Jobs / United States / Sanofi US Services INC
Quality Control Biochem / Chemistry Testing L1-1
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 Control Biochem / Chemistry Testing L1-1 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. Sampling & Analysis • Sampling of Raw Material, intermediate and as per the relevant SOP’s • Ensuring proper storage as per Storage conditions for Raw Material, intermediate, stability samples and Finish Product as per the relevant SOP’s • Handling and confirming external testing of Raw material samples. • Management of samples in sample cabinet as per Storage conditions for Raw Material, intermediate, stability samples and Finish Product as per the relevant SOP’s • Analysis of Raw Materials, stability samples, finished goods as per the required specifications on time. • Ensure cGLP in the laboratory activities. • Carry out instrumental analysis of stability samples, Raw materials, Finished Goods such as HPLC, GC, Dissolution, potentiometer, IR spectrophotometer, Raman Analyzer, Dissolution tester, Disintegration tester, Viscometer, Tap density apparatus, Microscope, UV-Vis Spectrophotometer, Conductivity meter, pH Meter, Sieve shaker, Melting point etc. • Ensuring audit readiness in Quality control laboratory. Documentation • Prepare and maintain raw data and analytical records in compliance with the current regulatory requirements. • Maintain the raw data as per regulatory requirements. • Scanning and Proper Storage of Raw Material ATR in documentation store. • Filling and documentation of ILI/Deviations at site. • Review of logbooks, Calibration records, Qualification documents etc. • Review and revise the specifications and test procedures based on the pharmacopeia. • Raising deviations and implementation of CAPAs through Qualipso • Carry out result recording, Review of data, printing of ATRs, Sampling instruction transactions in SAP ATHENA • Perform qualification of new instruments. • To support in Simplification and digitalization of activities in Quality control laboratory. • To support in OOS/OOT and deviations related to Quality control. Qualification/Calibration/Validation • Carry out the calibrations and preventive maintenance of instruments as per SOP and maintain records. • Perform qualification of instruments • Carry out the validation of analytical methods as per the testing procedure • Supporting in chromatographic trouble shooting *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 culture of continuous improvement. • Conducting daily training in the +QDCI meeting address any unsafe condition. • Take suggestion from associates to improve the work conditions with great safety and zero risk. • Periodic review of the implemented procedures and evaluation of the same. • Train people on safety and their job to ensure zero LTI and IWLT at workplace. • Carry out activities related to HSE applicable to the laboratories at side • Support the team to comply with requirements of ISO 14001 standards with respect to laboratories. • Ensure HSE compliance in the laboratory at all times About you • Experience : 3 Years • Techni