{"id":4272955,"url":"https://alion.io/job/catalent-quality-assurance-supervisor","title":"Quality Assurance Supervisor","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":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Philadelphia, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-11-13T18:24:59Z","employer_posted_date":"2026-11-13","last_verified_at":"2026-11-13T18:24:59Z","board_verified":true,"closed_at":null,"days_open":0,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":0},"description":"QA Supervisor\nPosition Summary\nWork schedule: M-F 8am-5pm\n\n100% based on-site in Philadelphia, PA\n\nCatalent’s 206,878-square-foot Philadelphia-area facility serves as the global Center of Excellence for Clinical Supply Packaging, offering GMP secondary packaging and clinical labeling services. The site provides manual to fully automated packaging solutions, including temperature-controlled options for sensitive products. Come and be part of a team that delivers industry-leading quality and innovation.\nThe Quality Assurance department is responsible for ensuring compliance with quality system and product quality requirements defined by international regulations and corporate, network, and local standard operating procedures. The Quality Operations department supports this by providing oversight and guidance on matters affecting the quality system or product quality in daily operations.\nThe Role\nResponsible for all QA activities related to incoming, distribution and destruction and process auditing\n\nAssist In ensuring the quality and identity of pharmaceutical products during all aspects of the incoming, distribution, or packaging processes\n\nAct as the Quality partner to support the Supply Chain and Operations department\n\nEnforce Catalent policy and regulatory requirements\n\nAct as site subject matter expert for \"Good Manufacturing Practices\" and \"Good Distribution Practices\"\n\nWork to schedule a daily resource plan to support Supply Chain/Operations activities\n\nAct as lead investigator for all compliance issues regarding incoming, distribution, returns, destruction, or packaging/production\n\nDevelop process excellence and efficiencies prior to the beginning of a project\n\nTrack and report metrics and identify trends and predictive models\n\nAll other duties as assigned\n\nThe Candidate\nHS Diploma/GED and 5+ years of Production QA experience required.\n\nCollege degree preferred (BA, BS)\n\nProven track record of monitoring/auditing quality and identifying potential efficiencies in a production environment.\n\nPrevious supervisory experience of 5 years or more preferred.\n\nExperience in a regulated field - pharma, food, automotive, etc.\n\nExperience working on continuous improvement activities in partnership with other functions (e.g. Production, Validation, etc.)\n\nGood Computer Skills. Knowledge of MS Office and Inventory Management system are a plus.\n\nBasic knowledge of Lean Six Sigma methodologies an advantage\n\nGood knowledge of the application of FDA cGMP’s.\n\nAbility to be on feet and move easily throughout the Operations facilities.\n\nAbility to quickly learn and implement QA Auditing techniques.\n\nKnowledge reading engineering drawings/material specifications, a plus.\n\nIndividual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds.\n\nBe accessible to production floor, supply chain and office staff and to use required office equipment.\n\nSpecific vision requirements include reading of written documents and use of computer monitor screen frequently.\n\nWhy you should join Catalent\nDefined career path and annual performance review and feedback process\n\nDiverse, inclusive culture\n\nPositive working environment focusing on continually improving processes to remain innovative\n\nPotential for career growth on an expanding team within an organization dedicated to preserving and bettering lives\n\n152 hours of PTO + 8 paid holidays\n\nSeveral Employee Resource Groups focusing on D&I\n\nDynamic, fast-paced work environment\n\nCommunity engagement and green initiatives\n\nGenerous 401K match\n\nMedical, dental and vision benefits\n\nTuition Reimbursement - Let us help you finish your degree or start a new degree!\n\nWellHub- program to promote overall physical wellness\n\nPerkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories\n\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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Docs: https://alion.io/developers"}}