Jobs / United States / Sanofi US Services INC
Batch Release Lead Qualified Person
Sanofi US Services INC · 🇺🇸 Waterford
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: Batch Release Lead Qualified Person Location: Waterford, Ireland Working Pattern: 3 days onsite, 2 days remote per week About This Job As Qualified Person within our Quality Lyo APU team, you'll play a critical role in ensuring that sterile pharmaceutical products are manufactured and released in full compliance with cGMP regulations. Reporting directly to the Head of Quality Lyo APU, you'll provide expert oversight of quality systems, lead improvement initiatives, mentor QA specialists, and ensure timely batch certification and release. This is an opportunity to be instrumental in shaping best practices at our award-winning Waterford site as we continue to grow and expand our capabilities. Ready to get started? 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 • Make sure all products released from the site meet strict quality and safety standards before they reach patients • Review and sign off on quality documents to confirm everything meets required standards • Work closely with other teams to resolve quality issues and close out actions in a timely manner • Investigate any product issues thoroughly, making sure they're fully resolved before a product is released • Follow all safety procedures carefully and speak up if you notice any safety concerns • Lead projects aimed at improving how quality processes work across the site • Support and guide quality team members, helping them grow their skills and expertise About You • You've worked as a Qualified Person, certifying and releasing batches on a manufacturing license — ideally within sterile product manufacturing • You're familiar with current regulatory requirements for sterile manufacturing, including Annex 1, and you stay up to date through ongoing professional development • You're a strong communicator who can influence others across teams and are genuinely results-driven, following through until quality outcomes are achieved • You hold a Master's degree or Pharmacy qualification that meets the eligibility criteria for Qualified Person status (Ireland-based qualification or UK equivalent) • You're fluent in English • You're comfortable working on-site with flexible days based on production schedules, and you're based in Ireland Why Choose Us • 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 scale. • Transform lives worldwide by delivering life-changing treatments anywhere, anytime. • Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride. • Work with AI, robotics, and next-gen automation to redefine global manufacturing and supply. • Be part of world-first initiatives like our Modulus factory, smart factories, and AI-driven supply chain solutions. • Help deliver 30+ new product launches by 2030, ensuring patients get treatments faster than ever. • Develop new skills, explore cross-functional roles, and work in an environment that values growth and discovery. Pursue Progress . Discover Extraordinary . Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’l