Medical Device Regulatory Affairs Manager

Los Angeles, CA

Job ID: 131508 Industry: Regulatory & Scientific

 

Medical Device Regulatory Affairs Manager

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 regulatory affairs managers and oversee three regulatory affairs specialists. Specific areas that they would be working In would be submissions for class two devices.

Duties/Responsibilities:      

They will be managing a team of three regulatory affairs specialists and managing the submissions for their department. Specifically this client works with 510k submissions in Class II medical devices so experience in these areas is a necessity. While this role is a management type role, the expectation is that this person will conduct hands on regulatory work when necessary. Other areas that this manager would be working with labeling, registrations and other domestic regulatory affairs activities.

Required:             

-      Class 2 device experience

-      510k submission experience

Job Type: Contract

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