Syringe Process Manager

Sanofi Genzyme

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: High-quality healthcare, wellness programs, 14 weeks 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
  • Experience with SAP and Lean Manufacturing principles
  • Strong analytical and problem-solving skills

Nice-to-have

  • Background in Aseptic Processing strongly preferred
  • Mechanical and engineering competency
  • Intermediate proficiency in MS Office Suite
  • Ability to inspire and develop teams
  • Excellent verbal and written communication skills

Key Requirements

  • Bachelor's degree in Life Sciences, Engineering, or Business
  • 7+ years equivalent experience in manufacturing/filling of biological products
  • 1+ years relevant experience in leadership roles
  • FDA-regulated industry experience with cGMP knowledge
  • Shift flexibility required for Tuesday-Saturday coverage

Work Rights

Not specified

Tailored Resume

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