Quality Operations Supervisor

Quality Operations Supervisor

The Quality Operations Supervisor is a hands-on leadership role responsible for overseeing daily quality operations activities and ensuring compliance with cGMP and regulatory requirements across multiple sites. This position involves operational quality oversight, direct engagement in batch record review, deviation management, and on-the-floor support, while managing staff. The role serves as the primary interface between site operations and Quality Operations leadership, providing proactive support to Manufacturing, Warehousing, and QC operations, and ensuring product quality and compliance objectives are consistently met.

Responsibilities :

• Ensure site-wide GMP compliance and product quality.
• Apply advanced knowledge of GMP, quality, and risk management to identify and mitigate potential risks or process gaps.
• Serve as the Quality primary point of contact between site operations and QO leadership.
• Provide hands-on, on-the-floor QO support in manufacturing cleanrooms, warehouse operations, and QC laboratories.
• Review and approve deviations, CAPAs, and Change Controls.
• Oversee critical quality activities including apheresis material receipt, production document issuance, batch record review, and final product shipment.
• Review and approve GMP documentation to ensure compliance and accuracy.
• Supervise, mentor, and develop QO staff.
• Promote a strong culture of quality, compliance, teamwork, and accountability within the QO team.
• Coordinate with cross-functional teams to allocate resources and resolve operational challenges.
• Contribute to continuous improvement of QO processes.
• Support audit and inspection readiness, and serve as SME during client and regulatory interactions.
• Lead continuous improvement initiatives to enhance compliance, efficiency, and operational excellence.

Essential Skills :

Additional Skills & Qualifications :

Work Environment :

The work environment is a growing Contract Development and Manufacturing Organization (CDMO) specializing in Cell / Gene Therapy at a brand-new site. The role involves working in manufacturing cleanrooms, warehouse operations, and QC laboratories. Flexibility to work varying hours, including evenings, weekends, and shifts, is required.

Job Type & Location :

This is a Permanent position based out of New Jersey.

Pay and Benefits :

The pay range for this position is $100000.00 - $110000.00 / yr.

Workplace Type :

This is a fully onsite position in Princeton, NJ.

Application Deadline :

This position is anticipated to close on Nov 6, 2025.

About Actalent :

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.