Jobs / United States / Regeneron Pharmaceuticals INC
Sr. Scientist - Drug Product Process Development (siRNA & mAb)
Regeneron Pharmaceuticals INC · 🇺🇸 TARRYTOWN
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 roles7 certified filings for “Scientist-Research & Tech Development” (Molecular and Cellular Biologists) in MA: $124k–$188k, median $130k. Most were filed at wage level II (71%) — 2 lottery entries, ≈31% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- Last confirmed live 1 day agoWhen 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 — 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
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a highly motivated Sr. Scientist to join our Process Development (PD) team within the Drug Product Development and Technology (DPDT) department. In this role, you will plan and execute drug product (DP) process development activities, developing cross-scale models, supporting risk assessments, and leading technology transfer to manufacturing sites, while helping set up in-house drug product process development capabilities. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. When & where: • Location: Tarrytown, NY • Flexibility & travel: Soml travel to CMO partners and to conferences; must be available on-site consistently, including to maintain coverage during staff absences and critical site events • Other requirements: Routine lifting of items over 30 lbs will be necessary What you'll do: • Lead DP process development activities for different unit operations across multiple programs • Support implementation of cross-scale models to successfully bridge the gap between lab and manufacturing while supporting the increasing pipeline of new modalities • Ensure effective characterization of different unit operations for a seamless technology transfer to the manufacturing sites • Support setup of in-house DP process development capabilities in the Formulations Development Group, including laboratory layout and setup, procuring tools and equipment, overseeing equipment installation and operation, and working closely with formulation development, manufacturing, and facility management teams to develop full functionality of the DP process laboratory • Independently design, execute, and document formulation, fill and finish development studies to understand the impact of process parameters on product quality attributes • Write complete internal and/or external "publications" that require minimal revisions (i.e., peer reviewed publications, patents, business plans) • Routinely author and review guidelines, protocols and reports, regulatory sections, and risk assessments to support technology transfer to manufacturing sites • Present work at group, department, and cross-functional meetings, and contribute as a process lead in drug development team meetings • Seek out, recognize, and assess existing and new technologies to improve process development capabilities in the Formulations Development Group, serving as a knowledgeable resource on prevalent manufacturing-related technologies and processes Let's find out if we're a fit: Must-haves: • Ph.D. in Pharmaceutical Sciences, Pharmaceutics, Chemical or Biomedical Engineering (or related subject area) with 0-3 years of relevant industry working experience, a MS with 8+ years, or a BS with 10+ years • Ability to work effectively in a team environment and capacity to quickly adapt to changes in project direction • A consistent record of publications with creative, productive, and insightful statistical-based analysis • Excellent oral/written communication skills and interpersonal skills to support frequent interactions with collaborators Preferred / nice-to-haves: • Experience with biologics drug product (formulation and process) development and characterization • Strong capability with analytical instruments in characterizing protein therapeutics • Proven skills and understanding in support of GMP manufacturing, quality, and regulatory functions • Hands-on experience and know-how of DP process related unit operations • Experience in developing and implementing small-scale models Thrive today. Grow tomorrow. • Studen