You will work in a multidisciplinary, international environment of researchers, engineers and physicians in support of our common goal to make high-tech innovation quickly accessible to patients.
Your primary responsibilities will include:
- Regulatory support of academic research teams from the EKFZ working on developing innovative medical devices
- Development of regulatory strategies in compliance with relevant legal regulations (MDR/ IVDR)
- Support in the creation of technical documentations in preparation of clinical trials
- Project management of publicly funded research projects
- Support in the implementation and maintenance of a Quality Management System that conforms to ISO 13485
For more details please refer to the link below.