Senior Regulatory Affairs Lead Medical Devices Submissions

3 weeks ago


California, United States Bayside Solutions Full time

A medical device company is seeking a Senior Regulatory Affairs Specialist to manage regulatory submissions and ensure compliance with industry standards. This role involves preparing regulatory documents, collaborating with New Product Development teams, and maintaining regulatory approvals. Candidates should have a bachelor's degree in a scientific discipline, 6+ years of relevant experience, and strong knowledge of FDA regulations. This full-time position is based in California.#J-18808-Ljbffr



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