication and Interpersonal Skills
* Excellent Academic Achievement, Analytical Ability
* 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.

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 # CHE003240.

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
Other Locations: US-PA-West Point, US-NJ-Summit
Employee Status: Regular
Number of Openings: 5]]>http://jobs.merck.com/job/Rahway-Senior-Process-Engineer-Job-NJ-07065/1463442/146344214634422012-03-04Merck/MSDfull-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.


Sales position within the Inside Sales team for Merck Animal Health Companion Animal division focusing primarly on Equine or Companion Animal veterinary customers. Candidate will be responsible for but not limited to:

* Contacting veterinary customers via the telephone to initiate sales relationships and promote, position, and sell the companion animal line of products.
* Inside Sales representatives will be accountable for developing and maintaining account relationships and managing account growth for assigned veterinary, animal shelter, or other accounts.
* The Inside Sales representative is responsible for contacting decision makers to discuss product needs, increase product occupancy, expand market penetration, and acquire sales.
* Performance is measured on sales goal achievement vs. goal, as well as targeted promotions and other performance standards consistent with operating objectives.

1 Position is an Equine Inside Sales position

3 Positions are Companion Animal Inside Sales position

Qualifications

Education Minimum Requirement:

* Bachelors' degree

Required Experience and Skills:

* Minimum 4 year's sales related experience
* Proven ability to set goals and exceed targets
* Highly self motivated and achievement oriented.
* Proven ability to set and adjust schedule for maximum sales performance.
* High level of prioritization and organizational skills
* Sales focused and motivated.
* Excellent interpersonal communication skills a must

Desired Experience and Skills:

* Animal Health experience
* Equine or Companion Animal oriented and 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 # TEL000131.

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-NE-Omaha
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 4]]>http://jobs.merck.com/job/Omaha-Inside-Sales-Rep-Job-NE-68046/1694172/169417216941722012-03-04Merck/MSDfull-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 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.

Primary Location: US-NE-Omaha
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Omaha-Distribution-Analyst-Job-NE-68046/1558419/155841915584192012-03-04Merck/MSDfull-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.


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 performing, interpreting, reviewing and approving equipment/process validation/qualification and change control activities. Perform a variety of regulatory document reviews, participate on site change control committee and set Quality Operations requirements. Other responsibilities include the development of production and customer complaint investigations. This analyst position must demonstrate solid leadership capability as demonstrated by, but not limited to, ensuring timely completion of change control and 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:

* Minimum Bachelors degree
* 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:

* Master's 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 # REG000883.

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-NC-Wilson
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Wilson-Quality-Assurance-Coordinator-Job-NC-27893/1679787/167978716797872012-03-04Merck/MSDfull-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 Leader 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 Leader is an integral position for our solid oral dosage manufacturing and packaging facility (packaging operations also includes secondary packaging of vial, syringe, and inhaler configurations). The Quality Assurance Leader reports directly to the site Quality Operations Director and leads a team of approximately 15 employees who are responsible for a variety of activities including release of finished product to both domestic and international markets.

Primary areas of responsibility include:

* Quality Assurance functions for plant wide systems/processes to include direct line support to production areas, batch record review and release, investigations and defect resolution. Ensures Quality Assurance responsibilities for audits, regulatory document reviews, SOPs, change control and other Quality Assurance related systems are properly implemented, conducted and documented.
* Responsible for the control and ultimate disposition of finished goods both to the international and domestic markets. Ensures proper root cause analysis and corrective action identification for deviation events occurs. Provides final approval of investigations.
* 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 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.
* Ensures Quality Assurance and overall site compliance 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 to meet production demands.
* Acts as a key regulatory compliance liaison to interface with domestic and international regulatory agencies during audits/inspections (CDER and CBER).
* Ensures that Quality Assurance maintains the necessary human and capital resources to meet present and future needs and manages those resources to meet annual profit plan. Interviews and hires personnel, ensuring proper training of personnel is completed.

Qualifications

Required Skills:

* Bachelors or Masters degree
* Minimum of 2 years supervisory experience in a Quality function that support 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.

Preferred Skills:

* Degree field in science or engineering
* Minimum of 5 years experience in Quality 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.

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 # QUA002704.

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-NC-Wilson
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Wilson-Quality-Assurance-Coach-Job-NC-27893/1538428/153842815384282012-03-04Merck/MSDfull-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.


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.

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 # QUA002737.

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-NC-Wilson
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Wilson-Senior-Analytical-Chemist-Job-NC-27893/1643327/164332716433272012-03-04Merck/MSDfull-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.


We currently have a Quality Operations Laboratory Quality Assurance Coordinator (Stability) vacancy at the Merck Facility in Wilson, North Carolina. 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®, FOSAMAX®, 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 Quality Operations Laboratory is a 40,000 square foot facility that provides support to the Wilson plant site operations through raw material and finished product testing and release; additionally, the Laboratory supports Merck & Co., Inc. on a worldwide basis through performing stability testing on finished products, API's and Components.

The Quality Assurance Coordinator (Stability) is an integral position for our worldwide Stability Laboratory that reports to the Stability Laboratory Manager. The Quality position manages stability samples from receipt to delivery to the laboratory for testing.

Specific areas of responsibility include, but are not limited to the following:

* Manages stability study set-up: Key studies in Laboratory Information Management System (LIMS) chamber management of samples, and procures required study information from sites sending samples to NASU-Wilson.
* Responsible for interacting with the laboratory personnel to pull samples to meet required due dates.
* Responsible for writing study protocols based on the General Stability Protocol
* Receives Finished Product and Active Pharmaceutical Ingredients (APIs) from multiple national and international sites, which requires knowledge of import/export regulations/documentation.
* Develops/revises SOPs based on Merck policies/guidelines.
* Responsible to interact with sites to secure required annual/PCRsamples.
* Working knowledge of GMP, NDA, and related regulations. Ability to interpret those regulations for implementation in the workplace. Ability to interpret Merck Quality Policies/Guidelines for daily application. Knowledge and understanding of pharmaceutical operations systems.

Qualifications

Required:

HS Diploma plus 6 years pharmaceutical industry experience

Preferred:

B.A./B.S. in scientific area

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 # REL000238.

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-NC-Wilson
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Wilson-Quality-Assurance-Coordinator-Job-NC-27893/1556999/155699915569992012-03-04Merck/MSDfull-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 Coordinator 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 QA Coordinator reports to the Quality Assurance Coach and has primary responsibilities of supporting various activities for our packaging facility, which includes secondary packaging of vial, syringe, and inhaler configurations. The QA Coordinator will have responsibilities of controlling to material, defect resolution, batch record review, finished product release, data compilation/support for internal/external audits and regulatory inspections, complaint investigations, 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 QA Coordinator will function as the primary contact on second shift to interact and provide support to production personnel.

Specific areas of responsibility include, but are not limited to the following:

* Performs batch record review and bulk/finished product release activities for both domestic and international distribution.
* Responsible for defect resolution and the control of material throughout the plantsite.
* Develops and implements basic operational SOP's.
* Completes complaint and production investigations and recommends disposition of affected material.
* Participates in internal GMP audits.
* Ensures job responsibilities are conducted in a timely and reliable manner to meet production demands.
* Primary contact on second shift to interact and provide Quality Assurance support to production personnel.

This position is 2nd shift

Qualifications

Required Skills:

* Bachelors degree, preferably in science
* Good organizational and time management skills

Preferred Skills:

* Experience in a Quality function within a pharmaceutical manufacturing facility
* 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 # QUA002752.

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-NC-Wilson
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 2nd]]>http://jobs.merck.com/job/Wilson-Quality-Assurance-Coordinator-Job-NC-27893/1669053/166905316690532012-03-04Merck/MSDfull-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.


We currently have an Incoming Materials Inspection Lead vacancy at the Merck Facility in Wilson, North Carolina. The Wilson facility, located at the intersection of I-95 and US 264 Alternate, is a 500,000 square foot solid dosage / packaging facility on 225 acres. As Merck's Packaging Center of Excellence, the facility packages a variety of finished goods types for both domestic and international supply. The Wilson facility also includes Merck's Global Stability Center 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 Incoming Materials Inspection Lead is an integral position for our packaging facility. The Incoming Materials Inspection Lead reports directory to the site Quality Operations Director and leads a team of approximately 10 employees who are responsible for a variety of activities supporting sampling, testing copyreading and release of (but not limited to) incoming components, bulk products and labeling. Responsibilities include timely and compliant release of bulk components, product and labeling to support both domestic and international markets. The Incoming Materials Inspection Lead must also ensure accurate completion of vendor-related investigations, including root cause analysis and identification of appropriate corrective actions to prevent recurrence. This position is responsible for ensuring compliant business processes are established and adhered to on a daily basis.

Specific areas of responsibility include, but are not limited to the following:

* Direct coaching/supervisory responsibilities for a group of approximately 10 employees who support incoming supplies inspection, copyreading and retention room activities.
* Performs statistical sampling for components, bulk APIs and raw materials. Stages samples in the Operations Laboratory for chemical testing.
* Tests, interprets, and reports results for packaging components, APIs, and raw materials per Quality Standards.
* Dispositions/releases bulk material, packaging components, APIs, and raw materials.
* Reviews and approves data associated with pending release of packaging components, APIs, raw materials, and bulk material.
* Plans and coordinates projects and develops/updates systems and policies relevant to Supplies Inspection and Copyreading. Seeks opportunities for continuous improvement in the quality of release systems.
* Facilitates completion of vendor-related investigations, identifying proper root cause and corrective actions.
Ensures knowledge of cGMP, CFR and other regulations in order to assure compliance within Supplies Inspection. Able to evaluate SOPs and recommend improvement opportunities to maintain compliance with corporate and regulatory guidelines. Develop or revise SOPs as required.

Qualifications

Required Skills:

* Bachelors degree, preferably in science
* Minimum 2 years previous supervisory experience.
* Minimum of 4 years experience in a Quality function within a pharmaceutical manufacturing facility
* Excellent written and oral communication skills, leadership and teamwork skills
* Excellent organizational and time management 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

Preferred Skills:

* SAP experience
* Experience in writing vendor related investigations
* Self-starter and initiator of change

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 # QUA002751.

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-NC-Wilson
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Wilson-Incoming-Materials-Inspection-Coach-Job-NC-27893/1658096/165809616580962012-03-04Merck/MSDfull-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 incumbent is responsible for statistical planning and data analysis of clinical 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 worldwide regulatory submissions. This position involves interaction with Medical, Data Coordination, Merck Research Laboratory (MRL) scientists, and Regulatory staffs in designing and analyzing clinical trials and providing the statistical support for clinical projects.

Primary Activities:

* Reports to Manager/Associate Director, Biostatistics and Research Decision Sciences (BARDS).
* Provides biostatistical support for a drug/vaccine project under the supervision of management. This includes the following activities:
* Is involved in early development planning to ensure that study designs are consistent with clinical program objectives and meet worldwide regulatory and marketing needs.
* Independently identifies and anticipates technical or other potential problems arising in the design, conduct, and analysis of clinical or pre-clinical trials, and pursues solutions.
* Develops individual protocols and data analysis plans, or collaborates with nonclinical scientists. Independently determines appropriate statistical methodology for data analysis.
* Participates in Worksheet development, database (collector and view) design meetings to ensure that the data evaluated are free of bias, contain maximum information (minimum variance) and satisfy the analysis requirements.
* Writes programs to retrieve data and perform statistical analyses and organizes the programming activities to ensure that all programs meet analysis requirements, internal SOP's, validation, and external regulatory requirements.
* Evaluates appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology.
* Analyzes data and interprets results from experiments to meet objectives of the study protocol. Independently applies and implements basic and complex techniques to these analyses.
* Prepares oral and written reports to effectively communicate results of clinical trials or non-clinical experiments to the project team, Merck Management, regulatory agencies, or individual investigators.
* Provides responses to queries relating to study design, analysis, and interpretation posed by the medical monitors, regulatory agencies, or investigators.
* Is responsible for ensuring the accuracy of Statistical Review Aids ted to regulatory agencies.
* Participates in discussions with corresponding technical personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.

* Collaborates in publication of research results in areas of applications.
* Conducts research on statistical methodology, pursues solutions to various technical problems, adapts known methods and develops new ones.
* Maintains technical skills and increases own knowledge of new methods or areas of applications by reading journals and attending professional society meetings.
* Presents own research at meetings and seminars.
* Communicates with statisticians outside Merck concerning technical problems.
* Participates in department activities including recruiting and training other statisticians, providing statistical training for non-statistical groups, department research effort, and other committee works, etc., as needed.

Qualifications

Education Minimum Requirement:

* Master in Statistics or related areas required
* PhD preferred

Required Experience and Skills:

* Masters degree with 5 years related experience or a PhD
* Strong technical skills and interest in applications to clinical research
* Strong interpersonal skills, as well as the ability to function in a team environment

Preferred:

* Experience in clinical research and/or basic science would be 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 submit your resume for requisition # BIO003425.

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
Other Locations: US-NJ-Rahway
Employee Status: Regular

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

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Upper-Gwynedd-Biometrician-Job-PA-19436/1653013/165301316530132012-03-04Merck/MSDfull-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.


This position will support the Neuroscience clinical research activities by providing medical support of early development activities (Preclinical to Phase I) and oversight in the design, execution and analysis of clinical trials in late stage clinical (Phases II through V), participation in biomarker development activities, and through review of licensing opportunities. In addition, this position would work closely with basic scientists, clinical pharmacologists, regulatory and other basic research functions, while participating in the development of new compounds as the clinical/medical representative of early and late product development teams.

Primary responsibilities include but are not limited to:

* Reports to a Senior Director or above level manager
* Supervise the activities of other team members, Clinical Associates and/or Medical Program Coordinators for specific research project
* Responsible for initiation of clinical Operational Plans for the development of new Merck drugs or for the completion of projects involving marketed drugs
* 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
* The team member is 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
* May travel on company business about twenty (20%) percent of the time of order to visit clinical investigators in regard to potential or active clinical research projects

Qualifications

Education:

* MD or MD/PhD

Required:

* US Board certified/eligible in Neurology
* Strong interpersonal skills, as well as the ability to function in a team environment
* Demonstrated record of scientific scholarship and achievement

Preferred:

* Experience in clinical research and/or basic science

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 # CLI002486.

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
Employee Status: Regular

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

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Upper-Gwynedd-Associate-Director-Clinical-Research-Neuroscience-Job-PA-19436/1429404/142940414294042012-03-04Merck/MSDfull-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 incumbent is responsible for statistical planning and data analysis of clinical trials.

This position requires a solid knowledge of statistical methodology, experimental design, computing software and data management; a general understanding of worldwide regulatory requirements and clinical trial expertise from phase I to V. 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 worldwide regulatory submissions.

This position involves interaction with Medical, Data Coordination, Merck Research Laboratories scientists and Regulatory staffs in designing and analyzing clinical trials and coordinating the statistical activities for clinical drug projects. Supervises a statistical or programming staff assigned to a development project as needed.

* Reports to Manager/Associate Director/Director, Biostatistics & Research Decision Sciences (BARDS).
* Develops, coordinates, and provides biostatistical support for related drug/vaccine projects under the supervision of management. Supervises staff assigned to the project as needed. This includes the following activities:
* Is involved in early clinical development planning to ensure that study designs are consistent with program objectives and meet worldwide regulatory and marketing needs.
* Independently identifies and anticipates technical or other potential problems arising in the design, conduct, and analysis of clinical trials, proposes solutions, and carries them out.
* Develops individual protocols and data analysis plans and independently determines appropriate statistical methodology for data analysis.
* Participates in Worksheet development, database (collector and view) design meetings to ensure that the data evaluated are free of bias, contain maximum information (minimum variance), and satisfy analysis requirements.
* Determines the statistical programming needs and organizes the programming activities to ensure that all programs meet analysis requirements, internal standard operating procedures, validation, and external regulatory requirements
* Evaluates appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology.
* Analyzes data and interprets results from experiments to meet objectives of the study protocol. Independently applies and implements basic and complex techniques to these analyses.
* Prepares oral and written reports to effectively communicate results of clinical trials to the project team, Merck Management, regulatory agencies, or individual investigators.
* Provides responses to queries relating to study design, analysis, and interpretation posed by the clinical monitors, regulatory agencies, or investigators.
* Is responsible for ensuring the accuracy of Statistical Review Aids ted to regulatory agencies.
* Participates with management in discussions with corresponding technical personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.

* Collaborates in publication of research results in areas of applications.
* Independently conducts research on statistical methodology, pursues solutions to various technical problems, adapts known methods and develops new methods.
* Maintains technical skills and increases own knowledge of new methods or areas of applications by reading journals and attending professional society meetings. Presents own research at meetings and seminars. Communicates with statisticians outside Merck concerning technical problems.
* Participates in departmental activities including recruiting and training other statisticians, providing statistical training for non-statistical groups, department research effort, and other committee works, etc., as needed.

Qualifications

Education Minimum Requirement:

* PhD, MS, or equivalent in statistics/biostatistics or related field

Required Experience and Skills:

* 3 years experience for PhD (6 years for MS) in the design and evaluation of clinical trials.
* Sound knowledge of computers and statistical software (e.g., SAS, R).
* Excellent communication skills as well as the ability to function in a team environment.

Preferred:

* Publications in peer reviewed statistical/medical journals are 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 submit your resume for requisition # BIO003434.

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
Other Locations: US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Upper-Gwynedd-Senior-Biometrician-Job-PA-19436/1669048/166904816690482012-03-04Merck/MSDfull-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 guidance of the Senior Leadership of MRL Finance, the position is responsible for the establishment of an aligned, operational vision and mission within the assigned business area. The position will lead clients (including EC+2 level and their organizations) through the development of strategic, operational and financial plans and establish capability to deploy resources to critical business drivers, including annual functional objectives and the long term strategic goals. The position is responsible for:

* Facilitating the development, execution and analysis of strategy and business plans for a Functional business area, including their assessment, priorization and aggregation;
* working with Functional leadership to create, monitor and cascade performance objectives/scorecards into functional areas;
* Assuring alignment and integration of other support functional groups (e.g. IT) into Functional plans to ensure realization of the stated strategic intent; and
* Ad hoc analysis and support of change initiatives.

Qualifications

Education:

* Bachelors in Business, Finance, Science or Engineering

Required:

* Minimum of 5-10 years of operations or equivalent is required, with that of a leadership nature in a research organization being highly desirable.

Preferred:

* MBA, or other Masters/PhD in Business, Finance, Science or Engineering.
* Demonstrated experience in broad areas such as business administration, strategic planning and analysis, managing and allocating resources, and operational and financial planning and management.
* Background in management consulting highly valued.
* Ability to provide strategic direction for business operations models.
* Strong Financial accumen.
* Demonstrated ability to develop, evaluate, organize, direct, and deliver on operational objectives in the areas of planning, finance, and metric setting leading continuous operational improvement.
* Proactive approach to problem solving.
* Results and process-driven orientation.
* Proven track record in drving large organizational change initiatives.
* Demonstrated ability to build and effectively manage and motivate a team in a challenging and complex environment.
* Excellent interpersonal skills and ability to influence; Ability to build internal and external relationships; proven negotiation skills.
* Sound and balanced judgement; able to assess and handle risks; decisive.
* Excellent communications 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 # FIN000764.

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
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Upper-Gwynedd-Finance-Manager%2C-Vaccines-Job-PA-19436/1682101/168210116821012012-03-04Merck/MSDfull-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.


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 Director M&S has a key integrating function and assures that advanced modeling and simulation is conducted 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 (NONMEM)
* Mechanistic/Disease modeling
* Comparator modeling
* Absorption and biopharmaceutical modeling
* Biological pathway analysis
* Physiological modeling
* Statistical modeling
* Trial simulation
* Quantitative decision analysis
* Data curation and data mining.

The M&S Director plans and executes advanced research in his/her own or related scientific specialty and makes significant, timely and impactful contributions to research programs. He/she will need to develop and manage collaborations with internal teams, outsource providers, vendors, contractors, and academics. Completes agreed upon research objectives independently and is an effective leader who can lead teams through strategy development and execution of M&S work. He/she should be recognized as an expert in his/her field, stay abreast of developments within his/her own field of specialization, and apply this state-of-the-art knowledge in recommending innovative research approaches, coaching subordinates and peers, and meeting Divisional objectives.

Qualifications

Education Minimum Requirements:

* PhD in a scientific discipline (e.g. biology, chemistry, PK/PD, computational biology/chemistry, pharmaceutics, mathematics, biochemical/bioengineering, physics or the like) coupled with a minimum of 8 years industry experience (or a combination of industry & academic experience),
* MSc degree coupled with a minimum of 10 years industry/academic experience.

Reqiured Experience & Skills:

- Experience in modeling & simulation e.g. PK and PK/PD modeling

- Possess strong leadership, communication, interpersonal, problem solving & planning and business skills necessary to participate in and lead interdisciplinary teams in collaboration with key partners.

- Enthusiasm and facility for learning new skills and applications will be 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 # QUA002633.

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
Other Locations: US-NJ-Rahway
Employee Status: Regular
Number of Openings: 3]]>http://jobs.merck.com/job/Upper-Gwynedd-Director-Modeling-&-Simulation-Job-PA-19436/1479909/147990914799092012-03-04Merck/MSDfull-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 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.

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-07065/1542238/154223815422382012-03-04Merck/MSDfull-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.


In this role, you will use knowledge of statistical methodology, experimental design, computing software, data management, drug discovery or worldwide regulatory requirements, non-clinical collaborations or clinical trial expertise from phase I to V to ensure that sound scientific principles and statistical methods are applied to designing and analyzing clinical trials or non-clinical studies in support of discovery and worldwide regulatory submissions. Previous experience working in the Early Development Space in clinical pharmacology studies including initial safety, and pharmacokinetic studies, as well as experience in the conduct and design of late stage clinical pharmacology studies including drug drug interaction studies, special population studies and selective proof of pharmacology and/or proof of concept studies (IB) research in patients is desired.

This position involves interaction with Medical, Data Coordination, Merck Research Laboratories (MRL) scientists and Regulatory staffs in designing and analyzing clinical trials or non-clinical experiments and coordinating the statistical activities for clinical or non-clinical drug projects. Supervises a statistical or programming staff assigned to a discovery or development project as needed.

Qualifications

Education Minimum Requirement:

* MS or PhD in statistics/biostatistics

Required Experience and Skills:

* Knowledge of biomedical sciences and at least 3 years (for PhD, 6 years for MS) experience in the design and evaluation of drug/vaccine discovery, non-clinical development or clinical trials.
* Sound knowledge of computers including the capability of programming on your own without the dedicated support of a SAS programmer, statistical and data processing software.
* Excellent communication skills.

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 # BIO003443.

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
Other Locations: US-PA-Upper Gwynedd
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Sr-Biometrician-Biostatistics-Job-NJ-07065/1691712/169171216917122012-03-04Merck/MSDfull-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 with Franchise/Area Heads to understand Research & Development (R&D) Strategies and prioritize detailed Knowledge Discovery/Knowledge Management needs.
* Develop and execute a KD/KM Research Services 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 Biologics, Chemistry, and Vaccines.

· 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 is highly desirable.

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 # SER000267.

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
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-Franchise-Area-Lead-Job-NJ-07065/1598875/159887515988752012-03-04Merck/MSDfull-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 Analytical Chemistry department within Merck Research Labs located in Rahway, NJ is seeking undergraduate and graduate summer interns. The summer interns will be exposed to core instrumentation critical to modern pharmaceutical analysis, process characterization, and drug substance physical attributes determination. Additionally, interns will learn the fundamentals of sound analytical and physical chemistry method development necessary to problem solve as a member of an integrated team in support of the Merck small and large molecule pipeline. The Analytical Chemistry Department will expose the intern to various expert groups in the area of screening and high-throughput analysis, molecular and materials characterization, structural elucidation including high end mass spectrometry and NMR techniques, labeled-compound analysis, and trace metals analyses, further broadening the experience. The intern will also attend departmental and team meetings to provide a wider perspective on the drug development process in the pharmaceutical industry. The intern will be responsible for accurate electronic notebook recording of critical experimental details which may be used in internal or external scientific publications and presentations which may follow from the internship.

We are seeking interns with strong academic performance, communications skills, teamwork, and the ability to work in a multi- functional environment.

This is a paid internship targeted to start in June 2012 for 9-11 weeks, whereby a weekly stipend will be provided. Housing is available for those interns meeting the housing distance guideline.

Qualifications

Required:

* Currently pursuing a Bachelor's or graduate degree in chemistry, chemical engineering, materials science, pharmaceutical science or related field.
* Candidate must have completed at least two years of studies toward BS/BA degree in Chemistry or related field.
* Basic laboratory skills and research experience preferred, including experience with electronic notebooks, high performance gas or liquid chromatography using various detection techniques, chiral separations, mass spectrometry, nuclear magnetic resonance spectroscopy, x-ray powder diffraction, infrared and Raman spectroscopy, or thermal analysis.
* Applicants 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 #PRE000280.

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


Primary Location: US-NJ-Rahway
Employee Status: Regular
Number of Openings: 4]]>http://jobs.merck.com/job/Rahway-Analytical-Chemistry-Intern-Job-NJ-07065/1694171/169417116941712012-03-04Merck/MSDfull-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.


We seek a talented professional to join a team of scientists involved in the automation of biochemical assays for the purposes of pharmaceutical Lead Identification and Optimization. Qualified candidates will have a BS in biochemistry or a related degree in the life sciences and 4 or more years experience or an MS and 2 years of experience. As this role is weighted towards the IT components of our process, demonstrated aptitude in computer programming or an advanced degree in computer technology is required.

Working in a laboratory setting, you will have the ability to rapidly design, code, and maintain custom software products developed in VB.net and C# which link to SQL server or Oracle databases. Knowledge of laboratory automation equipment and hands-on laboratory experience are required. Design or configuration of ActiveX controls, or XML for instrument control or data processing is also highly desired. The ability to work with Web services and applications (ASP.NET, SharePoint) would be a plus, as would be knowledge of LIMS and data reporting methods through the use of tools such as Pipeline Pilot, Spotfire and ActivityBase. Excellent organizational and communications skills are essential.

Qualifications

Education Minimum Requirement:

* BS or MS in life sciences

Required Experience and Skills:

* 4 or more years as a scientist in a laboratory setting.
* Demonstrated aptitude in computer programming or an advanced degree in computer technology is required.
* The ability to rapidly design, code, and maintain custom software products developed in VB.net and C# which link to SQL server or Oracle databases.
* Knowledge of laboratory automation, robotics and hands-on laboratory experience are required.
* Excellent organizational and communications skills are essential.

Preferred:

* Design or configuration of ActiveX controls, or XML for instrument control or data processing is also highly desired.
* The ability to work with Web services and applications (ASP.NET, SharePoint) would be a plus, as would be knowledge of LIMS and data reporting methods through the use of tools such as Pipeline Pilot, Spotfire and ActivityBase.
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 # BIO003436.

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
Other Locations: US-NJ-Kenilworth
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Radioactive materials, Biohazards and Solvents will be present in the lab. Training will be provided.]]>http://jobs.merck.com/job/Rahway-Team-Member-In-Vitro-Pharmacology-Job-NJ-07065/1666991/166699116669912012-03-04Merck/MSDfull-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:

* 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.

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-07065/1299128/129912812991282012-03-04Merck/MSDfull-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 directly to the Biologics CMC Site Head, the Senior Manager 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.

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-07033/1708742/170874217087422012-03-04Merck/MSDfull-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 Senior Biometrician will be responsible for statistical planning and data analysis of clinical trials or non-clinical experiments. This position involves interaction with Medical, Data Coordination, Merck Research Laboratory scientists and Regulatory staffs in designing and analyzing clinical trials or non-clinical experiments and coordinating the statistical activities for clinical or non-clinical drug projects. Supervises a statistical or programming staff assigned to a discovery or development project as needed.

Primary Activities:

* Develops, coordinates, and provides biostatistical support for related drug/vaccine projects under the supervision of management. Supervises staff assigned to the project as needed. This includes the following activities:
* Is involved in early development planning of Basic Medical Plan/ Clinical Development Strategy to ensure that study designs are consistent with program objectives and meet worldwide regulatory and marketing needs.
* Independently identifies and anticipates technical or other potential problems arising in the design, conduct, and analysis of clinical trials or non-clinical experiments, proposes solutions, and carries them out.
* Develops individual protocols and data analysis plans, or collaborates with nonclinical scientists. Independently determines appropriate statistical methodology for data analysis.
* Participates in Worksheet development, database (collector and view) design meetings to ensure that the data evaluated are free of bias, contain maximum information (minimum variance), and satisfy analysis requirements.
* Determines the statistical programming needs and organizes the programming activities to ensure that all programs meet analysis requirements, internal Standard Operating Procedures, validation, and external regulatory requirements
* Evaluates appropriateness of available software for planned analyses and ascertains needs for potential program development of novel statistical methodology.
* Analyzes data and interprets results from experiments to meet objectives of the study protocol. Independently applies and implements basic and complex techniques to these analyses.
* Prepares oral and written reports to effectively communicate results of clinical trials or nonclinical experiments to the project team, Merck Management, regulatory agencies, or individual investigators.
* Provides responses to queries relating to study design, analysis, and interpretation posed by the monitors, regulatory agencies, or investigators.
* Is responsible for ensuring the accuracy of Statistical Review Aids ted to regulatory agencies.
* Participates with management in discussions with corresponding technical personnel at regulatory agencies and with investigators concerning proposed or ongoing studies.

* Collaborates in publication of research results in areas of applications.
* Independently conducts research on statistical methodology, pursues solutions to various technical problems, adapts known methods and develops new methods.
* Maintains technical skills and increases own knowledge of new methods or areas of applications by reading journals and attending professional society meetings.
* Presents own research at meetings and seminars.
* Communicates with statisticians outside Merck concerning technical problems.
* Participates in department activities including recruiting and training other statisticians, providing statistical training for non-statistical groups

Qualifications

Education Minimum Requirement:

* Ph.D or M.S or equivalent in statistics or biostatistics

Required Experience and Skills:

* Knowledge of biomedical sciences and at least 3 years (for PhD, 6 years for MS) experience in the design and evaluation of drug/vaccine discovery, non-clinical development or clinical trials.
* Excellent communication skills
* This position requires a solid knowledge of statistical methodology, experimental design, computing software and data management
* A general understanding of drug discovery or worldwide regulatory requirements, and non-clinical collaborations or clinical trial expertise from phase I to V. The knowledge must be sufficient to ensure that sound scientific principles and statistical methods are applied to designing and analyzing clinical trials or non-clinical studies in support of discovery and worldwide regulatory submissions.

Preferred:

* Publications in peer reviewed statistical/medical journals are 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 submit your resume for requisition # BIO003429.

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

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Kenilworth-SR-RSCH-STATISTICIAN-Job-NJ-07033/1672539/167253916725392012-03-04Merck/MSDfull-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 the Category Insights Manager and Customer Business Manager, the Customer Category Manager is accountable for the development, implementation, and evaluation of Merck sales, category management and business building initiatives. As category expert, provides and interprets category data analysis and insights across multiple sources in support of recommendations for assortment, planogram, promotion, and planning.

Main areas of responsibility include:

* Sources, analyzes, and interprets account and market data in support of customer teams including shipment, financial, panel and POS data
* Develops hypotheses on drivers of trends and presents findings / recommendations to team and retailers.

* Presents data on account, market and brand performance utilizing all data sources.
* Provides Plano gram development, category data analysis, customer opportunity analysis to the customer and Merck Consumer Care (MCC) team
* Penetrates and influences customers relative to MCC / Category business development opportunity analysis and presentation.
* Leverage category expertise to maximize the success of sales initiatives.
* Builds conceptual and tactical customer presentations
* Works with other CBA's and CCM's to share best practices

This job supports HEB, Kroger and Publix accounts on the Footcare/First Aid franchises.

Qualifications

Education:

* Required: Bachelor's degree

Required:

* Minimum (2) years work experience in Consumer Products industry
* Proven knowledge, utilization and application of syndicated data
* Solid analytical and creating problem solving skills
* Technical skills with the ability to manage multiple tasks

Preferred:

* Category Management / Key Account experience
* Planogram 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 # DIR003930.

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-OH-Cincinnati
Employee Status: Regular

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

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Cincinnati-Customer-Category-Manager-%28Grocery%29-Job-OH-45201/1666995/166699516669952012-03-04Merck/MSDfull-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.


Under the direction of the Team Leader, the Customer Category Manager (CCM) is accountable for working in collaboration with the customer to develop and implement Merck's Consumer Care (MCC) sales and marketing programs for tops brands within Signature and Power Categories. The CCM is responsible for identifying and pursuing additional customer focused, business-building opportunities and providing analytical insights to help improve MCC market share and sales.

Key accountabilities include but are not limited to:

* Source, analyze and interpret account and market data in support of customer teams including but not limited to shipment, financial and POS data
* Analyze and present data on account and market category and brand performance
* Identify business-building opportunities
* Assist CBMs in developing and presenting strategic business plans and annual customer business review
* Build credibility with customer through category expertise

* Utilize shelf management tools to lead planogram development at the customers
* Initiate and support all all other necessary Category Management requirements
* Penetrate key decision makers at the customer relative to business development opportunities and build strong partnerships with customer
* Work with other Customer Category Managers to gain additional prospective on industry trends and developments
* Handle all administrative responsibilities in a timely and thorough fashion.
* Any other responsibility as assigned by the Sales management

Qualifications

Education:

* Required: Bachelor's degree

Required:

* Minimum (2) years experience in consumer sales, marketing or marketing/sales support
* Solid analytical with creative problem solving skills
* Strong leadership skills
* Technical skills with the ability to manage multiple tasks
* Strong presentation/communication skills
* Ability to build strong partnerships with customer
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 # DIR003897.

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-AR-Bentonville
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Bentonville-Customer-Category-Manager-%28Walmart%29-Job-AR-72712/1646171/164617116461712012-03-04Merck/MSDfull-timeUSDstarting0BSBentonville, AR, 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 play a leadership role for Merck, representing Informatics in Merck's relationships with one or more hospitals and academic institutions, collaborating with Merck Global Clinical Development, Regulatory Affairs, and IT organizations to implement a cohesive strategy for incorporating real world healthcare data and capabilities to benefit Merck's R&D pipeline and patients with unmet medical needs.

