Connecting...

QA/RA Officer

Excellent job opening for a Regulatory Affairs Specialist who loves to work on constantly improving the quality of the organization and make sure their product gets to market.

We have a great client who is looking for a Regulatory Affairs Specialist. This project is based in Eindhoven.

Regulatory Affairs Specialist

Project overview

In this Regulatory Affairs Specialist role, you will work at an international Medical Device organisation. This project will enable you to use your skills to:

  • Manage registrations in an array of countries
  • work on supporting user requirement definitions
  • support with technical file compilation
  • register products at authorities of different international markets

Details

  • start date: June 2019
  • project length: 6 months
  • hours per week: preferably 40 hours

Skills

  • 5 years' work experience in a highly regulated environment, preferably medical device
  • experience in a senior role (senior, supervisor, manager)
  • knowledge of MDR
  • experience with registration of medical devices in mainly Russia and the Middle-East
  • experience with technical files
  • good English communication skills
  • independent/analytical/problem solving skills/critical/result driven
  • BA-degree in Engineering, Life Sciences, or equivalent

Apply now

Are you the new Regulatory Affairs Specialist in Eindhoven? Apply online or to speak to a consultant about this project or similar projects, contact Jesse Hendriks via +31 (0)20 522 1588 or j.hendriks[at]realstaffing.com