Regulatory Affairs Professional Medical Devices (x|f|m) - Hybrid
Sartorius(1 month ago)
About this role
A fixed-term Regulatory Affairs Professional (Medical Devices & IVD) at Sartorius Stedim Biotech GmbH based in Göttingen. The role supports regulatory affairs and technical documentation for EU medical devices and in vitro diagnostics, is full-time, and combines on-site and remote work until 05/31/2027.
Required Skills
- Clinical Evaluation
- Performance Evaluation
- Post-Market Surveillance
- Risk Assessment
- Regulatory Submissions
- Scientific Writing
- Regulatory Interpretation
- Process Development
- Procedure Writing
- Compliance Monitoring
+2 more
Qualifications
- Master's Degree in Natural Sciences, Medical Technology or Biotechnology
About Sartorius
sartorius.comSartorius offers solutions for the biopharmaceutical industry and laboratories, from drug discovery and development to production platforms for biomanufacturing.
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