This role may include:

* Helping develop and manage partnerships with Global Clinical Development & Regulatory Affairs to understand their strategic objectives and help prioritize and incorporate these objectives into a cohesive informatics/IT roadmap
* Aligning partner and internal objectives and capabilities in order to identify opportunities for collaborative development of health informatics capabilities and/or fill gaps in real-world healthcare data access
* Developing and managing a portfolio of internal & external Informatics/IT projects, including responsibility for cost, timeline, and results.
* Developing and applying methods, tools, and systems for analysis, modeling, and visualization, and/or automating information pipelines
* Working with existing technical and project management resources to deliver new IT capabilities, either through commercial solutions, internal development, external partner sourcing, or crowd sourcing.
* Developing hypotheses, analyzing data, and providing direct analytical support to multiple business areas, and/or automatics information pipelines.
* Building relationships with peers across healthcare and other information industries to actively monitor trends, build partnerships, and identify innovative opportunities to improve drug discovery and development.

Qualifications

Education:

* Minimum Master's degree required in biostatistics, epidemiology, medical informatics/clinical informatics, or related scientific field
* PhD preferred in biostatistics, epidemiology, medical informatics, or related scientific field, or MD plus informatics/quantitative research experience.

Required:

* At least 2 years of experience and demonstrated effectiveness in health informatics including the design or implementation of informatics and/or IT solutions into clinical workflows.
* Experience manipulating and analyzing large data sets.
* Experience interacting with clinicians in healthcare organizations and/or in clinical settings.
* Demonstrated success at managing complex scientific partnerships and large multi-phase projects spanning multiple organizations.
* Self-motivated
* Strong communication and interpersonal skills
* Outstanding attention to detail
* Broad technical background, preferably hands-on experience with UNIX/LINUX, one or more scripting languages, SQL, and high performance computing (cluster and/or cloud-based computing).
* Motivated to make a difference in human health
* Documented history of direct contribution to clinical healthcare, e.g. peer-reviewed publications, teaching, academic advising for an academic hospital, etc.
* Experience capturing and analyzing business requirements in a research /clinical 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 # BIO003993.

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

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

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/San-Francisco-Lead-Analyst-Clinical-Health-Informatics-Job-CA-94101/1515974/151597415159742012-03-04Merck/MSDfull-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.


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.

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-27893/1540440/154044015404402012-03-04Merck/MSDfull-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.


Position Overview

The basic function of this position is to work with the site Training Team, COE's and IPT's to develop, coordinate, manage and implement training support for all employees. The incumbent will work closely with site organizations to identify skill gaps and develop and implement training programs encompassing regulatory, technical/mechanical, computer, business and/or lean manufacturing principles.

Additional responsibilities are as follows:

* Support the business goals and ensure alignment of training activities.
* Stay abreast of new and changing technology, procedures, and management practices to maintain a highly skilled workforce.
* Develop and maintain Job Position Training Requirements/ Curricula and coordinates training needs for employees.
* Develop new, and/or update and revise existing Standard Operating Procedures and other training materials, including job aids, to keep them aligned with source documents and current practices.
* Conduct needs analyses to identify technical and employee needs for obtaining desired job skills performance.
* Design and create competency-based training materials and associated compliance documentation for job skills, utilizing appropriate subject matter experts and personal expertise.
* Collaborate with people managers, engineers, subject matter experts and vendors, as necessary, to coordinate and/or facilitate training for employees.
* Monitor workforce performance for feedback to identify and address training gaps; communicate with leadership personnel and subject matter experts to identify training project needs and objectives, desired results, and potential limitations.
* Maintain training documentation.
* Actively integrate with the site teams to stay abreast of training needs and skills needed to align with the business and take appropriate actions to maintain a highly skilled workforce.

Qualifications

Educational requirements:

* BS/BA degree required (business, industrial psychology, organizational development, or science).

Required:

* Minimum of 3 years of experience in a training capacity in a industrial or military environment to include training methodologies and adult learning principals.
* Ability to achieve objectives requiring a high level of cooperation from others throughout the organization, along with customer orientation.
* Excellent verbal communication skills, facilitation skills, and technical writing skills.
* Able to work independently and as a team member.
* High personal integrity, credibility, and energy.
* Proficiency in Microsoft Office products (Excel, PowerPoint, and Word).
* Flexibility to perform other training related tasks to support the business.

Preferred:

* Knowledge of Human Error Prevention and web-page design knowledge and skills.
* Experience in a federally regulated 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 # EMP000424.

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-NC-Wilson
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Wilson-Training-Coordinator-II-Job-NC-27893/1653023/165302316530232012-03-04Merck/MSDfull-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.


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.

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-27893/1605058/160505816050582012-03-04Merck/MSDfull-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 4 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 # QUA002708.

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-NC-Wilson
Employee Status: Regular
Number of Openings: 2

Shift (if applicable)
: 2nd]]>http://jobs.merck.com/job/Wilson-Analytical-Chemist-Job-NC-27893/1551191/155119115511912012-03-04Merck/MSDfull-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 4 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 # QUA002736.

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-NC-Wilson
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Wilson-Analytical-Chemist-Job-NC-27893/1643326/164332616433262012-03-04Merck/MSDfull-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.


We currently have a Quality Operations Laboratory Quality Assurance Coordinator (Stability) vacancy at the Merck Facility in Wilson, North Carolina. 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®, FOSAMAX®, 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 Quality Operations Laboratory is a 40,000 square foot facility that provides support to the Wilson plant site operations through raw material and finished product testing and release; additionally, the Laboratory supports Merck & Co., Inc. on a worldwide basis through performing stability testing on finished products, API's and Components.

The Quality Assurance Coordinator (Stability) is an integral position for our worldwide Stability Laboratory that reports to the Stability Laboratory Manager. The Quality position manages the approval and disposition of stability samples.

Specific areas of responsibility include, but are not limited to the following:

Manages annual summary reports for APIs and Finished Product Stability Studies.

Responsible for approval/release of stability studies and laboratory data within LIMS.

Responsible for writing study protocols based on the General Stability Protocol

Responsible to trend/evaluate stability data per time-point and study.

Develops/revises SOPs based on Merck policies/guidelines.

Assists with laboratory investigations and integrates appropriately personnel into investigation meetings to determine root cause and path forward.

Working knowledge of GMP, NDA, and related regulations. Ability to interpret those regulations for implementation in the workplace. Ability to interpret Merck Quality Policies/Guidelines for daily application. Knowledge and understanding of pharmaceutical operations systems

Qualifications

Competencies/Leadership Behaviors/Skills: Position requires proficiency in the following competencies: Empowering leadership; Flexibility; Motivation; Functional Excellence; Teamwork/Collaboration; Results-Oriented; Problem-Solving; Communication.

Education Required:

Scientific B.A./B.S.

Experience Required:

Minimum 4 years pharmaceutical industry experience preferably in stability release/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 # REL000243.

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-NC-Wilson
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Wilson-Quality-Assurance-Coordinator-Job-NC-27893/1653015/165301516530152012-03-04Merck/MSDfull-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.


Under the general direction of the CRM Leader, the Clinical Risk Management Physician is an expert in drug and/or vaccine safety and is responsible for the overall clinical risk management and safety surveillance of assigned investigational and marketed drugs/vaccines.

* Includes all aspects of safety monitoring, including assessing safety information and ensuring completeness of safety information in worldwide package circulars.
* Responsible for the development of worldwide post-market risk management plans and pharmacovigilance strategies/specifications.
* The physician is a member of the Product Development Teams for products in phase II & III of development and chairs the Risk Management and Safety sub-team.
* Partners with appropriate Merck departments and therapeutic area heads to ensure efforts are aligned to meet our global risk management strategies for assigned products.
* Works with the CRM Leader, to plan direction for risk management function of the department, helps develop processes for the function of the program, and implements specific programs to achieve identified goals.

Qualifications

Education:

* MD from a recognized school of medicine

Required:

* Demonstrated analytic skills as well as medical writing skills

Preferred:

* Board certification in Medical Specialty, Epidemiology, Clinical Pharmacology, or other related subspecialty
* Pharmacovigilance or 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 # DRU000166.

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
Other Locations: US-NJ-Springfield
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Upper-Gwynedd-Clinical-Risk-Management-Physician-Job-PA-19436/1705734/170573417057342012-03-04Merck/MSDfull-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.


Manage organization's resource planning, headcount, & capacity in support of world class trial execution, based on consolidated clinical portfolio prioritization plans.

* Development, management, & maintenance of functional level resource algorithms in order to perform quarterly analysis & develop assumptive scenarios & mitigation recommendations.
* Maintain & track approved full time equivalent headcount, their related skill sets & capacity by collaborating with respective area contacts
* Process headcount requests, including reviewing all submissions for completeness & accuracy, providing supporting documentation/analysis & consolidation, routing & tracking of all global requests in alignment with approved staffing plans.
* Support functional area by reviewing & cascading time reporting compliance reports, & analyzing time data as a source to validate algorithms.
* Ensure adherence to GDP's, SOP's, internal processes.

Qualifications

Education Minimum Requirement:

* BS/BA

Required Experience and Skills:

* 5+ years combined experience in clinical development, operations, resource management, or project management
* Deep understanding of Clinical Development, Operations, and Resource Management
* Proven project management experience
* Familiarity with resource planning tools & processes
* Effective communication skills both orally and written
* Strong Analytical skills, including advanced MS Excel capabilities
* Business acumen
* Strong understanding of customer and ability to focus on customer needs.
* Ability to drive strategic partnerships with Functional Areas and support teams.
* Strategic thinker
* Attentive to details
* Open minded and flexible
* Process oriented
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 # CLI002607.

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
Other Locations: US-NJ-Rahway
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Upper-Gwynedd-HeadcountResource-Planning-Specialist-Job-PA-19436/1691722/169172216917222012-03-04Merck/MSDfull-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 Senior Director, the Associate Director/Director of Clinical Risk Management and Safety Surveillance is an expert in drug and/or vaccine safety and is responsible for the overall clinical risk management and safety surveillance of assigned investigational and marketed drugs/vaccines.

* This includes all aspects of safety monitoring, including assessing safety information and ensuring completeness of safety information in worldwide package circulars.
* Responsible for the development of worldwide post-market risk management plans and pharmacovigilance strategies/specifications.
* Is a member of the Product Development Teams for products in phase II & III of development and chairs the safety subcommittee as needed.
* Partners with appropriate Merck departments and therapeutic area heads to ensure efforts are aligned to meet our global risk management strategies for assigned products.
* Works with the Senior Director, CRMSS to plan direction for risk management function of the department, helps develop processes for the function of the program, and implements specific programs to achieve identified goals.

Qualifications

Education:

* M.D. - Graduate of a recognized school of medicine

Required:

* Demonstrated analytic skills as well as medical writing skills

Preferred:

* Board certification in medical specialty and clinical experience
* Additional training in Epidemiology, Clinical Pharmacology, or other related subspecialty
* Pharmacovigilance or 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 # DRU000150.

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
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Upper-Gwynedd-CRM-Physician-Job-PA-19436/1439387/143938714393872012-03-04Merck/MSDfull-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.


* Develop and validate immuno-based assays within the Clinical Development Lab (CDL) in Rahway, NJ supporting all therapeutic areas.
* Assist in the transition of biomarkers from Basic Research to Clinical by providing technical guidance on fit-for-purpose assay validation.
* Interface with scientists and physicians in both early and late stage clinical development, clinical pharmacology and experimentation medicine to deploy biomarker strategies in clinical trials.
* Writing memos, final reports and publications summarizing data, and writing/updating lab SOPs.
* Serve as the subject matter expert in immuno-assay development and validation within Merck collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in early- and in mid- stage clinical trials.

Qualifications

Education Minimum Requirement:

* BS, BA or MS in a life sciences discipline (Biochemistry, Immunology, Molecular Pathology, Cell Biology etc.) or Chemistry with broad knowledge of biomarker science.

Required Experience and Skills:

* A minimum of 10 (BS or BA) or 7 (MS) years of industry experience.
* A minimum of 5 years of direct experience in assay development on multiple immunoassay platforms such as MesoScale, Luminex, Gyros, SearchLight, Singulex etc.
* Demonstrated record of scientific achievement (publications, patents, etc).
* Strong interpersonal, verbal and written communication skills.
* Be able to work independently; strong leadership skills.
* Ability to execute within a matrixed organization.

Preferred:

* Experience with Regulated Clinical bioanalysis
* Experience with assay automation
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 # CLI002575.

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
Employee Status: Regular

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

Hazardous Materials
: Yes]]>http://jobs.merck.com/job/Rahway-Research-Immunochemist-Job-NJ-07065/1653021/165302116530212012-03-04Merck/MSDfull-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 support the Neuroscience clinical research activities by providing medical support of clinical development activities and oversight in the design, execution and analysis of clinical trials in late stage clinical (Phases II through V), participation in biomarker development activities, and through review of licensing opportunities. In addition, this position would work closely with basic scientists, clinical pharmacologists, regulatory and other basic research functions, while participating in the development of new compounds as the clinical/medical representative of early and late product development teams.

Primary responsibilities include but are not limited to:

* Reports to a Senior Director or above level manager
* Supervise the activities of other team members, Clinical Associates and/or Medical Program Coordinators for specific research project
* Responsible for initiation of clinical Operational Plans for the development of new Merck drugs or for the completion of projects involving marketed drugs
* 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
* The team member is 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
May travel on company business about twenty (20%) percent of the time of order to visit clinical investigators in regard to potential or active clinical research.

Qualifications

Education:

* MD or MD/PhD

Required:

* US Board certified/eligible in Psychiatry, Neurology, or Anesthesia
* Strong interpersonal skills, as well as the ability to function in a team environment
* Demonstrated record of scientific scholarship and achievement

Preferred:

* Experience in clinical research and/or basic science
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 # CLI002540.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Director-Clinical-Research-Neuroscience-Job-NJ-07065/1528628/152862815286282012-03-04Merck/MSDfull-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.


In this role you will be a member of a global structure elucidation team providing support to Merck's chemistry organization, including medicinal chemistry, process chemistry and labeled compound synthesis groups. Work performed in the global structure elucidation group includes, but is not limited to, structure elucidation and characterization of compounds being developed by medicinal chemistry project teams, validation of structure and purity of lead compounds under evaluation by exploratory chemistry teams, support for process chemistry as well as the development and implementation of NMR and LC-MS methods for open access and automation usage. You will interact with world-class scientists in a professional work environment at our state-of-the-art research facilities.

The successful candidate will provide structure elucidation support to our medicinal chemistry group. We are looking for a highly skilled and motivated individual, who, while capable of working independently, understands and values cross-functional team-work and our common mission to develop new therapeutic solutions to unmet medical needs. You will collaborate with synthetic, purification and analytical chemists in solving challenging structural problems. The ideal candidate will have expertise in small molecule structure elucidation using instrumentation such as NMR and mass spectrometry and the use of chromatography for sample isolation and purification.

Qualifications

Education Requirements:

* PhD in chemistry or equivalent degree from an accredited university

Required Skills and Experience:

* A minimum of 5 years experience in structure elucidation with a proven track record of accomplishments in the area of small organic molecule structure elucidation (e.g., natural products, pharmaceuticals, etc.)
* Good knowledge of organic chemistry with experience in a medicinal or process chemistry environment
* Comprehensive knowledge of NMR spectroscopy
* Highly skilled in the use of Bruker and Varian NMR software and hardware including cryo-probes and the application of automation.
* Experience in mass spectrometry and chromatography is highly desirable
* Technically inclined with the ability to troubleshoot complex instrument problems (e.g., automation, robotic systems, etc.)
* IT literate with the ability to manipulate data work-flows in a networked environment (e.g., Linux OS, macros, scripts, etc.)
* Excellent oral and written communication skills.
* Customer focused and driven to continually work towards technical and process improvements
* Excellent interpersonal and leadership 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 # CHE003332.

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
Other Locations: US-NJ-Kenilworth
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-NMR-Specialist-Job-NJ-07065/1596736/159673615967362012-03-04Merck/MSDfull-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 Basic Pharmaceutical Science (BPS) group in NJ is seeking applicants for an entry level Ph.D. scientist position. BPS is a multidisciplinary research group that provides drug delivery, solid state and solution chemistry tools in Discovery and early Development. The successful candidate will have key responsibilities including characterization of potential pre-clinical drug candidates' physicochemical properties and the identification of suitable oral and parenteral preclinical formulations for early pharmacology and toxicology studies. The candidate will also plan and execute studies for elucidating API chemical degradation pathways and phase optimization. The candidate will closely interact with Discovery, Safety Assessment, Process Research, Analytical Research and Drug Metabolism and Pharmacokinetics, as well as other members of Pharmaceutical Sciences

Qualifications

Education Minimum Requirement:

* Ph.D. degree or anticipated Ph.D. degree in January 2012 in pharmaceutical sciences, chemistry, or a related discipline

Required Experience and Skills:

* 0-5 years of experience in industry within preformulation, analytical chemistry or formulation development.
* Excellent verbal and written communication skills, demonstrated creativity, strong leadership/interpersonal skills
* Ability to work in a team environment with cross-functional interactions are essential.

Preferred:

* Experience with enabled formulations, solid state characterization, polymorphism, and solution chemistry is desirable.
* Candidates with experience in analytical techniques (e.g., X-Ray diffraction, differential scanning calorimetry (DSC), and high pressure liquid chromatography (HPLC)) and/or drug delivery (e.g., controlled release, transdermal) 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 # PRE000262.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Potent compounds]]>http://jobs.merck.com/job/Rahway-Sr-Research-Chemist-Job-NJ-07065/1603010/160301016030102012-03-04Merck/MSDfull-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 support the cardiovascular clinical research activities by providing medical support of early development activities (Phase Ib through IIa) and oversight in the design, execution and analysis of clinical trials in late stage clinical (Phases IIb through V), participation in biomarker development activities, and review of licensing opportunities.

The position would work closely with basic scientists, clinical pharmacologists and other research/development functions and would participate in the development of new compounds as the clinical/medical representative of early and late product development teams.

Primary responsibilities include but are not limited to:

* Reports to a Director or higher level manager.
* May supervise the activities of other team members, Clinical Associates and/or Medical Program Coordinators for specific research project to which assigned by the Senior Director.
* Initiation of clinical Operational Plans for the development of new Merck drugs or for the completion of projects involving marketed drugs.
* Planning and initiating clinical trials involving new Merck drugs or marketed products.
* Development of approved protocols for clinical studies to which assigned and is responsible for the initiation, monitoring and completion of the clinical studies.
* 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 (20%) percent of the time of order to visit clinical investigators in regard to potential or active clinical research projects.

Qualifications

Education:

* Required: MD or MD/PhD
* Preferred: MD Cardiology or Nephrology

Required:

* Strong interpersonal skills
* Ability to function in a team environment

Preferred:

* Board certification in Cardiology
* Experience in cardiovascular drug development
* Demonstrated record of scientific scholarship and achievement
* Experience in clinical research and/or basic science
* Subject matter expertise in lipids, vascular biology and/or hypertension
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 # CLI002529.

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
Employee Status: Regular

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

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Rahway-Assoc_-DirectorDirector%2C-Clinical-Research-Cardiovascular-Disease-Job-NJ-07065/1510515/151051515105152012-03-04Merck/MSDfull-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 will develop and implement enabling technologies with the goal of reducing product development cycle-times, and lowering the cost of advancing/ commercializing products. This position will be instrumental in creating cost-savings and support and implementation of key-intiatives in the field of biologics. The position will be a member of the Biologics-New and Enabling Technologies (B-NET) team and be responsible for developing novel upstream processes to provide innovative processes for biologics. This will include working with multiple expression systems including CHO, Pichia and E.coli. This will include colloboration with purfication technology teams aswell as basic research and manufacturing commericialization.

Qualifications

Minimum Education Requirement:

* BSc in Science is required in the field of upstream/fermentation processing of large molecules

Minimum Experience and Skills Required:

* Development experience of upstream processes for large molecules
* Demonstrated experimental design with DOE approaches and interactions to upstream development
* QbD understanding, and expertise in at least one upstream unit operation
* Demonstrated experience of leadership and rapid, smart 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 # BIO003426.

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
Other Locations: US-NJ-Union
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Biochemical-Engineer-Job-NJ-07065/1646165/164616516461652012-03-04Merck/MSDfull-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 Maintenance Technician will be responsible for the overall maintenance, inspections, and repairs for equipment, facilities, and utilities in a fast paced, team oriented Industrial/Production environment.

This position will perform the following duties and other tasks as needed:

* Must be attentive to his/her own safety and the safety of others in the workplace.
* Perform other related duties as assigned, by supervisor or manager

*** This is a 1st Shift position, working Tuesday-Saturday, 7:00am - 3:30pm.

Qualifications

Education Minimum Requirement:

* High School Diploma or equivalent required
* Technical or trade school training in HVAC-R or electrical/mechanical with PLC experience strongly preferred.

Required Experience and Skill:

* Minimum 2 years experience in Industrial Mechanical field
* Ability to communicate both verbally and written, and follow instructions

Desired Experience and Skills:

* 3rd Grade Boiler Operator license preferred or ability to obtain license within 18 months from date of hire.
* Analytical and mechanical troubleshooting skills required
* Ability to work independently without direct supervision 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 # TEC000399.

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-NE-Elkhorn
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Maintenance-Mechanic-Elkhorn%2C-NE-Job-NE-68022/1510517/151051715105172012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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.


The Maintenance Technician will be responsible for the overall maintenance, inspections, and repairs for equipment, facilities, and utilities in a fast paced, team oriented Industrial/Production environment.

This position will perform the following duties and other tasks as needed:

* Must be attentive to his/her own safety and the safety of others in the workplace.
* Perform other related duties as assigned, by supervisor or manager

*** This is a 2nd Shift position, working Tuesday-Saturday, from 3pm-11:30pm.

Qualifications

Education Minimum Requirement:

* High School Diploma or equivalent required
* Technical or trade school training in HVAC-R or electrical/mechanical with PLC experience strongly preferred.

Required Experience and Skill:

* Minimum 2 years experience in Industrial Mechanical field
* Ability to communicate both verbally and written, and follow instructions

Desired Experience and Skills:

* 3rd Grade Boiler Operator license preferred or ability to obtain license within 18 months from date of hire.
* Analytical and mechanical troubleshooting skills required
* Ability to work independently without direct supervision 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 # TEC000400.

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-NE-Elkhorn
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Maintenance-Mechanic-Elkhorn%2C-NE-Job-NE-68022/1510516/151051615105162012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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.


The Director reports to the Vice President in the MBV/Early Biologics Clinical Group. Under the guidance of a supervisor, the Director has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology biologics or marketed biologics for diabetes. Merck's Oncology/Diabetes biologics span all phases of clinical development (pre-clinical to post-licensure). The Director will manage the entire cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.

Specifically, the Director may be responsible for:

* Evaluating pre-clinical and translational work for the purpose of generating early clinical development plan and Investigational New Drug applications
* Developing of clinical development strategies for investigational or marketed Oncology or marketed Diabetes biologics
* 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 or marketed Diabetes biologics
* 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 biologics, and the further study of marketed biologics

In executing these duties, the Director may:

* Supervise the activities of Early Clinical Development Specialists 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 Vice President in ensuring that appropriate Corporate personnel are informed on 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 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 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

Qualifications

Education:

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

Required:

* Board Certified or Eligible in Oncology (and Hematology) OR Endocrinology
* Experience in pharmaceutical industry or academia
* 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 are essential

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 # CLI002473.

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
Other Locations: US-PA-Upper Gwynedd
Employee Status: Regular

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

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Rahway-Director%2C-Clinical-Research-Biologics-Job-NJ-07065/1415924/141592414159242012-03-04Merck/MSDfull-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.

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

Travel
: Yes, 15% of the time
Number of Openings: 2]]>http://jobs.merck.com/job/Rahway-Senior-EngineerScientist-Job-NJ-07065/1708743/170874317087432012-03-04Merck/MSDfull-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:

* Planning and execution of assigned clinical programs on new or marketed drugs - includes all phases of clinical development, study design, and study monitoring.
* 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 Requirements:

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

Required:

* Strong interpersonal skills, as well as the ability to work well in a team environment are essential

Preferred:

* Experience/training/Board certification/eligibility in Endocrinology or Reproductive Endocrinology
* Experience in industry or academia
* Demonstrated record of scientific scholarship and achievement with peer-reviewed publications
* Prior specific 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. 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 # CLI002465.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Director-Clinical-Research-Women's-Health-Job-NJ-07065/1391283/139128313912832012-03-04Merck/MSDfull-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 Clinical M&S Scientist 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 curation and data mining

The Clinical M&S Scientist is a member of clinical development teams and may lead M&S sub-teams, where he/she applies M&S experience together with good understanding of drug development, roles of functional areas and franchises. He/she is expected to be proficient in key standard M&S software (such as NONMEM, R, MATLAB, S-Plus) and beginning to broadening and deepen understanding of M&S software and methods. He/she will participate in collaborations with outsource providers, vendors, contractors, and academics. Completes agreed upon research objectives independently with limited supervision. He/she stays abreast of developments within his/her own field of specialization, and applies this state-of-the-art knowledge in recommending innovative research approaches and meeting Divisional objectives.

Qualifications

Education Minimum Requirements:

* MSc degree coupled with a minimum of 5 years industry/academic experience.
* PhD in a scientific discipline (e.g. biology, chemistry, PK/PD, computational biology/chemistry, pharmaceutics, mathematics, biochemical/bioengineering, physics or the like) preferably coupled with industry experience

Required Skills and Experience:

* Strong leadership, communication, interpersonal, problem scoping and planning, and business skills necessary to participate in and lead interdisciplinary teams in collaboration with key partners.
* Enthusiasm and facility for learning new skills and applications will be 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 # CLI002498.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Modeling-&-Simulation-Scientist-Job-NJ-07065/1483110/148311014831102012-03-04Merck/MSDfull-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 successful applicant for this position will be an expert in organic synthesis, with particular specialization in catalysis. Applicants will have completed minimally a PhD (preferably a postdoctoral fellowship) focused on the development of either transition metal or enzyme catalyzed reaction capabilities. In this role, the successful applicant will be responsible for collaborating across the Merck Global Chemistry network, developing innovative solutions to catalytic challenges. In addition to strong technical skills, the successful applicant will need to exhibit strong leadership and interpersonal skills.

Qualifications

Education Minimum Requirement:

* PhD

Required Experience and Skills:

* Organic Chemistry, Catalysis
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 # CHE003335.

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
Employee Status: Regular

Travel
: No
Number of Openings: 2]]>http://jobs.merck.com/job/Rahway-Sr_-Research-Chemist-Enabling-Technology-Job-NJ-07065/1601351/160135116013512012-03-04Merck/MSDfull-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 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.

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-27893/1538422/153842215384222012-03-04Merck/MSDfull-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 Specialty Representative - HCV is a key member of the HCV Specialty Team and plays a critical role in supporting Merck's customer centric business model. He/she is responsible for working with the HCV 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 Las Vegas, Nevada.

The ideal location to reside is within the territory.

Qualifications

Education:

* Requried: 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
* HCV 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 # DIR003946.

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-NV-Las Vegas
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Las-Vegas-Specialty-Representative-HCV-%28Las-Vegas%2C-NV%29-Job-NV-89044/1679790/167979016797902012-03-04Merck/MSDfull-timeUSDstarting0BSLas Vegas, NV, 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:

* Responsible for the development and leadership of an Animal Health Research & Development (R&D) Species Research team comprised of scientists up to the Ph.D. level
* Responsible for the scientific leadership of research projects providing guidance, risk analysis, planning and interpreting results
* Provide in-depth knowledge and advice to research staff and management in areas of scientific species, setting standards, timeframes and priorities
* Oversees proper execution of laboratory and animals vaccine development studies
* Responsibilities focus on resource management and technical troubleshooting
* Manages development of complex project plans and timelines.
* Responsible to oversee timely execution of work by subordinates
* Writes and reviews protocols and reports for vaccine development studies.
* Prepares progress reports for upper management
* Works on departmental and interdepartmental teams (Regulatory Affairs, Quality Control, Manufacturing, Animal Care, Sales/Marketing, and Technical Services) to develop strategies and oversee project execution
* Assist with legal activities including patent filings/assessments, outside research contracts, material transfer agreements, secrecy agreements, and licensed technology
* Performs self-directed literature searches and reads scientific literature.
* Prepares manuscripts for publication and presentations for scientific or marketing meetings
* Seek and stay abreast of external advances and technologies than can enhance the species product development or portfolio
* Source and manage the R&D relationships and deliverables of 3rd party/external contractors needed to leverage talent, space, time, resources and results
* Key interface with Discovery and Technology (D&T) in the planning and delivery of products and new technologies transferring from D&T to R&D
* Understanding and knowledge of industry practices, familiarity with competitors to contribute on design of competitive species research program

Qualifications

Education Minimum Requirement:

* Doctorate in biology, microbiology, virology, immunology, or related field (Ph.D.) and or Doctorate in Veterinary Medicine (DVM) plus M.S.

Required Experience and Skills:

* Minimum 5 years experience in biology, microbiology, virology, immunology, or related field
* Experience licensing veterinary vaccines and supervising doctorate level scientists.
* Knowledge of Regulatory Requirements for Vaccine Registration

* Strong verbal and written communication skills in order to convey, influence and negotiate at high levels in the organization

* Must be able to work effectively with peers in other R&D facilities in the world
* Effective interpersonal/collaboration skills for developing and retaining top talent

* Proven problem solving and listening skills along with sound judgment and business integrity

* Must be able to work effectively with upper management and manage intra- or inter departmental teams.

Desired Experience and Skills:

* Experience with feline infectious diseases preferred.
* Additional knowledge of the International Vaccine Registration is preferred
* Knowledge of GLP, GCP, and GMP requirements 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 # BIO003361.

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-NE-Elkhorn
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Sr-Principal-Scientist-Feline%2C-Bio-Research-Elkhon%2C-NE-Job-NE-68022/1463446/146344614634462012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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 is responsible for but not limited to the following
DUTIES:

* Coordinates agency submissions for existing and new veterinary biological products
* Maintains and controls files for all biological submissions to and from regulatory agencies
* Ensures that all in-house USDA documents/logs/Sharepoint sites are maintained appropriately
* Maintains and s changes to all blueprints, legends and personnel forms as required
* Assists with preparation and submission of labels
* Tracks budgets and expenses for departments
* Preparation of Requests 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
* Prepares and updates outlines

Qualifications

Education Minimum Requirement:

* Bachelors degree (Bachelor of Science preferred)

Required Experience and Skills:

* Computer skills and working knowledge of Microsoft Office products (Word, Excel, PowerPoint, Outlook & Access) and Internet searches.

* Excellent written and oral communication skills in English

Preferred:

* Science degree, preferably in a biology field or animal science.
* Experience in the animal health industry
* Ability to meet critical deadlines and to organize work to meet the deadlines.
* Some understanding of USDA requirements and 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 submit your resume for requisition # REG000878.

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-NE-Elkhorn
Other Locations: US-NE-Omaha
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Regulatory-Affairs-Associate-Job-NE-68022/1647707/164770716477072012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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.


Under general supervision, this position assists professional laboratory personnel by performing routine biological testing with relative independence. Duties include but are not limited to:

* Assure testing compliance according to site, corporate and USDA regulations
* Investigate and report testing issues as needed
* Operate and maintain laboratory equipment using approved Standard Operating Procedures
* Assist in self-audits and participate in Corporate and USDA audits as directed
* Other duties as assigned

Qualifications

Education Minimum Requirement:

* Associate's Degree in Biology or related field
* Bachelor's Degree in Biology or related field strongly preferred

Desired Experience and Skills:

* Biologic Laboratory Experience - Enzyme-Linked Immunosorbent Assay (ELISA)
* Viral / Bacterial Potency and Identification, Aseptic Technique, Polymerase Chain Reaction (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 # QUA002738.

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-NE-Elkhorn
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Quality-Control-Tech-Job-NE-68022/1660004/166000416600042012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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.


· Coordinate closely with Disease Franchise/Functional Area Heads, Merck Senior Leadership, and other internal as well as external partners to define requirements for Knowledge Management 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 Biologics, Chemistry, and Vaccines.

· 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.

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-07065/1598880/159888015988802012-03-04Merck/MSDfull-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.


Design, modify, and document clinical databases and their supporting systems for the support of clinical trials. Provide technical expertise in the design and development of protocols, case record forms, and other methods of capturing and transferring data in support of clinical research. Primary customers are Global Clinical Data Management and Clinical Research.

Qualifications

Education Minimum Requirement:

* Bachelor's degree in computer science or related field with exposure to software design and development theory, techniques, testing methodologies, and software documentation.

Required Experience and Skills:

* At least 2 years of experience as a clinical database developer utilizing Inform and/or Clintrial.
* At least 2 years experience with Oracle databases and SQL.
* Solid knowledge of MS Windows and exposure to web based applications.
* Expected to have a strong technical proficiency in a Clinical Data Management System. Particularly in Clintrial/Oracle, InForm, and SQL-PL/SQL, VBS.
* Ability to establish and maintain good working relationships with different functional areas.
* Strong sense of urgency and customer focus.
* Desire and ability to learn new processes and technologies
* Ability to multi-task, work independently, and good communication skills

Preferred:

* Level of proficiency: InForm - Architect, PF export, rules, special formatting
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 # CLI002562.

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
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-CDS-Developer-Job-NJ-07065/1646174/164617416461742012-03-04Merck/MSDfull-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 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

Required:

* Bachelors degree in Microbiology, Biological Sciences, Chemistry or relevant area.
* Minimum of 5 years directly related laboratory experience

Preferred:

* Masters Degree
* 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 # MAN001285.

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-NC-Durham
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: BL2 Micro organisms]]>http://jobs.merck.com/job/Durham-Laboratory-Analyst-EM-Lab-Job-NC-27701/1553315/155331515533152012-03-04Merck/MSDfull-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.


