Jobs / United States / Sanofi US Services INC
Head of Quality Compliance
Sanofi US Services INC · 🇺🇸 Restricted Posting
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).
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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: Head of Quality Compliance • Location: Waterford, Ireland • Job Type: Permanent, Full-time • Working Arrangement: On-site About the job As Head of Quality Compliance within our Quality team at Waterford , you'll take ownership of ensuring our site operates in full compliance with pharmaceutical regulations, industry standards, and internal quality requirements. Leading a dedicated compliance team, you'll be the driving force behind our inspection readiness, risk management, and continuous improvement agenda — building strong relationships with regulators and stakeholders while championing a culture of compliance that puts patients at the heart of everything we do. 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: • Develop, implement, and maintain an effective site compliance programme, ensuring adherence to all applicable pharmaceutical laws, regulations, and standards • Lead inspection readiness activities and represent the company during regulatory inspections and audits, ensuring timely and effective follow-up on all findings • Proactively identify, track, and mitigate compliance and quality risks, managing any issues or allegations with appropriate corrective and preventive actions • Build and maintain strong relationships with regulators, industry associations, customers, and suppliers, representing the company on all compliance-related matters • Establish and monitor KPIs and compliance metrics, reporting performance to senior management and driving data-led continuous improvement initiatives • Coordinate quality alerts and batch recall processes in collaboration with global teams, ensuring timely reporting to relevant authorities • Lead, coach, and develop the compliance team, fostering a high-performance culture and supporting professional growth across the function About you • Significant experience in compliance, quality, or regulatory affairs within the pharmaceutical industry, ideally in a senior leadership role, with experience as a Qualified Person being highly desirable • Extensive knowledge of local, national, and international pharmaceutical regulations and standards, including FDA, EMA, and ICH guidelines • Proven track record of managing internal audits and hosting external regulatory inspections, from preparation through to execution and follow-up • Strong analytical and problem-solving skills, with the ability to assess complex compliance issues, identify root causes, and implement effective, sustainable solutions • Excellent communication and stakeholder management skills, with the confidence to convey compliance requirements clearly across all levels of the organisation • Demonstrated ability to lead and inspire a team, with experience in coaching, performance management, and building a culture of quality and compliance • Highly organised with strong attention to detail, able to manage multiple compliance projects simultaneously and deliver to deadlines Why choose us? • Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply. • 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 Better is out there. Better medications, better outcomes, better