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Regulatory Affairs Specialist II – On-Site Medical Devices

Abbott, Minneapolis, MN, United States


Abbott is hiring a Regulatory Specialist II in Plymouth, MN. The role includes preparing regulatory submissions for medical devices, ensuring compliance with FDA regulations, and collaborating with the Regulatory Operations team. Candidates should have a Bachelor’s degree and 2-3 years of relevant experience. Preferred qualifications include a Master's in Regulatory Affairs and experience with capital equipment. Benefits include medical plans, 401(k), and more.
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