Regulatory Clinical Affairs Expert

We are looking for a creative and solution-oriented personality who can support our clients in regulatory affairs, registration of medical devices (europe and USA-510k), clinical evaluation (CEP, CER) and technical documentation.

The position is described in detail here

Axxos GmbH continues to follow its successful path and is constantly looking for new talents

Sustainable, continous development is important to us. We thus focus on the following core questions:

  • Are you honest and straightforward?
  • Do you relate to our core values?
  • Do you look back on multi year expertise in the medical device area?
  • Can you picture yourself as a consultant and team member of Axxos GmbH?

Fluent in spoken and written German and English are a must. Operational experience with the FDA is getting more and more important. There is always a wealth of ongoing tasks at hand, planning is therefore crucial.

When you see your personal scrabble in your mind's eye then please send it to me together with your CV.

I am looking forward to reading from you,

Markus Wipf

m.wipfnoSpam@axxos.noSpamch