Deputy Director Of Manufacturing Planning And Support

Sanofi UK

Pearl River, NY, United States
Base: $133,500.00 - $192,833.33; bonus/equity: not...
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Oversee manufacturing quality systems
Lead production planning team
Manage manufacturing support operations
** Sanofi UK is seeking a Deputy Director of Manufacturing Planning and Support in Pearl River, NY, to oversee manufacturing quality systems, production planning, and support functions in a biopharmaceutical environment. The ideal candidate will possess extensive experience in GMP settings and strong leadership skills, focusing on compliance, operational efficiency, and continuous improvement. **

Job Summary

  • The role provides strategic leadership and operational oversight of manufacturing quality systems, production planning, and manufacturing support functions within a GMP biopharmaceutical environment.
  • Candidates will be responsible for ensuring compliance, operational efficiency, and continuous improvement across three distinct functional teams supporting manufacturing operations.
  • Sanofi offers a thoughtful rewards package including high-quality healthcare, prevention programs, and at least 14 weeks' gender-neutral parental leave.

Matching Summary

Match Score: 75

** Sanofi UK is seeking a Deputy Director of Manufacturing Planning and Support in Pearl River, NY, to oversee manufacturing quality systems, production planning, and support functions in a biopharmaceutical environment. The ideal candidate will possess extensive experience in GMP settings and strong leadership skills, focusing on compliance, operational efficiency, and continuous improvement. **

Salary

Base: $133,500.00 - $192,833.33; Bonus/Equity: Not specified; Benefits: Eligible for Company employee benefit programs

Skills & Requirements

Must-have

  • Oversee manufacturing quality systems
  • Lead production planning team
  • Manage manufacturing support operations
  • Ensure cGMP compliance
  • Drive continuous improvement initiatives

Nice-to-have

  • Strong leadership and people development skills
  • Excellent cross-functional collaboration abilities
  • Strategic thinking with strong execution capabilities
  • Problem-solving and continuous improvement mindset

Key Requirements

  • Bachelor's degree in Life Sciences or related field
  • Minimum 10+ years biopharmaceutical manufacturing experience
  • Minimum 5+ years progressive leadership experience in GMP
  • Deep understanding of cGMP regulations (21 CFR Parts 210, 211, 600)
  • Experience with deviation management and batch record systems

Work Rights

Not specified

Tailored Resume

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