Regulatory Affairs Manager

Highly Competitive
Frankfurt am Main, Hessen
Posting date: 13 Nov 2018
This vacancy has now expired

ProClinical is currently looking for a Regulatory Affairs Manager for a leading biotech based in Germany.

Job Responsibilities:

  • Documentation preparation (clinical) in order to gain a CE Mark for their product
  • Management of team directly involved in obtaining CE Mark
  • Project Management, creation of invoicing and offers

Skills and Requirements:

  • 5 Years' experience within Regulatory Affairs
  • Strong Medical Device background
  • Experience within European markets
  • CE Marking experience

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Hugh Pickerill on +44 203 854 1079 or upload your CV on our website -
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.