Job Summary

An information technology and professional staffing and services company is filling a position for a Remote European Medical Device Regulatory Specialist.

Candidates will be responsible for the following:

• Writing MDR technical documentation
• Working on PMA/Class II/Class III medical devices
• Authoring submissions for Class III or Class II medical devices

Position Requirements Include:

• An engineering/scientific education background
• Experience working on PMA/Class II/Class III medical devices
• Comfortable writing MDR technical documentations
• Working knowledge of EU MDR
• 2-3 or more  of experienced working as a regulatory affairs professional authoring submissions for Class III or Class II medical devices