Why work for MedTech Europe?
Are you passionate about healthcare and innovative medical testing technologies?
In that case MedTech Europe, has the ideal job for you.
You will contribute (under the strategic direction of the Director IVDR/MDR, Petra Zoellner) to MedTech Europe’s work for the implementation of the In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746.
This is a role with a strong regulatory focus where you will interface with members, the European Commission and national regulatory authorities.
You need to follow technical dossiers thoroughly in order to achieve concrete outcomes, communicate and explain complex issues to different audiences, build consensus with members and contribute to the successful outcome of projects.
You will not only have the opportunity to be a member of a motivated, dynamic, and international team (regular team events), but also have:
We are looking forward to receiving your CV.
For more information:
Call EMMA WAITES
at the number: 02 738 02 63; GSM 0475 614967