European Union Medical Device Regulation (EU MDR) Specialist Consultant

Job Overview

Our client has an excellent year-long contracting opportunity for a European Union Medical Device Regulation (EU MDR) Specialist Consultant!

 

Responsibilities / Requirements:

  • Coordination and execution of Post Market Surveillance activities aligned with global regulations with a focus on the EU Medical Device Regulation (MDR).
  • Ensure assigned regulatory tasks are completed accurately and in a timely manner while maintaining compliance to internal standards/procedures and applicable external industry regulations.
  • Perform high-level post-market surveillance activities and projects associated with global regulatory compliance and quality improvements.
  • Detail oriented.
  • Data oriented.
  • Quality and Regulatory experience.
  • Clinical focus.
  • Risk Management.
Job Detail
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