Medical Device International Regulatory Affairs Sr. Specialist

Chicago, IL

Job ID: 131385 Industry: Regulatory & Scientific

Medical Device International Regulatory Affairs Sr. Specialist

 

Background: The client is a medical device company that is looking to bring on a consultant to help manage international regulatory work for their medical device product line. They are doing CE marking, change control, life cycle management and need a Sr. Regulatory Affairs Specialist who has experience in these areas.

Project: This consultant will need to be onsite for the duration of this role to help the client manage a product line.  Primarily this work will be supporting their EU and ROW markets, therefore international experience is a must.  They will be responsible for CE Marking, international registrations, regulatory licenses, etc.  This person should be able to work with little to no direction and have significant experience in international RA for the medical device industry.

Required:

International Regulatory Affairs

Medical Device

CE Marking

Life Cycle Management

Regulatory Licensing

Job Type: Contract 

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