Under the direction of the Site Services Lead, provide facility maintenance and services supporting the Durham Vaccine Manufacturing Operations. Maintain all facility related maintenance equipment and processes located throughout the entire site. Takes appropriate action to correct facility maintenance opportunities which includes but not limited to painting, general construction, door repair, plumbing issues, furniture maintenance, minor electrical repairs, grounds maintenance, fire/security equipment and any other general maintenance tasks as requested by management. Candidate must have excellent communication skills (verbal and written). Must be able to function in a team-based empowered culture. Seeks ideas and information on how to improve customer service involving internal and external customers.

The Facility Maintenance Technician has the following
DUTIES:

* Performs general maintenance repairs including carpentry, installing locks, plumbing, sheetrock, cement and minor electrical repairs.
* Small general construction projects including painting and wall repair
* Operates a variety of power, pneumatic, hydraulic and mechanical tools and equipment.
* Performs maintenance and repair on site vehicles and golf carts.
* Maintains facility equipment by developing and performing PM's
* Participates in new equipment installations by interfacing with equipment vendors
* Works on PLC's as needed and adds points
* Maintains Electric Doors within the facility
* Maintains specility wall, flooring and ceiling systems and makes repairs as necessary
* Responsible for Biologic and Hazardous Waste Programs and movement
* Responsible for loading, unloading and staging SD3A Alcohol

Qualifications

Required:

HS Diploma or GED equivalent

Three years of Facility Maintenance Experience

Basic electrical and mechanical troubleshooting skills.

Ability to read basic electrical and piping drawings

Ability to use Microsoft Windows Computer Programs

Preferred:

Two year Technical 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.

merckmanufacturing-durham.com/ to create a profile and your resume for requisition # FAC000309.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Durham-Facilities-Maintenance-Technician-Job-NC-27701/1691709/169170916917092012-03-04Merck/MSDfull-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 will provide the primary Quality support deviation management process for the bulk live virus vaccine manufacturing facility at the Durham site. The candidate will work independently from the Quality Director to support the IPT for timely investigation and resolution of deviation events in the bulk vaccine manufacturing facility. Individual will be responsible for final Quality approval of most deviation investigation reports. The individual may also provide direct Quality support for SOP development and review, direct support of regulatory inspections and audits, and direct support of other associated Quality functions.

Qualifications

Required:

* B.S. or B.A. required, or M.S. degree (preferred) in Science, Engineering, or Business.
* Minimum of 6 years experience in pharmaceutical operations, technical operations, and/or quality operations with at least 4 years in a Quality function.

Desired:

* Minimum of 2 years managerial experience recommended.
* Thorough knowledge of plantwide systems / areas.
* 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.
* Has in-depth knowledge of cGMPs and domestic and international regulatory requirements.
* Is expected to possess a high degree of problem solving ability.
* Experience with presenting and interacting with inspectors during regulatory audits.
* Knowledge of profit plan activities.
* Previous experience in conducting/approving deviation investigations 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 # QUA002672.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Durham-VBF-Deviation-Management-Lead-Job-NC-27701/1508962/150896215089622012-03-04Merck/MSDfull-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 role of Operational Coach - Mechanical at Merck's Durham facility is a manufacturing leadership role in Preventative Maintenance and Calibration of Process Equipment. The individual in this role provides guidance, cross-functional development and technical expertise to operations and administrative support personnel in various stages of team development responsible for the manufacturing processes. They must become proficient in the use of plant systems to resolve issues affecting equipment performance, to minimize equipment downtime, and to ensure product quality. The individual will anticipate shifting priorities to meet customer needs and will identify the need for new equipment and/or modifications to existing equipment to optimize throughput.

The individual is responsible for overall equipment reliability in various process areas. The individual provides oversight of preventative and unplanned maintenance of production equipment, instrumentation, and controls. Develops standard operating procedures (SOP's) and preventative maintenance (PM's) plans as required. Troubleshoots equipment failure to determine root cause and develop corrective actions. Actively support, participate and embrace an empowered team culture including significant interaction with Quality, Automation, Engineering, Maintenance and other groups as required. Position will also support the following systems:

* Automated Systems (e.g. Distributed Control System (DCS), Programmable Logic Controllers (PLC), robotics)
* SIP/CIP Systems (automated and manual)
* Process Vessel Equipment (e.g. tanks, cell bank manipulators, roller bottle carts)
* Environmental Monitoring Equipment (e.g. SMA, particle counters)
* Computer Systems (e.g. SAP, MES, Delta V)
* Autoclaves/Washers
* Benchtop Labratory Equipment
* Any other systems and equipment as necessary

Employee Development/People Management

* Coaches production employees in an Empowered Culture
* Assists the team with development of objectives and ensures alignment with site goals
* Assesses employee training and development needs, assesses the maturity of the team, and adjusts leadership style to enhance team performance

Information Transfer

* Attends departmental and team meetings focused on equipment/process improvement
* Serves as operations representative for technical group discussions

Compliance

* Completes accountability investigations
* Reviews and approves safety investigations
* Participates in internal and external audits and inspections
* Identifies quality-related trends and facilitates implementation of corrective actions

Financial

* Participates in development of profit plan and forecasting
* Assures IPT headcount is accurate and meets production and company needs
* Recognizes and investigates opportunities for financial savings

Qualifications

Required:

* Bachelors Degree in a Science, Engineering, or related field with minimum 1-5 years coaching/supervisory experience or position of demonstrated leadership OR
* Associates Degree in a Science, Engineering, or related field or Journeyman's Certification or similar certification with minimum 7 years coaching/supervisory experience or position of demonstrated leadership.
* Strong communication (written/verbal), and multi-tasking abilities
* Computer fluency (internet browsers, e-mail, word processing, spreadsheets, databases, CMMS) and Microsoft Outlook
* 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 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.

merck.com/careers to create a profile and your resume for requisition # PRO009013.

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-NC-Durham
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Durham-Operations-Coach-Maintenance-Job-NC-27701/1528622/152862215286222012-03-04Merck/MSDfull-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 an Operational Coach, this role will provide leadership, cross-functional development and technical expertise to operations, maintenance and clerical personnel in various stages of team development in the manufacturing of Durham live vaccine products. Responsible for operations teams, process equipment and all activities affecting them. Maximizes the potential of all team members. Fosters an environment that allows for progressive, continuous improvement of skills and honest, open feedback. Ensures team members have tools available to them to accomplish the team's mission statement.

Because of the entry-level nature of this operations role, the incumbent will work closely with more senior members to accomplish the goals set forth for the operations team.

Major Responsibilities

Line Performance -

* Coordinates production/maintenance operation with minimal coaching support.
* Prepares daily work assignments and coordinates work team and human resource related activities.
* Gains and uses general knowledge of plant systems (equipment, financial, planning, etc.) to monitor and execute production schedules.
* Responsible for ensuring compliance to government regulations through a demonstrated understanding of SOP's and a general knowledge of company policies/guidelines, safety/environmental regulations, and GMP's.
* Coordinates resources to ensure that equipment remains in operating condition.
* Gains a working knowledge of the production process by becoming qualified to operate equipment.
* Serves as point of contact for respective area.

Compliance -

* Troubleshoots root cause of problems and identifies/implements corrective actions.
* Completes quality observation investigations independently and atypical investigations with coaching support.

Qualifications

Education :

B.S./B.A. degree required (science, engineering or other technical field preferred) OR minimum, Associate Degree with 10 years related technical industry experience required.

Desired :

* Demonstrated leadership, interpersonal, technical aptitude, and problem solving skills.
* Willingness to work off-shift and/or weekends
* Computer literacy in MS Office, Word, Outlook, Excel
* Strong team skills, including ability to coach/develop work teams, provide training, motivate/empower others, and resolve conflict.
* Must be flexible and able to manage multiple priorities.
* Must be goal-oriented and able to manage risks.
* Good verbal and written 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 # MAN001297.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-Operations-Coach-Job-NC-27701/1566041/156604115660412012-03-04Merck/MSDfull-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.


Provide product costing & analytical support to clients in Latin America. Lead consolidation process. Review new & existing product standard costs, production variance. Responsible for forecasting, reporting, cost consolidation & valuation of projected inventory transfers. Develop communication processes & service metrics to measure performance. Liaise with manufacturing division. Develop & deliver training to staff.

Qualifications

Education;

BS in Accounting, Business Administration, Finance, or Economics

Required:

5 years experience in financial reporting & accounting, including inventory & costing.

Knowledge of business cultures & accounting rules in Latin American markets.

Proven quantitative, analytical, & presentation skills.

Expert user of Data3/JDE systems.

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 # FIN000667.

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-NC-Durham
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/Durham-Senior-Financial-Analyst-LA-Job-NC-27701/1642249/164224916422492012-03-04Merck/MSDfull-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.


Responsibilities include but are not limited to:

* Preparation of reagents, antigens and vaccines with minimum supervision
* Assist with or conduct laboratory and animal testing under the supervision of senior level scientist
* Development of in vitro and in vivo assays with minimum supervision
* Follow experimental procedures, SOPs, etc.
* Assist with or perform basic data analysis
* Preparation of study protocols and reports with minimum supervision
* Coordinate and complete assigned tasks in a timely manner/established timelines

Qualifications

Education Minimum Requirement:

* Bachelor Degree in Veterinary science, Microbiology, Immunology, Virology, Parasitology or related area with 1 year of related lab experience

Required Experience and Skills:

* Good oral and written communication skills and appropriate computer skills.
* Ability to interact with team members across multiple teams
* Good time management skills

Preferred Experience and Skills:

* Experience with veterinary vaccine formulation is preferred
* Understanding of animal diseases 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 # BIO003360.

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-NE-Elkhorn
Other Locations: US-NE-Omaha
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Assistant-Scientist-Canine-Job-NE-68022/1647708/164770816477082012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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.


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.
* 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 Requirements:

* M.D or M.D./Ph.D, plus Board Certification in Obstetrics/Gynecology

Required:

* Strong interpersonal skills, as well as the ability to work well in a team environment are essential

Preferred:

* Board certification/eligibility in Reproductive endocrinology
* Experience in industry or academia
* Demonstrated record of scientific scholarship and achievement with peer-reviewed publications
* Prior specific 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. 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 # CLI002463.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Associate-DirectorDirector-Clinical-Research-Women's-Health-Job-NJ-07065/1391285/139128513912852012-03-04Merck/MSDfull-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 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.

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-Sr_-Manufacturing-Engineer-Job-NC-27701/1525481/152548115254812012-03-04Merck/MSDfull-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.

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-27701/1650159/165015916501592012-03-04Merck/MSDfull-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

Primary Location: US-NC-Durham
Employee Status: Regular

Travel
: No
Number of Openings: 25

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/Durham-Bio-Process-Technician-Job-NC-27701/1505467/150546715054672012-03-04Merck/MSDfull-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.

Under the direction of an Operations Coach, this individual is responsible for partnering with business clients (business unit focus) or appropriate site level learning professionals (core curriculum focus) to improve human performance within their client/curriculum area through performance analysis and the designing, development and delivery of appropriate learning solutions.

Key Responsibilities include:

Engaging Leadership (15%)

· Partner with the department management team to create and execute departmental learning strategies that supports design, development, delivery and evaluation of training and development programs.

Building Relationships (10%)

· Build effective partnerships and team relationships within the department to effectively and efficiently utilize SMEs, understand needs of fellow team members and recognize opportunities to introduce training to support the effective operation of the department.

Driving Excellence (50%)

· Analyzing and implementing initiatives, training programs, and systems that will help to increase overall success within the department.

· Oversee design and facilitate training programs that emphasize active learning, customer needs, department integration, and appropriate organization.

· Effectively use metrics and measurement to ensure that training programs result in needed behaviors on-the-job.

· Participate in training for new hire training programs.

Applying Manufacturing Technical Skills (15%)

· Collaborates with internal customers to ensure training materials and workshops are current, effective, and compliant with regulatory guidelines.

· Ensure that training records are maintained in inspection ready status.

Mastering T&D Functional Skills (10%)

· Lead Learning Management System (LMS) utilization for the programs/trainings implemented within the department.

· Evaluate trainee performance and the effectiveness of learning programs and provide recommendations for improvement.

· Creates training programs based on analyzing tasks (i.e. TQR database, LMS) and basic e-learning technology where appropriate.

Qualifications:

Engaging Leadership

· Strategic and analytic capabilities as well as the ability to execute tactical training needs

· Demonstrated leadership ability within pharmaceutical or biotech industry

· Ability to effectively coach trainees to build their skills so that they may become one-on-one trainers

Building Relationships

· Collaborative team player

· Team player able to develop rapport and credibility with key stakeholders

Driving Excellence

· Demonstrates a sense of urgency by responding urgency and direction

· Holds self and others accountable for high standards

· Understands the business impact of decisions

· Takes a stand on tough issues to drive business performance

· Natural ability to flex and adapt in real time based on multiple channels of feedback

· Delivers commitments

Applying Manufacturing Technical Skills

· Excellent operational knowledge

· Through the exceptional understanding of state of the art manufacturing biologics including regulatory and compliance skills, the ability to develop programs to transfer knowledge to the shop floor or other technical teams.

Mastering T&D Functional Skills

· Can engage in basic performance consulting processes identifying training needs.

· Can design and develop training programs that use best practices in technical training

· Must have ability to effectively manage a project from its initiation to delivery, either as live training or as a deliverable.

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.

Other Requirements

· BS/BA degree in science or engineering is preferred.

· 1+ years in a current/past Operations related role.

· Minimum of two years in a highly regulated industry (preferably pharmaceutical).

· Instructor-led training experience preferred.
Biotech/pharmaceutical manufacturing experience at the line level preferred

merck.com/careers to create a profile and your resume for requisition # MAN001379.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1

Hazardous Materials
: Not Specified]]>http://jobs.merck.com/job/Durham-Bulk-Operations-Coach-Job-NC-27701/1703546/170354617035462012-03-04Merck/MSDfull-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 Coordinator is responsible for all Quality related functions that directly support the Durham VMF (Vaccine Manufacturing Facility) Integrated Process Team (IPT) and the site value stream map, while actively supporting, participating in and embracing an empowered team culture.

Responsibilities to include:

* Sample management
* Conduct periodic process simulation observation
* Direct in-line Quality support for all compliance, release and environmental monitoring matters
* Review atypical investigations
* Assist regulatory groups by providing documentation to support the approval of licensure supplements and new product license registrations.

Specific to Environmental Monitoring (EM), the coordinator will be responsible for maintaining the EM program to include the following:

* Performing environmental sampling of aseptic areas, personnel and utility systems
* Investigate OOS results and/or laboratory atypicals
* Evaluate environmental data for adverse trends
* Develop and participate in media challenges
* Preparation of Performance Qualification protocols and reports

Other:

* SOP and CJA development and review
* Direct support of regulatory inspections and audits
* Direct support of validation activities and all other associated quality functions

This position requires the incumbent to work a night shift.

Qualifications

Requirements:

* Bachelor degree in Science or Engineering.
* 2 years experience in a quality compliance role in a GMP environment
* Availability to work night shift

Preferred:

* Knowledge or experience in a product release position
* Understanding of aseptic processing, compliance requirements, and environmental monitoring practices would be beneficial.
* Strong leadership and communication skills.
* Knowledge of CFR, Eudralex and other regulatory guidance specific to the pharmaceutical industry.
* Experienced in the methods and approaches of conducting environmental monitoring and product release 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 # QUA002781.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 3rd]]>http://jobs.merck.com/job/Durham-Quality-Assurance-IPT-Coordinator-Job-NC-27701/1691718/169171816917182012-03-04Merck/MSDfull-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.


To that extent, we are pleased to let you know that our Durham Vaccine Facility will be hiring approximately 200 new employees between 2011 and 2012. The facility is located in Durham, North Carolina.

Entry level positions will be available in Quality Operations, Manufacturing Operations and Technical Operations.

For the remainder of 2012 we will be hiring for these functional areas and others and at different levels. If you have interest in any of these areas or types of roles please apply to this position and check off which areas you would have interest in pursuing when applying. Once an opening is posted we will contact you based on your interest and ask you to apply to the official job opening. We also encourage you to visit our careers page often as positions will be posted on an on-going basis.

Qualifications

Please Note: Required and Preferred Qualifications will be determined upon each unique positions level and its functional area of expertise.

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 # CHE003374.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Durham-Entry-Level-Technical-Operations-Engineer-Job-NC-27701/1682099/168209916820992012-03-04Merck/MSDfull-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.


Responsibilities include but are not limted to:

* Provide animal care and good husbandry practices for poultry, small animals, and large animals. Feeding and watering of animals: Ability to lift and dispense buckets of water and feed bags (minimum 50 lbs.). Cleaning of animal cages, pens, rooms, and other quarters, not limited to scooping, bagging, hosing, and operation of mechanized equipment (high-pressure sprayer, feed wagon, bobcat, tractors)
* Ensure the well-being of a variety of animals in accordance with SOP's and following compliance with the Animal Welfare Act
* Capable of working in inclement weather conditions, capable of taking multiple on-site showers when working in certain buildings, capable of wearing full body coveralls, full face respirators and other tight fitting personal protective equipments.
* Documentation of receiving, transferring, sale, and disposition of animals. Maintain feed supplies and inventory. Oversee animal inventory records for QC and R&D.
* Make and record accurate test observations of animals. Maintain daily observation and housekeeping records in accordance with study protocol.
* Should have valid driver's license and knowledge of stock truck with trailer.
* Assist other personnel (R&D, QC, QA, Maintenance, Contractors, Security) as directed in animal testing.
* Work independently. Provide training on procedures to junior staff. Assist in maintaining calibrations of weights and scales. Follow-up on maintenance work orders.
* Ensure animal care technicians are performing duties safely and efficiently

This is a Monday - Friday, 1st Shift Position, over-time will be required including some weekends and holidays.

Qualifications

Education Minimum Requirement:

* Veterinary Technician license or Bachelors degree required. AALAS certification preferred

Required Experience and Skills:

* Minimum 6 years experience working with and caring variety of animals.
* Preference will be given to the work experience gained in research setting.
* Minimum of 2 years experience as a Senior Animal Care Technician or equivalent.

Desired Experience and Skills:

* Must possess strong communication and multi-tasking skills.
* Demonstrate ability to work well as team.
* Must have good understanding of USDA and Animal Welfare guidelines

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 # ANI000117.

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-NE-Elkhorn
Other Locations: US-NE-Omaha
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Lead-Animal-Care-Tech-Job-NE-68022/1655968/165596816559682012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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 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.

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-68022/1460281/146028114602812012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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.


Job Responsibilities:

* Under general supervision, performs standard and semi- routine laboratory procedures and experiments.
* Works on problems of moderate scope where analysis of situation or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action.
* Performs routine data analyses (may include creation of graphs, tables and charts) and maintains accurate and detailed records (notebooks and computer).
* With guidance from supervisor, prepares written status reports and presents orally at department or project meetings.
* Understands studies, experiments, and processes well enough to monitor for unusual occurrences. Reports such occurrences to supervisor.
* May maintain laboratory equipment and supplies.
* With instruction from supervisor or co-worker, is able to acquire new technical skills and carry out new assignments.
* Reads selected literature.

Qualifications

Education Minimum Requirement:

* Requires a Associates/Bachelor'sdegree in a life science and a minimum of 2 years relevant experience or Master's degree

Required Experience and Skills:

* Has basic understanding of biochemistry, molecular biology, cell biology, immunology, or related scientific discipline and use of laboratory equipment and procedures commonly used in these disciplines such as pipettors, pH meters, centrifuges, microscopes, biosafety hoods and incubators.
* Is familiar with aseptic techniques, laboratory safety procedures, and principles of Good Laboratory Practice.
* Good oral and written communication skills and appropriate computer skills.
* Ability to interact with team members across multiple teams.
* Good time management skills.

Preferred:

* Experience in one or more of the following areas: protein analysis, molecular biology, immunoassays, cell culture, virus propagation/titration, bacterial fermentation.
* An understanding of animal infectious agents and diseases.

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 # BIO003440.

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-NE-Elkhorn
Other Locations: US-NE-Omaha
Employee Status: Regular

Travel
: No
Number of Openings: 2

Shift (if applicable)
: 1st

Hazardous Materials
: standard chemical and biological laboratory hazards]]>http://jobs.merck.com/job/Elkhorn-Assistant-Scientist-Job-NE-68022/1691711/169171116917112012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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.


Responsibilities include but are not limited to:

* Responsible for the development and leadership of multiple Poultry Parasitology US R&D Projects leading to licensure of new or improved products
* Responsible for the scientific leadership of projects providing guidance, data analysis, planning and interpreting results
* Provide in-depth knowledge and advice to research staff and management in the science of Poultry Parasitology
* Key interface with Discovery and Technology in the planning and delivery of products and new technologies transferring from D&T into R&D, as needed
* Manage the intellectual property (patents/product information) to meet corporate guidelines
* This position will require strong knowledge of general parasitology and basic knowledge of molecular parasitology and parasite antigen expression, in addition to the general Qualifications.
* Experience in Poultry product development will be highly desirable.

Qualifications

Education Minimum Requirement:

* M.S. with at least 7 years vaccine development experience including parasite vaccines.

Desired Education:

* Ph.D. degree in Parasitology or related biological field with post-doctoral experience in parasitology
* D.V.M. or equivalent with at least 2 years research experience in parasitology

Required Experience and Skills:

* Ability to manage cross-functional teams and provide supervision and training to less experienced colleagues
* Good project management skills. Must have aptitude to manage technical and logistical aspects of assigned research projects.
* Must have aptitude to provide interdepartmental leadership in product development and licensing; chair interdepartmental team meetings.
* Good problem-solving and decision-making skills.
* Knowledge of government regulations required for product licensure.
* Strong oral and written communication skills and appropriate computer skills.

Desired Experience and Skills:

* Preference will be given to candidates with molecular parasitology background and at least 3 years vaccine development industry experience.
* Knowledge of manufacturing processes is preferred.
* Experience in working with animals in vaccine development research 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 # BIO003358.

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-NE-Elkhorn
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Sr_-Scientist-Parasitology%2C-Bio-Research-Job-NE-68022/1463445/146344514634452012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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.


Responsibilities include but are not limited to:

* Responsible for the scientific leadership of projects providing guidance, data analysis, planning and interpreting results
* Provide in-depth knowledge and advice to research staff and management in the science of Companion Virology
* Interface with Discovery and Technology in the planning and delivery of products and new technologies transferring from D&T into R&D, as needed
* Assists with the intellectual property (patents/product information) to meet corporate guidelines
* This position will require strong knowledge of Virology in addition to the general Qualifications. Experience in companion animal product development will be highly desirable.

Qualifications

Education Required Minimum:

* Ph.D. degree in Virology, Microbiology, Veterinary Science or related biological field; D.V.M. or equivalent with at least 2 years research experience in virology; or M.S. with at least 7 years vaccine development experience. Preference will be given to candidates with at least 3 years vaccine development industry experience.

Required Skills and Experience:

* Ability to manage cross-functional teams and provide direction and training to less experienced colleagues
* Good project management skills. Must have aptitude to manage technical and logistical aspects of assigned research projects.
* Must have aptitude to provide interdepartmental leadership in product development and licensing; chair interdepartmental team meetings.
* Good problem-solving and decision-making skills.
* Knowledge of manufacturing processes is preferred.
* Knowledge of government regulations required for product licensure.
* Strong oral and written communication skills and appropriate computer skills.
* Experience in working with animals in vaccine development research is preferred.
* Must be able to work effectively with upper management and manage intra- or inter- departmental 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 # BIO003392.

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-NE-Elkhorn
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Sr_-Scientist-Virology%2C-Bio-Research-Elkhorn%2C-NE-Job-NE-68022/1531830/153183015318302012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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.


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 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 two 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

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 # MAN001258.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-Manufacturing-Engineer-Job-NC-27701/1525480/152548015254802012-03-04Merck/MSDfull-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 a highly motivated individual as Quality Assurance (QA) Coordinator. This individual will partner with Manufacturing Operations, Automation and Technology as a member 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.

The Quality Assurance Coordinator for our bulk live virus vaccine manufacturing facility is responsible for a range of Quality related functions that directly support the Durham VBF (Vaccine Bulk Facility) demonstration. Initially this will primarily involve supporting the set-up of the environmental monitoring, release programs, compliance oversight of the capital project and implementation of mandatory system requirements. Longer term, this role will support the Integrated Process Team (IPT) charged with routine production within an empowered team culture that is consciously cultivated at the Durham site.

Typical areas of responsibility:

* Sample management

* Conduct periodic shop floor process simulation observation

* Direct in-line Quality support for all compliance, release and environmental monitoring matters

* Prepare and review atypical investigations

* Assist regulatory groups by providing documentation to support the approval of licensure supplements and new product license registrations

* Performing environmental sampling of aseptic areas, personnel and utility systems

* Provide training for environmental sampling to production and other Quality personnel

* Investigate OOS results and/or laboratory atypical events

* Evaluate environmental data for adverse trends

* SOP development and review

* Direct support of regulatory inspections and audits

* Direct support of validation activities and all other associated quality functions

* Evaluate utility environmental monitoring data for adverse trends

* Assessment of facility and utilities for development of Performance Qualification requirements

* Preparation of Performance Qualification Protocols and Final Reports

* Review of HVAC documentation

* Support qualification of Environmental Monitoring equipment and calibration

*
Responsible for scheduling of sampling and oversite of EM Technician activities

Qualifications

Requirements:

* Bachelor in an Engineering or Science field

* 5 years experience within a quality assurance role supporting a GMP manufacturing process

Preferred:

* Understanding of aseptic processing, compliance requirements, and/or environmental monitoring practices in a GMP environment

* Strong leadership, teamwork and communication skills.

* Knowledge of CFR, Eudralex and other regulatory guidance specific to the pharmaceutical industry.

* Experienced in the methods and approaches of conducting environmental monitoring, product release and/or auditing

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 # QUA002782.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-Quality-Assurance-IPT-Coordinator-Job-NC-27701/1691719/169171916917192012-03-04Merck/MSDfull-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 role of Operational Coach at Merck's Durham facility is similar to a Manufacturing Supervisor role. The individual in this role provides leadership, cross-functional development and technical expertise to operations and administrative support personnel in various stages of team development in the manufacturing and/or packaging of Durham live virus vaccine products. Responsible for operations teams, process and/or packaging equipment and all activities affecting them. Maximizes the potential of all team members. Fosters an environment that allows for progressive, continuous improvement of skills and honest, open feedback. Ensures team members have tools available to them to accomplish the team's mission statement.

EMPLOYEE DEVELOPMENT/PEOPLE MANGAGEMENT

* Coaches Bio-Process Technicians in an Empowered Culture
* Assists the team with development of objectives and ensures alignment with site goals;
* Assesses employee training/development needs, assesses the maturity of the team, and adjusts leadership style to enhance team performance;

LINE PERFORMANCE

* Support the start-up, IQ, OQ, PQ and PPQ for the Varicella Bulk Facility Expansion (VBE)
* Troubleshoots equipment problems, identifies need for new equipment and/or modifications to existing equipment to optimize throughput and reduce process cycle times;
* Maintains qualification on all applicable equipment;
* Approves IQ/OQ/PQ/CC documents;
* Facilitates focus on continuous improvement activities;
* Oversees coordination of resources to implement suggestions/ideas of merit;;
* Manages adherence to Merck Production System (MPS) metrics, design standards and performance utilizing downtime tracking, MOE, SMED, and other available tools;
* Oversees coordination of preventive maintenance, reactive maintenance and plant shutdown activities;
* Participates in Event Management and Renewal

INFORMATION TRANSFER

* Attends departmental and team meetings focused on equipment/process improvement;
* Serves as operations representative for technical group discussions;
* Participates in Daily Walk Through of IPT (Integrated Process Team), and in plant tours as needed

COMPLIANCE

* Provides input review and approval for atypical , observation, and process capability investigations;
* Completes bulk accountability investigations;
* Reviews and approves safety investigations;
* Participates in internal and external audits and inspections;
* Identifies quality-related trends and facilitates implementation of corrective actions

FINANCIAL

* Participates in development of profit plan and EAs;
* Reviews and oversees charges;
* Assures IPT headcount is accurate and meets production and company needs.
* Determines appropriate work centers/staffing for new products, and provides input into development of capital plans

Qualifications

Education:

Bachelor's degree in science or engineering field.

Required:

* Minimum 4 years coaching/supervisory experience.
* Minimum 6 years experience in a manufacturing role in an FDA regulated environment.
* Demonstrated leadership, interpersonal, technical aptitude, and problem solving skills.
* Strong team skills, including ability to coach/develop work teams, provide training, motivate/empower others, and resolve conflict.
* Must be flexible and able to manage multiple priorities.
* Must be goal-oriented and able to manage risks.
* Good verbal and written communication skills.

Desired:

* Previous experience in bulk vaccine production including cell culture, inoculation, growth, harvest and/or purification

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 # MAN001238.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-VBE-Start-up-Coach-Job-NC-27701/1517902/151790215179022012-03-04Merck/MSDfull-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.


Vaccine Manufacturing Science and Commercialization, Durham, NC

* Development and Transfer of analytical methods appropriate for the characterization and release of vaccines for both drug substance and drug product.
* Provide oversight and direction to Bionalytical Lean Laboratory operation from start-up to license and commercial product testing
* Provide oversight and direction for all Viral and Bacterial Vaccines Assay development, assay qualification, product and process characterization through precise analytic methods applications; in-process and final product testing.

o Included cell-based, molecular and other high-precision chromatography-based assays

o General assay trouble-shooting and improvement. Implementation of new testing schemes and approaches in Vaccines development and commercial manufacturing

* Profound experience in GMP Quality systems (including and not limited to assay method validation, specifications setting, applied Statistics) for release of drug substance and drug product for evaluation of vaccines in late stage of development and commercialization
* Direct experience in preparation of CMC sections for regulatory filings.
* Development and execution of in-process monitoring assays to support vaccines process and formulation improvements.
* Understanding of local testing requirements by global BoHs
* Transfer of analytical methods to or from global manufacturing sites in Europe, Asia-Pacific and Latin American Countries
* Management scope includes supervising and directing technical and routine assay support groups

Qualifications

Required:

* BS in Biochemistry, Industrial Biotechnolgy, Molecular Biology, Analytical Chemistry, Pharmaceutical Chemistry, or related field.
* Minimum 10 years Leadership / Managerial experience in applied Industrial GMPs required for Vaccine analytical and formulation development, particularly understanding of the real regulatory expectations for filing for approval and for filing for process/analytical changes with global boards of health

Preferred:

Master or Ph.D.

For the role is also expected that the prospective candidates have demonstrated career managerial and leadership success in:

* Managing budget processes to allocate resources wisely to meet company goals
* Have keen strategic thinking-from examining situations to interpreting information-and how to apply those on the job.
* Contributing to company's strategic planning process and then support strategic initiatives by developing and executing action plans.
* Identifying underlying issues related to decisions, generate and evaluate multiple alternatives, and then communicate and implement decision.
* Making a team genuinely work well together to improve business processes and meet goals associated with short and long term business strategies
* Master the art and science behind successful persuasion-and begin changing other people's attitudes, beliefs, or behavior to create win-win solutions.

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 # QUA002769.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Durham-Bio-Analytical-Laboratory-Director-Job-NC-27701/1708751/170875117087512012-03-04Merck/MSDfull-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 Tech 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.
* Provides oversight and final review of investigations to ensure adherence to cGMP's, rigorous technical content, and investigation clarity and completeness.
* 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 4 years experience in manufacturing or process/technical support role.
* Working knowledge of cGMP's 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.
* Demonstrated leadership and teamwork skills, experience managing and motivating teams, excellent analytical abilities, and proven written and verbal communication skills.

Preferred:

* 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.
* Experience with isolator filling, lyophilization, and automated inspection equipment/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 # MAN000705.

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


Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 2

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Durham-Technical-Support-Engineer-Job-NC-27701/950154/9501549501542012-03-04Merck/MSDfull-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.

As an Operational Coach, this role will provide leadership, cross-functional development and technical expertise to operations, maintenance and clerical personnel in various stages of team development in the manufacturing of Durham live vaccine products. Responsible for operations teams, process equipment and all activities affecting them. Maximizes the potential of all team members. Fosters an environment that allows for progressive, continuous improvement of skills and honest, open feedback. Ensures team members have tools available to them to accomplish the team's mission statement.

Because of the entry-level nature of this operations role, the incumbent will work closely with more senior members to accomplish the goals set forth for the operations team.

Major Responsibilities

Line Performance -

* Coordinates production/maintenance operation with minimal coaching support.
* Prepares daily work assignments and coordinates work team and human resource related activities.
* Gains and uses general knowledge of plant systems (equipment, financial, planning, etc.) to monitor and execute production schedules.
* Responsible for ensuring compliance to government regulations through a demonstrated understanding of SOP's and a general knowledge of company policies/guidelines, safety/environmental regulations, and GMP's.
* Coordinates resources to ensure that equipment remains in operating condition.
* Gains a working knowledge of the production process by becoming qualified to operate equipment.
* Serves as point of contact for respective area.

Compliance -

* Troubleshoots root cause of problems and identifies/implements corrective actions.
Completes quality observation investigations independently and atypical investigations with coaching support.

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.

Education :

B.S./B.A. degree required (science, engineering or other technical field preferred) OR minimum, Associate Degree with 10 years related technical industry experience required.

Desired :

* Demonstrated leadership, interpersonal, technical aptitude, and problem solving skills.
* Willingness to work off-shift and/or weekends
* Computer literacy in MS Office, Word, Outlook, Excel
* Strong team skills, including ability to coach/develop work teams, provide training, motivate/empower others, and resolve conflict.
* Must be flexible and able to manage multiple priorities.
* Must be goal-oriented and able to manage risks.
Good verbal and written communication skills.

merck.com/careers to create a profile and your resume for requisition # MAN001370.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1

Hazardous Materials
: Not Specified]]>http://jobs.merck.com/job/Durham-Bulk-Operations-Coach-Job-NC-27701/1703547/170354717035472012-03-04Merck/MSDfull-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.


