Regulatory Affairs Professional Medical Devices (x|f|m) - Hybrid

For the Regulatory Compliance department within Sartorius Stedim Biotech GmbH we are looking to fill immediately on a limited basis until 05/31/2027 a Regulatory Affairs Professional Medical Devices (x|f|m) at the location Goettingen. In this position you are responsible for the preparation and execution of clinical and performance data as well as post-market surveillance documents. As a Regulatory Affairs Professional Medical Devices (x|f|m) you support the Regulatory Affairs Specialist in the technical documentation in the EU.



The job is to be filled full-time and is performed remotely on some days as well as on site at the campus in Göttingen.

After the fixed-term assignment there is the possibility to return to a comparable position.









For the Regulatory Compliance department within Sartorius Stedim Biotech GmbH we are looking to fill immediately on a limited basis until 05/31/2027 a Regulatory Affairs Prof...