Medical Device Regulatory Affairs Specialist

Denver, CO

Job ID: 123503 Industry: Med

Regulatory Affairs Specialist

Environment:
Our client is a  developer and international supplier of blood component and cellular technologies. They need someone to offer support to their Regulatory team. 

Principle Duties and Responsibilities:
Our client seeks a Regulatory Affairs Consultant from the Medical Device industry, with experience planning and writing Regulatory Submissions and PMAs, They are looking for someone that is familiar with Asia’ s regulations – APEC. This person will be helping with ECOs from a regulatory affairs standpoint.

Required Experience:
  • Medical Device (Class III): 5 years
  • Regulatory Submissions: 5 years
  • APEC

Desired:

Class III devices

 

Job Type: Contract 

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