Job of the week: Senior Regulatory Affairs Specialist in Oberdorf

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.

 

 

 

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