Global SaMD Regulatory & Quality Lead (Flexible Hours)

regulatory affairs managers

regulatory affairs specialists

validation engineers

pangaea data

administration of environmental quality programs nursing care facilities skilled nursing facilities

South San Francisco, CA

March 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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