Jobs / United States / Regeneron Pharmaceuticals INC
Principal Analytical Scientist (Automation)
Regeneron Pharmaceuticals INC · 🇺🇸 RENSS - TEMPEL LN
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 roles60 certified filings for “Principal Scientist” (Biochemists and Biophysicists) in NY: $100k–$153k, median $136k. Most were filed at wage level II (85%) — 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
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Analytical Scientist to join our Quality Control team in Rensselaer, NY, supporting our IOPS organization on-site. In this role, you will shape the future of QC analytical testing by designing, developing, and scaling automated assay workflows across advanced laboratory platforms, while mentoring scientists and fostering a culture of technical growth and innovation. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When & where Location: Rensselaer, NY (Tempel Lane) Work Shift: Monday-Friday 1st shift Discover your role : • Lead the design, implementation, and optimization of automated assay workflows across modern laboratory platforms, applying deep expertise in mass spectrometry, chromatography, bioassay, electrophoresis, and ELISA. • Mentor and develop junior and mid-level scientists, building team capability in analytical science and laboratory automation. • Set priorities, coordinate work, and track progress on analytical and automation initiatives against key milestones. • Independently design and execute studies to evaluate emerging automation technologies and troubleshoot existing systems with limited supervision. • Lead complex investigations into automated method performance, supporting verification activities and driving continuous improvement. • Transfer automated workflows to QC and partner functions by developing training materials, transfer plans, and acceptance criteria. • Engage cross-functional collaborators and equipment vendors to evaluate new technologies and assess their fit for QC applications. • Prepare clear scientific reports, automation procedures, and SOPs; communicate findings, risks, and mitigation strategies to management and cross-functional teams. • Bring hands-on experience programming and optimizing automated liquid handling systems (e.g., Hamilton/Venus, Andrew+/OneLab, or Cellario) and scripting in Python, R, or VBA. • Apply strong troubleshooting skills across both analytical methods and automated instrumentation to resolve complex technical challenges. • Make sound, independent decisions and proactively recommend experiments or solutions based on deep expertise in analytical science and automation. This role requires : • 8+ years of industry experience in analytical development, laboratory automation, and QC method lifecycle management (or equivalent combination of education and experience). • Demonstrated hands-on expertise in automated liquid handling platforms and associated software programming. • Proficiency in scripting languages (Python, R, or VBA) for data analysis, workflow automation, or system integration. • Deep knowledge of QC analytical techniques including mass spectrometry, chromatography, electrophoresis, bioassay, or ELISA. • Proven ability to work independently, design scientifically sound studies from broad objectives, and drive projects to completion. • Level will be determined based on qualifications at the time of offer. Preferred: • PhD in Chemistry, Biochemistry, Biology, or a related field. • Previous experience working in a cGMP or cGLP regulated environment. • Familiarity with Cellario, Venus (Hamilton), or OneLab (Andrew+) automation platforms. • Experience developing and executing technology transfer plans across QC or partner functions. Physical Requirements: Ability to work in a laboratory environment, including standing for extended periods and handling laboratory equipment. Gowning & Environment: This role operates in a GMP analytical laboratory. Appropriate gowning and PPE are required in design