We offer a great opportunity for a Regulatory Affairs Specialist to join one of the leading medical devices companies in Switzerland.
This role is based in gorgeous Oberdorf, a charming town in Basel-Landschaft. This is a contract until the end of this year, with possibility of extension.
Responsibilities include:
- Supporting the preparation of technical documentation or design dossier documentation for submission to and review by Notified Bodies, as required (both MDD and MDR) as assigned
- Back up the compliance execution work in collaboration with local Regulatory Team.
- Offering of regulatory support
Find out more and apply here.
