Senior Program Leader, Early-stage

Sanofi

Cambridge, MA, United States
Base: $178,500.00 - $297,500.00; bonus/equity: not...
Onsite
Combination product development
Mechanical and electromechanical design
Cross-functional team leadership
Sanofi’s Global Medical Device and Packaging organization aims to lead the industry in device-mediated therapies by developing innovative drug-delivery systems that improve patient outcomes

Job Summary

  • Sanofi’s Global Medical Device and Packaging organization aims to lead the industry in device-mediated therapies by developing innovative drug-delivery systems that improve patient outcomes.
  • The Senior Program Leader will be responsible for leading device development from ideation through clinical readiness, managing cross-functional teams, and ensuring on-time, on-budget execution.
  • Sanofi offers a supportive, future-focused environment with extensive career growth opportunities, comprehensive health and wellbeing benefits, and a commitment to diversity and inclusion.

Matching Summary

Sanofi’s Global Medical Device and Packaging organization aims to lead the industry in device-mediated therapies by developing innovative drug-delivery systems that improve patient outcomes.

Salary

Base: $178,500.00 - $297,500.00; Bonus/Equity: Not specified; Benefits: Company employee benefit programs available

Skills & Requirements

Must-have

  • Combination product development
  • Mechanical and electromechanical design
  • Cross-functional team leadership
  • Device development project management
  • Regulatory knowledge for combination products
  • Technology innovation in drug delivery

Nice-to-have

  • Experience with pumps or infusion systems
  • Third party management skills
  • Strong leadership and communication
  • International business experience
  • Matrix environment decision making
  • SolidWorks design experience

Key Requirements

  • Bachelor's degree in Mechanical Engineering or related
  • 8+ years in combination product or medical device development
  • Technical lead experience on device projects
  • Preferred Master’s degree
  • Knowledge of 21 CFR parts 4 & 820, ISO 13485, 14971 & IEC 62366
  • Experience with clinical and research development teams

Work Rights

Not specified

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