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Merck Assoc. Principal Scientist, Operations/Pharmaceutical Development in Rahway, New Jersey

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

Merck’s Animal Health (MAH) Division works to improve the health of animals around the world through collaborative partnerships and a deep sense of responsibility towards our customers, consumers, animals, society, and planet. This team of energetic, independent thinkers offers one of the industry’s most innovative portfolios of products, services, and technologies that serve to prevent, treat, and control diseases across all major farm and companion animal species both domestically and internationally.

The Associate Principal Scientist’s role encompasses the following:

Responsibilities

  1. Support R&D development programs outside of the FLEx Center as an individual contributor. Incorporate scientific and technical knowledge to complete assigned tasks.

  2. Support internal (FLEx Center; commercial sites) and external (CMOs) transfer of manufacturing processes.

  3. Collaborate with internal stakeholders (Human Health, Quality, Environmental Health and Safety, etc.) to drive effective communication and completion of deliverables.

  4. Coordinate and supervise the daily activities of individual contributors

  5. Understand priorities from manager/supervisor to ensure task completion

  6. Understand/act on guidance from supervisor where decisions are guided by policies, procedure and business plan

  7. Interprets customer needs and assesses requirements

  8. Apply supervisory skills to improve efficiency and accomplish operational objectives

  9. Identify and resolve standard day to day quality, technical, and operational problems

  10. Set priorities to meet daily deadlines; develops plans to meet short-term objectives

  11. Work within budgetary/financial objectives

  12. Make decisions guided by policies and standard operating procedures

  13. Compliance – Responsible for creating and sustaining a culture that ensures that compliance (Safety, Environment, cGMP, etc.) are imperatives for the business. Responsible for driving continuous improvement and reviewing compliance documents, as per procedures or need.

  14. Exercise judgement and decision making to ensure quality product is reliably produced while managing cost.

  15. Continuous Improvement – Tie into overall FLEx Center metric across modalities to drive efficiency.

  16. Responsible for creating and sustaining a highly engaged workforce through utilization of Merck Leadership Behaviors and Inclusion. Provide feedback and input on performance evaluations for indirect staff.

  17. Keep all team members informed on current policies/procedures and all other FLEx Center communications.

  18. Enforce all prescribed safety rules and regulations and take prompt corrective action concerning potential safety hazards

  19. Provide leadership in establishing and maintaining a high efficiency and productivity level from the team members, while maintaining a focus on Safety First and Quality Always.

  20. Identify root causes of manufacturing issues and implement corrective action with a focus on Safety, Quality, Delivery and Cost, in that order.

  21. Actively develop members to obtain maximum potential

  22. Enhance operational and/or technical capability through project experience or outside learning.

  23. Author/review documentation related to operational procedures and/or reports/memos associated with supporting development projects.

Accountability

  1. First line quality/operations supervisor working with a team of individual contributor scientists/technicians

  2. Ensure that objectives are achieved while reliably supplying quality product while following Merck standards/procedures.

  3. Tactical and strategic Shift(s) management, including collaboration with indirect staff

  4. Promote the behaviors and principles that drive continuous improvement

  5. Delivering on-time work performance in support of operational and scientific experimental activities

Core Skillsets

• Ability to learn and enhance capabilities while developing others

• Ability to be flexible and understand risk

• Continuous improvement

• Conflict resolution

• Ability to adapt between operational manufacturing and lab experiment activities

• Good documentation practices

#LI-JS1

Education Minimum Requirement:

• Master’s Degree in Science, Engineering or another technical field

Required Experience and Skills**:

• Minimum (5) years’ experience in a functional area, such as Operations, Manufacturing, Engineering, Pharmaceutical Development

Preferred Experience and Skills:

• Minimum (3) years’ experience in relevant manufacturing or processing (bulk, solid oral dosage, solutions/suspensions, packaging, etc.)

• Experience of interacting with site, divisional or regulatory audits

Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life.

If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com .

Search Firm Representatives Please Read Carefully:

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

Visa sponsorship is not available for this position.

For more information about personal rights under Equal Employment Opportunity, visit:

EEOC Poster at http://www1.eeoc.gov/employers/upload/eeocselfprint_poster.pdf

EEOC GINA Supplement​ at http://www1.eeoc.gov/employers/upload/eeocginasupplement.pdf

OFCCP EEO Supplement at https://www.dol.gov/ofccp/regs/compliance/posters/pdf/OFCCPEEOSupplementFinalJRFQA508c.pdf

Merck is an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of it’s manifestations.

Job Pharma Process Development

Title: Assoc. Principal Scientist, Operations/Pharmaceutical Development

Primary Location: NA-US-NJ-Rahway

Requisition ID: PHA001517

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