🧪 Job Title: QC Lab Team Supervisor
📍 Location: Swiftwater, Pennsylvania, USA
💰 Salary Range: USD 84,750.00 – 122,416.66
🏢 Company: Sanofi
🔗 Application: [Apply Now]
🧭 About the Company
Sanofi is an innovative global healthcare company driven by one purpose — to chase the miracles of science to improve people’s lives. With cutting-edge technology, smart manufacturing, and a strong focus on quality, Sanofi delivers over 4 billion units of medicines and vaccines annually, ensuring life-saving treatments reach people faster and safer.
💼 About the Role
The QC Lab Team Supervisor (Incoming Quality Material Release – IQMR) will oversee daily operations to ensure timely material release, compliance with cGMP, and adherence to manufacturing schedules.
This role involves direct personnel management, quality oversight, and process improvement initiatives to maintain Sanofi’s high-quality standards in pharmaceutical manufacturing.
⚙️ Key Responsibilities
Operational Management
Supervise day-to-day activities of the IQMR department.
Ensure testing schedules align with production and release timelines.
Oversee accurate and timely testing of received materials.
Compliance & Quality Control
Maintain strict adherence to cGMP and regulatory requirements.
Review and approve test results, reports, and control logs.
Conduct investigations for quality events and implement corrective actions.
Team Leadership
Manage and develop department staff, ensuring all are qualified and trained.
Maintain an updated qualification matrix for personnel.
Conduct GEMBAs (on-site evaluations) to identify improvement opportunities.
Equipment & Process Oversight
Ensure calibration, qualification, and maintenance of lab equipment.
Approve raw material and finished goods batch disposition.
Support validation, transfer, and investigation protocols.
Continuous Improvement
Lead internal projects focused on operational excellence.
Implement CAPAs and monitor ongoing improvement outcomes.
🎓 Qualifications & Experience
Required:
Bachelor’s degree in Life Sciences (preferred) OR 8–10 years of relevant experience in a GMP-controlled environment.
3–5 years of relevant experience with a BA/BS degree in Life Sciences.
Proven experience in pharmaceutical quality control and GMP compliance.
Strong leadership, analytical, and communication skills.
Proficiency in SAP, LabWare, Veeva, and Microsoft 365 preferred.
Skills & Abilities:
Data-driven decision-making and attention to detail.
Ability to lead, train, and motivate a technical team.
Problem-solving and cross-functional collaboration skills.
🌍 Why Join Sanofi
Work in a future-focused, innovative environment where science meets impact.
Access career growth opportunities across departments and geographies.
Enjoy a competitive benefits package, including:
High-quality healthcare coverage
Prevention and wellness programs
14 weeks of gender-neutral parental leave
Global mobility and learning opportunities
⚖️ Equal Opportunity Statement
Sanofi and its U.S. affiliates are Equal Opportunity and Affirmative Action employers.
All qualified applicants will receive consideration for employment regardless of race, color, religion, national origin, gender, age, disability, sexual orientation, or veteran status.
🔖 Job Category:
Quality Control (QC) / Quality Assurance (QA) – Pharmaceutical Manufacturing
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