Jobs / United States / Sanofi US Services INC
Quality Assurance Specialist
Sanofi US Services INC · 🇺🇸 Verna
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.
- Confirmed live todayWhen 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).
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
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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 : Quality Assurance Specialist Location : Goa Site, Verna Industrial Estate, Salcete, Goa, India About the job 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 people’s lives. Main responsibilities: Management of Quality Systems • Compilation, Review & Management of overall Product Quality Reviews system. • Act as site coordinator for change controls & management of change control system. • Management of Deviation system. • Management of Market complaint investigation system. • Act as QA focal point for OOS/OOT management. • Management of Training system. • Oversight on Pest Control system. • To perform Nitrosamine Assessment & review. • Management of ICHQ3D requirements. • Site coordinaator for Implementation of Sanofi Global Standards (STDs) and Global Operating Procedures (GOPs) • Act as focal point for Subcontractors/ Service Providers management. • Management of overall Validation systems (Process, cleaning, transport & computerized system) • Management of CAPA System. Quality Management Systems • Coordinating for conducting self-inspection as per planner and associated self-inspection activities. • Review and Approval of GxP documents, batch manufacturing record and batch packing record in electronic-document system. • Implementation of quality documents, management, and control of documents, such as SOPs, Master Documents etc. • Coordination of cGMP training activity including training of the people & review of training module. • Initiation, implementation, and closure of change controls. • Initiation of deviation and support in deviation investigation. • Support in Market Complaint investigation. • Implementation of assigned CAPAs and support in closure. • Implementation of assigned Efficiency Reviews (ERs). • Act as PPO (Primary Process Owner) for QMI (Quality Maturity Index) as assigned. • Batch release & response to queries from QP. • Management of Data integrity aspects. • Participation and support in SMS initiatives. • Support for HSE activities. • Handling of Site Master File (SMF). • Calibration document review of Engineering/QC/PMTD. • User access management & review • Analytical method creation • Audit trail review • Document archival/retrieval management. Validation & Qualifications • Quality focal point for all validations [Process, cleaning, transport & computerized system] and qualification activities. • Quality focal point for temperature/ relative humidity mapping activities. • Quality focal point for study related to hold time of products, cleaned/uncleaned equipment hold time, campaign length. • Quality focal point for utilities & purified water system. • Management of Site Qualification & Validation Master Plan In-Process Quality Assurance [IPQA] • Review & Approval of Master Batch Records & executed Batch Records • Review and Approval of logbooks. • Line clearance in Production. • To perform In-process checks in Production. • Sampling of products during routine production and validation. • Quality oversight on shopfloor. HSE • Adherence to all health safety & environmental aspects as required by company policies and procedures. • Ensure that the implementation of HSE systems, safe working conditions and maintain a cultur