Regulatory Affairs Professional Medical Devices - Göttingen, Lower Saxony
vor 1 Monat
Job summary
We are looking for a Regulatory Affairs Professional to join our team in Göttingen. The successful candidate will be responsible for preparing and executing clinical and performance data documents as well as post-market surveillance documents.Responsibilities
- Create documents for clinical evaluation of Medical Devices (MDs) and In Vitro Diagnostics (IVDs)
- Develop schedules and ensure compliance
- Analyze market developments, perform research, and evaluate findings
Stellenbeschreibung
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