Manufacturing Associate III
Manufacturing Associate III
About Site
Catalent’s Princeton, New Jersey site is a key part of the company’s cell therapy network and serves as a U.S. commercial manufacturing facility for autologous and allogeneic cell therapies. The site is equipped to support the full product lifecycle, including late‑stage clinical development, process characterization, and commercial‑scale CGMP manufacturing across a wide range of cell types. With flexible cleanroom suites, quality control laboratories, and an experienced technical team focused on scalable, single‑use manufacturing approaches, the Princeton site enables reliable production and supply of advanced cell‑based therapies. As part of Catalent’s global Cell & Gene Therapy organization, the Princeton facility plays a strategic role in helping partners advance complex, personalized medicines toward commercialization.
Position Summary
We have an opportunity for a Manufacturing Associate III to join our team and contribute to the production of advanced cell therapies. This role involves supporting and performing GMP manufacturing processes, applying technical knowledge to ensure quality and compliance. The position requires collaboration with cross‑functional teams to maintain operational excellence and continuous improvement. The Manufacturing Associate III will play a key role in ensuring the success of both clinical and commercial manufacturing programs.
Shift: Monday - Friday, 7:30am - 4pm
Location: Princeton, NJ
100% Onsite
The Role
- Support manufacturing operations for clinical and commercial cell therapy programs through the execution of cGMP-compliant production activities.
- Coordinate daily production scheduling and resource planning in partnership with Manufacturing leadership.
- Execute and oversee key manufacturing processes, including cell culture, aseptic processing, cell expansion, separation, counting, and cryopreservation.
- Assist with the development, review, and maintenance of manufacturing documentation, including SOPs, work instructions, forms, and protocols.
- Train and mentor Manufacturing Associates in technical operations, aseptic techniques, and cGMP requirements.
- Serve as a subject matter expert in cell therapy manufacturing processes, media preparation, cryopreservation, and Biological Safety Cabinet operations.
- Lead deviation investigations, CAPA implementation, and manufacturing troubleshooting to resolve process and equipment issues.
- Drive continuous improvement initiatives to enhance process efficiency, quality, compliance, and operational performance.
- Support validation and qualification activities, including equipment, cleanroom, calibration, a...
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