Regulatory Affairs Consultant: Medical Device And Combination Product Expert

Parexel

Multiple Locations
Regulatory strategy development
Medical device regulations expertise
Regulatory interactions with health authorities
At Parexel, we are committed to improving the world's health through our work in clinical trials and regulatory consulting

Job Summary

  • At Parexel, we are committed to improving the world's health through our work in clinical trials and regulatory consulting.
  • The role involves leading regulatory strategy for medical devices and combination products.
  • We seek professionals who take their work personally and are dedicated to making a difference.

Matching Summary

At Parexel, we are committed to improving the world's health through our work in clinical trials and regulatory consulting.

Skills & Requirements

Must-have

  • Regulatory strategy development
  • Medical device regulations expertise
  • Regulatory interactions with health authorities

Nice-to-have

  • Experience with in vitro diagnostic devices
  • Strong communication skills
  • Proficiency with regulatory systems

Key Requirements

  • Minimum 5 years of regulatory affairs experience
  • University degree in a scientific discipline
  • In-depth knowledge of EU MDR

Work Rights

Not specified

Tailored Resume

Cover Letter