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Global SaMD Regulatory & Quality Lead (Flexible Hours)

regulatory affairs managers
regulatory affairs specialists
validation engineers
pangaea data
administration of environmental quality programsnursing 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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