Senior Regulatory Affairs - Software Medical Devices (Alameda)
Regulatory Toolkit
Abbott is seeking a Senior Regulatory Affairs Specialist to support Lingo product development and regulatory activities for US commercialization in Alameda, CA. You will collaborate with software and systems teams to prepare regulatory submissions and ensure compliance with post-market requirements. The role emphasizes cross-functional teamwork, problem solving, and rigorous documentation, with a focus on Class II software medical devices and 510(k)/PMA pathways. On-site opportunity in Alameda. #J-18808-Ljbffr Regulatory Toolkit
Vacancy posted 1 day ago
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