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Associate for Medical Device Regulatory Affairs

Posted on May 13, 2024 (over 1 year ago)

This job post is archived - the company is no longer hiring for this position.

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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.

Please apply by using the "apply button" in the job post linked below