Responsibilities include but are not limited to:

* Provide animal care and good husbandry practices, to include: feeding and watering, cleaning of animal cages, pens, rooms, and other quarters.
* Ensure the well-being of a variety of animals in accordance with SOP's and following compliance with the Animal Welfare Act.
* Receive training on Environmental Health & Safety, GLP, GMP, and OSHA standards.
* Provide feed and water daily, lifting feedbags or hay bales (up to 50 lbs). Clean animal quarters or cages with appropriate equipment such as hand washing or using non-mechanized/mechanized equipment including high-pressure spray equipment
* Capable of working in inclement weather conditions, capable of taking multiple on-site showers when working in certain buildings, capable of wearing full body coveralls, full face respirators and other tight fitting personal protective equipments.
* Make and record accurate test observations of animals. Maintain daily observation and housekeeping records in accordance with study protocol.
* Provide animal transport on and off site using livestock truck and trailer, skid loader and farm tractor (requiring on-site PIV certification).
* Other duties to be assigned.

This is a Monday - Friday, 1st Shift Position, over-time will be required including some weekends and holidays.

Qualifications

Education Minimum Requirement:

* High School Diploma or GED required, Associate degree or Veterinary Technician license preferred

Required Experience and Skills:

* Minimal one year experience working with animals required (small and large animals including poultry)

Desired Experience and Skills:

* Must possess strong communication and multi-tasking skills. Demonstrate ability to work well as team.
* Must have good understanding of USDA and Animal Welfare guidelines

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 # LAB000177.

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-NE-Elkhorn
Other Locations: US-NE-Omaha
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Animal-Care-Technician-Job-NE-68022/1655964/165596416559642012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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.


Responsibilities include but are not limited to:

* Responsible for the scientific leadership of projects providing guidance, data analysis, planning and interpreting results
* Provide in-depth knowledge and advice to research staff and management in the science of Poultry Virology
* Interface with Discovery and Technology (D&T) in the planning and delivery of products and new technologies transferring from D&T into R&D, as needed
* Assists with the intellectual property (patents/product information) to meet corporate guidelines
* This position will require strong knowledge of Virology and basic knowledge of Molecular Virology, in addition to the general Qualifications.
* Experience in Poultry product development will be highly desirable.

Qualifications

Education Minimum Requirement:

* M.S. with at least 7 years vaccine development experience including parasite vaccines.

Preferred Education Requiment:

* Ph.D. degree in Virology, Microbiology, Veterinary Science or related biological field
* D.V.M. or equivalent with at least 2 years research experience in virology

Required Experience and Skills:

* Ability to manage cross-functional teams and provide direction and training to less experienced colleagues
* Good project management skills. Must have aptitude to manage technical and logistical aspects of assigned research projects.

* Must have aptitude to provide interdepartmental leadership in product development and licensing; chair interdepartmental team meetings.

* Good problem-solving and decision-making skills.

* Knowledge of government regulations required for product licensure.
* Strong oral and written communication skills and appropriate computer skills.

* Must be able to work effectively with upper management and manage intra- or inter- departmental teams.

Desired Experience and Skills:

* Preference will be given to candidates with Molecular Virology background and at least 3 years vaccine development industry experience.

*
Knowledge of manufacturing processes is preferred.

*
Experience in working with animals in vaccine development research 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 # BIO003359.

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-NE-Elkhorn
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Sr_-Scientist-Virology%2C-Bio-Research-Elkhorn%2C-NE-Job-NE-68022/1463444/146344414634442012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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.


At Merck Animal Health's facility in Elkhorn, Nebraska, we currently have an Environmental, Health, and Safety Manager (EHS Manager) position available supporting the Nebraska Operations.

The successful candidate will be responsible for ensuring facility compliance with all local, state, federal and corporate guidelines as they pertain to Environmental, Health and Safety Activities. The EHS Manager is accountable for implementing and maintaining site level EHS programs, including the recognition and reporting of any potentially deficient situations/conditions with recommended corrective actions. This position requires good interpersonal skills to develop a cooperative relationship with colleagues, the ability to maintain confidentiality, and the ability to manage a complex workload.

The primary responsibilities are as follows:

* Provide leadership and management of site EHS programs, including routine assessments, facilitating corrective measures, as necessary and anticipating program needs based on relevant business conditions and developments
* Interact and communicate with corporate and site EHS, Compliance, Quality Assurances, Technical Services, Engineering, Manufacturing, Research & Development and Distribution representatives.
* Work with local, state, federal and corporate representatives in conducting and completing audits and corrective actions
* Ensure the improvement and implementation of site specific environmental, health and safety training to meet facility needs; including regulatory and best management practices.
* Conduct proper investigations to determine root cause for all facility incidents, spills, accidents, near misses, and injuries to prevent recurrence
* Coordinate the proper handling and disposition of facility waste materials.
* Advise management on upcoming environmental, health and safety regulations.

Due to the dynamic nature of our business, we are looking for a candidate who can do the following:

* Demonstrate integrity, credibility, and flexibility in their daily performance so as to motivate others to do the same.
* Collaborate with team members to identify and implement continuous improvement initiatives.
* Stay abreast of new technologies and trends of EHS
* Coach colleagues on company EHS values and opportunities

Qualifications

Minimum Education Required:

* BS Degree in Science, Engineering, or other relevant discipline or equivalent required

Preferred Education Required:

* MS Degree in EHS or Engineering strongly preferred

Minimum Skill or Experience Required:

* Minimum 5 years experience in the Animal Health, Manufacturing or Pharmaceutical Industry
* Minimum 3 years supervisory experience required
* Must be knowledgeable of Federal and State OSHA, EPA, and EHS laws and regulations
* Excellent communication, interpersonal, and organizational skills
* Leadership and teambuilding skills, with a focus on coaching and mentoring
* High analytical and logical problem solving abilities
* Ability to prioritize, focus on and obtain business results
* Flexibility to perform various tasks to support the business

Desired Skills and Experience:

* Experience with either multi-location or remote facilities preferred
* Six sigma Yellow or Green Belt certification preferred
* Proficiency in SAP and Microsoft Office 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 # IND000135.

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-NE-Elkhorn
Other Locations: US-NE-Omaha
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkhorn-Environmental-Health-&-Safety-Affairs-Manager-Job-NE-68022/1655965/165596516559652012-03-04Merck/MSDfull-timeUSDstarting0BSElkhorn, 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.


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:

* Prior work 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, or resolving manufacturing anomalies.

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 # MAN001212.

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-NC-Durham
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/Durham-Technical-Support-Engineer-Job-NC-27701/1479908/147990814799082012-03-04Merck/MSDfull-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

· 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.

Primary Location: US-NC-Durham
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: BL2 Micro organisms]]>http://jobs.merck.com/job/Durham-Laboratory-Analyst-EM-Laboratory-Job-NC-27701/1553316/155331615533162012-03-04Merck/MSDfull-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 MES Engineer is responsible for the technical development and support of a Manufacturing Execution System (MES) at the Vaccine Manufacturing Facility in Durham, NC. The Werum PAS-X MES system is the Merck standard electronic batch record (EBR) system used to document the manufacturing process steps. Use of the EBR will ensure cGMP compliance and data integrity of the systems and batch record. As part of a plant team, the engineer will provide direct process support for the manufacture of vaccine products using the MES system in an aseptic environment. Must embrace and help to establish an empowered team culture, including significant interaction on automation-related activities with manufacturing, material management, and quality. Also responsible for systems administration support of the local MES system.

Primary Activities include, but are not limited to:

* Constructs the content of VBF Master Batch Records (MBRs) with knowledge of vaccine products and critical process parameters (CPPs). Creates and maintains alignment between MBRs, corresponding SAP Production Variant and DeltaV recipes.
* Provides input to the MES development process team on technical aspects of MES functionality and becomes functional expert in the MES product application.
* Analyzes, defines and documents requirements for process interfaces, material flow, batch reporting, and operating procedures.
* Executes the appropriate change control documentation to assure the MES system is in a state of control and compliance.
* Develops and executes a comprehensive MES training strategy including identification of programs needed, the overall content of programs, the delivery methods and schedule.
* Assists in system administration for local MES solution
* Assists with troubleshooting and efficiently resolving manufacturing problems. Effectively develops and implements corrective actions to unplanned manufacturing events to ensure a consistent and reliable supply of vaccine products.
* Identifies and implements technology-driven productivity improvements. Exhibits behaviors focused on maintaining process consistency.
* Provides on-floor support of manufacturing activities
* Helps to foster empowered teams to achieve site mission, vision and goals through:
* Efficient and safe operation of process systems
* Compliance with current Good Manufacturing Practices
* Production of product that is safe and efficacious
* Supports all quality and safety initiatives.

Qualifications

Education:

* B.S., B.A., or M.S., preferably in Engineering, Science, or Information Technology

Required:

* Minimum 6 yrs of experience in Process Automation, Production, Technical Operations or equivalent is required.
* A positive Varicella titer is required prior to start date.

Preferred:

* Experience in Manufacturing Execution Systems and shop floor automation
* SAP ERP System Implementation and use in a GMP environment
* Emerson DeltaV
* Data base administration
* Crystal Reports
* Aseptic processing/sterile manufacturing
* Lean Manufacturing /Six Sigma 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 # TEC000436.

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-NC-Durham
Employee Status: Regular

Travel
: No
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-MES-%28Mfg_-Execution-Systems%29-Engineer-Job-NC-27701/1691721/169172116917212012-03-04Merck/MSDfull-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.

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-IPT-Quality-Assurance-Coordinator-Job-NC-27701/1689827/168982716898272012-03-04Merck/MSDfull-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.

As an Operational Coach, this role will provide leadership, cross-functional development and technical expertise to operations, maintenance and clerical personnel in various stages of team development in the manufacturing of Durham live vaccine products. Responsible for operations teams, process equipment and all activities affecting them. Maximizes the potential of all team members. Fosters an environment that allows for progressive, continuous improvement of skills and honest, open feedback. Ensures team members have tools available to them to accomplish the team's mission statement.

Because of the entry-level nature of this operations role, the incumbent will work closely with more senior members to accomplish the goals set forth for the operations team.

Major Responsibilities

Line Performance -

* Coordinates production/maintenance operation with minimal coaching support.
* Prepares daily work assignments and coordinates work team and human resource related activities.
* Gains and uses general knowledge of plant systems (equipment, financial, planning, etc.) to monitor and execute production schedules.
* Responsible for ensuring compliance to government regulations through a demonstrated understanding of SOP's and a general knowledge of company policies/guidelines, safety/environmental regulations, and GMP's.
* Coordinates resources to ensure that equipment remains in operating condition.
* Gains a working knowledge of the production process by becoming qualified to operate equipment.
* Serves as point of contact for respective area.

Compliance -

* Troubleshoots root cause of problems and identifies/implements corrective actions.
Completes quality observation investigations independently and atypical investigations with coaching support.

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.

B.S./B.A. degree required (science, engineering or other technical field preferred) OR minimum, Associate Degree with 10 years related technical industry experience required.

Desired :

* Demonstrated leadership, interpersonal, technical aptitude, and problem solving skills.
* Willingness to work off-shift and/or weekends
* Computer literacy in MS Office, Word, Outlook, Excel
* Strong team skills, including ability to coach/develop work teams, provide training, motivate/empower others, and resolve conflict.
* Must be flexible and able to manage multiple priorities.
* Must be goal-oriented and able to manage risks.
Good verbal and written communication skills.

merck.com/careers to create a profile and your resume for requisition # MAN001371.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1

Hazardous Materials
: Not specified]]>http://jobs.merck.com/job/Durham-Bulk-Operations-Coach-Job-NC-27701/1703548/170354817035482012-03-04Merck/MSDfull-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 are currently looking to fill the role of COE/GFS Support Specialist. This role performs advanced administrative tasks for Center of Excellence (COE) and Global Support Functions.

* Conducts research, analyzes and reviews data, and recommends action from various reports and/or statistics.
* Troubleshoots and resolves problematic systems and processes.
* Develops reports, tables, graphs, presentations and correspondence.
* Demonstrated knowledge of Microsoft programs (Word, Excel, PowerPoint, etc) required.
* May be responsible for various systems and requires in-depth knowledge of specialized confidential software applications such as Employee Data Management [SAP], Job Placement [Career Link], Financial systems [ SAP and my eTrip], SOP administration system [MIDAS] , CMMS [Maintenance Management], MRP [Materials Requirement Planning], MES [Manufacturing Execution System], LIMS [Laboratory Information Management System], etc.
* May be responsible, where applicable, for coordinating various events such as regulatory inspections, and environmental regulatory programs.
* Performs advanced administrative tasks for Plant Leadership Team, Integrated Process Team (IPT) and/or Center of Excellence (COE), including coordination of communication and assignments.
* Produces/completes various assignments requiring advanced analytical ability, independent judgment, creativity and problem solving skills.
* Coordinates special projects within the area/division. Provides functional guidance to individuals and work groups at the Durham site.
* Coordinates and/or facilitates key meeting and schedules

.

In addition, the following characteristics/traits are inherent to this role:

* Work priorities and activities are performed independently with minimal supervision.
* Communication skills must be at a level to effectively interact with internal/external customers to manage projects, assignments, and workflow.
* General administrative duties constitute approximately 30% of job responsibilities that include meeting/calendar management,
* Position may include business unit specific assignments; i.e., SOP administration, CMMS database, coordination of environmental regulatory programs, coordination of regulatory inspections, MRP system, etc.
* Assist with the coordination of community relations.

Please note, this position may require additional overtime hours to be worked.

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.

Required:

* Minimum of 3 years minimum administrative experience.
* High School Diploma/GED
* Advanced computer skills including the use of various software suites (MS Office, SAP, etc.) and hardware (scanners, faxes, etc.)
* Ability to perform complex administrative functions.
* Excellent verbal and written communication skills.
* Flexibility and the ability to work with a diverse group in a self directed work group.

Preferred:

Associate or higher degree in a business or science field

merck.com/careers to create a profile and your resume for requisition # ADM005018.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-COEGFS-Support-Specialist-Job-NC-27701/1691725/169172516917252012-03-04Merck/MSDfull-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 role of Detailed Scheduler at Merck's Durham facility is within VBF Operations' manufacturing support group. The individual provides expertise in the coordination of resources and equipment for the manufacture of live virus vaccine products. The individual has in-depth knowledge of equipment and processes. He or she must be able to identify and communicate improvement opportunities and results. Recognized as the subject matter expert, the detailed scheduler will also function as the liaison to Planning, Maintenance and Finance to name a few.

Line Performance

· Monitors forecast and delivers Production Schedule

· Assists coaches in identifying key equipment availability, training opportunities and allocates them accordingly

· Identifies opportunities to optimize throughput and reduce process cycle times

· Facilitates focus on continuous improvement activities

· Coordinates resources to implement suggestions/ideas of merit

· Assists in creating and continuous tracking of Merck Production System (MPS) metrics, designing standards and performance utilizing downtime tracking and available lean tools

· Coordinates preventive maintenance, reactive maintenance and plant shutdown activities

· Participates in Event Management and Renewal

Information Transfer

· Attends departmental and team meetings focused on equipment, process and training improvement

· Serves as operations representative for schedule change discussions

· Reports plan versus actuals

Compliance

· Completes accountability investigations

· Participates in safety initiatives and safety investigations

· Participates in internal and external audits and inspections

· Assists in identifying and Communicates quality-related trends and facilitates implementation of corrective actions

Financial

· Participates in development of profit plan and asset utilizations

· Reviews and oversees charges

· Assists in determination of appropriate work centers/staffing for new products, and provides input into development of capital plans

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.

Bachelor's degree in science or engineering fields.

Required:

* Must be flexible and able to manage multiple priorities
* Demonstrated interpersonal, technical aptitude and problem solving skills

Desired:

* Planning and/or detailed scheduling experience
* Experience with SAP and planning software. Experience with MRP/ERP systems
* Manufacturing experience with high-volume and Lean operations
* Prior work experience in a cGMP manufacturing environment

merck.com/careers to create a profile and your resume for requisition # QUA002789.

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-NC-Durham
Employee Status: Regular
Number of Openings: 1

Hazardous Materials
: Not specified]]>http://jobs.merck.com/job/Durham-Detailed-Scheduler-Job-NC-27701/1703552/170355217035522012-03-04Merck/MSDfull-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 a highly motivated individual to fill the entry level IPT Quality Assurance Coordinator role.

This role will allow you to apply your academic background to vaccine manufacturing operations and expand your skills in the area of Quality Assurance. Additionally, you will have the opportunity to learn aspects of pharmaceutical manufacturing which includes processes, procedures and policies.

You will have the responsibility for the following
DUTIES:

* Support the release of Product through the review of Batch Records and support process documentation
* Work on special projects
* Support the release of incoming supplies and raw materials

As you develop in your role, you will have the opportunity to provide support of regulatory inspections, internal corporate audits and participate in investigations.

Qualifications

Requirements:

* Bachelor of Science or Bachelor of Art's Degree with 5+ years relevant experience

Preferred:

* One (1) year of Experience in a Quality Assurance role supporting a GMP Manufacturing Process
* Understanding of Aseptic Processing, Compliance Requirements, Pharmaceutical Documentation and/or Environmental Monitoring

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 create a profile and your resume for requisition # QUA002274.

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-NC-Durham
Employee Status: Regular
Number of Openings: 3

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/Durham-IPT-QA-Coordinator-Job-NC-27701/1197416/119741611974162012-03-04Merck/MSDfull-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.

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/Durham-Technical-Support-Engineer-Job-NC-27701/1281991/128199112819912012-03-04Merck/MSDfull-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 Instrumentation Technician is responsible for providing instrumentation and controls support for the vaccine operations areas (weigh/dispense, media, stabilizer/prep, thaw/pool, filling, capping/inspection, etc.) located in aseptic and clean room environments. The instrument technician works within a team to perform maintenance and troubleshooting activities. Evaluates instrumentation performance, completes calculations, and resolves deviations. Develops standard operating procedures (SOPs) and preventative maintenance (PM) plans/calibration procedures, as required. Follows proper procedures for maintaining equipment, supplies and facilities in a clean room environment. Responsible for written documentation of activities. Actively supports, participates and embraces an empowered team culture including significant interaction with Quality, Technical Operations, Engineering and other support groups.

Must be flexible to perform all of the following functions and other tasks as needed:

* Design, assembly, installation, adjustment, testing, cleaning, calibration, maintenance, repair and troubleshooting of plant instrumentation and electronic systems such as controllers, transmitters, indicators, plant and laboratory analyzers, and weighing systems
* Perform on-going maintenance of aseptic/clean room area
* Follow instructions for completion of job tasks.
* Complete written documentation of work performed.
* Provide training to other site personnel
* Flexible schedule required to support start-up activities
* 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 procedures(cGMP), safety and environmental requirements/regulations/guidelines
* Effective communication

The successful candidate for this position will work day light hours in the beginning of his/her employment however it will be required to move to a non-day light shift position on a regular basis (12 hour night shift). You must be willing to be able to work in this capacity.

Qualifications

Education:

High School Diploma or GED required

Required:

* Operation/use of general hand and power tools, instruments and testing apparatus common to the electronic and instrumentation fields
* Ability to read P&ID's, electrical drawings, blueprints, PLC ladder logic, etc
* Effective calibration/troubleshooting skills
* Ability to communicate and work in a highly effective team environment
* Ability to manage multiple priorities and advance several tasks in parallel
* Demonstrated mechanical aptitude

Desired:

* Experience in aseptic or GMP/regulated manufacturing environment
* Ability to work with and troubleshoot computer control equipment, including Programmable Logic Controllers (PLCs) and Distributed Control Systems (DCS)
* Knowledge of SAP 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 #PRO009247.

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-NC-Durham
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/Durham-Instrumentation-Technician-Job-NC-27701/1689828/168982816898282012-03-04Merck/MSDfull-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

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 2]]>http://jobs.merck.com/job/Durham-Production-Associate-Job-NC-27701/1528616/152861615286162012-03-04Merck/MSDfull-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.


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-27701/963995/9639959639952012-03-04Merck/MSDfull-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.


Primary responsibility is to ensure cGMPs are utilized for all batch documentation and the day to day operation of areas. Conducts batch record reviews and audits. Supports sampling requirements for several areas. Performs quarantine functions and accountability reviews. Supports special projects as assigned. Supports GMP audit functions as required. Conducts complaint investigations as required.

Primary Activities:

Follows cGMP and routinely makes decisions/resolves issues using cGMP/process knowledge. Works with customers to resolve problems and to satisfy quality and production needs. Follows site safety requirements. Authors, reviews, and or approves data, and documents such as methods, procedures,and protocols. Completes assigned projects. Performs all work in a timely basis and is an active member of 1 or more teams.

Conducts 100% batch record reviews. Audits production areas for compliance to manufacturing formula, process, and for compliance to procedures. Audits other areas to assure conformance to procedures and cGMP's. Performs statistical sampling procedures to monitor and to ensure product quality. Follows American National Standard sampling sheets, SOP's, forms, change controls, PM/PV masters. Authors annual reviews. Represents QA at various manufacturing meetings.

Qualifications

Required:

Bachelor's degree required, concentrations Chemistry, Microbiology or other science related field preferred. Position supports 24x7 operations on a rotating shift schedule.

Minimum of 2 years manufacturing experience 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 # QUA002786.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/Elkton-QA-Project-Operations-Analyst-Job-VA-22827/1703553/170355317035532012-03-04Merck/MSDfull-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.


Performs analytical testing and second person review in a Quality Control laboratory on a variety of samples including drug substance, drug products, and/or incoming materials. Prevalent techniques include HPLC, GC, CE, UV/Vis, gravimetric, titrations and others. In addition to testing the Analyst is responsible for technical and administrative support for a team of 2 - 4 laboratory technicians. Works closely with laboratory team members to ensure the highest levels of GMP compliance and inspection readiness. Routinely participates in laboratory related activities such as validation, qualification, report writing, deviation investigations, training, and others. Must be able to work independently in an open team environment and have strong problem solving and communication skills.

Requires shift work, 12 hour rotating schedule that includes weekends

Qualifications

Required

* Bachelor degree in Chemistry, Biology or related area
* Minimum 3 years of analytical laboratory experience.
* Strong problem solving skills

Preferred

* Pharmaceutical testing experience
* Knowledge of relevant cGMP's
* LIMS and chromatography experience
* 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 # QUA002758.

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
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/Elkton-QC-Lab-Analyst-Job-VA-22827/1670757/167075716707572012-03-04Merck/MSDfull-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 Clinical Research Manager (CRM) position based in Summit New Jersey reports directly to the Director of US Clinical Research. The primary function of this CRM position is to design, coordinate, monitor, and report pre-clinical and clinical field studies that will support the approval, primarily in the USA, of new companion animal and livestock products. The position requires the candidate to be responsible for Good Clinical Practice (GCP) field studies, and occasionally Good Laboratory Practice (GLP) studies.

Other responsibilities include but are not limited to:

* Responsible for the creation and implementation of clinical development plans
* Responsible for the conduct of pre-clinical and clinical field studies
* Supports post-approval activities

Qualifications

Minimum Education Requirement:

* A Master degree may be sufficient with five years of relevant industry experience.

Preferred Education Requirement:

* DVM or Ph.D. in veterinary science, animal science, or related area.

Required Skills and Experience:

* Minimum three (3) years experience in designing and conducting pre-clinical and / or clinical field studies that supported the regulatory approval of new companion animal or livestock products.

* Must have demonstrated strong ability in scientific writing.

* Must have demonstrated strong ability to communicate effectively with both technical / professional and lay persons and also individuals with diverse backgrounds in the animal health field.

* Must be able to work in a team environment and lead a team of professionals to meet study objectives and company goals.

* Must be able to work independently and efficiently in a matrix organization (project team environment).

* Must have strong organizational skills and have strong attention to detail.

* Must have strong problem solving and communicative skills necessary to resolve issues and misunderstandings inherent of conducting regulatory-based clinical and pre-clinical studies.

* Must be able to combine technical background and training with a thorough knowledge of internal procedures and policies as well as government guidances and regulations.

* Must be proficient in MS Word, Excel. Knowledge of Power Point, SharePoint, and Adobe Acrobat applications preferred.

* Must be able to travel primarily nationally. Travel requirements will vary greatly depending on study activities (0% to 50%).

Preferred Skills and Experience:

* Although this CRM position does not supervise other individuals, previous managerial or supervisory experience is valued

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 # CLI002552.

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
Employee Status: Regular

Travel
: Yes, 50% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Summit-Manager%2C-Clinical-Research-Job-NJ-07901/1596742/159674215967422012-03-04Merck/MSDfull-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.


Merck is seeking Respiratory Product Development Interns and Co-Ops for our R&D facility in Summit, New Jersey. In this role, you will help transform molecules from discovery into marketed products (e.g., NasonexÒ, AsmanexÒ, DuleraÒ) that will enhance millions of lives.

The professional in this position will support the formulation, process, and analytical development of high priority drug candidates. You will design and perform studies to characterize key physical and chemical properties of pharmaceutical materials (e.g., active drug substances) and/or formulated drug products (e.g. dry powder inhalers, meter dose inhalers, nasal sprays). You will work as part of a team to develop and implement new formulation technology, manufacturing processes, process analytical technology (PAT), and/or novel analytical methods to guide product development. You will use novel approaches to solve challenging technical problems related to drug product performance, inhalation devices, stability, and manufacturing. Techniques often used by persons in these positions include separation techniques (e.g., UPLC, HPLC, GC), general/wet chemical methods, PAT, physical characterizations (e.g., particle size analysis, SEM and light microscopy), spectroscopy (e.g., UV/Vis, NIR, THz), and thermal methods (e.g., DSC, TGA). Other responsibilities may include manufacturing of respiratory products in a research environment, statistical data analysis, simulation modeling, compliance with pharmaceutical good manufacturing practices and the preparation of technical reports, presentations, and external publications (as appropriate).

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/PhD in chemistry, pharmaceutics, chemical engineering, or a related discipline.
* Must be available for a period of 9-11 weeks, beginning June 2012.
* Candidate will have demonstrated good laboratory skills and a solid understanding of analytical and physical chemistry.

Preferred:

* Respiratory/inhalation related experience 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 #PRE000285.

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


Primary Location: US-NJ-Summit
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Summit-Respiratory-Product-Development-Intern-Job-NJ-07901/1703540/170354017035402012-03-04Merck/MSDfull-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.


We currently have an exceptional career opportunity for a scientist in the area of Process Analytical Technology (PAT).

As a member of Global Science and Commercialization Technology-Analytical Chemistry in Development and Supply (GSTC-ACDS), you will be responsible for the following:

* Development and implementation of PAT methods supporting new and in-line products within Merck.
* Support strategic development and manufacturing initiatives, including Quality by Design and Lean Manufacturing.
* Work closely with various teams and departments across the company to support the development and technology transfer of advanced in-line, on-line, and at-line tools for the assessment of chemical and physical product and process parameters.
* Support the entire spectrum of the Merck product portfolio, including developing PAT applications for vaccines, biologics, and small molecule drug product manufacturing processes in the worldwide Merck research, commercialization, and manufacturing supply sites.

Qualifications

Education:

* B.S/M.S./Ph.D.

Required:

* Bachelor's Degree must have 8 years industrial experience
* Master's Degree must have 4 years industrial experience
* Ph.D can have between 0 - 15 years of industrial experience.
* Must possess diverse range of backgrounds and skill sets (Analytical Chemistry, Chemical Engineering, Biotechnology Engineering) are encouraged to apply due to the multidisciplinary nature of the position.
* Must have hands on experience with Process Analytical Technology (PAT).

Preferred:

* Demonstrated interest/experience in manufacturing process development and/or characterization of small molecules or 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 # CHE003272.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Summit-PAT-Senior-Analytical-Chemist-Job-NJ-07901/1490584/149058414905842012-03-04Merck/MSDfull-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.


In addition to developing and enhancing your analytical acumen, you will gain hands on experience interacting with retail customers and Merck sales teams. Additionally, you will be able to take advantage of the extensive professional and career development opportunities we offer.

MCC is seeking qualified individuals to fill a Retail Customer Business Analyst (CBA) that will be based in the Summit, NJ office supporting Alternate Channel.

Main areas of responsibility include:

* Sources, analyzes, and interprets account and marketing data in support of customer teams
* Analyzes and presents data on account, market and brand performance utilizing all sources of information.
* Develops category management analysis to customer teams and broker personnel
* Provides Planogram development, category data analysis , customer opportunity analysis to the customer and internal Senior Management
* Builds conceptual and tactical customer presentations
* Works with other CBA's and Customer Category Managers to share best practices

Qualifications

Education:

* Required: Bachelor's degree

Required:

* Minimum one (1) year Consumer Products Experience

Preferred:

* Proven knowledge, utilization and application of syndicated data
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 # PRE000267.

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
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Summit-Customer-Business-Analyst-Job-NJ-07901/1643322/164332216433222012-03-04Merck/MSDfull-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 team member within the Respiratory and Immunology group will be a member of a team of (4 to 7) scientists that uses biochemical, molecular, cellular and pharmacological techniques for the preclinical discovery and development of drug candidates for the treatment of respiratory and immunological diseases (e.g. asthma, rheumatoid arthritis).

The responsibilities of the team member include:

* Conducting preclinical experiments to support drug discovery efforts for new therapeutics at different stages of development including target identification and validation, lead identification and lead optimization
* Designing and executing preclinical research efforts to support the clinical development small molecule candidates
* Generating and integrating data from molecular, biochemical and cell biology experiments towards the discovery and validation of target engagement, pharmacodynamic and efficacy biomarkers as well as lead identification and lead optimization of drug candidates
* Collaborating with members from other functional groups including In Vitro Pharmacology, In Vivo pharmacology, Medicinal Chemistry, Basic Pharmaceutical Sciences, and Exploratory and Translational Sciences
* Working with external academic, biotech, and contract research organizations.
* Monitoring the external research environment and helping establish collaborations that are consistent with R&I franchise and functional strategies.
* 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 the summarization and consolidation of experimental data
* Ensuring that this information is communicated in a concise, easy to understand manner to the appropriate teams and committees
* Managing the design of research protocols and the 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 R&I franchise discovery groups
* May have scientific management responsibilities of other scientists within their group

Qualifications

Education:

M.Sc. degree in biological sciences with ≥ (10) years industry experience or equivalent academic credentials

OR

Ph. D. (biological sciences), MD, or D.V.M. degree in with ≥ (2) years industry experience or equivalent academic credentials, such as post-doctoral research

Required:

* Subject matter expertise in the biology and pathophysiology associated with respiratory and or immunological disorders
* Subject matter expertise preclinical research approaches in respiratory and/or immunological research
* 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:

* Experience in target identification and validation for new respiratory and/or immunological therapeutic targets
* Experience in discovery of drug candidates at the preclinical stage

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 # BIO003344.

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-MA-Boston
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Boston-Team-Member-Respiratory-and-Immunology-Job-MA-02108/1567428/156742815674282012-03-04Merck/MSDfull-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 the recognized SME for Knowledge Engineering in the Knowledge Discovery/Knowledge Management (KDKM) Department, the candidate will be responsible for developing and executing KM strategy, including product/service portfolio definition and operations planning and delivery. Candidate will recommend a suite of preferred standards for knowledge engineering practice and develop policy to help ensure their use across the organization. Candidate will collaborate with colleagues in KDKM as well as other internal and external stakeholders to develop high-quality vocabularies, ontologies, associated repositories, and rule-bases in support of text mining, search, and knowledge engineering strategies.

Key business area stakeholders include but are not limited to KDKM franchise and function support researchers, the Licensing organization, Discovery organization scientists and project teams, the One-Merck Digital Library, and the Clinical Literature organization. The position will also collaborate with other support groups, including Informatics-IT, Project and Pipeline Management IT, and Innovation IT.

This position requires excellent leadership, written and oral communication, stakeholder management skills, and demonstrated experience delivering world-class knowledge engineering products/services in a pharmaceutical company.

Qualifications

Education:

BS/BA degree required, Ph.D. or equivalent experience in Knowledge Engineering with M.S. or equivalent experience in Natural or Life Sciences preferred.

Required:

A minimum of 5 years of experience in at least one Life Sciences area, plus broad drug R&D knowledge.

Preferred Skills:

Demonstrated ability to take on new projects and successfully deliver results in fast-paced, dynamic and multifunctional environments.

Proven record of innovative and critical thinking and excellent problem-solving ability.

Proven track record of high quality 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 # RES001252.

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-MA-Boston
Other Locations: US-NJ-Kenilworth, US-PA-West Point, US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Knowledge-Engineer-Lead-Job-MA-02108/1577188/157718815771882012-03-04Merck/MSDfull-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.


Under the general direction of the research veterinarian, the incumbent provides clinical and diagnostic technical support to achieve optimal laboratory animal health. The responsibilities also include the conduct of approved in vivo research protocols. The incumbent is able to apply fundamental principles, experience, and techniques to the solution of complex problems. Exercises a reasonable degree of initiative and independent in performing work. Provides training or guidance for one or more junior staff members or research staff in specific assignments. Exercises care to help insure personnel safety and animal welfare, in compliance with departmental Standard Operating Procedures (SOPs), MRL study requirements, and all applicable local, state and federal regulations and guidelines.

* Performs multiple animal surgical procedures; surgical and non-surgical procedural assistance along with surgical instrument and pack preparation; sterilization of instrumentation via various methods.
* Under the direction of the veterinarian, provides veterinary care for MRL research animals, including vaccination, grooming, and dental hygiene, consistent with professional standards. Assures compliance with all applicable federal, state, and local laws, regulations, and guidelines for animal care and use.
* Communicates effectively, both verbally and in writing, with departmental and research staff. Documents experimental data in technical notebooks or approved electronic formats. Maintains accurate, timely, and well-organized records.
* Initiates and pursues career development opportunities, including participation in recommended educational and training opportunities to expand skills and knowledge. Reviews the relevant veterinary, lab animal, and medical literature or order to advise and support the MRL community.
* Establishes and maintains collaborations with departmental and MRL research staff. This may include provision of professional and technical support for surgical model development, anesthesia protocols, various imaging modalities, and/or activities related to the pharmacokinetic drug metabolism assessment of test compounds. Assist in study design, data analysis and interpretation, and report generation.
* Maintains and provides inventory of surgical instruments, medical/surgical/procedural supplies
* Monitors the effectiveness of the environmental enrichment plan by performing regular behavior assessments of research animals. Provides feedback to senior staff on modifications needed to meet the behavioral needs of individual animals.
* Performs basic diagnostic testing procedures including sentinel animal processing, gross necropsy, microbiological testing, microscopy, parasitology, and other veterinary procedures.
* Is included in rotational weekend and holiday duty, including surgical animal care and treatments.

