Meissner Str. 191

01445 Radebeul

0351 25999 420

Specialist Regulatory Affairs (medical devices) (w/m/d)

Freelance or part/full-time, temporary position (parental leave replacement), effective immediately.



What will you do?

You will ensure a smooth flow of processes in the Regulatory Affairs division:

  • You will be in charge of the technical documentation and design dossiers of our medical devices class III.

  • You support the area of the change management process by processing change requests

  • You are responsible for the registration and approval of our products in the countries requested by our customers.

Who are you?

  • You have successfully completed your technical or scientific studies (or comparable training in the field)

  • You have acquired a sound knowledge of quality management and the relevant laws and standards

  • You have already gained professional experience in the field of regulatory affairs and quality management

  • You have a distinctive goal-oriented way of working and enjoy working in a team

  • You are communicative and speak or write a confident English

  • You are confident in using MS Office programs (such as Word, Excel, PowerPoint, Outlook)

  • You are confident in dealing with culture-specific differences

Who do you contact?

Please submit your informative documents preferably by email to Frau Tauchert.

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