Jobs / United States / Sanofi US Services INC
Visual Inspection Manager - 3rd Shift
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.
- What Sanofi US Services INC paid sponsored hires in similar roles1 certified filing for “Business Analyst Manager” (Management Analysts) in NJ: $157k–$157k, median $157k. Most were filed at wage level IV (100%) — 4 lottery entries, ≈61% 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 — 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 Visual Inspection Manager Location: Swiftwater, PA This is a 3rd Shift leadership role. About the Job The Manager, Visual Inspection Operations provides hands-on leadership and strategic oversight of visual inspection operations within a regulated vaccine manufacturing environment. This role is accountable for safety, quality, delivery, cost, and people performance while fostering a culture of ownership, compliance, and continuous improvement. The ideal candidate is an experienced visual inspection leader who sets clear expectations, holds teams accountable to defined standards, and drives measurable performance improvements. This individual brings strong technical knowledge of manual and automated inspection processes and leverages industry best practices to strengthen systems, elevate inspector capability, and enhance operational efficiency. This leader serves as a change agent—developing talent, improving processes, reinforcing right-first-time execution, and elevating inspection excellence across the shift. Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster. 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 lives. Main Responsibilities Safety: • Follows all procedures put into effect to ensure your safety as well as the safety of others. Participates in monthly safety meetings. • Reports all safety issues, concerns, incidents and near misses to the team leadership. • Actively participates in safety walkthroughs coordinated by the department’s safety team. • Provides input for potential safety issues as well as contributing ideas for corrective and preventative actions. • Follows effective procedures to ensure the production of a safe and efficacious product. • Utilizes +QDCI boards for Safety issues • Leads Safety Meetings. Quality: • FDA audit understanding and awareness. Ensures areas are always following proper procedures. • Identifies possible deviation occurrences and prevents or aids in investigations and root cause analysis. • Ensure compliance with cGMP, FDA, EU Annex 1, and regulatory requirements. • Review batch records and inspection documentation for accuracy and completeness. • Lead preliminary deviation investigations and support root cause analysis. • Support internal and external audits and regulatory inspections. • Maintain inspection standards and ensure audit readiness. Delivery: • Performs production in accordance with volume fluctuation, business need, and effective procedures. Must be flexible to ensure staffing for changing business volume and needs • Lead visual inspection operations during 3rd shift. • Establish clear expectations and drive accountability across the team. Cost: • Executes procedure as documented to avoid deviations. • Oversee production planning and scheduling to meet throughput and quality targets. • Drive efficiency improvements, waste reduction, and process optimization initiatives. • Implement best practices from industry benchmarking and prior experience. • Lead or support automation initiatives for visual inspection systems. • Collaborate cross-functionally with Manufacturing, Quality, Engineering, and Supply Chain. Involvement: • Has a thorough working knowledge of cGMP’s and works to help others understand. • Lead in S