QC Lab Team Supervisor

QC Lab Team SupervisorLocation: Swiftwater, PAThe 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.

Join 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.We'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.Main Responsibilities:Laboratory Operations ManagementCompliance & Quality AssuranceTeam Leadership & DevelopmentTechnical OperationsLaboratory & Quality SystemsAbout You:Basic qualifications:Bachelor's degree in Life Sciences, Pharmaceutical Sciences, Engineering or a related scientific field with at least 8 years of experience in a cGMP environment.Experience:Progressive QC experience within a pharmaceutical or vaccine manufacturing environment, spanning roles from laboratory technician through training management and laboratory management levelsComprehensive knowledge of Good Manufacturing Practices (GMP) and regulatory requirements (FDA, EMA, ICH guidelines)Direct, hands-on expertise in Particulate Isolation, Micro-FTIR, and SEM/EDS analysis within a regulated pharmaceutical environmentDemonstrated experience authoring and reviewing technical reports, memorandums, and quality documentsExperience in a regulated compendial testing environment (USP/EP/JP standards a plus)Active involvement in regulatory and internal inspections and audit support activitiesTechnical Skills:Advanced analytical skills with the ability to analyze complex data and laboratory results to make informed decisions and identify areas for improvementProficiency in identifying issues and implementing effective solutions to resolve quality control problemsExpert knowledge of laboratory instrumentation, maintenance, qualification, and calibration proceduresStrong understanding of method validation and transfer protocolsProficiency in laboratory information management systems (LIMS) and quality systems (Trackwise, SAP, iLearn, etc.)Experience with continuous improvement and Lean initiatives, including tracking cost and efficiency metrics, is a differentiating strength (e.g., demonstrated revenue/efficiency performance above target)Leadership & Soft Skills:Strong leadership abilities to manage and motivate a team, ensuring high performance and adherence to quality standardsExcellent written and verbal communication skillsKeen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirementsAbility to work effectively under pressure and manage multiple prioritiesStrong problem-solving and critical thinking capabilitiesCommitment to continuous improvement and quality excellenceHealth, Safety & Environment (HSE) — Valued Asset:Experience serving as an HSE safety representative or correspondent, including conducting regular lab area inspections as preventative actionsDemonstrated experience performing monthly GEMBA walks and Satellite Accumulation Area inspectionsExperience facilitating safety initiatives, presenting safety communications, and driving action item completion within a QC departmentAbility to provide safety metrics for department-level meetings (L1, L2, QDCI) and serve as backup to the QC HSE managerStrong commitment to maintaining a safe laboratory environment as a core operational priorityWorking Conditions:Laboratory environment with exposure to chemicals and specialized equipmentMay require the use of personal protective equipment (PPE)Standard working hours with flexibility based on operational needs, i.e. overtime may be requiredWhy choose us?Bring the miracles of science to life alongside a supportive, future-focused team.Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks'gender-neutral parental leave.Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.Power industry-leading performance by leveraging digital, data, and AI-driven innovation – at speed and scaleTransform lives worldwide by delivering life-changing treatments anywhere, anytime.Sanofi 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.