Associate Director - Quality Assurance

MSD; Rahway (NJ); Hybrid; USD 129,000 - 203,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Medical, dental, vision insurance

401(k) retirement plan

Paid holidays

Job summary

Merck in Rahway, NJ is seeking an Associate Director of Quality Assurance to lead quality operations for facilities, validation, and low bioburden programs supporting clinical development at the site.

The role ensures quality systems meet regulatory standards, oversees cross-functional capital projects, and drives quality from design through startup and operations. This position expects travel and offers a comprehensive benefits package.

Qualifications

• Bachelor's degree in science, engineering, or related discipline is required.
• Advanced degree is preferred for this role.

Responsibilities

• Lead QA activities for facilities, equipment, and automation for clinical trial material supply capabilities.
• Support design phases and readiness of capital projects aligned with site expansion.
• Drive quality from design through qualification, startup, and operations of new facilities; sustain existing operations.

Skills

Compliance Investigations

Conflict Management

Cross-Functional Project Management

Deviation Management

Good Manufacturing Practices (GMP)

Operational Quality

Project Leadership

Project Life Cycle Management

Project Risk Assessments

Quality Assurance Systems

Quality Auditing

Quality Management

Quality Oversight

Quality Risk Management

Quality Systems Compliance

Regulatory Compliance

Strategic Thinking

Education

Bachelor's degree in science, engineering, or related discipline

Advanced degree preferred

Job description

Job Description

The Associate Director, Quality Assurance will be responsible for quality leadership and subject matter expertise in Quality Operations, Facilities and Validation, and Low Bioburden facilities at the our company Rahway, New Jersey site. This position will serve an important role in supporting the expansion of clinical development activities at the site with responsibilities including, but not limited to the following:

The successful candidate will assure that quality systems and controls for investigational new drugs (investigational medicinal products) meet all relevant our company quality requirements and regulatory standards.

Essential Duties and Responsibilities:

• Execute GMP quality assurance activities directly related to facilities, equipment, and automation for clinical trial material supply capabilities.
• Support the design phases and operational readiness of one or more cross-modality capital projects that are aligned with the expanding site mission.
• Drive quality from design through qualification, start-up, and operations of new facilities as well as maintain and sustain existing operations and facilities.
• Develop relationships with and provide Quality oversight of key partner groups that are commensurately expanding in size and scope of work.
• Participate in a growing team of professionals enabling an expanding site asset base.

Education Minimum Requirement:

• Bachelor’s degree in science, engineering, or related discipline; an advanced degree is preferred.

Required Experience, Knowledge, and Skills:

• Minimum of 8 years of experience in Pharmaceutical / Biotechnology industry role(s). Experience in Quality, Operations, and/or related functions at pilot and/or commercial scale. Strong knowledge and application of Current Good Manufacturing Practice (cGMP). Working knowledge of capital projects and facility operations regarding the impact to health authority regulators as well as interpretation and application of GMPs. Interpersonal skills in verbal and written communications, collaboration, teamwork, negotiation, and conflict resolution.

Preferred Experience and Skills:

• Leadership of cross-functional teams and problem-solving situations. Technical knowledge or proficiency in one or more elements of validation, facilities, equipment, utilities, automation, systems, unit operations in various product modalities, or associated technologies. A combination of experiences foundational to knowledge of validation - in product or process development, engineering, scale-up, manufacturing, technical operations, technology transfer, facilities, equipment, automation, quality systems, and / or quality operations. Advanced ability to identify and solve complex problems in a timely and efficient manner. Knowledge and/or experience with capital project lifecycle. Experience in R&D or clinical supply areas and processes.

Required Skills:

Compliance Investigations, Conflict Management, Cross-Functional Project Management, Deviation Management, Good Manufacturing Practices (GMP), Operational Quality, Project Leadership, Project Life Cycle Management, Project Risk Assessments, Quality Assurance Systems, Quality Auditing, Quality Management, Quality Oversight, Quality Risk Management, Quality Systems Compliance, Regulatory Compliance, Strategic Thinking

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:

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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.

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The salary range for this role is

$129,000.00 - $203,100.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this 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.

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:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

10/12/2026

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