Qualifications

Education Minimum Requirement:

* Requires Bachelor's Degree in laboratory animal science, animal health technology, medical technology, biology, or a related life science.

Required Experience and Skills:

* A minimum of 5-7 years experience as an animal health technician or research technician
* AALAS certification as Laboratory Animal Technologist and participation in the certification Registry (RLATg) 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 # LAB000175.

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-MA-Boston
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Sr_-Veterinary-Associate-Job-MA-02108/1691717/169171716917172012-03-04Merck/MSDfull-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, translational informaticists. Successful candidates will have the opportunity to collaborate with talented and dedicated colleagues to make a difference to patient healthcare.

The Health Informatics Program Lead will be responsible for developing and managing partnerships and executing informatics programs relevant to utilization of real world, patient-driven, clinically-relevant data streams to enable Merck Research Labs drug discovery, development and commercialization objectives as part of Merck's Global Health IT strategy. This position will play a leadership role for Merck, representing Informatics in Merck's relationships with one or more partners and collaborating with Merck Global Clinical Development, Regulatory Affairs, the Chief Medical Office, IT organizations and other internal partners in realizing a coherent strategy for applying real world health data and capabilities to benefit Merck's R&D pipeline and patients with unmet medical needs.

Initial projects in the area of patient social networking will focus on psoriasis, expanding to other disease areas of interest to Merck's respiratory and immunology franchise. The program lead will be responsible for defining opportunities for deriving value and developing new informatics capabilities from patient social networking platforms and executing on and evaluating project outcomes in collaboration with functional area and therapeutic area teams. The role will also be responsible for identifying, evaluating, developing and executing on additional informatics partnership opportunities around consumer health and/or ubiquitous computing, particularly those taking advantage of existing Health IT partnerships, and may include working with Merck innovation and venture units to support informatics components of adjacency opportunities.

Qualifications

Education:

* Minimum of MS degree in medical informatics, health informatics, nursing informatics, biostatistics, bioinformatics, epidemiology, outcomes research, public health or other relevant field.

Required:

* A minimum of seven years of relevant work experience (can be obtained through school/industry) in clinical research informatics, health informatics, bioinformatics and/or drug discovery in an academic or industry environment.
* Significant experience with patient reported outcomes, real world outcomes, patient engagement and/or consumer health informatics in an academic, industry or healthcare setting.
* Outstanding written and verbal communication and presentation skills; excellent team-building and interpersonal/management capabilities; effective planning and organizational abilities.
* Demonstrated history as a self-motivating, productive, innovative, interdisciplinary leader in consumer 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 success at managing complex scientific partnerships and large multi-phase projects spanning multiple organizations
* Demonstrated ability to collaborate with external vendors and partner companies to develop innovative informatics and analytics solutions to meet emerging healthcare industry and patient/consumer needs.

Preferred:

* PhD
* Experience with mobile technologies, consumer health platforms and/or gaming approaches is highly desirable. Familiarity with patient social media is useful but not required.
* 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
* Experience and expertise in business development and/or organizational change management would be beneficial.
* Experience manipulating and analyzing large data sets.
* Disease expertise in the respiratory and/or immunology area would be beneficial but not 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 # QUA002720.

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-MA-Boston
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Program-Lead-Health-Informatics-Job-MA-02108/1603916/160391616039162012-03-04Merck/MSDfull-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 Boston Medicinal Chemistry department of Merck Research Labs is seeking 2 co-op students to take on a 6 months assignment. The successful candidate will work closely in a team environment at our state-of-the-art organic synthesis laboratory preparing and charactering new molecules of interest to the research program. The day-to-day work usually involve conducting multi-step synthetic sequencing techniques of chromatographic purification, H-NMR and mass spectrometry. Co-op students are expected to show presentation of results in both oral and written formats.

We are seeking co-op students with general computer knowledge, good communication and problem solving skills. Some basic laboratory skills preferred.

Merck Research Laboratories-Boston is located on the back of Emmanuel College campus. This is a full-time paid 6 month co-op assignment whereby a weekly stipend will be provided to the student. Housing subsidy is not available as part of this program and if housing is required by student, it must be funded 100% by the student.

Qualifications

Required:

* Pursuing degree in chemistry or a related field.
* Applicants must be available for full time employment for 6 months with target start date in June/July 2012.
* Applicant must be currently enrolled in an academic degree program and will be returning to school following this assignment.

Preferred:

* Candidates who have completed more than 2 years of college-level coursework are preferred
* Candidates with organic chemistry 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 #CHE003357.

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


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

Travel
: No
Number of Openings: 2]]>http://jobs.merck.com/job/Boston-Medicinal-Chemistry-Co-op-Job-MA-02108/1658088/165808816580882012-03-04Merck/MSDfull-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 Research Laboratories, an international pharmaceutical company, is currently seeking a Senior Scientist level position in the Biologics Therapeutic Protein Research Organization. In this role, you will assist in the transformation of high-priority biotechnology drug candidates from discovery into late stage development to enhance millions of lives.

In this position, the scientist will assist in development efforts for biotechnology therapeutic protein processes. The candidate will solve challenging characterization problems related to protein purification, fermentation, assay development, and product quality. This position will afford the selected candidate the opportunity to work in a leading edge department that utilizes a diversity of techniques including analytical, biochemical and biophysical methods to obtain and characterize proteins of interest.

The candidate should enjoy working both independently and with multidisciplinary research teams. The candidate should also take pride in communicating results effectively and clearly. Scientific excellence, team spirit, creativity, compliance with pharmaceutical best scientific practices, and enthusiasm for the drug discovery process are prerequisites for the position.

Qualifications

Minimum Education Requirement:

* PhD degree in Analytical Chemistry, Biochemistry or a related field

Minimum Skills and Experience:

* Proficient in developing HPLC-based analytical methods to support release and characterization testing of therapeutic proteins, in particular monoclonal antibodies

* Ion-exchange chromatography method development experience is required

* Experience developing methods suitable for use in a GMP laboratory

* Experience with isolation and collection of variants

* Experience with N- and/or O-glycan carbohydrate profiling

* Experience working on a cross-functional team

* Superior communication skills are Required -
verbal and written

* Prior experience (2-3 years) in the pharmaceutical industry

Desired Experience and Skills:

* Experience with project management 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 # RES001262.

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-Union
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Union-Sr-BioProcess-Analytical-Scientist-Job-NJ-07083/1646169/164616916461692012-03-04Merck/MSDfull-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.


This position is in a bioassay group responsible for the functional characterization of biopharmaceuticals in support of pre-clinical and clinical product development. Main responsibilities of this position involve the development of protein- and cell-based immunoassays and bioassays to assess biological activity or potency of biological product candidates for formulation development, stability studies and QC lot release. The successful candidate will be responsible for the development and qualification of bioassays or potency assays for evaluating receptor-ligand interactions, signal transduction pathways, effector functions of therapeutic antibodies or proteins. The candidate should have a strong background in cell biology and immunology with good understanding of in vitro assays for assessing biological activity of either therapeutics proteins or drug candidates. The candidate will also participate in the evaluation of cutting edge technology and development of novel assays. The candidate will be expected to communicate results effectively in presentation and written reports. The candidate will be expected to participate in cross-functional teams with Biologics Discovery Research and within Bioprocess Development and MMD manufacturing sites.

Qualifications

Education:

* Degree in Biological Sciences (e.g. Immunology, Biology, Cell Biology or related)
* Ph.D. with 0 - 5 years of experience in biological research or biologics development or MS with 5 plus years of relevant experience

Required:

* Experience with cell culture, immunoassays (e.g. ELISA, immunofluorescent assays, competitive binding assay, bioplex), and cell-based bioassays (e.g. cell proliferation assay, signal transduction assay, ADCC, CDC, apoptosis assay, gene reporter assays).
* Assay development experience at industrial settings or experience with GMP and method transfer to GMP labs is a plus.
* Must have good oral and written communication skills and ability to effectively work independently as well as within project 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 # BIO003432.

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-Union
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Union-Assay-Development-Senior-Scientist-Job-NJ-07083/1670753/167075316707532012-03-04Merck/MSDfull-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.


Position Overview

Utilizing information from Merck Research Labs (MRL) scientists and Merck Manufacturing Division (MMD) technology and quality personnel, the Senior Regulatory Coordinator prepares Chemistry, Manufacturing and Controls (CMC) sections for biotechnology product Clinical Trial Applications and Marketing Applications, and may assist with preparation of license supplements to existing biological product license applications (BLAs) or marketing authorization applications (MAAs) for US, Europe and most-of-world (MOW).

Under the direction of the Biologics CMC Site Lead, the Senior Regulatory Coordinator is responsible for implementing CMC regulatory strategies for Merck's biotechnology product franchise and Merck BioVentures in accordance with domestic and international regulations, and:

* Support project teams by providing strategic input into product development and supply plans and agency meetings. Serve as the regulatory CMC member of Integrated Development and Supply Teams and Global Regulatory Teams.
* Work independently to compile data and information in support of new and in-line biotechnology product licenses/registrations worldwide.
* Review proposed changes in the manufacturing, testing or packaging of a bio drug substance/product and provides recommendations regarding the potential regulatory impact on product registration.
* Manage product lifecycle by preparing documentation to assure compliance with existing registrations.

Qualifications

Educational requirements:

* B.S. in biological science or related engineering field (e.g. molecular biology, biochemistry, biochemical engineering, chemical engineering, mechanical engineering, or microbiology). Other fields may be considered, with appropriate experience.

Preferred:

* M.S. or Ph.D. in biological science or related engineering field (e.g. molecular biology, biochemistry, biochemical engineering, chemical engineering, mechanical engineering, or microbiology). Other fields may be considered, with appropriate experience.

Required skills and Experience:

* Minimum 4 years of experience in biological/pharmaceutical research or manufacturing to include activities directly related to manufacturing, testing, or licensure of biological or pharmaceutical products is required for this position.
* 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.
* Strong technical writing skills. Meticulous attention to detail.
* 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.
* Set clear priorities in support of departmental objectives. Demonstrates flexibility in responding to changing priorities or dealing with unexpected events.
* Demonstrated superior communication skills in multicultural settings and ability to communicate complex issues in a succinct and logical manner. Strong listening skills.
* Strong working knowledge of business systems and compliance requirements related to the manufacture of biologics.
* Demonstrated effective leadership, communication, interpersonal and negotiating skills.
* Understanding of the domestic and international regulations that govern the licensure of biotechnology products.
* Understanding of basic project management tools.
* Ability to clearly communicate complex scientific concepts, both in writing and orally.

Preferred:

* Regulatory CMC experience, especially with monoclonal antibodies or therapeutic 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 # REG000892.

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
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-19486/1691710/169171016917102012-03-04Merck/MSDfull-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 have an Internship opportunity within our Pharmaceutical Analytical Chemistry group located in West Point, PA location. The Intern in this role will have the opportunity to:

* Learn about essential drug development considerations, namely the impact of drug solubility, precipitation kinetics, and dissolution rate on bioavailability.
* Utilize standard analytical chemistry lab techniques , quantitative chemical analysis techniques (such as HPLC) and basic solid state characterization techniques (such as XRPD) to evaluate solubility of a range of compounds in medias that simulate human GI fluids.
* Optimize media composition to improve its ability to mimic conditions in the GI track, with the goal of developing a standardized media that can be prepared robustly and routinely.
* Participate in important research efforts aimed at strengthening the predictive power of in vitro models used to aid formulation development, thus minimizing reliance on animal studies.
* Interact with other technical and research groups.
* Learn new skills while advancing your academic career.

The Intern will also have the opportunity to work on general assignments or specific parts of overall projects related to:

* Process development support for the formulation of new products.
* Development and validation of methods for new Merck's products utilizing state-of-the-art technology.
* Investigating issues associated with manufacturing abnormalities.

This is a 9-11 week, paid internship beginning in June 2012. Housing will be provided to those who meet distance requirement.

Qualifications

Required:

* Candidate must be currently pursuing a minimum of a BS in Chemistry
* Candidate must have completed one year toward their degree
* Candidate must be available for a period of 9-11 weeks beginning in June 2012
* Candidate must be currently enrolled in a degree program as will return to school after the completion of the Intern assignment

Desired:

* GPA of 3.0 or higher

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 #PRE000276.

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


Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Analytical-Chemistry-Intern-Job-PA-19486/1703542/170354217035422012-03-04Merck/MSDfull-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.


Lead the design, development and implementation of a global digital library as part of the Knowledge Discovery/Knowledge Management (KD/KM) Library Services team. Develop the digital library strategy in alignment with KD/KM strategy to improve information access and decision-making throughout Merck.

* Partner with internal information management and information services groups across Merck to deliver a global, integrated "One Merck" Digital Library.
* Develop digital library strategy, design, delivery, and maintenance, and metadata schema management.
* Manage and implement digital rights management policies and practices in the digital library.
* Partner with KDKM and R&D leadership to translate business needs into functional project plans.
* Build and maintain leadership in the field of electronic content access, delivery, and use, including desktop applications, virtual workspaces, and mobile devices.
* Serve as the Merck subject-matter expert on techniques for information aggregation, organization, and linking.
* Benchmark the digital library against best practices, monitor usage and ROI.
* Manage digital library related vendors and outsourced operations.

Collaborate externally with standards bodies and content vendors to shape the development of emerging library products and services, including delivery platforms, digital rights management solutions, and APIs.

NOTE: Position can sit also in our KENILWORTH, NJ or RAHWAY, NJ locations.

Qualifications

Education:

* Minimum of a M.S. preferably in Information or Life Sciences

Required:

* Minimum of 5 years of experience developing and managing Digital Libraries.
* Knowledge of pharma related content resources and delivery platforms
* Demonstrated project and stakeholder management experience.

Preferred:

* Requires excellent leadership, communication, and stakeholder management skills
* Experience developing and managing Digital Libraries in the Pharmaceutical Industry.
* Demonstrated experience delivering world-class Digital Library Services capabilities in a pharmaceutical company.

* Sample problems include:

* Balancing multiple, competing, high-profile client/stakeholder requests against IT, budgetary, and time constraints.
* Providing guidance as a recognized Industry Expert on critical MRL projects
* Collaborating externally with vendors on the development of advanced content delivery tools and services to enable knowledge acquisition, search, and delivery.

* Excellent oral and written communication skills
* M.S. level knowledge and expertise in Information/Life Sciences
* Ability to design and deliver a Digital Library that will enable decision-making within, and collaboration between all levels of the 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 # RES001251.

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-Kenilworth, US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Digital-Library-Lead-Job-PA-19486/1566042/156604215660422012-03-04Merck/MSDfull-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 12 hour shift position (6am to 6pm) rotating days.

Qualifications

Education:

* Bachelor'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 # MAN001365.

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
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/West-Point-Manufacturing-Supervisor-Job-PA-19486/1705726/170572617057262012-03-04Merck/MSDfull-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 role of Operational Coach at Merck's Durham facility is a manufacturing leadership role. The individual in this role provides guidance, cross-functional development and technical expertise to operations and administrative support personnel in various stages of team development responsible for the manufacturing processes. They must become proficient in the use of plant systems to resolve issues affecting equipment performance, to minimize equipment downtime, and to ensure product quality. The individual will anticipate shifting priorities to meet customer needs and will identify the need for new equipment and/or modifications to existing equipment to optimize throughput.

This role will support the manufacturing process by providing leadership primarily in the area of sterile component supply. This includes ensuring on-time delivery of high-quality sterilized components and managing scheduling activities to meet that goal.

Employee Development/People Management

* Coaches production employees in an Empowered Culture
* Assists the team with development of objectives and ensures alignment with site goals
* Assesses employee training and development needs, assesses the maturity of the team, and adjusts leadership style to enhance team performance

Line Performance

* Identifies opportunities to optimize throughput and reduce process cycle times
* Facilitates focus on continuous improvement activities
* Oversees coordination of resources to implement suggestions/ideas of merit
* Manages adherence to Merck Production System (MPS) metrics, design standards and performance utilizing downtime tracking, MOE, SMED, and other available lean tools
* Must be able to identify and communicate improvement opportunities and results.

Information Transfer

* Attends departmental and team meetings focused on equipment/process improvement
* Serves as operations representative for technical group discussions
* Participates in Daily Walk Through of IPT (Integrated Process Team), and in plant tours as needed

Compliance

* Completes accountability investigations
* Reviews and approves safety investigations
* Participates in internal and external audits and inspections
* Identifies quality-related trends and facilitates implementation of corrective actions

Financial

* Participates in development of profit plan and forecasting
* Assures IPT headcount is accurate and meets production and company needs
* Determines appropriate work centers/staffing for new products, and provides input into development of capital plans
* Recognizes and investigates opportunities for financial savings

Qualifications

Education:

* B.S./B.A. degree required (science, engineering or other technical field preferred) OR minimum, Associate Degree with 10 years related technical industry experience required

Required:

* Minimum 1 year coaching/supervisory experience
* Minimum 2 years experience in a manufacturing role
* Must be willing to various shifts, including weekends.

Preferred:

* Aseptic manufacturing experience
* Experience in a regulated environment
* Manufacturing experience with high-volume and Lean operations
* Demonstrated leadership, interpersonal, technical aptitude, and problem solving skills
* Strong team skills, including ability to coach/develop work teams, provide training, motivate/empower others, and resolve conflict
* Must be flexible and able to manage multiple priorities

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 # MAN001156.

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


Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Durham-Operational-Coach-Job-NC-27701/1426294/142629414262942012-03-04Merck/MSDfull-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.

Primary Location: US-NC-Durham
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: BL2 Micro Organisms]]>http://jobs.merck.com/job/Durham-Laboratory-Analyst-EM-Lab-Job-NC-27701/1553317/155331715533172012-03-04Merck/MSDfull-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.

Position Description

Support Plant Engineering with trouble shooting, operating, and maintaining equipment which includes but not limited to HVAC equipment, water for injection systems, clean steam systems, compressed air systems, and chill/glycol water systems, BAS/PLC systems. Responsible for supporting MMD Divisional site mission by assuring quality of products and services are of the highest quality, optimal cost, and delivered on schedule. Responsible for supporting departmental vision that will provide for continuous improvement in all aspects of the operation. Must be able to function in a team-based empowered culture. Identifies and demonstrates a working knowledge of customers, suppliers and their requirements. Seeks ideas and information on how to improve customer service involving internal and external customers.

Major Responsibilities

* Support completion of Plant Engineering Projects (Capital and Expense)
* Responsible for assisting in the identification, development, and implementation of new systems which enhances the operation of Plant Engineering processes.
* Support site energy and EMAC initiatives
* Responsible for updating PE drawings and coordinating repairs utilizing in-house resources as well as outside contractors
* Facilitate HAZOPs and perform pressure safety valve calculation packages on an as needed basis.
* Perform engineering task as needed to maintain plant utilities equipment
* Responsible for assisting in the identification, development, and implementation of new systems which enhances the operation of Plant Engineering processes.
* Assist with trouble shooting Plant Engineering equipment on an as needed basis which includes but not limited to chillers, boilers, AHUs, AB programmable logic controllers, humidifiers/dehumidifiers, water systems, Square D controllers/monitors, clean steam generators etc.
* Develop technical documents (IQ, OQ, PQ, SOPs, Atypicals, Computer validation, etc.) that support the plant engineering processes.
* Develop & provide training to Plant Engineering mechanics involving equipment familiarization and trouble shooting on an as needed basis.
* Develops technical reports relating to equipment changes, reliability, downtime, efficiency, safety, and ROI

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.

Competencies/Leadership Behaviors/Skills: All positions require proficiency in the following competencies: Empowering leadership; Flexibility; Motivation; Functional Excellence; Teamwork/Collaboration; Results-Oriented; Problem-Solving; Communication. Actively supports, participates and embraces an empowered team culture

Other Requirements: (Knowledge; education/degree in what preferred field; min. years of experience in what work area; certification or license requirement, etc.)

Skills Required

* Extensive knowledge of industrial utility and building automation systems is required
* Proficiency in the use and knowledge of PCs (Hardware & Software) including project management, word processing, spread sheet applications, and Microsoft Windows platform is required.
* BAS, HVAC and instrumentation troubleshooting skills are essential: must possess the skills to be immediately effective in this area without further skills
* Must be able to read electrical prints, P&ID's, and understand P&ID control loops
* Strong technical skills
* Extensive industrial experience involving utility system generation, distribution and control are required, including a strong knowledge of steam, compressed air, refrigeration and water systems.
* This individual must have excellent documentation and verbal communication skills
* Must possess the ability to work effectively with peers, and display strong interpersonal and organizational skills.

Education Required

B.S. Degree in Mechanical or Electrical Engineering discipline preferred. Five years experience in Industrial Plant Engineering with emphasis on utility maintenance/operations, a working knowledge of BAS systems, instrument systems, plumbing systems, voltage distribution systems, steam systems, and all other Plant Utility Systems. Must have experience and a good working knowledge of good industrial maintenance practices. Must have good working knowledge of computer maintenance management systems.

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.

Primary Location: US-NC-Durham
Employee Status: Regular
Number of Openings: 1

Hazardous Materials
: Not Specified]]>http://jobs.merck.com/job/Durham-Utility-Engineer-Job-NC-27701/1705733/170573317057332012-03-04Merck/MSDfull-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 reports within the Merck Manufacturing Division, Global Technical Operations - Central Services organization and is responsible for providing technical support for the non-sterile dosage forms with the primary area of focus being oral solid dosage forms (tablet manufacturing, encapsulation and film coating experience required). The incumbent will work with the internal manufacturing sites within the Asia Pacific region to facilitate new and in-line technology transfer projects, develop and execute validation strategies, identify and support process improvement and value capture opportunities by utilizing six lean sigma tools and techniques, provide process and equipment trouble-shooting and root-cause analysis expertise, support change management process, and assist in equipment/facility upgrades and qualification. The incumbent will act as a liaison between the manufacturing plant personnel at multiple manufacturing sites and global technical groups to engage and solicit the support of relevant subject matter experts and leverage the technical knowledge across the vast global technical community when needed.

Key attributes for this position include:

* Expertise in non-sterile drug product manufacturing processes
* Root-cause analysis expertise
* Solid knowledge of cGMPs
* Good organization and communication skills
* Ability to work independently or as part of a cross functional team.

The position is based in US or Asia Pacific and requires 30-40% travel primarily within the Asia Pacific region.

Qualifications

Education Minimum Requirement:

* Bachelor's degree in Engineering or Science

Required Experience and Skills:

* Minimum of ten years of relevant experience in drug product manufacturing, development or related area
* Must be fluent in English

Preferred:

* Technical experience with manufacture of Oral Solid Dosage forms (tablet manufacturing, encapsulation and film coating experience) is desired.
* Additional language skills are 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 # ENG002329.

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: SG-Singapore-Singapore, US-PA-West Point
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Summit-Technical-Manager-Asia-Pacific-Region-Job-NJ-07901/1703537/170353717035372012-03-04Merck/MSDfull-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 with brand maketing and agencies to execute digital initiatives that were set forth from the organization and Center of Excellence. Educate and ensure all markets comply with best practices, guidelines, and policies.

Primary responsibilities will be to:

* Manage the implementation of digital assets (banner creative, online sponsorship assets, mobile apps and sites, websites and social media pages) with agencies, brand and Merck IT to ensure it executes on strategy, guidelines and best practices
* Develop and refine digital implementation best practices, guidelines and policies for website, SEO, social media, mobile, ad creative, etc.
* Apply optimization recommendations and findings from analytics agency to implement against digital campaigns and Merck assets
* Create white papers from the optimization recommendations and findings that would be applicable to local and regional markets (ie, Facebook ad buy, competitive branded keyword term bidding, etc)
* Assist in the development, mobilization and maintenance of the global KPI database
* Manage agency digital production projects in the US and core markets and provide counsel for all other markets
* Manage all digital production budgets for all agencies in the US and core markets, including agency fees, SOW, and projects. Additionally, this position will need to maintain a global view of digital budgets from all other markets
* Counsel all markets in the evaluation and selection of agency resources
* Work with Merck IT to implement all digital programs in the US and core markets and counsel other geographies on how to implement digital programs including the use of a CMS for website development

Qualifications

Education Requirement:

* Bachelor's degree required

Required Experience:

* Minimum of 5 years of work experience
* At least 3 years of digital experience
* Demonstrated experience in the production cycle of digital asset development: website, mobile, creative, etc.
* Ability to translate technical jargon into simple, easy to understand language.
* Strong leadership ability and previous client/agency relationship experience

Preferred Experience:

* Work independently and act as a change agent with strong influential 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 # MAR004128.

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
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-Social-&-Digital-Implementation-Job-NJ-07901/1700166/170016617001662012-03-04Merck/MSDfull-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.


Merck is seeking Respiratory Product Development Interns and Co-Ops for our R&D facility in Summit, New Jersey. In this role, you will help transform molecules from discovery into marketed products (e.g., NasonexÒ, AsmanexÒ, DuleraÒ) that will enhance millions of lives.

The professional in this position will support the formulation, process, and analytical development of high priority drug candidates. You will design and perform studies to characterize key physical and chemical properties of pharmaceutical materials (e.g., active drug substances) and/or formulated drug products (e.g. dry powder inhalers, meter dose inhalers, nasal sprays). You will work as part of a team to develop and implement new formulation technology, manufacturing processes, process analytical technology (PAT), and/or novel analytical methods to guide product development. You will use novel approaches to solve challenging technical problems related to drug product performance, inhalation devices, stability, and manufacturing. Techniques often used by persons in these positions include separation techniques (e.g., UPLC, HPLC, GC), general/wet chemical methods, PAT, physical characterizations (e.g., particle size analysis, SEM and light microscopy), spectroscopy (e.g., UV/Vis, NIR, THz), and thermal methods (e.g., DSC, TGA). Other responsibilities may include manufacturing of respiratory products in a research environment, statistical data analysis, simulation modeling, compliance with pharmaceutical good manufacturing practices and the preparation of technical reports, presentations, and external publications (as appropriate).

This is a paid 6 month co-operative assignment targeted to start in June 2012, whereby a weekly stipend will be provided. Housing subsidy is not available as part of this program and if housing is required it must be funded 100% by the student.

Qualifications

Required:

* Currently pursuing a minimum of a BS in chemistry, pharmaceutics, chemical engineering, or a related discipline.
* Student must be returning to school upon completion of Co-op.
* Applicant must be available for full-time employment for 6 months starting June 2012

* Candidate will have demonstrated good laboratory skills and a solid understanding of analytical and physical chemistry.

Preferred:

* Respiratory/inhalation related experience 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 #PRE000286.

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


Primary Location: US-NJ-Summit
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Summit-Respiratory-Product-Development-Co-Op-Job-NJ-07901/1703541/170354117035412012-03-04Merck/MSDfull-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.

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-07901/1525475/152547515254752012-03-04Merck/MSDfull-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 Human Resources Business Partner acts as a partner to Global Pharmaceutical Sciences and Clinical Supplies leadership team and will develop and implement effective human resources strategies programs or plans (organization design and effectiveness, change management, leadership and team development, talent planning and development, performance management, diversity etc) to support the areas overall business objectives. Additionally, this role will provide pull through support of Human Resources processes for Animal Health Research organization located in Summit NJ Facility.

Primary responsibilities of the business partner include but are not limited to:

* Provide Human Resources support to the Global Pharmaceutical Science and Clinical Supplies; participate in the development of strategic direction with the leadership team. Includes a solid understanding of the business strategy and recognition of implications on HR plans and programs.
* Partners with leaders to support business results by maximizing performance management, talent planning and development, and leadership development.
* Coach Leader and member of Leadership team to successfully manage all annual people management processes (performance management, talent management, compensation planning, etc.).
* Coach Leaders and Managers to improve leader effectiveness and teamwork.
* Execute change initiatives based on local client needs (retention, deployment, compensation, organizational design, etc.).

Qualifications

Education Minimum Requirement:

* Bachelor's degree in Human Resource Management or related field is required.

Required Experience and Skills

* A minimum of 7 years demonstrated HR experience in related fields ( eg: HR BP , Compensation, Benefits, Employee Relations)
* The ability to understand the business function's operating model, business priorities and talent needs. The ability to stay informed about the trends affecting the business, and to create HR/division management agreements based on them.
* The ability to understand and assess business needs and the relevant HR components impacted by the challenges. The ability to identify opportunities where HR processes, programs and initiatives can further the business strategy. The ability to translate HR issues clearly and articulately into business terms.
* The ability to build and maintain relationships with key customers and stakeholders, and to apply appropriate steps to understand the "customer's" problem, identify root causes and develop solutions based on data, facts and sound judgment..
* The ability to identify appropriate HR solutions to support business needs. The ability to appropriately utilize knowledge, tools, programs, and CoE specialists (e.g., Talent Management, Comp & Benefits), to sufficiently understand, adapt, create / co-create, innovate, recommend, gain buy-in for and deliver the appropriate solution.
* The ability to align leaders and employees, engage them, minimize risks, and maintain an open dialogue to enable them to adopt and accept the change.

Preferred Skills / Qualifications:

* MBA or Masters degree in Human Resource Management or Industrial and Labor Relations 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 # HR 000277.

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-NJ-Rahway
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Rahway-Human-Resources-Buisness-Partner-%28HRBP%29-Job-NJ-07065/1698522/169852216985222012-03-04Merck/MSDfull-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 support Merck's drug discovery in the department of In Vitro Pharmacology, focusing on development and implementation of high quality screening cell-based assays. Under scientific and administrative direction, the candidate is expected to grow, maintain and manipulate common cell lines, and primary cell cultures. The candidate will be responsible for the implementation of the reproducible cell-based assays and execution of the most appropriate semi- and fully automated assay standard procedures. The candidate will conduct laboratory procedures in compliance with established protocols and laboratory requirements. The candidate will provide analysis, evaluation and initial data interpretation. The candidate will work with other scientists within department and across functional teams to help to address In Vitro Sciences related issues in support of lead ID and lead optimization programs, and will provide scientific contribution to research programs including accurate determinations of compound potency, selectivity and mechanism of action.

Merck Research Laboratories-Boston is located on the back of Emmanuel College campus. This is a full-time paid 6 month co-op assignment whereby a weekly stipend will be provided to the student. Housing subsidy is not available as part of this program and if housing is required by student, it must be funded 100% by the student.

Qualifications

Required:

* Currently enrolled in a minimum of a Bachelor's program in: Life Sciences, Biotechnology, Pharmacology, or related field.

* This position requires hands-on expertise in the areas of cell culture and familiarity with cellular biological assays.

* Solid analytical and problem solving skills are essential for this position.

* Computer literacy (e.g. MS Word, MS PowerPoint)

Preferred:

* Experience with data analysis software programs 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 #BIO003435.

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


Primary Location: US-MA-Boston
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Cell-Pharmacology-Co-op-Job-MA-02108/1666992/166699216669922012-03-04Merck/MSDfull-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.


At Merck & Co., Inc Manufacturing facility in Elkton, Virginia, we currently have a Senior Process Protein Scientist position available in the Global Vaccine Technology & Engineering Center of Excellence. The Stonewall Plant 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 Stonewall Plant is a multi-discipline site for Merck & Co., Inc. The site currently operates processes to support Vaccine manufacturing (Fermentation and Downstream Purification), Active Pharmaceutical Ingredient manufacturing: Organic Synthesis, Traditional, Large Volume Fermentation, Bulk and Antibiotic processing. The site also has a newly installed high speed Finished Antibiotic filling line. Employees working at the Stonewall Plant have the opportunity learn many aspects of pharmaceutical, vaccine and chemical manufacturing.

Most recently, the Stonewall Plant has been afforded the opportunity to support Merck's work in Therapeutic Proteins (TP). The Senior Process Protein Scientist will play a key role in the implementation and establishment of TP process development and manufacturing at the site in support of both clinical stage, and commercial production. The person in this role will serve as a Subject Matter Expert and have the opportunity to function in a leadership role.

The Senior Process Protein Scientist will provide expertise in all areas of therapeutic protein assay and characterization through a variety of analytical methods including, but not limited to HPLC, LC-MS, immunoassays and other immunological based techniques, gel electrophoresis, size analysis, conformational studies, and peptide mapping by way of HPLC and other methodologies. The analyses will be conducted on samples obtained during and following bench, pilot and commercial-scale purification for the purpose of supporting clinical evaluations (Phase III) and manufacturing objectives that include the consistent supply of quality protein therapeutics as well as the development and scale-up new biologics processes.

The individual will play key roles in:

· Expansion of bioanalytical capabilities at the site;

· Investigations into unique protein chemistry-related issues;

· Maintaining awareness of cutting-edge advances in protein analytical methods and capitalizing on those that show potential as tools to advance our knowledge and understanding of a therapeutic protein's structure and/or mechanism of action.

Proteins to be analyzed will include, but not be limited to novel and "biosimilar" therapeutic proteins produced via fermentation processes using recombinant bacteria and yeast. The candidate will have a considerable knowledge of protein analytical methods and strong practical experience which they will be able to apply to support protein purification experimentation for troubleshooting and process improvement. They will also be expected to act as a Company resource in applying their technical knowledge to projects that involve protein characterization and analysis.

The successful candidate will have the opportunity to:

· Apply their enthusiasm for the scientific process to design and carry out studies requiring protein analysis.

· Use techniques such as, liquid chromatography (HPLC / FPLC), LC-MS, particle size analysis, electrophoresis, immunoblotting, as well as other

general chemical, biochemical and immunological analyses, to quantify and characterize proteins of interest.

