Clinical & Regulatory Affairs Compliance Coordinator

vor 17 Stunden

Port BE, Bern, Schweiz Ziemer Group Vollzeit

Tasks

  • Preparation of clinical evaluations for Class I, IIa, IIb, and IIb implantable products
  • Ensuring compliance with all regulatory requirements relating to products and their documentation
  • Coordination of the maintenance of all MDR tech files and clinical evaluations (pre-market, post-market, and product changes)
  • Carrying out project work in consultation with the supervisor
  • Active cooperation with internal and external specialists
  • Central interface to the PMS, PMCF, literature search and clinical investigation processes
  • Supporting and moderating strategic discussions in the CA & RA environment

Profile

  • Technical university degree (university or university of applied sciences)
  • Several years of experience in clinical AND regulatory affairs in medical technology
  • Ideally, experience with FDA registration processes
  • Sound knowledge of MS Office
  • Very good German and English skills, other languages are an advantage
  • Analytical and conceptual thinking skills
  • Structured, independent and precise way of working
  • Communicative, open personality with a passion for interdisciplinary collaboration

We offer you an exciting challenge in the growth-oriented medical technology market. As a committed and proactive personality, you can help shape the future of our dynamic company.

Have we aroused your interest? Then we look forward to receiving your complete online application.

For further information, please contact Mr. Richard Büchi, Director Human Resources,

Ziemer Ophthalmic Systems AG

Allmendstrasse 11

CH-2562 Port, Switzerland

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