Syringe Process Manager

Sanofi Consumer Healthcare

Swiftwater, PA, US
Base: $78,000.00 - $112,666.66; bonus/equity: not ...
Bachelor's degree in life sciences or engineering
7+ years manufacturing experience in biological products
1+ years leadership experience in fda-regulated industry
The Syringe Process Manager is responsible for overseeing all personnel and operational activities within their assigned shift to ensure full team adherence to QDCI standards

Job Summary

  • The Syringe Process Manager is responsible for overseeing all personnel and operational activities within their assigned shift to ensure full team adherence to QDCI standards.
  • This role drives continuous improvement of line performance by leading strategic projects and developing robust Corrective and Preventive Actions (CAPA) to prevent recurrence.
  • Sanofi offers a thoughtful rewards package including high-quality healthcare, prevention programs, and at least 14 weeks' gender-neutral parental leave.

Matching Summary

The Syringe Process Manager is responsible for overseeing all personnel and operational activities within their assigned shift to ensure full team adherence to QDCI standards.

Salary

Base: $78,000.00 - $112,666.66; Bonus/Equity: Not specified; Benefits: Eligible for company employee benefit programs including healthcare and parental leave

Skills & Requirements

Must-have

  • Bachelor's degree in Life Sciences or Engineering
  • 7+ years manufacturing experience in biological products
  • 1+ years leadership experience in FDA-regulated industry
  • Working knowledge of cGMP standards
  • Shift flexibility for Tuesday-Saturday coverage

Nice-to-have

  • Experience with aseptic processing preferred
  • Familiarity with Lean Manufacturing principles
  • Mechanical and engineering competency
  • Intermediate proficiency in MS Office Suite
  • Strong analytical and problem-solving skills

Key Requirements

  • Bachelor's degree required
  • 7+ years equivalent experience in manufacturing
  • 1+ years relevant leadership experience
  • FDA-regulated industry background
  • cGMP working knowledge

Work Rights

Not specified

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