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Global SaMD Regulatory & Quality Lead (Flexible Hours)
South San Francisco, CAMarch 26th, 2026
A health technology company in South San Francisco is seeking a Quality Assurance & Regulatory Affairs Specialist to build a robust regulatory and quality framework. The role involves developing regulatory strategies for SaMD approval and implementing a Quality Management System aligned with industry standards. Candidates should have experience in quality assurance within the medical device space, expertise in regulatory submissions, and be able to collaborate cross-functionally. Flexible hours and benefits include private medical insurance and more.
J-18808-Ljbffr
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