· Employ their strong verbal and written communication skills, including the skill of listening to others.

· Effectively work both independently and within a multidisciplinary team.

· Employ their leadership skills to recruit, teach, and develop team members

· Develop plans and regulatory documentation in support of analytical method technology transfer, qualification, change control, and validation

· Interact with internal and external partners to interpret and evaluate data

· Utilize and further develop their project management skills.

Additionally, the successful candidate would keep abreast of innovative and novel developments, particularly of a bioanalytical nature, in the bio-processing industry by presenting papers at symposia, attending scientific seminars, and maintaining awareness of the scientific literature. Some supervision of junior level personnel will be required.

Qualifications

Required

* Ph.D. in Analytical Chemistry, Biological Chemistry, Biochemistry or other life science and experience with the analysis of proteins or peptides

or

* Masters degree in a Life Science or Analytical Chemistry field of study and three (3) years of experience with the analysis of proteins or peptides

Desired

* Ph. D. in Biological Chemistry, Biochemistry or other Life Science discipline with extensive specialization in, and experience with, protein analytical methods.
* Expertise in a broad range of protein analytical / characterization methods and their application to the development and maintenance of pilot and commercial-scale therapeutic protein purification processes as well as experience with investigations and troubleshooting of unique protein chemistry related issues.

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 # CHE003289.

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
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Elkton-Senior-Process-Bioanalytical-Scientist-Job-VA-22827/1514885/151488515148852012-03-04Merck/MSDfull-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.


Position Overview:

The Associate Scientist / Engineer will be an important member of the Technical Operations Department at the Elkton, VA site. The Elkton plant, also known as Stonewall, is located in Virginia's Shenandoah Valley and opened in 1941. The site employs a wide array of manufacturing technologies to support the production of medicines. Organic synthesis and biotechnology operations are used to chemically manufacture many intermediate products. Sterile operations include bulk and finished manufacturing/packaging steps. Pharmaceutical operations involve tableting, encapsulation and packaging operations. The most recent addition to Elkton's manufacturing spectrum, vaccine operations, is also supporting the company's first exploration into therapeutic proteins and the positions will be a part of the technical support groups in these areas.

Responsibilities of a Technical Operations Associate Scientist / Engineer are:

* Demonstration of process improvements, monitoring process performance, investigating deviations and implementing corrective actions, creating standard work for operations, and assisting in troubleshooting.
* Day-to-day technical support for the manufacturing areas involves assignments related to quality, safety, environmental, and operating cost goals.
* Frequent validation, equipment and process related projects will also be required.

Please note: This position may be required to work some shift work on a periodic basis.

Qualifications

Education Requirement:

* B.A. degree in Engineering or Life Sciences field.

Preferred:

* M.S. degree in Chemical or Mechanical Engineering, Biotechnology, Chemistry/Biochemistry, or Microbiology.

Required skills and Experience:

* The successful candidate must have strong problem solving skills and a hands-on approach to problem solving, with a bias toward going to see problems for oneself in the field.
* Excellent organizational, interpersonal, and verbal/written communication skills.
* Ability to examine an issue from diverse perspectives (safety, compliance, automation, equipment, process, people) in order to best understand and resolve it and have an enthusiasm for continuously learning.

Preferred:

* 0 - 2 years experience in an engineering, technical operations or operations position supporting a manufacturing process through one or more of the following roles: process improvements, monitoring process performance, investigating deviations and implementing corrective actions, creating standard work for operations, and assisting in troubleshooting of the process.

* Experience with technical support of a GMP (good manufacturing practices) manufacturing process.

* Experience in bioprocess, vaccine, or sterile manufacturing.

* Experience with Lean and Six Sigma methodologies.

* Experience with SAP and/or Trackwise.

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 # CHE003245.

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
Employee Status: Regular
Number of Openings: 4]]>http://jobs.merck.com/job/Elkton-Associate-Engineer-Technical-Operations-Manufacturing-Job-VA-22827/1466968/146696814669682012-03-04Merck/MSDfull-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 a Principal Engineer position available 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.

Position overview:

Under the coaching of the Director of Technical Operations, the Technical Lead manages available resources to provide technical support and direction to manufacturing operations with a focus on aseptic processing and finished product filling operations. Responsibilities include but are not limited to: problem solving manufacturing issues, providing technical direction to the demonstration of new and / or improved processes, project management and coordination, assisting the manufacturing area in achieving production schedule and financial targets, supporting efforts on regulatory compliance, and focusing on improving the efficiency of the work environment, with special emphasis on leadership and activities associated with employee development and involvement.

Primary activities:

1) Provide supervision for technical resources in designated production area. This will include providing team vision, one to one coaching and feedback for employee development, and training / developmental assignments allowing for employee development.

2) Provide the necessary resources to address technical issues identified in the manufacturing area. Focus on root cause problem solving, thorough technical report writing, and application of systematic tools, such as those associated with LSS (Lean Manufacturing and Six Sigma). Assist with effectively resolving unplanned manufacturing events, as well as develop and implement corrective actions.

3) Provide technical support for capital activity in production area, through contributing to scope development, design, construction completion, qualification, licensing, and operational start up.

4) Support all GMP, safety, and environmental compliance objectives for area of support. This includes monitoring all activities to ensure the manufacturing area remains in compliance with respect to all regulatory requirements.

5) Install a culture of continuous improvement with respect for cost, quality, delivery, and other appropriate measures.

Qualifications

Required:

* BS degree in life sciences or engineering discipline and 8 years experience in GMP Technical, Quality, or Operational Support role

or

* Advanced degree (M.S. or Ph.D.) and at least 6 years of experience in pharmaceutical and / or biotechnological industry.
* Demonstrated interpersonal skills, leadership, and bility to solve difficult problems in a complex, highly regulated manufacturing arena
* Experience in Sterile / Aseptic, Biologics, or Vaccine Manufacturing, Quality, or Technical Support.

Preferred:

* Experience in group leadership, management, and supervisory role.
* Regulatory inspection presentation experience with external regulatory authority representatives.

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 # ENG002303.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkton-Aseptic-Processing-Principal-Engineer-Job-VA-22827/1670750/167075016707502012-03-04Merck/MSDfull-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 the Biotech's Integrated Process Team Business Process Expert position available 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 Business Operations Leader within the Biotech Integrated Process Team at the Elkton, VA Manufacturing Plant is responsible for ensuring products are produced in accordance with established procedures while adhering to all domestic and international quality, safety, and environmental guidelines.

This individual will utilize a high degree of independent judgment and decision-making to direct production or support operations personnel to ensure customer supply requirements are achieved and maintain cost control in assigned area.

The individual will manage area within Company policies and within the framework of the local bargaining unit agreement and the responsibility for guiding/supporting talent management activities for direct reports and support personnel.

The successful candidate will have the ability to coach, influence and support others through a culture of inclusion, continuous improvements, feedback, and empowerment.

The successful candidate will have 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

Qualifications

Required:

* Bachelor degree or higher required.Chemistry, Biological Science, Engineering or related discipline preferred.
* Six (6) years of cross functional experience in Quality, Operations and Technical Operations in a GMP environment
* Five (5) years of People Management responsibilities, with some experience managing multi layered organization
* Experience in Continuous Improvement, Lean Manufacturing and Right the First Time Methodologies
* Demonstrated strong leadership and interpersonal skills with ability to coach, influence and support others through a culture of inclusion, feedback and empowerment
* Demonstrated ability to motivate people to achieve stretch goals
* Demonstrated experience holding self and others accountable to the Merck Leadership Behaviors
* Demonstrated experience using analytical, organizational and project management skills
* Strong written and verbal communication skills
* Demonstrated ability to work independently as a team leader and team member

Preferred

* SAP working knowledge
* Management of organizations under bargaining unit agreement preferred
* Green or Black Belt Certification in Lean Six 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 # MAN001348.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Elkton-Biotech-IPT-Business-Process-Expert-Job-VA-22827/1658092/165809216580922012-03-04Merck/MSDfull-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 Lean Six Sigma Senior Analyst positions available 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 Stonewall Plant in Elkton, Virginia is a multiple disciplined site for Merck & Co., Inc. The site currently operates the following processes to support Active Pharmaceutical Ingredient manufacturing: Organic Synthesis, Traditional, Large Volume Fermentation, Vaccine Fermentation, Bulk and Antibiotic processing. The site also has a newly installed high speed Finished Antibiotic filling line. Employees working at the Stonewall Plant have the opportunity learn various aspects of pharmaceutical and chemical manufacturing.

The Lean Six Sigma Senior Analyst has the opportunity to work with the Integrated Process Teams to apply fundamental LEAN and Six Sigma tools to solve problems and implement process improvement initiatives. The Senior Analyst understands the concepts of LEAN manufacturing and is able to teach others. While working with the production teams to eliminate efficiency losses, reduce operating costs, and maximize throughput, the Senior Analyst will have the opportunity to influence the financial bottom line while sustaining and improving product quality. The Senior Analyst will use his or her understanding of Six Sigma tools and mentor others.

The Lean Six Sigma Senior Analyst will have the following responsibilities:

* Lead kaizen teams
* Manage shop floor improvement initiatives
* Conduct training sessions
* Develop and execute a LEAN transformation strategy for a specific production area that incorporates educational awareness as well as individual project management.
* Manage the basics of Change Execution

Qualifications

Required:

* Bachelor degree
* 5 years experience with manufacturing operations with knowledge of the application of LEAN tools

Preferred:

* Green Belt certification
* Experience within 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 # OE/000281.

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
Employee Status: Regular
Number of Openings: 2

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Elkton-LEAN-Six-Sigma-Senior-Analyst-Job-VA-22827/1505471/150547115054712012-03-04Merck/MSDfull-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.


Responsible include but are not limited to:

* Leadership and management of all Marketing activities in the US Small Animal Business Unit.
* The position currently has 8 direct reports (Product Directors, Product Managers, Market Research Manager) however, a revised organization design has been proposed that could result in this position having 2 additional direct reports and a total organization of 15 professionals.

Qualifications

Education Minimum Requirement:

* Bachelors Degree with MBA a plus

Required Experience and Skills:

* 15+ years of sales and marketing management experience
* 10 + years of leadership experience
* Motivating, Inspiring and Encouraging work style
* Creative marketer with a bias for execution, action and results
* Strong record of developing, mentoring and managing talent to drive individual, team and business performance
* Demonstrated Leadership skills as a team manager and with cross functional groups
* Proven track record of success in general marketing strategy, business planning and business development
* Experience in financial and production forecasting, pricing analysis and strategy, new product launches and marketing communications planning & strategy
* Able to mobilize and orchestrate a plan that ensures effective Field Sales Team & Customer alignment and execution
* Strong financial and business acumen
* Driver and Leader for change management
* Self starter, able to work and manage effectively in a fast paced environment, and able to tolerate stresses of a rapidly growing business
* Effective listener, excellent communication and presentation skills, and high customer/colleague impact
* Proven record of market & product analysis, plan development, competitive evaluation & assessment
* Experienced in market research design and analysis - for existing & new products and latent market development
* Effective negotiator
* Experience in channel marketing (distributor, vet, shelter) and in OTC/Retail marketing

Desired Experience and Skills:

* Veterinary Pharma/Vaccine experience and industry knowledge, and specifically experience in Flea&Tick and Heartworm product marketing
* MBA and/or DVM

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 # PRO009106.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Summit-Director-Marketing-US-Companion-Animals-Job-NJ-07901/1543932/154393215439322012-03-04Merck/MSDfull-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.


Responsibilities include and not limited to the following:

* Developing sterile formulations for small molecule and small peptide drugs for injectable and ophthalmic routes of administration to support both preclinical or early clinical development.
* Primary duties to support both early and late stage development candidates will include screening and developing formulations to define a robust drug product composition, developing scalable process (including terminal sterilization) and defining primary packaging.
* Supporting appropriate compatibility characterization to enable processing of drug product and dosage administration in toxicology and clinical study and drafting formulation development reports.
* Active participation and leadership on formulation development teams and interfacing with other functional areas to drive project milestones
* Generate and test hypothesis
* Strong communication skills
* Good interpersonal skills
* Ability to multi-task
* Mentor fellow scientists
* Strong desire to learn and contribute

Qualifications

Education:

* BS/MS/Ph.D. Degree in Pharmaceutics, Pharmaceutical Chemistry, Pharmaceutical Sciences, Chemical Engineering,
Chemistry, or related field.

Required:

* BS/MS with atleast 4 years working experience in sterile formulation development / parenteral drug delivery
* Ph.D with working experience in sterile formulation development / parenteral drug delivery
* Good understanding of sterile dosage form requirements (sterility, endotoxins, particulates, and tonicity) from a composition (solubilization and stabilization approaches) and processing (liquid fill and lyophilization) perspective with insight on critical attributes for scale-up of sterile dosage forms.

Preferred:

* Course work in physiology, pharmacokinetics, biochemistry, microbiology, chemical kinetics, physical pharmacy and knowledge in sterile formulations
* Understanding of formulation development and analytical testing requirements for peptide therapeutics and experience with regards to sterile process scale-up and non-conventional drug delivery technologies (e.g. emulsions, suspensions, injectable depot)
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 # RES001237.

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
Employee Status: Regular

Travel
: No
Number of Openings: 2

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Summit-Senior-Research-Pharmacist-Job-NJ-07901/1601357/160135716013572012-03-04Merck/MSDfull-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.

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-%28SkincareFootcare%29-Job-NJ-07901/1385043/138504313850432012-03-04Merck/MSDfull-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.


Responsibilities include and are not limited to the following:

* Evaluate R&D pipeline to identify gaps and leverages opportunities broadly across US, Emerging and Developed Markets to optimize speed to market and maximize value of assets
* Ensure an alignment with R&D Operations and Center of Excellence Groups for DH and WH pipeline on realization of strategy.
* Facilitates development of Business cases for projects within for Digestive Health and Women's Health franchises
* Ensures adherence to global product development
* Work with internal and external partners to uncover Innovative New Technologies and Category Trends
* Link to internal and external SMEs to ensure access to best in class specialists, equipment and laboratories.
* Pro-actively develop, solicit and investigate new areas of opportunity that align with Digestive Health and Women's Health Franchise strategies
* Monitor global competitive landscape as input for franchise strategy development
* Link to Universities and set Collaboration and Publications, as appropriate
* Ensure ongoing communication to Senior Management, internal (R&D franchise Team) and external stakeholders (marketing and GMP) on all issues and risks on Franchise strategy

Qualifications

Education:

* Required: Master's degree (preferably in Chemistry, Biology, Pharmaceutics or equivalent)

Required:

* Minimum 10 years of work experience
* Product development/Research & Development experience
* Thorough knowledge of all the aspects of product delivery, including safety, regulatory, finance and supply chain.
* Ability to work independently and build relationships across all levels of the organization and with technical partners across different functions and within the region.

Preferred:

* Project/Program Management
* Work experience in digestive health or women's health franchises
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 # PRO009219.

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
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Summit-DHWH-Pipeline-Development-Lead-Job-NJ-07901/1666998/166699816669982012-03-04Merck/MSDfull-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.


In support of the Product Leader, the Product Manager actively collaborates with the MCC Franchise and Business teams to optimize product supply chains, identify and implement business support strategies and processes, and facilitate the flow of information between the MCC Franchise and MMD functional organizations. This role in engaged with the MCC Franchise teams for designated products, develops / implements supply strategies for new and in-line products to support divisional objectives, collaborates with MCC Global Project Management to achieve on-time commercialization objectives, and develops process solutions to enable MMD support of business growth.

Primary activities include, but are not limited to:

1. Actively engaged MCC and MMD team-member, responsible for translating consumer product development, manufacturing and packaging requirements into MMD strategies to support commercialization and ongoing optimization of the production supply chain.
2. For designated products and/or Franchises, defines physical and financial supply chain flow and develops supply chain strategies to optimize consumer business objectives, customer / distributor relationships.
3. Supports the Product Leader in collaborating cross-functionally to identify, develop, implement and manage global, regional and local business support targeted at enabling the growth and ongoing support of the MCC business.
4. Provides strategic analysis for MCC Supply Chain activities, including lifecycle management, productivity and innovation opportunities.
5. In support of MCC commercialization activities, assumes Site Selection and Launch Team functional support responsibilities for assigned products, including establishing consumer-focused success factors (lead time / MOQ), coordinating pre and post launch supply chain support activities, and other product-specific tactical support requirements; collaborates with Marketing, R&D, GPM Franchise leads and in-market team members to support product commercialization objectives.
6. Assists with the development and implementation of harmonized MCC supply chain reporting processes, collaborating with markets to link to various information platforms to provide MCC Supply Chain Management visibility to inventory and sales data as well as key performance indicators, highlighting opportunities for improvement in the metrics and process itself.

International travel is expected approximately 30% of the time.

Qualifications

Required:

* B.S. degree in Supply Chain, Industrial Engineering, Engineering, Business, or a relevant discipline is required.
* 10 years of total work experience is required.
* 5 years experience within a Supply Chain/Procurement or Manufacturing role is required.
* Knowledge of the Supply Chain business and processes are required.

Preferred:

* Experience within Consumer Product industry is a plus.
* Advanced degree 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 # SUP000305.

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
Employee Status: Regular

Travel
: Yes, 25% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Summit-Product-Manager-Job-NJ-07901/1540445/154044515404452012-03-04Merck/MSDfull-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 Category Strategy Manager (CSM) is responsible for the development of MCC Category strategy founded in analytics and insights for their assigned categories (Suncare, Footcare, Upper Respiratory). The CSM will lead the category vision and strategy for assigned categories to provide category thought leadership and to influence retail partners' decision making. The CSM develops and institutes strategic category insights plans for sales and category teams that integrate, align, and achieve retailer and MCC Consumer goals. The incumbent collaborates with and influences partners within the Sales, Marketing and cross-functional Customer Solutions teams as well as retail Customers.

Key responsibilities may include, but are not limited to:

* Develops and leads the MCC organization to create a category vision and long-term category strategy that influences planning at the HQ and field sales level
* Is the internal source of expertise of category/shopper insights and analytics for account teams and counterparts within MCC Sales
* Leads the acquisition and integration of information and insights from a variety of sources to build and shape effective category strategies
* Provides direction and expertise to field sales category and analytical functions to optimize analytical data utilization and application.
* Manages the development of data-based category selling stories to influence retailers decision making and drive sales growth
* Provides input for use of analytical tools and integration of actionable insights for MCC.
* Foster cross-functional collaboration and team work when developing and utilizing analytics and insights
* Identifies MCC category-specific shopper insights needs and manages third-party vendors for research development, execution and retailer presentations
* Manages a process to share category insights, analytics best practices, and templates to streamline processes and accessibility of resources and tools
* Optimizes category information and leads best practice sharing
* Provides oversight to analytical community database
* Responsible for knowledge of marketplace category trends and implications for MCC
* Partners and provides guidance to account teams on creation, development and presentation of category selling stories.

Qualifications

Education:

* Bachelor's degree required

Required Skills:

* Minimum of 7 years work experience
* Demonstrated work experience within consumer products industry
* Expertise in data analysis and application
* Ability to devise and deliver persuasive presentations
* Demonstrated ability to partner with sales account teams
* Understanding of retailer and category strategies
* Prioritization, time management, and multitasking skills
* Understanding of market research and application to category sales tools
* Knowledge of market research process
* Verbal and written communication skills
* Strong computer proficiency, including MS Office and database applications

Preferred Skills:

* Experience with category management & sales

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 # MAR004130.

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
Employee Status: Regular
Number of Openings: 3

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/Summit-Category-Strategy-Manager-Job-NJ-07901/1708747/170874717087472012-03-04Merck/MSDfull-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 successful candidate will be responsible for developing formulations primarily for respiratory dosage products (e.g., dry powder inhalers, metered dose inhalers, nasal sprays and nebulizers). Primary duties to support both early and late stage development candidates will include screening and developing formulations to define a robust drug product composition, process and primary packaging. The candidate will use innovative approaches to design robust formulations and manufacturing processes for respiratory dosage forms. The candidate will originate research ideas and design, execute & interpret complex laboratory experiments with broad priorities set by supervisor. Other responsibilities include statistical experimental design & data analysis, completion of technical reports, regulatory submissions and patent applications. Active participation on formulation development teams and interfacing with other functional areas to drive project milestones will be required. The candidate should have strong communication skills, good interpersonal skills, ability to multi-task and a strong desire to learn and contribute.

Qualifications

Education Minimum Requirement:

* Ph.D. degree in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, Material Sciences, Chemistry or a related field.

Required Experience and Skills:

* Ph.D. degree
* Familiar with requirements of formulation development including composition, processing & scale-up considerations.

Preferred:

* Some respiratory formulation development experience preferred.
* Pharmaceutical process development understanding is a plus.
* Strong scientific skills with practical experience in physical and mechanical characterization of pharmaceutical liquid, solid and aerosols, and a good understanding of the relationship between physical/mechanical properties and drug product process/performance 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 # RES001239.

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
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 3

Hazardous Materials
: Laboratory Chemicals and Potent Pharmaceutical Actives]]>http://jobs.merck.com/job/Summit-Respiratory-Formulation-Development-Job-NJ-07901/1598877/159887715988772012-03-04Merck/MSDfull-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 Staff Scientist / Engineer will be an important member of the Technical Operations Department at the Elkton, VA site. The Elkton plant, also known as Stonewall, is located in Virginia's Shenandoah Valley and opened in 1941. The site employs a wide array of manufacturing technologies to support the production of medicines. Organic synthesis and biotechnology operations are used to chemically manufacture many intermediate products. Sterile operations include bulk and finished manufacturing/packaging steps. Pharmaceutical operations involve tableting, encapsulation and packaging operations. The most recent addition to Elkton's manufacturing spectrum, vaccine operations, is also supporting the company's first exploration into therapeutic proteins and the positions will be a part of the technical support groups in these areas.

Typical routine responsibilities of a Technical Operations Scientist / Engineer are demonstration of process improvements, monitoring process performance, investigating deviations and implementing corrective actions, creating standard work for operations, and assisting in troubleshooting. Day-to-day technical support for the manufacturing areas involves assignments related to quality, safety, environmental, and operating cost goals. Frequent validation, equipment and process related projects will also be required.

This position may be required to work some shift work on a periodic basis.

Qualifications

Education Requirement:

* Bachelor degree in Engineering or Life Sciences field

Required:

* The successful candidate must have strong problem solving skills and a hands-on approach to problem solving, with a bias toward going to see problems for oneself in the field.
* Excellent organizational, interpersonal, and verbal/written communication skills are needed.
* Be able to examine an issue from diverse perspectives (safety, compliance, automation, equipment, process, people) in order to best understand and resolve it and have an enthusiasm for continuously learning.
* 1 - 2 years experience in an engineering, technical operations or operations position supporting a manufacturing process through one or more of the following roles: process improvements, monitoring process performance, investigating deviations and implementing corrective actions, creating standard work for operations, and assisting in troubleshooting of the process.

Preferred:

* BS or MS degree in Chemical or Mechanical Engineering, Biotechnology, Chemistry/Biochemistry, or Microbiology
* Experience with technical support of a GMP (good manufacturing practices) manufacturing process
* Experience in bioprocess, vaccine, or sterile manufacturing
* Experience with Lean and Six Sigma methodologies
* Experience with SAP and/or Trackwise
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 # CHE003201.

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
Employee Status: Regular

Travel
: No
Number of Openings: 3

Shift (if applicable)
: 1st

Hazardous Materials
: No]]>http://jobs.merck.com/job/Elkton-Staff-Engineer-Technical-Operations-Manufacturing-Job-VA-22827/1412553/141255314125532012-03-04Merck/MSDfull-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 the Biologic's Integrated Process Team Business Process Expert position available 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 Business Operations Leader within the Biologic's Integrated Process Team at the Elkton, VA Manufacturing Plant is responsible for ensuring products are produced in accordance with established procedures while adhering to all domestic and international quality, safety, and environmental guidelines.

This individual will utilize a high degree of independent judgment and decision-making to direct production or support operations personnel to ensure customer supply requirements are achieved and maintain cost control in assigned area.

The individual will manage area within Company policies and within the framework of the local bargaining unit agreement and the responsibility for guiding/supporting talent management activities for direct reports and support personnel. The successful candidate will have the ability to coach, influence and support others through a culture of inclusion, continuous improvements, feedback, and empowerment.

The successful candidate successful candidate will have 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

Qualifications

Required:

Bachelor degree or higher required

Six years of cross functional experience in Quality, Operations and Technical Operations in a GMP environment

Five years of People Management responsibilities, with some experience managing multi layered organization

Experience in Continuous Improvement, Lean Manufacturing and Right the First Time Methodologies

Demonstrated strong leadership and interpersonal skills with ability to coach, influence and support others through a culture of inclusion, feedback and empowerment

Demonstrated ability to motivate people to achieve stretch goals

Demonstrated experience holding self and others accountable to the Merck Leadership Behaviors

Demonstrated experience using analytical, organizational and project management skills

Strong written and verbal communication skills

Demonstrated ability to work independently as a team leader and team member

Preferred

Biological Science or Engineering major preferred.

SAP working knowledge

Management of organizations under bargaining unit agreement preferred

Green or Black Belt Certification in Lean Six 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 # MAN001329.

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
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/Elkton-Biologic's-IPT-Business-Process-Expert-Job-VA-22827/1643323/164332316433232012-03-04Merck/MSDfull-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.


As the recognized SME for Text Mining & Analytics (TMA) in the Knowledge Discovery/Knowledge Management (KDKM) Department, the candidate will be responsible for the development and delivery of advanced data and text analytics capabilities and services to enable knowledge acquisition, search, and hypothesis generation. This position influences the KD/KM technology platform and preferred vendor portfolio and helps define and execute KM Services strategies and policies across all Franchises/Areas in Merck Research Labs in order to: 1) Deliver industry-leading TMA capabilities; 2) Establish best practices, maintenance, and governance for development of full-text corpora; and 3) Develop productive, ongoing relationships with leading text mining and analytics vendors.

Key business area stakeholders include but are not limited to KDKM franchise and function support researchers, the Licensing organization, Discovery organization scientists and project teams, the One-Merck Digital Library, and the Clinical Literature organization. The position will also collaborate with other support groups, including Informatics and Analysis, Informatics-IT, and Innovation IT.

This position requires excellent leadership, written and oral communication, stakeholder management skills, and demonstrated experience delivering world-class text mining analytics products/services in a pharmaceutical company.

Qualifications

Education:

BS/BA required, Ph.D. or equivalent experience in computational linguistics, text mining, with M.S. or equivalent experience in Natural or Life Sciences preferred.

Required Experience:

A minimum of 5 years of demonstrated substantive experience in text mining analytics in support of pharmaceutical R&D.

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.

Proven record of innovative and critical thinking, and excellent problem-solving ability.

Proven track record of high quality 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 # RES001253.

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-MA-Boston
Other Locations: US-NJ-Kenilworth, US-PA-West Point, US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Text-Mining-and-Analytics-Lead-Job-MA-02108/1577189/157718915771892012-03-04Merck/MSDfull-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.


Under the direction of a Research Contracts Management Lead, the Scientific Liaison Coordinator [also known as Research Contracts Manager (RCM)] will be responsible for but not limited to:

* Liaising with Merck Research Scientists, Senior Management, Legal and Patent to prepare and negotiate agreements (contracts), including but not limited, to confidentiality, consultant, material transfer, license, evaluation, study, and research collaboration.
* The RCM will also interact with other ESA personnel and Corporate Licensing to facilitate appropriate related agreements to support commercial transactions.
* Responsibilities will include customization of template legal agreements based upon scientific work plans and budgets, business needs, intellectual property and legal considerations, and due diligence of third party rights.
* The RCM will negotiate agreements with outside academic, government, and industry partners while working closely with Legal and Merck scientists at all levels to align scientific and business needs and protect Merck's Intellectual Property and other rights.
* In addition, the RCM will maintain up-to-date records and communications in the Licensing Knowledge Repository (LKR) database.
* The candidate will be located at the Merck Research Laboratories Boston, MA facility

Qualifications

Minimum Education Requirement:

* MS or Ph.D. in a biomedical science and at least 5-10 years experience in laboratory research, licensing, or equivalent.

Minimum Skills and Experience Required:

* Candidate must demonstrate excellent written, verbal, organizational, judgment and interpersonal skills.
* Strong leadership qualities and the ability to work independently is a necessity.

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 # LIC000108.

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-MA-Boston
Employee Status: Regular

Travel
: Yes, 5% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Scientific-Research-Contracts-Manager-%28Boston%29-Job-MA-02108/1682108/168210816821082012-03-04Merck/MSDfull-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 team member within the Respiratory and Immunology group will be a member of a team of 4 to 7 scientists that uses biochemical, molecular, cellular and pharmacological techniques for the preclinical discovery and development of drug candidates for the treatment of respiratory and immunological diseases (e.g. asthma, rheumatoid arthritis).

The responsibilities of the team member include:

* Conducting preclinical experiments to support drug discovery efforts for new therapeutics at different stages of development including target identification and validation, lead identification and lead optimization
* Designing and executing preclinical research efforts to support the clinical development small molecule candidates
* Generating and integrating data from molecular, biochemical and cell biology experiments towards the discovery and validation of target engagement, pharmacodynamic and efficacy biomarkers as well as lead identification and lead optimization of drug candidates
* Collaborating with members from other functional groups including In Vitro Pharmacology, In Vivo pharmacology, Medicinal Chemistry, Basic Pharmaceutical Sciences, and Exploratory and Translational Sciences
* Working with external academic, biotech, and contract research organizations.
* Monitoring the external research environment and helping establish collaborations that are consistent with R&I franchise and functional strategies.
* Managing internal and external resources to accomplish scientific goals in a rigorous and cost effective manner

Additional responsibilities of the team member include: (i) oversight of the summarization and consolidation of experimental data; (ii) ensuring that this information is communicated in a concise, easy to understand manner to the appropriate teams and committees; (iii) managing the design of research protocols and the execution of experimental studies using standard and innovative scientific approaches and techniques; (iv) may represent franchise biology on cross-functional project teams; (v) monitors external trends and developments; (vi) works with and communicates with all levels of individuals within the DPS functional and R&I franchise discovery groups.

The R&I team member may have scientific management responsibilities of other scientists in his/her group.

Qualifications

Education Requirements:

* Ph. D. (biological sciences), MD, or D.V.M. degree in with minimum 2 years industry experience or equivalent academic credentials, such as post-doctoral research
* M.Sc. degree in biological sciences with minimum 10 years industry experience or equivalent academic credentials

Required Skills and Experience:

* Subject matter expertise in the biology and pathophysiology associated with respiratory and or immunological disorders
* Subject matter expertise preclinical research approaches in respiratory and/or immunological research
* 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 skills and experience:

* Experience in discovery of drug candidates at the preclinical stage
* Experience in target identification and validation for new respiratory and/or immunological therapeutic targets

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 # BIO003459.

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-MA-Boston
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Biology-Program-Team-Member-Job-MA-02108/1708746/170874617087462012-03-04Merck/MSDfull-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 Respiratory and Immunology (R&I) project teams, the individual, under general supervision and direction, conducts in vitro experiments to study the function of target genes in a biochemical and cellular environment using a variety of analytical and in silico approaches to build a comprehensive profile of the target. Develops and utilizes biochemical and cell based assays to define mechanism of action of pharmacological agents.

The primary responsibilities of the R&I Program Team Member include:

* Conducts in vitro cellular assays to support validation of multiple targets
* Under general supervision, designs research protocols and conducts experimental studies using standard and innovative techniques
* Analyzes data, troubleshoots problem, and interpret experimental results.
* Writes study reports to effectively communicate purpose, methods, findings and conclusions of experiments
* Publishes and presents findings and conclusions.
* Independently balances activities for multiple projects.
* Collaborates with other discovery groups, Central Teams and Centers of Excellence.
* Contributes to planning work and ensuring that team and group goals are met in a timely fashion

Qualifications

Education Requirements:

* B.Sc. degree in biological sciences with minimum 3 years industry experience or equivalent academic credentials (required)
* M.Sc. degree in biological sciences with 0 - 2 years industry experience or equivalent academic credentials (preferred)

Required Skills and Experience:

* Demonstrated skills and track record of research in in vitro sciences
* Skilled in studying function of target gene in a cellular environment using a variety of analytical approaches (biochemistry, molecular and cellular biology)
* Skilled in conducting experiments using small molecules, proteins, disruptive nucleic acids, and antibodies to determine their effects (phenotype) on the target gene
* Demonstrated ability to accurately record data/experiments and to communicate in written and oral forms
* Demonstrated ability to thrive in a team environment
* Demonstrated ability to communicate clearly and candidly

Preferred Skills and Experience:

* Demonstrated relevant subject matter expertise in the area of immunological-based disorders with specialization in respiratory diseases or arthritis
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 # BIO003460.

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


Search Firm RepresentativesPlease 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-MA-Boston
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Biology-Program-Team-Member-Job-MA-02108/1708744/170874417087442012-03-04Merck/MSDfull-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 the Safety Assessment (SA) representative to Merck Research Laboratories discovery research teams at the Boston, MA site, the SA discovery scientist leads the collaboration to define the preclinical SA strategy for programs prior to the approval of First-In-Man enabling GLP toxicity studies. With excellent leadership and collaborative skills, a broad expertise in preclinical safety assessment and an intimate understanding of the science and objectives of the assigned discovery programs, the SA discovery scientist assesses the safety risk using available literature, internal and external data and guides discovery and SA scientists to execute on the appropriate non-GLP SA studies to support selection of therapeutic targets and new molecular entities (NCE) with the highest probability of success for the intended indication. In addition, the SA discovery scientist is part of the scientific team that discovers and implements novel biomarkers and screening strategies. The SA discovery scientist is encouraged to participate in SA functional group activities aligned with their area of scientific expertise.

