Regulatory Affairs Specialist -neuro

Medtronic UK

Minneapolis, United States
Base: $73,600.00 - $110,400.00; bonus/equity: mip ...
Onsite
Medical device experience
Regulatory submission expertise
Fda, eu mdr, global submissions
Onsite 4 days a week to drive performance, foster an environment of belonging, and collaborate to inspire as we engineer the extraordinary

Job Summary

  • Onsite 4 days a week to drive performance, foster an environment of belonging, and collaborate to inspire as we engineer the extraordinary.
  • The Regulatory Affairs Specialist develops strategies for worldwide product registration with Medtronic Geography Regulatory partners and global regulatory agencies to introduce products and changes to market.
  • Medtronic offers a competitive Salary and flexible Benefits Package including health, dental, vision insurance, 401(k) plan plus employer contribution and match, and paid time off.

Matching Summary

Onsite 4 days a week to drive performance, foster an environment of belonging, and collaborate to inspire as we engineer the extraordinary.

Salary

Base: $73,600.00 - $110,400.00; Bonus/Equity: MIP eligible; Benefits: Health, Dental, Vision, 401(k) match, PTO, etc.

Skills & Requirements

Must-have

  • Medical device experience
  • Regulatory submission expertise
  • FDA, EU MDR, global submissions
  • ISO 14971, ISO 13485 knowledge
  • MS Office, MS Project, Adobe Acrobat, Agile

Nice-to-have

  • Strong communication skills
  • Organizational and time management skills
  • Ability to work independently
  • Passion for healthcare innovation

Key Requirements

  • 2 years relevant experience or advanced degree
  • Bachelor's degree in scientific discipline
  • Class II/III medical device experience
  • FDA 510(k) and PMA experience
  • EU MDR experience
  • Unrestricted US work authorization (for non-Principal roles)

Work Rights

Unrestricted US work authorization for non-Principal roles

Sponsorship: available

Tailored Resume

Cover Letter