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
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,