* Uses literature and data-base resources to understand and define safety risks associated with therapeutic targets.
* Defines the appropriate in silico approaches and in vitro and in vivo studies, including design, dose selection, compound requirements and timing to help innovate and select NCE with the highest probability of success.
* Collaborates with SA and Discovery scientists to assure the appropriate conduct of in silico assessments and in vitro and in vivo studies that support discovery programs.
* Effectively communicates the safety de-risking strategies, study data and conclusion to discovery teams, governance committees and management.
* Collaborates with the discovery and SA scientists to address all scientific issues including assessment of efficacy, metabolism, formulation and purity of drug product and substance.
* Provides consultation and guidance to discovery scientists on complex scientific problems and in general is available for consultation and advice on research approaches.
* Works closely with the SA development compound and therapeutic leaders to assure smooth transition and knowledge transfer for NCE approved for the development and understands safety data from NCE in development to build appropriate derisking strategies to support the innovation of improved back-up molecules.
* Provides due diligence support for licensing efforts of targets and NCE in the discovery space.
* May contribute as study pathologist to exploratory and mechanistic studies supporting discovery teams, if compatible with training and experience.

Qualifications

Education:

* MD, DVM and/or PhD. Degree from an accredited college or university with graduate and/or post-graduate work and/or residency training in Toxicology, Pathology, or related field.

Required:

* 10 or more years experience in Toxicology or related field and 5 or more years of demonstrated experience as pre-clinical SA scientist and team representative in the pharmaceutical industry with an extensive expertise and/or an excellent understanding of regulatory expectations, genetic toxicology, safety pharmacology, reproductive and developmental toxicology and general toxicology and pathology.

Preferred:

* Pharmaceutical experience in leading the pre-clinical safety assessment of small molecule programs for Respiratory, Immunology or Oncology indication in the discovery space.

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 # RES000976.

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-MA-Boston
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/Boston-Discovery-Scientist-Safety-Assessment-Job-MA-02108/1006308/100630810063082012-03-04Merck/MSDfull-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.


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 $19.29/hr.

Openings may be for 1st, 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 #USW000961.

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-PA-West Point
Employee Status: Regular

Travel
: No
Number of Openings: 14

Shift (if applicable)
: Other (see Work Schedule)]]>http://jobs.merck.com/job/West-Point-Pharmaceutical-Tech-Level-1%28continuous-recr_%29-Job-PA-19486/1658090/165809016580902012-03-04Merck/MSDfull-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 Field Engineer to join Specialty Products and Support (SP) team Technology Operations in West Point, PA.

Responsibilities are as follows:

* Provide technical support for vaccine and sterile manufacturing.
* Primarily responsible for reliable day-to-day 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 leading complex technical investigations. Specifically, this individual may be responsible for providing scientific support for Culture Media, Black Widow Spider Antivenin and Poultry areas within Merck's Manufacturing Division (MMD) Vaccine Manufacturing.
* Lead initiatives to ensure continuous supply of products part of SPS Integrated Process Team (IPT) in vaccine manufacturing.
* Troubleshooting and root cause analysis of laboratory test failures and manufacturing atypical, implementation of corrective actions, timely response to supply issues, compliance initiatives, test and specification updates to quality standards for SPS products.
* Must have the ability to establish good relationships with internal and external stakeholders.
* Analysis of complex processing problems through critical analytical thinking and the design/execution of laboratory/pilot scale experiments.
* Development of sound scientific justification to ensure uninterrupted supply of vaccines.
* Technology transfer of products and processes to Merck manufacturing plants.
* Development of working relationship with areas out of MMD for technology transfer issues and significant manufacturing issues.
* Development of working relationship with MMD manufacturing sites 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 and proposed environmental and drug and/or biological product regulatory requirements and determination of the applicability and impact on Merck operations.
* Documentation preparation and maintenance including SOPs, process descriptions, deviations, technical documents, and change requests.
* Effectively determine root cause and corrective/preventive actions for atypical events assigned.

Please note: Limited off-shift or weekend coverage may be required based on specific assignments.

Qualifications

Education:

* Required: B.S. degree in Engineering/Scientific field
* Preferred: M.S. degree in Engineering field

Required:

* Minimum (5) years post-bachelors degree experience in Production, Development or related field.
* Good interpersonal skills including flexibility and ability to work in a team environment.
* Demonstrated analytical abilities.
* Good written and verbal communication skills.
* Skillful in writing investigations for atypical events in a manufacturing environment.
* Proven experience with troubleshooting in a manufacturing or pilot plant environment

Preferred:

* Experience with deviation management organization in pharmaceutical companies.
* Previous experience with cell culture techniques, virology, aseptic processing and sterile manufacturing, biologics process development or manufacturing and/or process equipment.
* Familiar with Lean Six 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 # PRO009258.

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
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Field-Engineer-Spec_-Products-&-Supp-Job-PA-19486/1670758/167075816707582012-03-04Merck/MSDfull-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 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.

Additional responsibilities are as follows:

* 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.

Please note: This position is 3rd shift - Monday - Friday.

Qualifications

Required Education:

HS Diploma

Bachelor's degree preferred

Required Experience and Skills:

* 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

Preferred Experience:

Some experience in responsible line or staff position related to pharmaceutical production 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 # MAN001306.

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
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 3rd]]>http://jobs.merck.com/job/West-Point-IPT-Associate-Manufacturing-Supervisor-Job-PA-19486/1575127/157512715751272012-03-04Merck/MSDfull-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 image segmentation, image registration, machine learning and pattern recognition algorithms for quantitative analysis of images for applications in biomedical imaging and biomarker development to support drug discovery. Project areas include development of biomarkers for various disease and functional areas and analysis of images in various projects for manufacturing division. 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 concentration in one of the following studies is required; mathematics, electrical engineering, biomedical engineering, physics, computer science, or another area applying math, computer science, and/or image analysis techniques to biology, biomedical applications, preclinical or clinical medical research.

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: Machine learning and automated pattern recognition, signal and/or image processing, computer vision, 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:

* Research experience in applications of signal/image processing, machine learning, pattern recognition to biomedical imaging methods such as MR/CT/ultrasound/microscopy/histology are preferred.
* Experience in software packages such as Matlab, ITK, VTK, Amira, ImageJ, Definiens, MRIcro 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 # BUS000435.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Research-Associate%2C-Imaging-Applied-Mathematics-&-Modeling-Job-PA-19486/1577192/157719215771922012-03-04Merck/MSDfull-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 Business Analyst for MRL IT Discovery and Pre-Clinical Sciences is accountable for providing support to the Business area through a variety of means and to create value by enabling information technology to achieve outcomes and strategic goals. The BA must have strong business acumen and understand RNA Therapeutic, Screening and Protein Sciences both strategically and within day-to-day operations, and its relationship to Merck and Customers.

The BA must be able to anticipate and influence needs of the Business and is responsible for development of business cases to support technology investments, which at times will involve active demand management and facilitation of trade off decisions. The BA must understand the current portfolio of technology, including suitability and life-cycle status of solutions.

The BA is responsible for requirements specifications for solutions and engaging with solutions delivery on how these requirements will be met. They will receive ad-hoc requests for support and must be able to address or re-direct these as appropriate, and will be required to facilitate prioritization discussions with the business, and ensure Service Level Agreements and other support parameters are identified and in place.

This is a client-facing role which has a high level of interaction with the Business at all levels and as such, a strong customer service mindset is imperative. They must possess change management skills and be strong in developing and articulating the case for change, including being able to speak in business terms. The BA must maintain awareness of industry trends and of the focus of partner groups in MRL. The BA must be able to work independently with a clear understanding of the boundaries of the role, both with the Business and with other IT functions.

Primary activities include, but are not limited to:

* Reporting to the DPS IT Account Manager, the Business Analyst (BA) is responsible for enabling the business to maximize its technology investment to realize business outcomes.
* Support the Account Manager in relationship and demand management with the Business
* Receive and appropriately respond to service requests, questions, etc. by business clients
* Manage the RNA Therapeutic portfolio, including demand management, portfolio planning & reporting, forecasting, budget estimates
* Document current and future state business process and information flow map
* Identify key performance indicators for business processes and develop appropriate process measures and metrics
* Is a subject matter expert as it relates to client business processes and the current business environment in which they operate in, and initiate improvements, including the ability to perform root cause analysis to identify current state process inefficiencies
* Once the need for a solution is identified:
* Develop qualitative and quantitative business cases for process improvement and automation initiatives
* Develop detailed functional requirement specification from high level business concepts
* Develop solution alternatives for business requirements and ensure alignment with IT Architecture
* Lead or oversee the validation activities for solutions across all phases of the Merck SLC
* Participate in business assessment reviews and walk-throughs for complex projects
* Apply effective risk management techniques
* Planning for benefits and how they will be measured, including development and tracking of benefits realization plans as appropriate

* Understand the Enterprise Architecture and help the Business apply for maximum benefit
* Understand and be able to navigate Merck's IT function, including engagement of solution delivery and other services
* Ensure business continuity, via properly addressing issues that affect running the business day-to-day and also as new solutions are deployed
* Network with other BAs (formally and/or informally) to establish best practices
* Execute basic project management for local or small projects that do not require a Program Manager

Position will be located at our West Point, PA site. General travel will be required between Merck locations.

Qualifications

Education:

* A Bachelor's Degree is required. Concentration in Sciences, Information Systems or related field preferred.

Required:

* A minimum of 4 years experience in the areas of business requirements analysis and gathering, and business process engineering in a client facing role
* Project management experience
* Demonstrated requirements gathering skills through development of use cases and other methods and skills used in business analysis such as negotiation, decision making / trade off analysis, and problem solving skills
* Demonstrated success in building strong relationships with client organizations and across technology centers
* Must be able to effectively lead a cross-functional core team in a matrix organization
* Demonstrated skills in risk-based approaches, including ability to facilitate a robust risk analysis
* Demonstrated ability to succeed in a complex and dynamic work environment
* Process mapping experience
* Facilitation / workshop management skills
* Knowledge, content Management, and data mining experience
* Change Management experience

Preferred:

* Knowledge of Discovery and Preclinical Sciences
* Knowledge of RNA Therapeutics
* Experience with Merck SLC or equivalent validates systems approaches preferred
* Proven leadership and people management skills are preferred, along with excellent written, communication, and presentation skills
* Ability to understand and align IT architecture with business solutions
* Must be able to develop and articulate a plan of action, whether in support of strategy development or planning a roadmap. This plan must be clear, compelling and understandable, and flow in a logical fashion with supporting rationale as appropriate.

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 # SER000255.

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
Employee Status: Regular

Travel
: Yes, 15% of the time
Number of Openings: 1

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/West-Point-Business-Analyst-Job-PA-19486/1700164/170016417001642012-03-04Merck/MSDfull-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 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.

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-19486/1703557/170355717035572012-03-04Merck/MSDfull-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 committed to developing RNA-based therapeutics to bring groundbreaking new medicines to the clinic. We are currently seeking an entry level chemist in the RNA Therapeutics group within the Pharmacokinetics, Pharmacodynamics, and Drug Metabolism organization to support the discovery and development of RNA therapeutics using a variety of in vitro and in vivo LC/MS based assays. This individual will be part of a departmental team providing in vitro and in vivo data on the stability, metabolism and quantitation of RNA utilizing high resolution LC/MS and LC/MS/MS. The successful candidate will be involved in the conduct of in vitro metabolic stability assays and in vivo tissue metabolite identification. The ideal candidate will have experience in bioanalytical methods for isolating, detecting and characterizing potential therapeutics using High Resolution Mass Spectrometry.

Qualifications

Education Minimum Requirement:

* BA/BS

Required Experience and Skills:

* Educational background in chemistry, analytical chemistry, biochemistry, or related field.
* Strong skills in experimental design, bioanalysis, and critical data analysis/interpretation are required.
* Hands-on experience with LC/MS instrumentation.
* Experience with sample preparation of biological samples (e.g. plasma and tissues) using both liquid-liquid and solid phase extraction
* Solid proficiencies in written and verbal communication, as well as strong ability to work in teams, are critical.

Preferred:

* Prior experience in HRMS-based identification of unknown biological macromolecules (e.g., oligonucleotides, proteins, etc…) is highly desired.
* Knowledge of the chemistry and enzymology of metabolism, and experience with automation platforms is desired.
* Prior experience using High Resolution Mass Spectrometry (HRMS) to support identification of unknown metabolites/degradants at trace levels in biological matrices.
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 # PHA001049.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Research Chemicals, radioactivity, biohazards]]>http://jobs.merck.com/job/West-Point-Chemist-Job-PA-19486/1700169/170016917001692012-03-04Merck/MSDfull-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.

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-19486/1577193/157719315771932012-03-04Merck/MSDfull-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 reports directly to the IT Leader responsible for Safety and Regulatory Capability Delivery.

For solution strategy / envisioning / planning, the Solution Architect will drive decision making on the future state solution landscape and develop plans (road maps) for evolving the solutions to meet future business objectives or enable business strategy. For high level design, the Solution Architect will have overall responsibility for delivering high level solution designs that serve as the guiding structure for all subsequent solution design and build activities in this space. The Solution Architect will work across multiple large programs and projects as needed to cover the solutions that are in scope.

The incumbent must work closely with business leadership, IT leadership, and IT Shared Services organizations and peers to understand the key business capabilities required by the business, to assess the current state, and to develop and align target state and roadmaps with the business strategy. The incumbent stays current with both internal and external solution architecture best practices.

Position can be located in West Point, PA, Rahway, NJ, Springfield, NJ, or Whitehouse Station, NJ

Qualifications

Education:

* Bachelors degree required; degree in Computer Science or equivalent preferred. Advanced degree preferred.

Required:

* A minimum 8 years of experience in systems analysis, application development, and/or architecture working with regulated, validated systems.
* A minimum of 5 years of work experience working in architecture
* Demonstrated understanding and proficiency in enterprise architecture, business architecture and/or solutions architecture.
* Demonstrated proficiency in developing strategic solution roadmaps.
* Demonstrated proficiency in influencing and impacting overall design recommendation/direction from multiple solutions/applications/platforms to a single platform/technology suite.
* Demonstrated skills in implementing COTS, vendor solutions, data mapping to a vendor specification, and implementing large scale transformational solution initiatives.
* Demonstrated experience in developing multi-year plans to evolve technology capabilities, based on evolving and transformational business strategy.
* In depth knowledge of Global Safety and/or Regulatory Affairs and/or Medical Affairs business/functional areas.
* In depth knowledge of large, complex platforms and COTS applications and technologies used in pharmaceuticals, specifically Global Safety and/or Regulatory Affairs and/or Medical Affairs

Preferred:

* Experience working in pharmaceuticals and/or biotechnology.
* Strong leadership, decision-making and communications skills.
* Exceptional interpersonal skills, including teamwork, facilitation and negotiation.

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 # SOL000120.

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-Springfield, US-NJ-Whitehouse Station, US-NJ-Rahway
Employee Status: Regular

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

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/West-Point-Solution-Architect-Job-PA-19486/1488544/148854414885442012-03-04Merck/MSDfull-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 will be responsible for performing daily preclinical in vivo electrophysiology (EP) recordings in rodents. Animal preparation, data collection, analysis and interpretation, communication of results to drug discovery teams and planning of next studies are all primary responsibilities of this position. Testing animals for pain sensitivity using von Frey filaments, heat stimuli or mechanical pressure is needed prior to EP sessions. Performing periodic system upgrades, assay optimization and enhancement of techniques is required.

Qualifications

Education Minimum Requirement:

* Masters degree and 6 years related experience or a PhD is required

Required Experience and Skills:

* The candidate must have considerable experience with in vivo electrophysiology recording and analysis methods in preclinical pain models.
* Pain-related experience with in vivo single-unit, single-fiber or ectopic discharges is required.
* Familiarity with both spinal cord and peripheral nerve recording methods in rodent is advantageous.
* The qualified individual must be able to work as part of a matrix organization with other subject matter experts.

Preferred:

* Familiarity with ex vivo peripheral nerve or spinal cord electrophysiology preparations 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 # PHA001044.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Working with novel chemical entities in small (mg) amounts]]>http://jobs.merck.com/job/West-Point-Neurophysiology-&-Pain-Team-Member-Job-PA-19486/1655970/165597016559702012-03-04Merck/MSDfull-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 currently seeking a qualified PET modeler within the Department of Imaging located at our West Point, PA site in suburban Philadelphia. This innovative team consists of chemists, imaging physiologists, PET modelers and other biological and computational scientists. The group currently has state-of-the-art PET radiochemistry facilities and imaging instrumentation (PET, SPECT, CT, MRI, and optical) for in vivo imaging in preclinical species.

The successful candidate will be responsible for the kinetic modeling and parameter estimation of PET and SPECT data from preclinical and clinical imaging studies. A Ph.D. or equivalent in Mathematics, Physics or Engineering is required; directly relevant experience in an industrial setting is preferred. Expertise with quantitative kinetic modeling of CNS PET data and image processing is required. Experience with MATLAB, various image formats, study design for both occupancy studies and tracer characterization is a plus. The candidate must have a proven track record of successful research and have strong written and oral communication skills as well as interpersonal skills necessary for working in a cross functional working environment. Flexibility and the ability to adapt to a fast paced research environment are required.

Duties would include:

* Responsibility for the kinetic modeling and parameter estimation of PET and SPECT data from preclinical and clinical CNS imaging studies.
* Study design for occupancy studies and tracer characterization.
* Contribution to imaging protocols in regulatory documents required for clinical PET tracer filings.
* Presentation of research results to discovery, preclinical and clinical teams, including writing of manuscripts for submission to peer-reviewed journals.
* Collaboration with Imaging Department personnel, drug discovery program team leads, and clinical scientists.

Qualifications

Education Minimum Requirement:

* PhD or equivalent in Mathematics, Physics or Engineering

Required Experience and Skills:

* Quantitative kinetic modeling of CNS PET data.
* Image processing.
* Proven track record of successful research.
* Strong written and oral communication skills.

Preferred:

* Experience with MATLAB.
* Experience with various image formats.
* Experience with study design for occupancy studies and tracer characterization.
* Relevant research experience in an industrial 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 # IMA000120.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Sr-Research-Biologist-Job-PA-19486/1453386/145338614533862012-03-04Merck/MSDfull-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 # REL000239.

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
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-19486/1560772/156077215607722012-03-04Merck/MSDfull-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 vision is to make a difference in the lives of people globally through our innovative medicines, vaccines, biologic therapies, consumer health and animal products. The Vaccine Product & Technical Operations (VaPTO) organization is responsible for providing business and technical support for vaccine manufacturing within the Merck Manufacturing Division. Within VaPTO, the Technology Development group provides technical support for vaccine products and sites to the GVSM network. We identify unmet needs, respond to emerging issues, communicate and implement harmonized best practices and leading edge innovations to enable global vaccine supply across the GVSM network. Our current areas of focus are raw materials, components, technical systems, new technologies and technology transfer.

As part of the VAPTO organization, the Process Technology Team is seeking a highly motivated individual to be the Technical Lead for process improvements in aseptic processing and sterility assurance. In partnership with other technical groups in the network, identify implement new technologies that could simplify and/or improve robustness within GVSM.

In this role you will be:

* Providing technical support for manufacturing of licensed vaccine bulk products initially focusing on sterility assurance and aseptic processing.
* Project managing key manufacturing improvement projects including responsibility for charter development, execution and monitoring effectiveness.
* Collaborating with Procurement, Operations and other Technology Groups to, identify implement new technologies that could simplify and/or improve robustness for manufacturing processes.
* Utilizing sound scientific and engineering principles for problem solving and execution of continuous process improvements within the context of cGMP practices.
* Supporting, as needed, risk assessments to identify continuous improvement actions for the manufacturing shop floor.
* Individual will be part of a matrix team, responsible for driving strong collaboration and communication across Operations, Quality and Technology organizations.
Directly impacting the Vaccine business performance, from a Compliance, Supply and Strategy and Profit Plan standpoint.

Qualifications

Education:

* Required: B.S. in Microbiology, Biological Sciences or Chemical/Biochemical Engineering
* Preferred: M.S. and/or PhD in Microbiology, Biological Sciences or Chemical/Biochemical Engineering

Required Experience:

* Minimum 5 years experience in biological/pharmaceutical/chemical manufacturing
* Travel may be required up to 20%
* Role predominantly on first shift may require weekend/off shift coverage depending on project support and responsibility

Preferred Experience:

* Proven analytical and technical problem-solving abilities
* Strong collaboration and leadership skills, including previous experience in personnel and/or project management
* Demonstrated capability to analyze data, highlight exceptions and provide useful insights
* Ability to lead large cross-functional and complex initiatives using strong collaboration and communication skills
* Demonstrated knowledge and application of Lean six sigma methodology and tools
* Demonstrated effective written and verbal communication skills
* 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 # CHE003366.

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
Employee Status: Regular

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

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Process-Engineer-Job-PA-19486/1694170/169417016941702012-03-04Merck/MSDfull-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 selected candidate will join the clinical operations team within the Merck Research Labs (MRL) Pharmacokinetics, Pharmacodynamics, and Drug Metabolism (PPDM) Regulated Bioanalytical Group. Their responsibilities will include assisting with the entry of clinical study designs into the Drug Metabolism Lab Information Management System (Watson LIMS) and collaborating with bioanalytical scientists and other PPDM operations group members on the compilation, formatting, and publishing of reports documenting the results of preclinical and clinical bioanalytical studies. The selected candidate will also be expected to assist with the computer tracking, inventory, storage, and final disposition of samples of biological fluids collected during preclinical and clinical studies. Finally, they will, on occasion, be asked to be "on call" during non-working hours to deal with the management of emergencies resulting from the failure of sample storage freezers.

Qualifications

Education Minimum Requirement:

* Bachelors Degree or Equivalent in a Scientific or Health Care Related Field

Required Experience and Skills:

* Understanding of Clinical Study Designs, Knowledge of Documentum based document management systems, knowledge of Microsoft Office Programs (Word, Excel, PowerPoint), basic understanding of scientific report authoring.

Preferred:

* Knowledge of Watson LIMS and Cambridgesoft based Electronic Lab Notebook systems.
* Human clinical sample handling.
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 # PHA001037.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Human Clinical Samples, Pre-Clinical biological fluid samples, dry ice.]]>http://jobs.merck.com/job/West-Point-Technical-Coordinator-PPDM-Job-PA-19486/1691726/169172616917262012-03-04Merck/MSDfull-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 filling this position will be responsible for leading a group of technical and PhD molecular toxicologists in Molecular and Investigative Toxicology within the department of Safety Assessment. In this role, the candidate will:

* Formulate and execute novel strategies to decrease attrition of drug development candidates due to toxicity.
* Plan experimental approaches to gain mechanistic understanding around safety signals observed in preclinical toxicity studies and place in context of human risk.
* Develop translatable biomarkers to effectively monitor and manage safety in humans.
* Lead and mentor a highly-skilled and motivated team of scientists.
* Provide technical and strategic scientific leadership within Merck through strong cross-functional communication.
* Actively participate in weekly investigative strategy meetings, contributing expertise in developing approaches to overcome issues of toxicity and develop paths forward for successful development of drug programs.

The ideal candidate will possess a PhD in molecular toxicology or a closely related field and a preferred minimum 7 years experience in preclinical pharmaceutical or biotechnology drug development. Demonstrated scientific research ability and strong communication skills are essential. GLP experience is desirable.

This position is located at the Safety Assessment site in West Point, PA

Qualifications

Education Minimum Requirement:

* PhD

Required Experience and Skills:

* 3+ years of relevant experience
* Experience in molecular toxicology or a closely related field.
* Demonstrated scientific research ability and strong communication skills.

Desired Experience and Skills:

* 7+ years experience in preclinical pharmaceutical or biotechnology drug development.
* GLP 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 # BIO003421.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Research-Fellow-Job-PA-19486/1648271/164827116482712012-03-04Merck/MSDfull-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 Business Analyst acts as the key point of contact between the MES COE and site based project teams to ensure that deployments of the Werum PAS-X software are installed to maximize business benefits and are in line with Merck business process and technical standards. The Business Analyst is responsible for supporting MES implementations across the full systems lifecycle, from identifying the business needs of clients and stakeholders to help build business cases and determine appropriate implementation of the technology, through support to project implementation and ongoing operations. The Business Analyst will have regular direct interaction with Directors and other stakeholders in the Client organization, plus collaborate with the COMET program and representatives from the Process Council. In this 'above site role' the Business Analyst will also be accountable for driving standardization and collaboration across sites.
This specific role will be US based and primarily support projects at sites throughout North and Latin America.

Under the management and supervision of the Senior Director MMD IT MES COE, the Business Analyst is responsible for activities that include the following:

* Partner with local business leadership and project teams to develop business case for MES deployments bringing knowledge of process standardization and standard Werum configuration
* On-board local project teams into standard methods of working with the Merck Core Werum environment and set up project execution framework
* Understand and educate local project teams on MES standards as they relate to PAS-X system configuration, SLC, validation, hardware, software environments and business processes.
* Gain detailed knowledge of application of Werum software to enable production execution processes in order to work in concert with site teams to speed up project implementation
* Drive efficiencies in site execution of projects to reduce costs and cycle times based on standards
* Identify and ensure that best practices are leveraged from site to site. Actively participate in MES user groups within Merck
* Represent Merck in external forums as it relates to MES eg Werum user groups (PFU and SIG) as appropriate
* Educate sites in COMET deployment and operational methodology as it relates to Merck PAS-X Core environment to ensure that the interface between SAP and Werum works as planned. Develop and apply detailed knowledge of the Manufacturing Systems Architecture as it relates to the ERP and MES interface
* Partner with Process Council stewards to drive business process standardization across sites. Identify and resolve process standardization issues
* Provide level 2 support to ongoing operations and manage the interface with Werum for local site needs
* Actively participate in the MES COE activities and take ownership of aspects of global standards and requirements
* Actively participate in the development of PAS-X end-user training requirements and deliverables as it relates to maintenance and operational activities.

Qualifications

Education Requirement:

* BS in Engineering, Computer Science, or other technical degree.

Experience Requirements:

* 1-4 years of experience in Vaccines / Pharmaceutical Manufacturing front line supervision and/or project/automation/IT support.
* Proven record of proficiencies associated with business analysis on small sized projects.
* Excellent understanding of cGMP's, System Life Cycle methodologies and LEAN/MPS/ Sigma principles.
* Excellent facilitation, problem solving, and decision making skills.
* Demonstrated ability to analyze and define business problems, develop business cases, and identify appropriate process and technological solutions is essential.
* Proven facilitation, meeting/workshop management, project management and change management skills are essential, along with excellent written and oral communication skills, as well as strong presentation skills.
* Familiarity with implementation of Manufacturing Execution Systems and associated business benefits.

Desired:

* MS in Computer Science or related field/MBA a plus.
* Ability to understand and align IT Architecture and business strategy with business solutions.
* Familiarity with Merck Core Werum environment a plus.
* Project Management experience required, PMP certification 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 # BUS000449.

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-TN-Cleveland, US-NC-Durham, US-NC-Wilson, US-VA-Elkton, US-NJ-Whitehouse Station
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Manufacturing-Execution-Systems-%28MES%29-Business-Analyst-Job-PA-19486/1682104/168210416821042012-03-04Merck/MSDfull-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.


Join our dynamic Informatics incorporating real-world healthcare data, computational sciences, modeling, analytics, and agile engineering to benefit patients with unmet medical needs.

Position Overview:

The Research Associate in the Applied Mathematics and Modeling group, within Informatics IT, will work with colleagues to accelerate progress in research and development in relevant disease areas, in vaccine, biologic, and pharmaceutical manufacturing, and also in marketing, consumer care (over-the-counter), animal health, and corporate areas. The incumbent will develop and apply quantitative mathematical, computational and statistical modeling and simulation methodologies to a wide range of problems in the pharmaceutical industry. Work may include, but is not limited to: disease modeling, (translational) PK and PK/PD modeling, fluid dynamics and bioreactor modeling, process optimization, quantitative decision analysis, pattern recognition and data mining, image analysis, epidemiological modeling, computational immunology, mass spectrometry- and NMR-based proteomics and metabolomics, and trial simulation and prediction.

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 concentration in one of the following studies is Required: mathematics, computational biology, computer science, statistics, or another area applying math, statistics, computer science, and/or optimization techniques to biology, biotechnology, chemistry, genetics, biochemistry, process optimization, or manufacturing strategy development.

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: mathematical analysis and modeling, fluid dynamics, computational biology, probability, stochastic processes, scientific software engineering, 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:

• Experience in the use of scientific, statistical and/or modeling and simulation software (e.g. Matlab, R, Java, Mathematica and/or more specialized software such as ANSYS in particular research domains)

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 # BUS000433.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Research-Associate%2C-Mathematical-Modeling-Applied-Mathematics-&-Modeling-Job-PA-19486/1577194/157719415771942012-03-04Merck/MSDfull-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 6-month Co-op student position in Pharmaceutical Research Department in Pharmaceutical Research & Development (PR&D), Merck Research Laboratories. The Pharmaceutical Research Department identifies and implements best practices in formulation and process selection related to pharmaceutical dosage form development. This team interfaces with a variety of preclinical development groups including bulk drug synthesis, safety assessment, drug metabolism, pharmaceutical analysis, pharmaceutical scale up, and manufacturing.

Successful candidates will work together with multi-disciplinary scientists and engineers to study some common formulation and processing issues for a number of process trains in solid dosage form development at the laboratory to pilot scale such as material, physical, and mechanical property characterization, mixing, granulation, lubrication, tablet compression, powder flow and segregation, compaction behavior, and sticking problem, etc. The Co-op student will gain knowledge and experience in pharmaceutical industry especially in solid dosage formulation development by working closely with supervising scientists, learning and practicing a number of material characterization tools and processing unit operations that are important to pharmaceutical development.

There is one position available at our West Point, PA site. Merck's West Point site is located approximately 25 miles north of Philadelphia. The site is easily accessible via car or public transportation. Housing and transportation are not provided.

Qualifications

Required:

* Pursuing degree in Materials Science and Engineering, Mechanical Engineering, Chemical Engineering or a related field.
* At least completed sophomore year of BS; students completed junior year or pursuing an advanced degree preferred.
* Grade Point Average (GPA) of 3.0 or higher preferred.
* Strong academic performance, communication skills, teamwork, and the ability to work in a multi- functional environment are particularly important.
* Applicants must be legally authorized to work in the United States.
* Must be available for a period of 6 months.

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 #ADM005017.

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


Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Pharmaceutical-Research-Co-op-Job-PA-19486/1682106/168210616821062012-03-04Merck/MSDfull-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 Incineration Operations group within Energy and Environmental Services is seeking a qualified individual for a position as a Utility Technician - Powerhouse Operator at our West Point, PA facility

PLEASE NOTE:

· This is a Union position in a manufacturing environment.

· The hourly rate for this position is $30.51.

· This opening is for 3rd shift, 12:00 a.m. to 8:00 a.m. from Sunday to Thursday. (Hours/shift are subject to change).

Under the supervision of the Utility Supervisor and direction of the Maintenance Team Leader, the Utility Technician - Power House Operating (PHO) Engineer operates and maintains equipment and machinery used in a high pressure, superheated cogeneration power plant which includes steam and gas turbine and diesel generators. Monitors and operates auxiliary systems including main steam and condensate distribution, feedwater treatment, fuel, potable water, fire prevention, compressed air, chilled water, condenser water, waste water treatment, and electrical grid. Maintains logs and/or necessary paperwork as required by the operation. PHO Engineers will perform maintenance on any equipment or facilities which their skills support in a compliant quality manner. PHO engineers are part of the Utilities Technician work group and will primarily share work assignments within their job grouping with no inherent or "system imposed" limits. Based on business needs Utilities Technicians will perform maintenance activities including crossing between job groupings where skills are common. Work assignments, buildings, and equipment are not exclusive to any craft, job grouping, or employee. Position may include some responsibility for maintaining significant business systems (e.g. Maximo data, planning, procurement, and scheduling) including the authority to assign, coordinate, and maintain work for others.

