A leading German Medical Device Consultancy is looking to grow its expanding team across Germany. They are looking for candidates who have implemented their skills with a manufacturer and are now willing t share their knowledge with the wider Medical Device space as we continue to prepare for the MDR.
Your tasks:
- Creation of the technical documentation according to the EU MDR
- Introduction of new processes to meet the necessary requirements
- Support with existing documentation on the new requirements
- Consulting on clinical evaluations, post market surveillance and other changes,
What you need:
- A degree in engineering, ideally with a focus in a medical field,
- Knowledge and experience of international standards such as: MDR, ISO 13485, 14971
- Willingness to travel
- Proficiency in spoken and written German and English
What we offer:
- Interest in your personal and professional development
- An innovative, open-minded and team culture
- Demanding projects in an international environment
- Performance Bonus
- Home-office
