Jobs / United States / Sanofi US Services INC
QC Lab Team Supervisor
Sanofi US Services INC · 🇺🇸 Swiftwater, PA
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 47 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 29 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- Last confirmed live 2 days agoWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
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Sponsor Radar — Sanofi US Services INC
The US Department of Labor certified 47 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 29 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Sanofi US Services INC →
About the role
Job Title : QC Lab Team Supervisor • Location: Swiftwater, PA About the Job : The 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. About Sanofi: 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 : 1. Laboratory Operations Management • Oversee daily operations of the quality control laboratory to ensure adherence to committed scheduled plans • Conduct routine shopfloor reviews of the laboratory to identify improvement opportunities • Ensure accurate and timely testing of received samples according to designated perimeter • Assist in scheduling laboratory work to meet the demands of production and operational timelines • Serve as a qualified reviewer for key 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. 2. Compliance & Quality Assurance • Maintain the laboratory in compliance with GMPs and quality control processes defined according to internal and external quality requirements and regulations . • Ensure the use of validated methods within the designated perimeter and execute any validation/transfer protocol as receiving unit . • Investigate in a timely manner and resolve any quality control events, issues, or discrepancies from the designated perimeter . • Implement remediation actions from findings and CAPAs (Corrective and Preventive Actions) • Author and review quality documents as a technical reviewer, including procedure revisions, protocols, reports, change controls, CAPAs, and deviations • Support internal and external audits through scribing, backroom documentation support, and participation in management walkthroughs for audit preparation and readiness . • Investigate customer product complaints and conduct deviation investigations, including interpretation and reporting of results • Assist with logbook creation, certification, logbook review, stability dispensing laboratory operations, and file retention management . 3. Team Leadership & Development • Manage and train laboratory staff, ensuring they follow best practices and safety guidelines • Ensure laboratory staff is qualified to perform testing execution by maintaining the lab qualification matrix • Foster a culture of continuous improvement and high performance • Oversee training compliance • Actively mentor colleagues to support professional development opportunities • Participate in the interview and selection process for new hires, including QC production workers, salaried