Jobs / United States / Regeneron Pharmaceuticals INC
Assoc Fill/Finish Engineer
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 roles5 certified filings for “Staff Engineer” (Chemical Engineers) in NY: $125k–$159k, median $145k. Most were filed at wage level II (40%) — 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
Summary: The Fill/Finish MFG Engineer will serve as an expert for formulation, aseptic filling, visual inspection (manual and automated), assembly, and/or packaging processes as assigned, directly supporting the operations team. They will support equipment design and selection as well as process development activities. They will be hands-on, solving issues during technology transfer, cGMP start-up, and routine manufacturing for Regeneron internal operations. This role will also support validation and training activities for the assigned equipment, processes, and operators. Essential Duties and Responsibilities: • Acts as technical SME for assigned equipment and areas in fill/finish manufacturing facility. • Interfaces with other departments such as Engineering, Validation, DP Process Development, Process Analytical Sciences, Combination Products, Regulatory, Quality Assurance and Quality Control. • Leads tech transfer / tech transfer studies, investigations, innovative technology adoption and continuous improvement initiatives. • Designs and executes cycle development and other studies on manufacturing equipment as defined by end user needs. • Supports equipment / new technology design, install, and qualification. • Manages change parts and recipe creation for new product introduction. • Leads material and component selection, design, and approval. Works with internal stakeholders and external vendors to design, source, and implement materials. • Performs functional evaluation of new components and raw materials for feasibility of use on manufacturing equipment. • Reviews Standard Operating Procedures, specifications, regulatory filing, or other controlled documents as needed. • Supports SOP development and revision for assigned equipment and process operations. • Drives innovation in fill/finish manufacturing equipment and techniques by keeping abreast of latest technological advancements. • Recommends capital expenditures and aids in the realization of capital projects. • May represent manufacturing during regulatory and client audits. • Tracks and trends relevant technical and business process metrics to ensure operations are performing effectively and efficiently. • Up to 30% travel (domestic and international) may be required (during project phase). • May lead others Education and Experience: • Associate Engineer: BS in engineering with 0+ years industry experience; MS with 0+ years industry experience or equivalent combination of education and experience. • Engineer: BS in engineering with 2+ years industry experience; MS with 1+ years industry experience or equivalent combination of education and experience. • Sr. Engineer: BS in engineering with 5+ years industry experience; MS with 4+ years industry experience or equivalent combination of education and experience. Knowledge, Skills and Abilities: • Knowledge of cGMP manufacturing environment and familiarity with formulation, aseptic filling, visual inspection (manual and automated), assembly, labeling, and/or packaging of liquid and lyophilized injectable products. • Demonstrated strong interpersonal, cross-cultural, communication, negotiation, and problem-solving skills. • Exhibits confidence, has a high emotional IQ, and demonstrated ingenuity, creativity and resourcefulness. • Ability to gain understanding from provided instructions and work towards established goals individually or as part of a team. • Ability to understand and listen to team members and stakeholders’ needs while supporting a positive team environment • Technology transfer and equipment / process validation experience of aseptic, parenteral fill/finish operations preferred. • Previous experience providing technical support preferred. • Experience with lyophi