Cmc Synthetics Clinical Manufacturing Leader

Sanofi Genzyme

Cambridge, MA, USA
Base: $148,500.00 - $214,500.00; bonus/equity: not...
Onsite
Drug substance manufacturing expertise
Gmp regulatory compliance knowledge
Cdmo sourcing and vendor management
The role is responsible for coordinating and overseeing internal and external GMP clinical manufacturing activities to supply drug substance and product for clinical trials

Job Summary

  • The role is responsible for coordinating and overseeing internal and external GMP clinical manufacturing activities to supply drug substance and product for clinical trials.
  • Candidates will act as a representative of clinical manufacturing within the CMC core project team and support local outsourcing activities for US-based CDMOs.
  • Sanofi offers a competitive rewards package including high-quality healthcare, wellness programs, and at least 14 weeks of gender-neutral parental leave.

Matching Summary

The role is responsible for coordinating and overseeing internal and external GMP clinical manufacturing activities to supply drug substance and product for clinical trials.

Salary

Base: $148,500.00 - $214,500.00; Bonus/Equity: Not specified; Benefits: High-quality healthcare, wellness programs, 14+ weeks parental leave

Skills & Requirements

Must-have

  • Drug substance manufacturing expertise
  • GMP regulatory compliance knowledge
  • CDMO sourcing and vendor management
  • Internal and external manufacturing coordination
  • Process transfer from CDMO to internal pilots

Nice-to-have

  • Strong cross-functional collaboration skills
  • Experience with AI-powered research environments
  • Ability to prioritize in dynamic portfolio settings
  • Technical scientific input capabilities

Key Requirements

  • Pharm. D. or PhD in Pharmaceutics, Chemistry, or Chemical Engineering
  • Minimum 5 years of industry experience in Drug Substance/Drug Product manufacturing
  • Trained and experienced in working in a GMP environment

Work Rights

Not specified

Tailored Resume

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