Top 81 Quality assurance manager Jobs in Lawrenceville Nj

Manager Quality Assurance Operations
Catalent —Princeton, NJ
- $130,000 - $160,000 a year
- Email
- Engineering
- English
- 3 years
- Paid holidays
- Health insurance
QA Manager/Associate Director – Quality Assurance (Job Code: QA)
Primera Analytical Solutions —Princeton, NJ
- 5 years
- Bachelor of Science
- Bachelor's degree
5d
Food Safety Quality Manager / QC Manager
iSpice Foods Inc. —East Brunswick, NJ
- $75,000 - $95,000 a year
- Full-time
- 3 years
- Supervising experience
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
10d
Quality Control Manager
Kelly Pipe CO, LLC Fairless Hills, PA —Fairless Hills, PA
- $50,000 - $60,000 a year
- Full-time
- Bachelor's degree
- Warehouse
- In-person
Quick Apply
Director, Data Quality and Process, External Data Clinical Data Management
Genmab —Princeton, NJ
- $189,200 - $283,800 a year
- Online Application
- 5 years
- Bachelor's degree
- Doctor of Philosophy
- Commuter assistance
- Paid parental leave
Quality Assurance Lead - (CMM, PC-DMIS, GD&T)
Harold Beck & Sons Inc. —Newtown, PA
- From $83,000 a year
- Full-time
- Management
- Ability to walk for extended periods
- Mid-level
- Health savings account
- Health insurance
Quick Apply
8d
Quality Manager- GMP Analytical Testing Site
Pace Analytical Life Sciences —Lebanon, NJ
- $115,000 - $135,000 a year
- Full-time
- 3 years
- Bachelor's degree
- Senior level
- Wellness program
- Health savings account
11d
Quality and Records Manager
HDR —Pennington, NJ
- $89,114 - $127,305 a year
- Full-time
- 6 years
- Management
- Office
- Paid holidays
- Disability insurance
Area Manager - Quality Assurance/Systems
Walmart —Westampton, NJ
- $72,050 - $108,000 a year
- High school
- Writing skills
- Mid-level
- Paid jury duty
- Disability insurance
9d
Manager, Quality Assurance - GxP (GLP)
PTC Therapeutics, Inc. —Pennington, NJ
- $123,000 - $154,800 a year
- Full-time
- 6 years
- Writing skills
- Bachelor's degree
- Dental insurance
- Vision insurance
Quick Apply
4d
Quality Assurance Manager
Princeton BioMeditech Corporation —Middlesex County, NJ
- Mid-level
- 1 year
Customer Quality Manager
Mettler Toledo —Princeton, NJ
- $110,000 - $130,000 a year
- Mid-level
- Office
- Training & development
- Disability insurance
- Health insurance
Sr Quality & Compliance Manager- North America
CBRE —Raritan, NJ
- $130,000 - $158,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor's degree
Senior Quality Specialist (Document Control and Record Management)
Insmed Incorporated —Bridgewater, NJ
- $100,000 - $126,500 a year
- Full-time
- Hybrid work
- Office
- 3 years
- Bachelor's degree
- Employee stock purchase plan
- Disability insurance
12d
QA Team Lead
ANI Pharmaceuticals —East Windsor, NJ
- $80,000 - $100,000 a year
- Full-time
- Inventory management
- Writing skills
- Mid-level
- Paid holidays
- Disability insurance
Manager, Global Quality Compliance
Sun Pharmaceutical Industries, Inc (USA) —Princeton, NJ
- $101,000 - $112,500 a year
- Microsoft Excel
- Microsoft Outlook
- 5 years
- Disability insurance
- Health insurance
Senior Manager, Quality Assurance and Audit, North America Claims, Claims Shared Services
AXIS Insurance —Princeton, NJ
- $140,000 - $160,000 a year
- Full-time
- CPA
- Office
- 3 years
- Health insurance
- Tuition reimbursement
2d
Manager, Quality Control
Insmed Incorporated —Bridgewater, NJ
- $124,000 - $161,000 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Travel
- Senior level
- Employee stock purchase plan
- Disability insurance
Director, Corporate Quality Management System (QMS)
Integra LifeSciences —Princeton, NJ
- $166,750 - $228,850 a year
- Email
- Engineering
- 11+ years
- Office
- Disability insurance
- Health insurance
Inventory Quality and Control Manager - Lumberton, NJ
CVS Health —Lumberton, NJ
- $66,330 - $145,860 a year
- Full-time
- PMP
- 5 years
- Microsoft Office
- Health insurance
- Dental insurance

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Manager Quality Assurance Operations

Catalent -
Princeton, NJ

Apply Now

Job Details

Full-time
$130,000 - $160,000 a year

Benefits

Paid holidays
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Vision insurance
Benefits from day one

Qualifications

Team member evaluation
Team leadership
Coaching
GMP
Performance management
Manufacturing facility experience
Team development
Supervising experience
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Managing product quality assurance teams
Pharmaceutical manufacturing facility experience

Full 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 in Gosselies, 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 leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs 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.

Visit Catalent Careers to explore career opportunities.

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 [email protected]. 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.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to [email protected] for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.

Apply Now

Refine Your Search

quality assurance manager jobs in lawrenceville nj

Manager Quality Assurance Operations

QA Manager/Associate Director – Quality Assurance (Job Code: QA)

Food Safety Quality Manager / QC Manager

Quality Control Manager

Director, Data Quality and Process, External Data Clinical Data Management

Quality Assurance Lead - (CMM, PC-DMIS, GD&T)

Quality Manager- GMP Analytical Testing Site

Quality and Records Manager

Area Manager - Quality Assurance/Systems

Manager, Quality Assurance - GxP (GLP)

Quality Assurance Manager

Customer Quality Manager

Sr Quality & Compliance Manager- North America

Senior Quality Specialist (Document Control and Record Management)

QA Team Lead

Manager, Global Quality Compliance

Senior Manager, Quality Assurance and Audit, North America Claims, Claims Shared Services

Manager, Quality Control

Director, Corporate Quality Management System (QMS)

Inventory Quality and Control Manager - Lumberton, NJ

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