Medical Device Platform Technical Lead

Genentech

South San Francisco, CA, US
Base: $157,000 to $291,600; bonus/equity: discreti...
Systems engineering fundamentals
Mechanical product and process design
Cross functional matrix team collaboration
The Medical Device Platform Technical Lead is a senior level individual contributor role responsible for driving design excellence across a diverse range of device platform technologies

Job Summary

  • The Medical Device Platform Technical Lead is a senior level individual contributor role responsible for driving design excellence across a diverse range of device platform technologies.
  • This role involves leading platform initiatives to support product design and development teams across development and commercial lifecycles while collaborating with global cross-functional teams and external partners.
  • The position offers a salary range of $157,000 to $291,600 with a discretionary annual bonus and benefits, but relocation benefits are not available.

Matching Summary

The Medical Device Platform Technical Lead is a senior level individual contributor role responsible for driving design excellence across a diverse range of device platform technologies.

Salary

Base: $157,000 to $291,600; Bonus/Equity: Discretionary annual bonus; Benefits: Provided as detailed in company link

Skills & Requirements

Must-have

  • systems engineering fundamentals
  • mechanical product and process design
  • cross functional matrix team collaboration
  • platform design history file management
  • risk management and traceability
  • regulatory compliance and documentation
  • drug-device combination product development

Nice-to-have

  • entrepreneurial spirit
  • hands-on approach
  • excellent communication skills
  • collaboration with external partners
  • continuous improvement methods

Key Requirements

  • BS in Mechanical Engineering or equivalent
  • 10+ years experience in medical device development
  • knowledge of surgical implants and drug delivery devices
  • experience with medical device regulations
  • requirement management expertise
  • experience with CDMO/CMO collaborations

Work Rights

Not specified

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