Process Engineer MS&T 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 Process Engineer MS&T to join our team and provide technical leadership and support to our Princeton, NJ cGMP manufacturing facility. This role ensures cell therapy processes are robust, scalable, and compliant with cGMP standards. You will drive seamless technology transfer, reliable manufacturing, and continuous improvement to deliver safe, high-quality therapies to patients. The position reports to the Manager, MS&T and plays a key role in operational excellence and innovation. Shift: Monday - Friday, 8:00am - 4:30pm Location: Princeton, NJ 100% Onsite The Role Serve as the Manufacturing Science & Technology (MS&T) process subject matter expert, leading technology transfer, new product introduction, and lifecycle management activities. Evaluate facility, equipment, process, and workflow readiness through fit-gap analyses, risk assessments, and manufacturing feasibility reviews for new programs. Author, review, and approve cGMP technical documentation, including batch records, SOPs, protocols, validation documents, sample plans, and technical reports. Lead process validation activities, including validation strategy development, PPQ support, regulatory compliance, and ongoing process monitoring. Provide hands-on manufacturing support through process troubleshooting, deviation management, root cause investigations, quality event triage, and CAPA implementation. Analyze, trend, and interpret manufacturing data using statistical and data-driven methodologies to support process understanding and performance improvements. Identify and implement process optimizations, operational efficiencies, and new technologies to enhance productivity, quality, and compliance. Partner with Manufacturing, Supply Chain, Process Development, and Engineering teams to support equipment implementation, material assessment, validation, and operational readiness. Represent MS&T as a technical expert on cross-functional and client-facing project teams, maintaining effective relationships with vendors and stakeholders. Support site performance objectives related to quality, delivery, cost, and safety while contributing to employee training and technical development initiatives. Other duties as assigned. The Candidate Minimum Requirements Bachelor of Science in Science or Chemical/Biological Engineering. Minimum 5 years of industry experience, including 3 years in cGMP biologic or cell therapy manufacturing, technical, or process development roles. Strong scientific understanding of bioprocessing principles. Strong knowledge of FDA cGMP regulations (21 CFR Parts 11, 210, and 211) and their application to manufacturing facilities, equipment, systems, and processes. Experience supporting equipment qualification, process validation, and compliance-driven operational strategies within regulated environments. Proven ability to collaborate with clients, external partners, and cross-functional teams while building effective stakeholder relationships. Excellent verbal and written communication skills, with the ability to influence stakeholders, think strategically, prioritize competing demands, and execute effectively in dynamic environments. Proficient in Microsoft Office applications and capable of working safely and effectively in controlled manufacturing environments, including adherence to Good Documentation Practices (GDP), gowning requirements, and applicable safety protocols. Visual acuity requirements, including willingness to undergo visual acuity and color deficiency testing. Occasional exposure to moving mechanical parts, biohazardous agents, and electrical Ability to work safely and effectively in controlled manufacturing environments requiring visual acuity, color discrimination, full gowning compliance, and occasional exposure to mechanical equipment, biohazardous materials, and electrical hazards. risk; work in controlled environments with full gowning requirements. Preferred Skills & Background Advanced degree in Science or Chemical/Biological Engineering. Familiarity with cell therapy processes, cleanroom facilities, and equipment. Experience with autoclaves. Experience with cell culturing using T-Flask or G-REX. Experience with start-up, validation, and licensure of new biopharmaceutical manufacturing facilities. Experience with data aggregation, processing, and analysis software and statistical tools. Experience with Data Historian and Distributed Control Systems. Pay The anticipated salary range for this position in NJ is $105,000 – $125,000 Plus Bonus. 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 with annual performance reviews and feedback. Diverse and inclusive culture. Opportunities for career growth within an organization dedicated to improving lives. Competitive paid time off plus 8 paid holidays. Community engagement and green initiatives. Medical, dental, and vision benefits effective from day one. Tuition reimbursement program. 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. Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis. Massachusetts Lie Detector Test Notice: 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. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

Process Engineer MS&T.

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