Currently partnering with a large client in the Medical Device Industry, we are looking for a Regulatory Affairs Specialist / Consultant for a 11 month contract with a high chance of extension in Switzerland.
Main responsibilites are:
- All kind of technical documentation (Design, Risk, Validation, CER, Performance, Labelling)
- Support MDR Compliance
- Strong understanding of Risk Management process
- Review Submission content
- Prepare documents for Notified Body
If you are interested in this position and want to discuss it in more details, please apply via the link below.
