Manager Quality Assurance Operations

Catalent Pharma Solutions; Princeton (NJ); On-site; USD 130,000 - 160,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

401K benefits

152 hours PTO + 8 holidays

Job summary

Catalent is seeking a Manager, Quality Assurance Operations for our on-site cell therapy manufacturing facility in Princeton, NJ. You will provide on-the-floor QA oversight, review batch records, manage deviations, and support release decisions for clinical and commercial products.

The role requires a bachelor's in science/engineering with 7+ years in GMP pharma, 3+ years in leadership, strong regulatory knowledge, and excellent communication.

Qualifications

• Bachelor’s degree in Science, Engineering, or related discipline required; advanced degree preferred.
• Minimum 7+ years in GMP-regulated pharma/biologics manufacturing.
• Minimum 3 years of leadership or supervisory experience.
• 5+ years QA experience supporting manufacturing operations; on-the-floor QA required.
• Experience with batch records, deviations, CAPAs, change control in manufacturing.
• GMP regs knowledge incl. 21 CFR Parts 210/211, 600-series, EU GMPs, ICH; cell therapy/aseptic preferred.
• Excellent English written and verbal communication; cross-functional collaboration.

Responsibilities

• Provide real-time QA on-the-floor support for cell therapy manufacturing.
• Perform GMP walkthroughs and ensure GDP compliance.
• Review batch records, logbooks, and release decisions for products.
• Support supplier qualification activities and material investigations.
• Participate in regulatory inspections and client audits.
• Lead QA team guidance and training within QA Operations.

Skills

QA on-the-floor leadership

Regulatory GMP knowledge

Batch record review

Deviation investigations

Change control experience

Leadership / coaching

Cross-functional collaboration

English communication

Education

Bachelor’s degree in Science, Engineering, or related discipline

Advanced degree preferred

Job description

Job Description

Manager, Quality Assurance Operations

Position Summary:

• Work Schedule: Monday – Friday, 8:00am-5:00pm.
• 100% on-site

Catalent is a leading global CDMO, trusted by pharma, biotech and self-care companies to accelerate the development, manufacturing and delivery of products that improve lives.

With advanced technologies, deep expertise and a worldwide network, we partner with innovators to transform bold ideas into life-changing therapies and self-care solutions.

Our U.S. commercial cell therapy manufacturing facility is located in Princeton, NJ, and is part of Catalent’s cell therapy network including our European Center of Excellence for cell therapy inGosselies, Belgium.

The Manager, Quality Assurance Operations – Cell Therapy provides on-the-floor Quality Assurance (QA) oversight for GMP cell therapy manufacturing operations. This role ensures compliant execution, review, and disposition of manufacturing activities, materials, and documentation associated with clinical and commercial cell therapy products. Responsibilities include QA presence in processing areas, batch record review, lot disposition, raw material release, deviation management, and direct support of aseptic and cell processing operations.

The Manager, QA Operations, reports to the Director, Quality and may have direct reports including QA Specialists or Senior Specialists supporting manufacturing operations.

The Role:

• Provide real‑time QA on‑the‑floor support for cell therapy manufacturing operations, including aseptic processing, cell handling, cryopreservation, fill/finish, and material handling activities.
• Perform GMP walkthroughs and observe critical manufacturing steps to ensure compliance with approved procedures, batch records, and Good Documentation Practices (GDP).
• Support manufacturing personnel during execution of complex or high‑risk operations to ensure quality, compliance, and right‑first‑time execution.
• Review executed batch production records, logbooks, and associated GMP documentation for accuracy, completeness, and regulatory compliance.
• Support timely batch record review and participate in lot disposition and release decisions for clinical and commercial products.
• Perform QA review, approval, and release of raw materials, consumables, and critical reagents used in cell therapy processing.
• Review, assess, and approve deviations, nonconformances, investigations, CAPAs, and change controls impacting manufacturing operations, facilities, equipment, or materials.
• Support supplier qualification activities, material‑related investigations, and ensure material qualification documentation meets internal and regulatory requirements.
• Support inspection readiness activities and participate in regulatory inspections and client audits to ensure adherence to the Catalent Quality Management System (QMS), site SOPs, and global standards.
• Provide day‑to‑day leadership and QA guidance while collaborating cross‑functionally with Manufacturing, Supply Chain, MS&T, Validation, and Regulatory Affairs, and supporting QA Operations training and development.
• Other duties as assigned.

The Candidate:

• Bachelor’s degree in Science, Engineering, or related discipline required; advanced degree preferred.
• Minimum of 7 years of experience in a GMP-regulated pharmaceutical, biologics, or cell/gene therapy manufacturing environment.
• Minimum of 3 years of Prior leadership or supervisory experience required, with demonstrated ability to coach and manage performance.
• 5+ years of Quality Assurance experience supporting manufacturing operations; direct QA on-the-floor experience required.
• Demonstrable leadershipexperience at Catalent (including but not limited to participation in Catalent-sponsoredleadershipprograms such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.
• Demonstrated experience supporting GMP operations, including batch record review, lot disposition, deviation investigations, change control, and work performed in manufacturing and cleanroom environments.
• Strong knowledge of GMP regulations and guidance, including 21 CFR Parts 210/211, 600‑series (biologics), applicable EU GMPs, and ICH guidelines; cell therapy, ATMP, or aseptic processing experience strongly preferred.
• Experience with raw material qualification and release activities; supplier quality experience preferred.
• Strong written and verbal communication skills in English, with the ability to work cross‑functionally under tight timelines, manage multiple priorities with high attention to detail, and willingness to successfully complete required visual acuity testing (including Graham Field Eye Test Chart and Ishihara Color Vision Test).

The anticipated salary range for this position in New Jersey is $130,000 - $160,000 plus annual bonus, when eligible. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.

Why you should Join Catalent:

• Defined career path and annual performance review and feedback process.
• Diverse, inclusive culture.
• Potential for career growth on an expanding team.
• Cross-functional exposure to other areas within the organization.
• 152 hours of paid time off annually + 8 paid holidays.
• Medical, dental, vision and 401K benefits effective day one of employment.
• Tuition Reimbursement.

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [e-mail]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

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It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.