Director, Large Molecule Analytical - GMP Operations

MSD; Rahway (NJ); On-site; USD 173,000 - 273,000; Full time

Job summary

MSD in Rahway, NJ is seeking a Director to lead a growing GMP analytical team supporting biologics manufacturing. You will drive development of people, lab capability, and a culture of quality and compliance during rapid expansion into sterile drug-product filling and ADCs.

Responsibilities include overseeing batch-release, stability testing, method validation, and cross-functional partnerships with Manufacturing, Quality, and Regulatory to align testing priorities and scale operations.

Qualifications

• Ph.D. in analytical chemistry, biochemistry, biotechnology, pharmaceutical sciences, or a related discipline with 8+ years of pharmaceutical experience; or
• MS with 10+ years; or
• BS with 14+ years.

Responsibilities

• Lead and develop a growing team of scientists and people leaders responsible for GMP analytical testing and manufacturing support across multiple biologics operations.
• Build the organizational structure, workforce plan, technical expertise, and leadership capacity to support significant growth in portfolio demand and laboratory scope.
• Establish clear expectations and operating practices that allow growth while maintaining a culture of quality, scientific rigor, safety, data integrity, and accountability.
• Provide leadership for batch-release and stability testing, ensuring timely, reliable, and compliant delivery of analytical results for product disposition and supply.
• Oversee analytical support for manufacturing, including raw-material and in-process testing for standard monoclonal antibody production, ADC manufacturing, and sterile drug-product filling.
• Lead GMP Operations participation in early-stage analytical method validation and transition of methods from development into routine GMP use with Validation Strategy team.
• Provide laboratory input to validation plans and ensure readiness to execute studies and transition validated methods to routine use.
• Build analytical readiness for new manufacturing capabilities, including capacity, equipment, methods, materials, data systems, training, staffing, and expertise.
• Balance ongoing GMP operations with longer-term work to prepare for new facilities, technologies, and expanding portfolio.
• Maintain inspection readiness through documentation, disciplined practices, investigations, and CAPA.
• Proactively identify and manage quality and operational risks with increasing workload and new technologies.
• Provide technical leadership for analytical events, method-performance issues, and other risks affecting product quality or schedules.
• Partner with Manufacturing, Quality, analytical development, technical operations, and Regulatory teams to align testing priorities and risk mitigation.
• Establish performance measures and standardized ways of working to improve reliability, right-first-time execution, efficiency, and predictability.
• Develop scientific and leadership talent, strengthen succession plans, and foster an inclusive, high-performing organization.

Skills

Analytical Chemistry

Biologics

GMP

Leadership

Regulatory

Education

Ph.D. in analytical chemistry/biochemistry/biotechnology/pharmaceutical sciences

MS in a related field

BS in related field

Job description

Job Description

Position Overview:

This Director will lead a growing GMP analytical team supporting biologics manufacturing in Rahway. The organization is expanding to support sterile drug-product filling, antibody-drug conjugate manufacturing, and standard monoclonal antibody production in the Next Gen Bio facility. The role is accountable for reliable analytical delivery, development of people and laboratory capability, and maintaining a strong quality and compliance culture throughout this period of significant growth.

Key Accountabilities:

• Lead and develop a growing team of scientists and people leaders responsible for GMP analytical testing and manufacturing support across multiple biologics operations.
• Build the organizational structure, workforce plan, technical expertise, and leadership capacity required to support significant growth in portfolio demand and laboratory scope.
• Establish clear expectations and operating practices that allow the organization to grow while maintaining a strong culture of quality, scientific rigor, safety, data integrity, and accountability.
• Provide leadership for batch-release and stability testing, ensuring timely, reliable, and compliant delivery of analytical results in support of product disposition and supply.
• Oversee analytical support for manufacturing, including raw-material and in-process testing for standard monoclonal antibody production in the Next Gen Bio facility, antibody-drug conjugate manufacturing, and sterile drug-product filling.
• Lead GMP Operations participation in early-stage analytical method validation and the transition of methods from development into routine GMP use, in partnership with the dedicated Validation Strategy team.
• Provide laboratory and operational input to validation plans authored by the Validation Strategy team and ensure the GMP Operations team is prepared to execute the studies reliably and transition validated methods into routine use.
• Build analytical readiness for new manufacturing capabilities, including the required laboratory capacity, equipment, methods, materials, data systems, training, staffing, and technical expertise.
• Balance the immediate demands of ongoing GMP operations with the longer‑term work required to prepare for new facilities, technologies, and an expanding product portfolio.
• Maintain continual inspection readiness through robust documentation, disciplined laboratory practices, effective investigations, and timely corrective and preventive actions.
• Proactively identify and manage quality and operational risks associated with increasing workload, new employees, new technologies, and expanding laboratory capabilities.
• Provide technical and operational leadership for analytical events, method‑performance issues, and other risks that could affect product quality, manufacturing schedules, regulatory commitments, or supply.
• Partner closely with Manufacturing, Quality, analytical development, technical operations, and Regulatory teams to align testing priorities, capacity, readiness plans, and risk mitigation.
• Establish performance measures and standardized ways of working that improve laboratory reliability, right‑first‑time execution, efficiency, and predictability.
• Develop scientific and leadership talent, strengthen succession plans, and create an inclusive, high‑performing organization capable of sustaining continued growth.

Qualifications and Experience:

• Ph.D. in analytical chemistry, biochemistry, biotechnology, pharmaceutical sciences, or a related discipline with 8+ years of relevant pharmaceutical experience; or
• MS with 10+ years; or
• BS with 14+ years.
• Demonstrated leadership of scientists or laboratory teams in a GMP‑regulated biologics environment.
• Experience with biologics analytical testing, including method validation, manufacturing support, batch release, stability, investigations, and laboratory lifecycle management.
• Broad knowledge of analytical technologies used for biologics drug substance and drug product; experience with monoclonal antibodies, antibody‑drug conjugates, or sterile products is preferred.
• Strong knowledge of GMP requirements, data integrity, quality systems, and regulatory inspection expectations.
• Proven ability to lead through organizational growth, manage competing priorities, and deliver through cross‑functional partnerships.

Core Competencies and Skills:

• People leadership and organizational development
• GMP laboratory operations and inspection readiness
• Scientific judgment across biologics analytical platforms
• Operational planning, prioritization, and risk management
• Cross‑functional influence and clear communication
• Change leadership and continuous improvement

Required Skills:

Analytical Chemistry, Analytical Method Development, Analytical Testing, Antibody Drug Conjugates (ADC), Antibody Production, Biochemistry, Biological Manufacturing, Biologics, Biotechnology, Chromatographic Techniques, Monoclonal Antibodies, Monoclonal Antibody Development, Pharmaceutics, Process Analytical Technology (PAT), Regulatory Submissions

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

The primary location for this posting is:

USA - New Jersey - Rahway

Where required by law, the compensation range for this role is provided below.

The salary range for the primary location of this role is:

$173,200.00 - $272,600.00

This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

Additional location(s):

Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location.

Additional location(s) Compensation Information:

• San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
• Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Employee Status:

Regular

Relocation:

Domestic

VISA Sponsorship:

Yes

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

11/13/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.