{"id":4272973,"url":"https://alion.io/job/catalent-specialist-qa-otf","title":"Specialist, QA OTF","company":{"id":1785256,"name":"Catalent","domain":"catalent.com","url":"https://alion.io/company/catalent-com","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":null},"role":"QA","role_family":"QA","seniority":"junior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Princeton, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Cell Culture","optional":false},{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-11-12T00:00:00Z","employer_posted_date":"2026-11-12","last_verified_at":"2026-11-13T18:24:59Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"Specialist, QA OTF\nAbout Site\nCatalent’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.\nPosition Summary\nWe have an opportunity for a Specialist, QA OTF to join our team supporting GMP manufacturing of master and working cell banks, biological bulk drug substances, and finished drug products for human use. The role provides real-time quality oversight, documentation review, deviation management, and compliance monitoring to ensure product quality and patient safety. The Specialist will work closely with manufacturing and support teams to maintain high standards of GMP compliance and continuous improvement. This position reports to the Manager, QA.\nShift: Monday - Friday, 8am - 5pm\nLocation: Princeton, NJ\n100% Onsite\nThe Role\nPartner with Manufacturing and cross-functional teams, maintaining a strong floor presence (approximately 80%) to support GMP operations and ensure real-time quality oversight.\nPerform QA on-the-floor activities, including room release, observation of critical manufacturing processes, issue resolution, and real-time batch record review.\nConduct routine audits and walkthroughs of manufacturing, warehouse, and support areas to verify compliance, equipment readiness, material control, labeling, and housekeeping standards.\nMonitor adherence to cGMP requirements, Quality Management System procedures, aseptic behaviors, and Good Documentation Practices.\nReview manufacturing documentation and batch records for accuracy, compliance, and contemporaneous completion using controlled documents.\nProvide QA oversight for the manufacture of cell banks, drug substances, and final drug products, including Acceptable Quality Limit (AQL) visual inspections.\nMake independent quality decisions, identify risks, escalate issues appropriately, and drive continuous improvement initiatives.\nServe as a quality resource to GMP personnel by providing guidance on compliance, regulatory requirements, internal procedures, and industry best practices.\nBuild effective partnerships across operations and support functions to strengthen quality culture and operational excellence.\nEnsure timely completion of projects, documentation, and quality deliverables while maintaining professionalism and effectiveness in a dynamic team environment.\nThe Candidate\nMinimum Requirements\nHigh school diploma or General Educational Development required; Bachelor’s degree preferred.\n2+ years of experience within the biologic, biopharmaceutical, or regulated industry.\nKnowledge or exposure to biological manufacturing processes including microbial and cell culture cell banking, fermentation/cell culture, purification, and fill/finish.\nStrong knowledge of Good Manufacturing Practices, 21 CFR Parts 210 and 211, biological regulations per 21 CFR Parts 600s, ICH Guidelines, and EU GMPs.\nCreative and adaptable professional with strong troubleshooting, decision-making, and communication skills; able to quickly learn new manufacturing processes, interpret evolving global regulations, and deliver results independently or collaboratively in fast-paced GMP environments while effectively engaging personnel at all levels, including regulatory inspectors.\nAbility to work extended periods while standing or sitting in Grade B gowning, perform documentation and computer-based tasks, and meet required visual acuity and color vision standards.\nCapable of handling physical demands including lifting or pushing up to 50 lbs., working in confined spaces, and performing cleaning activities using disinfectants, sporicidal agents, and specialized equipment.\nComfortable working in GMP manufacturing environments with exposure to human blood components, biohazardous materials, moving mechanical equipment, and other controlled operational hazards.\nWork performed in grade A BSC or grade B, C, or D controlled environments with full gowning requirements and aseptic techniques.\nPreferred Skills & Background\n1+ years of experience in Manufacturing, Quality Assurance, or Quality Control preferred.\nKnowledge of pharmaceutical regulations relating to biologics preferred.\nExperience or knowledge in Trackwise preferred.\nExperience or knowledge with electronic batch records preferred.\nPay\nThe anticipated salary range for this position in NJ is $85,000 - $95,000 plus bonus. The final salary offered to a successful candidate may vary and will depend on factors such as experience, skillset, education, and business needs. Catalent is a multi-state employer, and this range may not reflect positions in other states.\nWhy You Should Join Catalent\nDefined career path with annual performance reviews and feedback.\nDiverse and inclusive culture.\nOpportunities for career growth within an organization dedicated to improving lives.\nCompetitive paid time off plus 8 paid holidays.\nCommunity engagement and green initiatives.\nMedical, dental, and vision benefits effective on day one of employment.\nTuition reimbursement program.\nCatalent 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.\npersonal initiative. dynamic pace. meaningful work.\nVisit Catalent Careers to explore career opportunities.\nCatalent is an Equal Opportunity Employer, including disability and veterans.\nIf 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 . 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.\nNotice 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.\nImportant Security Notice to U.S. Job Seekers:\nCatalent 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  for us to investigate with local authorities.\nCalifornia Job Seekers can find our California Job Applicant Notice HERE.\nVolunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.\nMassachusetts 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. 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