Global SaMD Regulatory & Quality Lead (Flexible Hours)

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