Jobs / United States / Regeneron Pharmaceuticals INC
Quality Control Microbiology Specialist
Regeneron Pharmaceuticals INC · 🇺🇸 2 Locations
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.
- What Regeneron Pharmaceuticals INC paid sponsored hires in similar roles1 certified filing for “Sr QA Validation Specialist” (Industrial Engineers) in MA: $120k–$120k, median $120k. Most were filed at wage level II (100%) — 2 lottery entries, ≈31% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- 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
Regeneron is currently looking for a Quality Control Microbiology Lab Operations Specialist to join our QC team. The QC Microbiology team performs microbiological assays, related to clean room monitoring, utility monitoring, raw material, and product testing in accordance with Standard Operating Procedures (SOPs) and cGMP/FDA regulation. The specialist serves as a technical resource for microbiological methods, laboratory processes, and compliance-related activities while supporting operational excellence across the QC Microbiology organization. When & where: • Monday–Friday, 8:00am–4:30pm • Location: Rensselaer, New York, United States Discover your role: • Serve as a technical resource and Subject Matter Expert (SME) for QC Microbiology laboratory operations, microbiological methods, and testing programs. • Evaluate, implement, and support new or revised microbiological methods, laboratory procedures, equipment, software applications, and reporting tools. • Lead and support laboratory studies, protocols, troubleshooting efforts, and technical assessments to improve testing effectiveness and operational efficiency. • Represent QC Microbiology on cross-functional teams and project initiatives • Lead and support complex laboratory investigations, deviations, non-conformances, and root cause analyses. • Perform data gathering, trend analysis, and technical assessments to support investigations and business decisions. • Initiate, execute, and close quality system records including Change Controls, CAPAs, deviations, and document revisions. • Ensure investigations and quality system activities are completed in compliance with cGMP requirements, company procedures, and regulatory expectations. • Author, revise, and review SOPs, technical reports, protocols, risk assessments, and other controlled documents. • Facilitate inspection readiness activities and participate in internal audits, regulatory inspections, and client audits. • Monitor regulatory and technical updates and incorporate applicable changes into laboratory procedures and practices. • Ensure laboratory activities, documentation, and data integrity practices remain compliant with applicable regulations and industry standards. • Monitor and analyze laboratory performance metrics and Key Performance Indicators (KPIs). • Identify and implement process improvements to enhance efficiency, compliance, data quality, and laboratory performance. • Support strategic initiatives aimed at improving microbiology testing, sampling programs, and laboratory operations. • Collaborate with internal stakeholders and external partners to resolve technical and operational challenges. • Advanced knowledge of pharmaceutical microbiology principles and practices. • Advanced knowledge of microbiological testing methods including endotoxin, sterility, bioburden, environmental monitoring, utility monitoring, and raw material testing. • Understanding of cGMP regulations, data integrity requirements, and laboratory compliance expectations. • Ability to navigate and interpret regulatory guidance documents and compendial requirements. • Experience conducting laboratory investigations and root cause analyses. • Knowledge of Change Control, CAPA, deviation management, and quality systems. • Strong analytical, technical writing, and problem-solving skills. This role requires: • BS/BA in Biology, Microbiology or related field, and 2+ years of relevant experience. • Experience with electronic quality management systems and laboratory software applications. • Proficiency with Microsoft Office applications (Word, Excel, PowerPoint). • Working knowledge of Laboratory Information Management Systems (LIMS), Learning Management Systems (LMS), and deviation management systems. Prefer