Jobs / United States / Sanofi US Services INC
Senior Production Technician
Sanofi US Services INC · 🇺🇸 Swiftwater, PA
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 47 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 29 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.
Or apply yourself on the official page →
Sponsor Radar — Sanofi US Services INC
The US Department of Labor certified 47 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 29 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 Sanofi US Services INC →
About the role
Job Title : Senior Production Technician Location: Swiftwater, PA Shift : Off Shift About the job Sanofi is seeking an experienced production technician for the role of Senior production technician. This is an exciting opportunity for a candidate to develop leadership skills and is a crucial role in overseeing the production process, ensuring products are manufactured according to established specifications, schedules, and quality standards. About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. Main Responsibilities: • Ensuring that processes are always compliant with FDA regulations. • Maintain and repair equipment and monitor software and hardware issues. • Train and guide Personnel in proper work procedures, use of equipment, cGMP’s, safe work techniques and SAP to assure timely signoffs and consistency in training. • Maintains qualified trainer status. • Identifying and preventing deviations and assisting in investigation and root cause analysis. • Ensures operational areas are always staffed adequately and breaks are managed accordingly. • Accountable for the completion of operations including Metasys and Lab watch, corresponding documentation, data entry, etc. • Acts as Liaison for Production and Lead Technicians to dictate support. • Works with Lead Technicians and managers to ensure continuous operation. • Continues Development by completing at least one developmental class annually. • Helping with deviation investigations, Corrective and Preventive Actions (CAPA), Change Control Requests (CCR), and other assigned projects. • Ensuring that quality documents like Batch Production Records (BPRs) and logbooks are completed accurately and on time. • Ensuring documentation is completed accurately and in real-time is crucial for compliance and quality control. • Preparing areas for the next shift helping to maintain smooth operations and efficiency. • Responsibly use material in an efficient matter to reduce waste. • Sharing improvement ideas, issues, concerns to team members along with providing solutions. • Proactive in identifying and solving production issues to ensure smooth operations. • Model and uphold HSEEn standards, ensuring compliance with all safety procedures. • Report safety concerns, near misses, equipment issues, and environmental incidents promptly. • Participate in safety meetings, walkthroughs, and improvement initiatives. • Maintain a clean, organized, and safe work environment, performing necessary checks and inspections. • Support continuous improvement by providing input on corrective and preventive actions. • Follows effective procedures to ensure the production of safe and efficacious products. • All other duties as assigned. About You Required Qualifications: • HS or GED with 3+ yrs in cGMP or pharmaceutical experience • Associates with 2 + yrs. in cGMP or pharmaceutical experience • Bachelors with 1 + yr. in cGMP or pharmaceutical experience • Good mechanical skills, computer skills and is detail oriented. • Must have basic mechanical aptitude, computer skills, good comprehension skills, retention skills, troubleshooting and manual dexterity. • Proficiency in at least but not limited to one area of operation or product line. • Must be a qualified trainer in one or more areas. • Must have access to systems in applicable buildings and processes which have these systems (SFD, PI, Metasys, Lab watch) Special Working Conditions: • Ability to l