JobDiva, Inc. seeks a contractor to provide regulatory affairs lifecycle support for a Class III medical device during a medical leave. The candidate should be based in Texas, with consideration for strong fits outside the area within budget. Responsibilities include strategic regulatory guidance for integration of a newly acquired entity, drafting procedures, and maintaining PMA/MDR/MDD files. Collaboration with international teams and consultants is essential.

Also on the board Same function, level within a rung

Level

Manager

Location

Port Reading, NJ

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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