{"id":1038218,"url":"https://alion.io/job/sanofi-qc-lab-team-supervisor","title":"QC Lab Team Supervisor","company":{"id":146,"name":"Sanofi","domain":"sanofi.com","url":"https://alion.io/company/sanofi","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":98,"open_postings":99,"ghost_share":0,"stale_share":0.283,"repost_share":0.02,"time_to_fill_p50_days":14,"computed_at":"2026-10-13T05:45:00Z"}},"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":["Swiftwater, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":90000,"max":130000,"currency":"USD","period":"year","gross":null,"usd_annual":130000},"salary_estimate":null,"experience_years_min":8,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-09-18T17:19:39Z","employer_posted_date":"2026-09-18","last_verified_at":"2026-10-14T03:34:52Z","board_verified":true,"closed_at":null,"days_open":25,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":25},"description":"Job Title:QC Lab Team Supervisor\nLocation: Swiftwater, PA\n\nAbout the Job:\nThe Quality Control Laboratory Team Supervisor plays a pivotal role in ensuring the highest standards of product quality and patient safety within a pharmaceutical/vaccine manufacturing environment. This position is ideally suited for a seasoned QC laboratory professional who has demonstrated progressive growth through hands-on technician roles, training management, and laboratory management responsibilities. The successful candidate will bring proven expertise in quality control operations, regulatory compliance, and team leadership - with a track record of driving continuous improvement while maintaining strict adherence to internal and external GMP requirements.\nJoin a global network that powers how Sanofi delivers - seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.\nAbout Sanofi:\nWe’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system and innovative pipeline - enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve lives. \nMain Responsibilities:\n1. Laboratory Operations Management\nOversee daily operations of the quality control laboratory to ensure adherence to committed scheduled plans\n\nConduct routine shopfloor reviews of the laboratory to identify improvement opportunities\n\nEnsure accurate and timely testing of received samples according to designated perimeter\n\nAssist in scheduling laboratory work to meet the demands of production and operational timelines\n\nServe as a qualifiedreviewer forkey testing areas to maintain operational continuity and testing coverage, including but not limited to: Wet Chemistry, Electrophoresis, HPLC, LCMS, CCIT, BLFG, ICP, FTIR, GC, MALs, and SEM/EDS.\n\n2. Compliance & Quality Assurance\nMaintain the laboratory in compliance with GMPs and quality control processes defined according to internal and external quality requirements and regulations.\n\nEnsure the use of validated methods within the designated perimeter and execute any validation/transfer protocol as receiving unit.\n\nInvestigate in a timely manner and resolve any quality control events, issues, or discrepancies from the designated perimeter.\n\nImplement remediation actions from findings and CAPAs (Corrective and Preventive Actions)\n\nAuthor and review quality documents as a technical reviewer, including procedure revisions, protocols, reports, change controls, CAPAs, and deviations\n\nSupport internal and external audits through scribing, backroom documentation support, and participation in management walkthroughs for audit preparation and readiness.\n\nInvestigate customer product complaints and conduct deviation investigations, including interpretation and reporting of results\n\nAssist with logbook creation, certification, logbook review, stability dispensing laboratory operations, and file retention management.\n\n3.Team Leadership & Development\nManage and train laboratory staff, ensuring they follow best practices and safety guidelines\n\nEnsure laboratory staff is qualified to perform testing execution by maintaining the lab qualification matrix\n\nFoster a culture of continuous improvement and high performance\n\nOversee training compliance\n\nActively mentor colleagues to support professional development opportunities\n\nParticipate in the interview and selection process for new hires, including QC production workers, salaried employees, and interns\n\n 4. Technical Operations\nMaintain laboratory equipment by applying maintenance, qualification, and calibration plans to ensure accuracy and reliability of lab activities\n\nEnsure lab facilities and instruments are kept in a quality and safety status to ensure appropriate use\n\nApply deep, hands-on expertise in specialized techniques including:\n\n**Particulate Isolation and Characterization** using optical microscopy, photographic analysis, and **Micro-FTIR**\n\n**FTIR (Fourier Transform InfraredSpectroscopy)** and **SEM/EDS (Scanning Electron Microscopy/Energy DispersiveSpectroscopy)**\n\n**Container Closure Integrity Testing (CCIT)**\n\n**BLGF Testing**\n\nAuthor technical memorandums and reports\n\n5. Laboratory & Quality Systems\nDemonstrate proficiency in laboratory and quality management systems including: **Opstrakker,Qualipso,iLearn, SAP, LIMS (LabWare),Trackwise,**and the **Adobe Software Suite**\n\nAbout You:\nBasic qualifications:\nBachelor’s degree in Life Sciences, Pharmaceutical Sciences, Engineering or a related scientific field with at least 8 years of experience in a cGMP environment.