Senior Director, Regulatory Affairs - FDA Class III Devices

A prominent recruitment firm is seeking a Regulatory Affairs Specialist in South San Francisco. This role involves supporting regulatory activities for US FDA class III medical devices, evaluating product changes, and preparing regulatory submissions. The ideal candidate has experience in the medical device industry and direct regulatory affairs experience, preferably with class III devices. Strong analytical and organizational skills are essential, along with a Bachelor's degree in a relevant field. A self-starter attitude is critical for success in this collaborative environment.
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