Medical Device Regulatory Affairs Specialist

Anaheim, CA

Job ID: 131509 Industry: Regulatory & Scientific

 

Medical Device Regulatory Affairs Specialist

Environment:

The client is a large medical device manufacturer that is looking for some help in the regulatory affairs department. This role is intended for someone to come in and act as a hands on regulatory affairs specialist. Specific areas that they would be working in would be submissions for class II devices.

Duties/Responsibilities:

They will be a regulatory affairs specialist working hands on to accomplish all duties related to the submission. Specifically this client works with 510k submissions in Class II medical devices so experience in these areas is a necessity. Other areas that this specialist would be working with labeling, registrations and other domestic regulatory affairs activities.

Required:

-      Class II device experience

-      510k submission experience

Job Type: Contract

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