\n\nExperience\nProgressive QC experience within a pharmaceutical or vaccine manufacturing environment, spanning roles from laboratory technician through training management and laboratory management levels\n\nComprehensive knowledge of **Good Manufacturing Practices (GMP)** and regulatory requirements (FDA, EMA, ICH guidelines)\n\nDirect, hands-on expertise in **Particulate Isolation, Micro-FTIR, and SEM/EDS** analysis within a regulated pharmaceutical environment\n\nDemonstrated experience authoring and reviewing technical reports, memorandums, and quality documents\n\nExperience in a regulated compendial testing environment *(USP/EP/JP standards aplus)*\n\nActive involvement in regulatory and internal inspections and audit support activities\n\n Technical Skills\nAdvanced analytical skills with the ability toanalyzecomplex data and laboratory results to make informed decisions and identify areas for improvement\n\nProficiency in identifying issues and implementing effective solutions to resolve quality control problems\n\nExpert knowledge of laboratory instrumentation, maintenance, qualification, and calibration procedures\n\nStrong understanding of method validation and transfer protocols\n\nProficiency in laboratory information management systems (LIMS) and quality systems (Trackwise, SAP,iLearn, etc.)\n\nExperience with **continuous improvement and Lean initiatives**, including tracking cost and efficiency metrics, is a differentiating strength *(e.g., demonstrated revenue/efficiency performance abovetarget)*\n\nLeadership & Soft Skills\nStrong leadership abilities to manage and motivate a team, ensuring high performance and adherence to quality standards\n\nExcellent written and verbal communication skills\n\nKeen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements\n\nAbility to work effectively under pressure and manage multiple priorities\n\nStrong problem-solving and critical thinking capabilities\n\nCommitment to continuous improvement and quality excellence\n\nHealth, Safety & Environment (HSE) - Valued Asset\nExperience serving as an **HSE safety representative or correspondent**, including conducting regular lab area inspections as preventative actions\n\nDemonstrated experience performing monthly **GEMBA walks** and **Satellite Accumulation Area inspections**\n\nExperience facilitating safety initiatives, presenting safety communications, and driving action item completion within a QC department\n\nAbility to provide safety metrics for department-level meetings (L1, L2, QDCI) and serve as backup to the QC HSE manager\n\nStrong commitment to maintaining a safe laboratory environment as a core operational priority\n\nWorking Conditions\nLaboratory environment with exposure to chemicals and specialized equipment\n\nMay require the use of personal protective equipment (PPE)\n\nStandard working hours with flexibility based on operational needs, i.e. overtime may be required\n\nWhy choose us?\nBring the miracles of science to life alongside a supportive, future-focused team.\n\nDiscover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.\n\nEnjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.\n\nTake good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention andwellness programs and at least 14 weeks’gender-neutral parental leave.\n\nShape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.\n\nPower industry-leading performance by leveraging digital, data, and AI-driven innovation - at speed and scale\n\nTransform lives worldwide by delivering life-changing treatments anywhere, anytime. \n\nSanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race;color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or militarystatus or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.\n#GD-SP \n#LI-SP\nPursue progress, discover extraordinary\nBetter is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.\nSanofi US endeavours to make our career center accessible to any and all users. If you are experiencing difficulty and need assistance applying online, please call 1-866-SANOFI2 (1-866-726-6342) or click here\nUS and Puerto Rico Residents Only\nSanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.\nNorth America Applicants Only\nThe salary range for this position is:\n$90.000,00 - $130.000,00All compensation will be determined commensurate with demonstrated experience. 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