Jobs / United States / Regeneron Pharmaceuticals INC
QC External Lab Coordinator
Regeneron Pharmaceuticals INC · 🇺🇸 Limerick
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 290 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 40 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 — Regeneron Pharmaceuticals INC
The US Department of Labor certified 290 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 40 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 Regeneron Pharmaceuticals INC →
About the role
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a QC External Laboratory Coordinator to join our Quality Control (QC) Support team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When & where: • Location: Raheen, Limerick, Ireland. • Flexibility & Travel: Occasional travel may be required to support external laboratory partnerships and audits. • Other Requirements: Ability to work cross-functionally in a highly regulated Good Manufacturing Practice (GMP) environment. What you’ll do: • Coordinate sample management and method transfer activities with external laboratories supporting manufacturing and quality control operations. • Serve as a technical subject matter expert for analytical and microbiological method transfers, ensuring successful execution and compliance. • Partner with Quality Assurance, Manufacturing, and external laboratories to resolve quality issues, investigations, and technical challenges. • Review and approve method transfer documentation, quality records, and laboratory reports to support regulatory compliance. • Drive continuous improvement initiatives while maintaining quality systems, including change controls, corrective and preventive actions, and Standard Operating Procedures (SOPs). The Environment and Physical Rhythms of This Role: • This role is primarily office and laboratory-based within a Good Manufacturing Practice (GMP) regulated environment. • May involve entering manufacturing, warehouse, or laboratory areas requiring appropriate gowning and personal protective equipment. • Requires routine use of computer systems and the ability to review technical documentation and laboratory data. Let’s find out if we’re a fit: • Bachelor's degree in Biology, Chemistry, Microbiology, or a related scientific discipline, or equivalent relevant experience. • Experience in quality control, analytical testing, microbiology, or external laboratory management within a regulated industry. • Knowledge of Good Manufacturing Practice (GMP) requirements and quality systems. • Experience with method transfers, investigations, change controls, or contract laboratory oversight is preferred. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship. Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonu