Principal Regulatory Affairs Specialist - Mervue

Medtronic

Mervue, Ireland
Irel + : 81,360.00 eur - 122,040.00 eur; bonus/equ...
Implementing regulatory strategies
Managing regulatory submissions
Assessing regulatory impact
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all

Job Summary

  • At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all.
  • This role entails implementing regulatory strategies, managing regulatory submissions, assessing the regulatory impact of product changes, and ensuring your team delivers high-quality results through providing guidance and mentorship to team members.
  • Medtronic offers a competitive Salary and flexible Benefits Package.

Matching Summary

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all.

Salary

Ireland: 81,360.00 EUR - 122,040.00 EUR; Bonus/Equity: MIP; Benefits: flexible Benefits Package

Skills & Requirements

Must-have

  • implementing regulatory strategies
  • managing regulatory submissions
  • assessing regulatory impact
  • collaboration with cross-functional partners
  • EU MDR implementation
  • FDA regulatory requirements
  • European Medical Devices Regulation (EU MDR)

Nice-to-have

  • dynamic team player
  • strong technical knowledge
  • critical thinking and sound decisions
  • ethical behavior
  • excellent attention to detail
  • proven problem-solving skills
  • good initiative

Key Requirements

  • 8 Honor’s Degree Science or Engineering bachelor's degree/master's
  • minimum of 7 years of relevant experience
  • Class III Medical Devices experience
  • Regulatory Affairs qualification desirable
  • Medical Devices, Pharmaceuticals or similar regulated industry experience
  • Experience with software and hardware medical devices

Work Rights

Not specified

Tailored Resume

Cover Letter