Duties include, but are not limited to:

* Operates and maintains proper operating conditions on boilers, power generating equipment, and associated auxiliaries including a high pressure feedwater and feedwater heater system, boiler superheater, desuperheater, major PRV station, compressed air, potable water and steam/electrical distribution systems in order to meet variable load conditions to maintain adequate supply to building systems.
* Operates and regenerates water softeners, deionized softeners, neutralization, and boiler feedwater treatment system making resin changes, as necessary, and insuring efficient operation. Operates and maintains associated deaerator and storage tank systems and auxiliaries.
* Operates and maintains steam driven and fossil fuel fired electric generating systems and associated equipment.
* Operates utility systems/equipment within specified environmental emissions monitoring limits. Responds to alarms/emissions exception reports by making proper system/ equipment adjustments. Notifies appropriate authorities.
* Checks yard piping systems including natural gas, fuel oil, steam and condensate, for proper operation. Monitors and maintains associated manholes, valves, connections, valve boxes, traps condensate receiver stations, etc. Performs appropriate maintenance and assures service reliability.
* Operates, as necessary, compressed air, chilled water and condenser water systems including associated auxiliaries in the utility system area.
* Operates and maintains proper operating conditions on all waste heat boiler, portable boilers and associated auxiliaries.
* Monitors and operates the waste treatment systems including pumps, blowers, tank levels, and hazardous material as necessary.
* Maintains proper equipment conditions by performing routine maintenance including oiling, changing oil as required, greasing, packing, cleaning, adjusting, changing and/or cleaning burners and strainers/filters, housekeeping, etc. Troubleshoots and makes general repairs, adjustments and corrections, as necessary for continuity of efficient service.
* Checks applicable equipment and operating instruments and takes necessary steps to maintain proper operating conditions. Maintains records of operating details including fuel, water, steam, chemical electrical data, etc., and daily shift report. Changes recording charts as required, and records appropriate daily, weekly, and monthly utility data. Provides written entries and logging as necessary in shift log book/and or data entry to automated/computerized systems.
* Maintains boiler water chemistry. Performs chemical test/analysis of boiler feedwater, condensate return, and as necessary to support the effective and efficient operation of the plant, chilled water, condenser water, and plant potable water system. Troubleshoots and takes appropriate actions to correct problem areas within the utility systems. Adds chemicals as required and maintains record conditions. Monitors and maintains supply of chemicals and informs supervisor when additional chemicals are to be reordered. Standardizes and checks water room test instruments.
* Prepares equipment and/or systems for modification, tie-in, or overhaul by shutting down as required. Returns systems to service.
* Maintains proper system and equipment operation in all utility areas to insure energy and water usage efficiency. Inspects and maintains boilers and power generating equipment as required and participates in scheduled maintenance and overhaul to provide continued reliable and efficient service.
* Evaluates power (steam and electrical) requirements, and operates system efficiently considering power generation plant demands, steam driven equipment, steam accessories, etc. Prints computer generated equipment efficiency and combustion test data on all boilers for proper plant set-up.
* Performs soundings of fuel oil storage tanks, caustic and acid tanks, receives and oversees bulk deliveries, and performs inspections of associated containment areas. Maintains required records of levels. Responds to spills and notifies proper authorities. Pulls required fuel oil, lube oil and hydraulic oil samples from tanks, vessels and equipment for analysis.
* Operates various communications equipment, monitors assigned systems, and responds to emergency alarms from the utilities monitoring systems and outside utility companies.
* Operates the boiler and power generation control system and associated equipment remotely, locally, automatically, or by hand as determined necessary under normal and emergency conditions. Monitors, troubleshoots and acts appropriately on input from boiler and power system graphics, panels and annunciator systems. Makes changes as indicated by diagnostics and makes adjustments on necessary controls to maintain proper water levels in boilers, deaerator and condensate tanks, steam pressure, combustion air/fuel, power generation, and distribution requirements.
* Provides coordination/direction/guidance for operations, maintenance and contract personnel as required to support powerhouse/plant operation, maintenance and projects. Resolves plant operational problems with Power Plant Technician and Power Distribution Electrician assistance.
* Works with minimum supervision. Generates data to immediate supervisor concerning condition and status of utility systems and associated equipment.
* Performs all other duties as necessary to insure continuity and maintenance of utility systems and conditions throughout the area. Completes assigned Preventative Maintenance work orders and system outage work orders. Verifies assigned systems drawings and P&IDs for accuracy.
* Monitors and operates high and low pressure natural gas and LPG systems and associated safety systems.
* Coordinates, monitors, and performs the Lockout/Tagout procedure as defined in site and operational Hazardous Energy Control Procedures.
* Performs job duties in accordance with site and departmental safety policies and procedures.
* Operates all necessary fire fighting equipment, as well as the fire suppression systems.
* Attend and actively participates in HAZOPS, waste walk-throughs, 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

Equipment or Machinery Operated:

Boilers, superheaters, desuperheaters, feedwater heaters, compressors, pumps, fuel handling equipment, heaters, water filters, all other equipment necessary for the operation of utility plant steam, potable water, compressed air and auxiliary systems, automated control systems, chillers, cooling towers, de-ionized water units, combustion/steam turbines, electric generators, synchronizers, computerized automated control systems, internal combustion engines, and electric generation/distribution.

Required:

* Qualified candidates must pass a computer-based Skills Assessment
* Ability to perform heavy lifting (100#); use solvents, acids, and chemicals: combustible fuel handling; heat and cold; bad odors, dust, dirt, and noise; safety shoes and glasses; superheated steam and hot water; flare back; controlled combustion with explosive potential; system emergency response; subject to emergency call-in and work in an area with confined space entry.

Required Education:

* High school diploma or GED
* Graduation from a recognized trade school with a minimum of 480 hours of course work in boiler operation and control similar to the Navy Boiler Technician (BT) "A" School or the Navy Machinist Mate "A" School that has been augmented with the BT curriculum, plus a minimum of 1500 hours of hands-on, operating casualty drill training and experience similar to the Navy Boiler Technician Petty Officer 3rd Class (E4), U.S.Merchant Marine QMED (Qualified Member of the Engine Department) with steam vessel discharge documentation, or the modified Navy Machinist Mate Petty Office 3rd class (E4) which includes BT job responsibilities.

Required Experience:

* Minimum 3 years recent (within last 10 years) full-time experience (6,000 hours) operating boilers/power plant equipment of comparable pressure, size, type (design, construction, fuels, controls, and equipment) to the boilers at West Point plant (see "Equipment or Machinery Operated") OR Recently served as a U.S. Navy Boiler Technician or as a U.S. Navy Machinist Mate (including BT job responsibilities), with a minimum of 3,000 hours as a Boiler Topwatch underway or Machinist Mate Topwatch underway and obtained a rank of BT2 (E5) or MM2 (E5).
* Candidate must be able to document previous full-time experience, and be able to correctly answer comprehensive questions about boiler operation, control, and power generation in an interview.
* Experience operating boilers, superheaters, desuperheaters, compressors, pumps, chillers, cooling towers, de-ionized water units, combustion/steam turbines, electric generators, computerized automated control systems, and electric generation/distribution equipment.
* Ability to read blueprints, drawings, etc.; ability to analyze equipment problems, and take appropriate corrective action; ability to operate computers to input or retrieve information as necessary; ability to safely use hand tools and various power tools in the performance of routine maintenance. Able to work unsupervised with effective communication skills.

Preferred:

* Boiler Technician Petty Officer 2nd Class (E5)/3rd Assistant Engineer Unlimited Tonnage License/Suitable State Seal/Machinist Mate Petty Office 2nd Class (E5) which includes BT job responsibilities.
* A minimum of 40 hours documented training plus operating experience in the following preferred:
* (1) De-ionized water system; (2) Gas and Steam Turbine generator operation and control, including synchronizers; (3) Centrifugal absorption chillers; (4) Refrigeration systems; (5) Cooling towers.

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 # USW000978.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 3rd]]>http://jobs.merck.com/job/West-Point-Utility-Technician-Power-House-Operator-Job-PA-19486/1708748/170874817087482012-03-04Merck/MSDfull-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.
* 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.

This is a 1st shift position.

No relocation is offered for this position.

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.
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 # QUA002794.

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
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Quality-Specialist-Job-PA-19486/1705731/170573117057312012-03-04Merck/MSDfull-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 committed to developing RNA-based therapeutics to bring groundbreaking new medicines to the clinic. We are seeking a Ph.D.-level molecular/cell biologist to join our team of scientists performing innovative drug discovery research. The candidate will have the ability to develop expertise needed to approach complex scientific challenges and shape drug discovery strategies. Ability and interest in providing mentorship and training to other scientists is also critical. Other requirements include a Ph.D. in a life sciences-related discipline, preferably in Nucleic acids biochemistry, strong scientific software and data analysis skills, excellent communication and problem solving skills, high level of motivation and flexibility to thrive in a dynamic environment, and ability to work both independently and in a team. The candidate will either have experience in or aptitude for technologies including siRNA, antisense oligonucleotides, aptamers, real-time PCR, assay development, mammalian tissue culture, rodent pharmacology, flow cytometry, and ELISA/Western/immunochemistry. Experience with in vivo models is preferred.

Qualifications

Education Minimum Requirement:

* Ph.D.

Required Experience and Skills:

* Background in Nucleic acids biochemistry
* Strong scientific software and data analysis skills
* Excellent communication and problem solving skills
* High level of motivation and flexibility to thrive in a dynamic environment
* Ability to work both independently and in a team.
* Experience in or aptitude for technologies including siRNA, antisense oligonucleotides, aptamers, real-time PCR, assay development, mammalian tissue culture, rodent pharmacology, flow cytometry, and ELISA/Western/immunochemistry.

Preferred:

* Experience with in vivo models
* Excellent scientific writing and presentation skills
* Scientific mentorship skills
* Familiarity with the drug discovery process.
* Post-doctoral training or industry experience of 2-4 years is 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 # RNA000148.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Hazardous Materials
: BSL2, blood borne pathogens, RAM]]>http://jobs.merck.com/job/West-Point-Senior-Research-Biologist-Job-PA-19486/1494054/149405414940542012-03-04Merck/MSDfull-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 in Merck Research Laboratories (MRL). The successful candidate will join the Formulation and Basic Pharmaceutical Sciences Group and be primarily responsible for development of robust drug product compositions, processes and primary packaging to support Merck's pipeline. Specifically, the candidate will:

* 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 Minimum Requirement:

* B.S., M.S., or Ph.D. in Chemical Engineering, Bioengineering, Mechanical Engineering and Material Sciences Engineering or other relevant discipline.

Required Experience and Skills:

* General knowledge of central aspects of formulation design including biopharmaceutics, stability, and manufacturability.
* Prior experience in pharmaceutical processing, including blending, wet granulation, roller compaction, compression, encapsulation and/or film coating.
* Strong team player with excellent communication and collaboration skills.
* Highly flexible and adaptable.
* Able to work independently and effectively to 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 dispersion technologies (extrusion, spray drying) and/or nanosuspensions.
* Prior experience in process development, scale-up, and technology transfer.
* Familiarity with Quality by Design.

Exemplary candidates with commensurate experience in the food/confection industry or polymer processing 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 # PHA001051.

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
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-Sr_-Research-Chemical-Engineer-Job-PA-19486/1705736/170573617057362012-03-04Merck/MSDfull-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.


Your role will be to work with a highly collaborative team consisting of scientists from vaccine basic research, bioinformatics, infectious disease and immunoassay development to conceive, design, plan and implement advanced microbial experiments/assays designed to advance vaccine development. The assays and approaches you develop will be critical to basic research and clinical development of vaccines.

Your duties will be to lead the development and implementation of assays and protocols allowing efficient analysis of immune responses against bacterial infections in various animal models and human studies. You will need to demonstrate your skills at developing sound microbial practices and techniques.

Applicants must have a PhD in Microbiology or related discipline and should be broadly trained with experience or research potential in assay development, microbial physiology and pathogenesis and host-microbe interaction.

Qualifications

Education Minimum Requirement:

* PhD in Microbiology or related discipline

Required Experience and Skills:

* The successful candidate will have 3-4 years of post-doctoral or 5 years of industrial experience
* Expertise in assay development and innovation
* Knowledge of host (human and animal) immune responses to infection
* Outstanding microbial experience including proper and safe growth, culturing and handling techniques. Experience with microbial physiology and pathogenesis
* Experience with people management and supervision of lab scientist

Preferred:

* The candidate will be expected to understand and solve challenging issues independently and to show a high degree of innovation.
* Critical to success will be the ability to design experiments, interpret and track results, and utilize this information to enable assay development.
* The candidate must demonstrate well-developed skills for effective communication of scientific information and should have a strong history of publication in peer-reviewed journals.
* The candidate is expected to participate in preparation of patents on novel methodology and manuscripts for 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 # RES001264.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: N/A

Hazardous Materials
: Infectious bacteria and Viruses]]>http://jobs.merck.com/job/West-Point-Research-Fellow-Job-PA-19486/1691714/169171416917142012-03-04Merck/MSDfull-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 will develop expertise in drug discovery pharmaceutics by characterizing physicochemical properties of drug substances from multiple programs as well as preparing conventional and enabled formulations of these compounds. The solid-state characterization techniques for drug and formulation include X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, microscopy, and particle size. The co-op will also learn to study solution properties by chromatography. In addition, the student will become proficient using the various techniques to produce wet or dry formulations with improved drug absorption properties.

This is a paid 6 month co-operative assignment targeted to start in June 2012, whereby a weekly stipend will be provided. Housing subsidy is not available as part of this program and if housing is required it must be funded 100% by the student.

Qualifications

Requirements:

* Applicant must be currently enrolled in a 4 year degree program (pursing a BS/BA degree in chemistry, chemical engineering or related fields)
* Must be returning to school upon the completion of the co-op.
* Applicant must be available for full-time employment for 6 months starting 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 #RES001269.

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


Primary Location: US-PA-West Point
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Basic-Pharmaceutical-Sciences-Co-op-Job-PA-19486/1689820/168982016898202012-03-04Merck/MSDfull-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.


As a member of Identity and Access Management (IAM) CoE. the incumbent is responsible for assisting in the development, design, management and application of Merck's identity and access management services. The incumbent is familiar with the complete range of IAM technologies including Directory Services, Provisioning, Federation, Role/Entitlement Reviews, Authentication and Access Management. These services allow Merck to protect, control and maintain identity information for employees, contractors, partners and customers. The incumbent stays current with both internal and external IAM best practices and strategies. The incumbent's core responsibilities have global implications and will work with infrastructure and systems development areas throughout the Company to provide the highest level of service to the customer areas.

Primary Activities include, but are not limited to:

1. Gather and understand divisional and site business requirements for IAM services. Maintain active and direct interaction with key customers.
2. Development of the Identity Management tools and services roadmap strategy
3. Perform Vendor / Technology assessments
4. Assist in the application of system lifecycle practices during IAM design and deployment
5. Engineer this environment throughout the Merck community, for all divisions and in all geographies in support of One Merck initiatives.

This position will also participate on cross-functional Information Security project teams designing and developing secure business computing services in these areas:

1. Access and Administration Automation
2. Certificate and Encryption services
3. Multi-Tier Authentication Services
4. External Identity Services

The individual will develop the appropriate technical and leadership skills to perform strategy, solution architecture, project management tasks, technical design and analysis in the delivery of these services.

Position can be located at West Point, PA or Lebanon, NJ

Qualifications

Education:

* Bachelors degree desireable or equivalent experience in related area

Required:

* Minimum of at least 5 years of relevant work experience to include any combination of IT Service Management, IT Operations, Customer Fulfillment, or Information Security/Risk Management experience.
* Demonstrated record of customer focus.
* In-depth understanding of the complex technical capabilities of the IAM product suite.
* The ability to shape and influence the evolution of IAM strategy.
* Ability to organize timely delivery of engineering assignments.
* Broad knowledge and practical experience with directory and identity management technologies.
* The ability to manage multiple high priority projects with minimal supervision and promote divisional strategies through the formation and support of appropriate action plans.
* Ability to become familiar with next generation of identity management products.
* Project management experience highly desirable.
* Ability to develop, articulate, and build support around a long term vision surrounding the benefit of directory integration, identity management and access controls.
* Excellent communication, negotiation and influencing skills.
* High personal integrity, credibility, and energy.
* Essential to this position are demonstrated leadership in achieving shared objectives in a matrix organization together the ability to work effectively on cross-functional teams.
* Strong skills in developing, operating and supporting high quality technology products & services.
* Demonstrates the Merck Leadership Principles.
* Working knowledge of web servers, provisioning products

Preferred:

* Understanding of at least one authentication protocols such as LDAP, Kerberos, SAML.
* Working knowledge of web servers such as Apache & IIS, Prior experience with databases, LDAP directories, hands on experience with Linux.
* Risk Management/Information Security certifications such as CISSP or CISM.
* Knowledge of: Privacy Laws & Safe Harbor framework; 21 CFR Part 11 are preferred.
* Experience in SDLC

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 # BUS000402.

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-Lebanon, US-NC-Charlotte
Employee Status: Regular

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

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/West-Point-Infrastructure-Management%2C-Sr-Analyst-Job-PA-19486/1708754/170875417087542012-03-04Merck/MSDfull-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.


Advance siRNA delivery vehicle formulation science to enhance potency, tolerability, stability, and robustness. Apply innovative thinking and technical depth to independently plan, conduct, and interpret laboratory experiments focused on formulation design and assembly process development. Support multiple delivery vehicle platforms, with particular emphasis on lipid-based systems, including incorporation of targeting ligands. Assure timely preparation and successful delivery of formulated materials and associated documentation for critical studies. This position offers the opportunity to work with a talented, diverse team of scientists, and develop one's career in an emerging and exciting area of drug delivery.

Specific Responsibilities:

* Develops robust, scalable, and stable parenteral lipid nanoparticle formulations and manufacturing
* processes to optimize potency and tolerability.
* Supervises manufacture and ensures on-time delivery of materials to partner groups to support critical studies.
* Authors and executes production records, standard operating procedures (SOPs), and other GLP/GMP records in support of pre-clinical and clinical studies.
* May support preparation of regulatory documentation.
* Develops innovative solutions to problems in frozen liquid and lyophilized liposomal formulations.
* Leads or participates in troubleshooting and technical investigations, as required
* Ensures clear communication of study plans, key data, analyses, and recommendations to team, program leads, partner groups, and management.
* Provides technical guidance and mentorship to junior staff
* Assures compliance with established policies/procedures of the Division and Corporation and complies with all applicable governmental regulations (GMP, etc.), both domestic and foreign
* Maintains a laboratory notebook in compliance with company policy
* Actively promotes a culture of safety

* Analyzes and optimizes systems and workflows to promote operational excellence and efficiency gains
* Ensures general laboratory upkeep and maintenance

Qualifications

Education Minimum Requirement:

* Ph.D. or equivalent in chemical/biochemical engineering, chemistry/biochemistry, pharmaceutics, or related field.

Required Experience and Skills:

* At least 1 year of relevant laboratory experience are required, preferably in the areas of lipid-based and/or nanoparticulate drug delivery systems, or formulation/processing of large molecules (nucleic acids, vaccines, biologics).
* Strong problem-solving and organizational skills, as well as attention to detail.
* Highly developed oral/written communication, facilitative leadership, and collaboration skills.
* Ability to thrive in a fast-paced, dynamic environment.

Preferred:

* Prior industry laboratory experience with process development, formulation, and manufacture of nanoparticulate, lipid-based (e.g. liposomal) drug delivery systems.
* Prior industry experience in GMP production of Phase I/II/III parenteral pharmaceutical products.
* Expertise in development of frozen liquid and lyophilized formulations.
* Working knowledge of analytical methodologies for characterization of drug product attributes.
* Expertise in Design of Experiments and statistical analysis of data.
* Prior experience with laboratory automation (hardware and software).
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 # PHA001011.

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
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Laboratory Chemicals]]>http://jobs.merck.com/job/West-Point-Sr-Research-Chemical-Engineer-Job-PA-19486/1494060/149406014940602012-03-04Merck/MSDfull-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.

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-19486/1488547/148854714885472012-03-04Merck/MSDfull-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.


Incumbent is a member of MMD GMP Training Department and acts under the general direction and guidance of the Director Process Improvement and Documentation Management to develop and implement GMP training programs and communications for use throughout MMD and by MMD business partners, where appropriate. Requires strong knowledge of cGMPs and MMD's Quality Management Systems. Working with Subject Matter Experts, applies this knowledge to lead the development of divisional quality training; supports the leveraging of training resources throughout the division; works with subject matter experts, professional trainers, and customer groups in a manner that promotes cooperation, synergy and fosters teamwork; works in a tactical environment between the operational site level and strategic senior management level; performs additional duties and participate in projects such as Quality Strategy Work streams as appropriate.

Primary activities include, but not limited to:

· Design/develop/modify/implement/evaluate programs to meet divisional/global needs, specifically focusing efforts in support of training needs associated with MMD Quality and MMD sites

· Support Quality lead in myLearning implementation and use. Be a subject matter expert on the use of the system. Be a department subject matter expert in and maintain the legacy TIS and SABA training programs and records until decommissioning.

· Support the training needs of the MMD Quality Management System

· Serve as Subject Matter Expert on QMS Chapter 11 - Training and Personnel and Merck Sterile Standard on Personnel Qualification and Training for Work in Sterile Processing

· Maintain Quality WebPages and Team sites

· Work independently, lead, and/or participate in cross-functional project and quality strategy teams.

· Collaborate with all levels of the organization to continually assess training needs; present training programs internationally in a cost effective manner; mentor/coach site GMP training liaisons.

No relocation is offered for this position.

This position can be located in either West Point, PA or Summit, NJ

Qualifications

Education

· BS/BA degree in Biology, Chemistry, Pharmacy, Engineering or related scientific discipline

· Minimum 5 years experience in the pharmaceutical industry

·

Required

· Proficient in MS Office software (Word, Excel, Power Point)

· Experience in the development of MS PowerPoint presentations

· Experience in the delivery of content such as SOPs or PowerPoint presentations including using ATT connect

· Strong technical writing skills

· Strong communication skills

· Demonstrated cross-functional teamwork, collaboration and negotiation skills

· Demonstrated skills in communicating (oral and written) effectively with diverse individuals/ groups,

· Time management skills, ability to conduct work assignments and projects with well defined scope in own discipline

· Demonstrates personal leadership and accountability in day to day interactions with an operational regard for customer needs and process requirements

· Demonstrates personal trustworthiness, courtesy, cooperation and flexibility in working, interacting, and communicating with diverse individuals/ groups and ability to develop and maintain effective trusting work and customer relationships.

Preferred

* Bachelors or Masters in learning design is desirable.

* Experience in working in the pharmaceutical industry preferably in a manufacturing or quality area
* 3 years training experience (design and delivery)
* Experience in working in a global cross-cultural environment and working on global team
* Proficiency in MS Project or Visio
* Familiarity with continuous improvement methodologies; ability to recognize improvement opportunities and make appropriate process improvement recommendations
* Experience in the manufacture of medical devices or sterile products
* Firm understanding of Quality Management Systems
* Experience in the regulatory requirements regarding training and required documentation.
* Experience in working with Subject Matter Experts to develop training materials for various subjects
* Experience in using myLearning, SABA and TIS (People Soft Training Information System)Experience in Dreamweaver and Articulate programs
* Experience in Web design and Trackwise or similar system
* Experience in MELS (Merck E-Learning System) or type of E-Learning system, course deployment for learning systems
* Familiarity with ATT Connect 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 # TEC000438.

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-Summit
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Compliance-Training-Coordinator-Job-PA-19486/1700168/170016817001682012-03-04Merck/MSDfull-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

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-19486/1703539/170353917035392012-03-04Merck/MSDfull-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 reports directly to the IT Lead responsible for Safety and Regulatory Services/BoB team.

The Technical Analyst will be assigned to the Safety and Regulatory Services team and be focused on support for our production platform applications. The Technical Analyst will be responsible for supporting, configuration, maintenance and management of assigned applications. The Analyst will also work with third party software vendors/providers on configuration, enhancements and ongoing maintenance on the platforms in response to ongoing business requirement changes and requests from health authorities and regulatory agencies.

The ideal candidate should have an understanding of drug safety processes and methodologies as well as in-depth technical knowledge of Oracle and other platforms, specifically Safety, Clinical and Regulatory. The position should expect to work collaboratively with business-facing IT colleagues and IT Shared Services organizations and peers to understand and assess ongoing service/support enhancements/changes to the platforms.

These 3 positions can be located in either West Point, PA, Rahway, NJ, Whitehouse Station, NJ, or Springfield, NJ

Qualifications

Education:

* Bachelors in Computer Science preferred or equivalent work experience.

Required:

* Experience in providing Level 2 and/or 3 support services for global enterprise business applications
* Experience in providing technical support to customers, business users and project development/deployment teams
* Ability to positively interact and communicate with software vendors, infrastructure shared services to maintain the global enterprise platform and/or troubleshoot issues
* Proactively and reactively coordinate with internal/external service teams in the areas of incident, program, change and release management
* Ability to effectively communicate issues to various levels of business and IT management
* Create (or maintain) implementation, deployment and maintenance plans and knowledge base articles / technical manuals for the global enterprise system
* Possess fine-tuned analytical and troubleshooting skills and/or programming experience and experience working with relational databases
* Possess system deployment/implementation/support expertise; preferably in a regulated/GxP/development environment
* Possess interpersonal skills including teamwork, facilitation, and the ability to influence others
* Possess organizational, decision-making and communications skills
* Ability to operate efficiently and effectively in a matrix team
* Proficiency in related, underlying technologies, including SQL, Oracle, XML, and integration technologies and standards
* Ability to produce documentation in a regulatory-compliant environment following Good Documentation Practices and all Merck related SOPs / standards

Preferred:

* Experience working on large, complex platforms and COTS applications and technologies used in pharmaceuticals, specifically Global Safety, Regulatory Affairs, or Clinical
* A minimum of 5 years of relevant work experience with demonstrated expertise in Oracle
* Familiar with Axway setup; community profiles and trading partner configurations; monitor Axway Message tracker and track ICSR submissions
* Experience with Argus Safety configurations and setup
* Experience with Global Safety Business process and management
* Experience with Regulatory Submission Management practices
* Familiarity with Regulatory Drug and Device Safety reporting regulations
* Familiarity with Registration 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 # TEC000388.

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-Springfield, US-NJ-Whitehouse Station, US-NJ-Rahway
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 2

Shift (if applicable)
: N/A]]>http://jobs.merck.com/job/West-Point-Technical-Analyst-Job-PA-19486/1646175/164617516461752012-03-04Merck/MSDfull-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.

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-19486/1577195/157719515771952012-03-04Merck/MSDfull-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 are currently seeking a Biologist/Chemist in the RNA Delivery group within the Pharmacokinetics, Pharmacodynamics, and Drug Metabolism department to support the discovery and development of siRNA delivery technologies. This individual will be part of a departmental team providing in vitro and in vivo data on the biodistribution, metabolism, and pharmacokinetics of siRNA delivery vehicles. The successful candidate will be involved in the conduct of PK, metabolism, and biodistribution studies including analysis of tissues and excreta from studies. The ideal candidate will have experience in conducting biodistribution studies and analysis of samples using liquid chromatography (LC), mass spectrometry (LC-MS), and/or radiometric analysis. A candidate with oligonucleotide or peptide experience and/or proficient in ELISA, Westerns, or other hybridization methods is also desirable.

Qualifications

Education Minimum Requirement:

* BA/BS

Required Experience and Skills:

* Educational background in biology, biochemistry, chemistry, analytical chemistry, or related field.
* Strong skills in experimental design, bioanalysis, and critical data analysis/interpretation are required.
* Prior experience in a similar position is expected.
* Solid proficiencies in written and verbal communication, as well as strong ability to work in teams, are critical.

Preferred:

* Knowledge or prior experience in developing assays to quantify or characterize large molecules such as oligonucleotides and/or peptides is highly desired.
* Some prior analytical experience(s) with autoradiography, tissue and excreta scintillation counting, HPLC, or LC-MS/MS to support identification of parent or metabolites in biological matrices is requisite.
* Other hands on experience with techniques such as ELISA, gel electrophoresis, western blotting, or other protein detection methods would be 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 # PHA001054.

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
Employee Status: Regular

Travel
: No
Number of Openings: 1

Shift (if applicable)
: 1st

Hazardous Materials
: Research Chemicals, radioactivity]]>http://jobs.merck.com/job/West-Point-Chemist-Job-PA-19486/1708755/170875517087552012-03-04Merck/MSDfull-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 MRL IT Innovation Team, the incumbent is responsible for executing projects to evaluate and apply innovative new technology to unmet Merck Research Laboratory needs. The incumbent will contribute to business analysis, technology sensing and selection initiatives, execution of agile experiments to test technologies in priority business contexts, and will be expected to emphasize wide dissemination of knowledge gained during project activity.

Primary Activities:

* Perform business analysis and technology evaluation to identify and select promising technologies to apply to unmet business needs.
* Design agile experiments to test new information technologies to develop empirical evidence that demonstrates value of those technologies in the context of MRL.
* Plan and execute experiments which pilot the application of promising new technologies to yield positive impact on MRL business outcomes, in collaboration with technology vendors, academic institutions, or other external research talent.
* Ensure that knowledge of the capability of the new technology is captured for wider use by populating an Innovation Repository with appropriate information and dissemination of that information through whitepapers, journal articles, and other presentations.

Ideal candidate will possess and aptitude for and interest in working with cutting-edge information technologies that have the potential to positively impact drug discovery and development; demonstrated business analysis, application development, and project management skills a plus. Flexible mindset essential, including openness to anything which enables unmet Merck Research needs and demonstrated hypothesis-based methodology for decisions with an engineering/metric-strong approach to technology evaluation. Good interpersonal skills; proficient oral and written communications skills; desire to work in a team environment; ability to adapt to new technologies, business (situations), ability to adapt to a rapidly changing work environment, and ability to solve problems by creative application of new and existing technology.

This is a 6 month co-op based in West Point, PA. Co-op will last for a period of 6 months, beginning between January- April 2012. No housing or relocation is provided. Open to U.S. Residents & Citizens only.

Qualifications

Required:

* Currently enrolled and in pursuit of an undergraduate or graduate degree in: Information Technology, Computer Science, Systems Engineering, or related field.

*
Eligible to work in U.S. on a permanent basis (US Citizen or Permanent Resident) without sponsorship.

*
Must be be available to work on a full time basis for 6 months, beginning April 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 # IT 000240.

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
Employee Status: Regular
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Research-IT-Innovation-Co-Op-Job-PA-19486/1364409/136440913644092012-03-04Merck/MSDfull-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.

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-19486/1703544/170354417035442012-03-04Merck/MSDfull-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.

Primary Location: US-PA-West Point
Employee Status: Regular

Travel
: Yes, 10% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Principle-Analytical-Scientist-Biologics-Analytical-Sciences-Job-PA-19486/1708753/170875317087532012-03-04Merck/MSDfull-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 Business Analyst acts as the key point of contact between the MES COE and site based project teams to ensure that deployments of the Werum PAS-X software are installed to maximize business benefits and are in line with Merck business process and technical standards. The Business Analyst is responsible for supporting MES implementations across the full systems lifecycle, from identifying the business needs of clients and stakeholders to help build business cases and determine appropriate implementation of the technology, through support to project implementation and ongoing operations. The Business Analyst will have regular direct interaction with Directors and other stakeholders in the Client organization, plus collaborate with the COMET program and representatives from the Process Council. In this 'above site role' the Business Analyst will also be accountable for driving standardization and collaboration across sites.
This specific role will be US based and primarily have the West Point site as the geographical area of accountability.

Under the management and supervision of the Senior Director MMD IT MES COE, the Business Analyst is responsible for activities that include the following:

* Partner with local business leadership and project teams to develop business case for MES deployments bringing knowledge of process standardization and standard Werum configuration
* On-board local project teams into stanare leveraged from site to site. Actively participate in MES user groups within Merck
* Represent Merck in external forums as it relates to MES eg Werum user groups (PFU and SIG) as appropriate
* Educate sites in COMET deployment and operational methodology as it relates to Merck PAS-X Core environment to ensure that the interface between SAP and Werum works as planned
* Develop and apply detailed knowledge of the Manufacturing Systems Architecture as it relates to the ERP and MES interface
* Partner with Process Council stewards to drive business process standardization across sites. Identify and resolve process standardization issues
* Provide level 2 support to ongoing operations and manage the interface with Werum for local site needs
* Actively participate in the MES COE activities and take ownership of aspects of global standards and requirements
* Actively participate in the development of PAS-X end-user training requirements and deliverables as it relates to maintenance and operational activities.dard methods of working with the Merck Core Werum environment and set up project execution framework
* Understand and educate local project teams on MES standards as they relate to PAS-X system configuration, SLC, validation, hardware, software environments and business processes.
* Gain detailed knowledge of application of Werum software to enable production execution processes in order to work in concert with site teams to speed up project implementation
* Drive efficiencies in site execution of projects to reduce costs and cycle times based on standards
* Identify and ensure that best practices

Qualifications

Education Requirements:

* BS in Engineering, Computer Science, or other technical degree.

Required Experience:

* 1-4 years of experience in Vaccines Manufacturing front line supervision and/or project/automation/IT support.
* Proven record of proficiencies associated with business analysis on small sized projects.
* Excellent understanding of cGMP's, System Life Cycle methodologies and LEAN/MPS/ Sigma principles.
* Excellent facilitation, problem solving, and decision making skills.
* Demonstrated ability to analyze and define business problems, develop business cases, and identify appropriate process and technological solutions is essential.
* Proven facilitation, meeting/workshop management, project management and change management skills are essential, along with excellent written and oral communication skills, as well as strong presentation skills.
* Familiarity with implementation of Manufacturing Execution Systems and associated business benefits.

Desired Experience:

* MS in Computer Science or related field/MBA a plus.
* Ability to understand and align IT Architecture and business strategy with business solutions.
* Familiarity with Merck Core Werum environment a plus.
* Project Management experience required, PMP certification 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 # BUS000450.

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
Employee Status: Regular

Travel
: Yes, 20% of the time
Number of Openings: 1]]>http://jobs.merck.com/job/West-Point-Manufacturing-Execution-Systems-%28MES%29-Business-Analyst-Job-PA-19486/1682105/168210516821052012-03-04Merck/MSDfull-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.

Additional responsibilities are as follows:

* 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.

Please note: This position is 3rd shift - Monday - Friday.

Qualifications

Education:

* HS Diploma
* Bachelor's degree preferred

Required:

* 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

Preferred:

* Some experience in responsible line or staff position related to pharmaceutical production 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 # MAN001369.

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
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 3rd]]>http://jobs.merck.com/job/West-Point-IPT-Associate-Manufacturing-Supervisor-Job-PA-19486/1705727/170572717057272012-03-04Merck/MSDfull-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.

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-19486/1324108/132410813241082012-03-04Merck/MSDfull-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 will be responsible for overseeing ongoing day to day preclinical in vivo electroencephalography (EEG) recording activities in rodents and large animal species. EEG data interpretation, communication of results to drug discovery teams, planning of next studies and participation/representation on core teams are all primary responsibilities of this position. Oversight of lab subject matter experts and occasional hands-on work with animals and custom electronics/computer systems is needed. Coordinating the implementation of periodic system upgrades and enhancements is required.

Qualifications

Education Minimum Requirement:

* PhD in biological sciences or related field

Required Experience and Skills:

* 5 years related experience
* The candidate must have extensive experience with in vivo electroencephalography (EEG) recording and analysis methods in preclinical animals.
* Familiarity with pharmaco-EEG methods in rodent and larger species, utilization of statistical methods and custom software development is advantageous.
* The qualified individual must be able to work as part of a matrix organization with other subject matter experts.

Preferred:

* A Neuroscience background and familiarity with cognitive test batteries is desirable.
* Experience with sleep-wake analysis, quantitative EEG and evoked potentials 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 # PHA001043.

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
Employee Status: Regular
Number of Openings: 1

Shift (if applicable)
: 1st]]>http://jobs.merck.com/job/West-Point-Neurophysiology-&-Pain-Team-Member-Job-PA-19486/1655969/165596916559692012-03-04Merck/MSDfull-timeUSDstarting0BSWest Point, PA, US