Beschreibung
Junior Regulatory Affairs SpecialistDuration: to (negotiable)
Location: Bern, Switzerland
Position duties & responsibilities:
-
International products registration in collaboration with our external partner -
Helping the team working to update our technical files (new MDR) -
Prepare and following legalization of regulatory documents -
Coordinate product testing with external laboratory
Professional experience requirements:
- Experience with ISO 9000, ISO 13485, MDR
Educational requirements:
- Biomedical background (Engineer or Technician)
Non-technical profile requirements:
- English spoken and written / French a plus
If you are interested in this position please send me your updated CV to my email address:
I am looking forward hearing back from you.
Kind Regards,
Marco Tvrdon
Recruitment Consultant
m.tvrdon(a)realstaffing.com
Tel.:
Sthree Switzerland is acting as an Employment Business in relation to this vacancy.