Principal Regulatory Affairs Project Manager, Medical Devices

West

Hybrid (on-site 3 days a week)
Hybrid work requiring onsite presence
Medical device regulatory expertise
Project management leadership skills
West is seeking a Principal Regulatory Affairs Project Manager for Medical Devices, offering a hybrid work model that requires on-site presence at least three days a week. The role focuses on navigating regulatory processes and ensuring compliance within the medical device sector

Job Summary

  • This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week.
  • The role involves managing regulatory affairs projects specifically within the medical devices sector.
  • The successful candidate will lead strategic initiatives ensuring compliance with industry regulations.

Matching Summary

Match Score: 85

West is seeking a Principal Regulatory Affairs Project Manager for Medical Devices, offering a hybrid work model that requires on-site presence at least three days a week. The role focuses on navigating regulatory processes and ensuring compliance within the medical device sector.

Skills & Requirements

Must-have

  • Hybrid work requiring onsite presence
  • Medical device regulatory expertise
  • Project management leadership skills

Nice-to-have

  • Strategic regulatory planning ability
  • Cross-functional team collaboration
  • Experience with global markets

Key Requirements

  • Minimum 3 days per week onsite attendance
  • Experience in medical device regulatory affairs
  • Proven project management capabilities

Work Rights

Not specified

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