<Back to Search
Vice President of Regulatory Affairs and Quality Assurance
Fremont, CAMarch 27th, 2026
Vice President, Regulatory Affairs & QualitySan Francisco Bay Area (Hybrid)We are partnering with a venture-backed, early-stage medical device company in the San Francisco Bay Area developing a next-generation software-driven surgical platform leveraging AI to transform procedural care.With strong early momentum and a clear path toward clinical and regulatory milestones, the team is looking to bring on a Vice President of Regulatory Affairs & Quality to build and lead the entire RA/QA function from the ground up.The OpportunityThis is a true foundational leadership role, reporting directly to the executive team, where you will:Own and define the regulatory and quality strategy for a novel AI-enabled medical device platformLead FDA interactions and act as the primary point of contact with the agencyDrive 510(k) submissions from scratch (including strategy, authoring, and execution)Build and scale a fit-for-purpose Quality Management System (QMS) aligned with FDA and ISO 13485Partner closely with R&D, Software, Clinical, and Executive leadership to align regulatory pathways with product developmentPrepare the organization for key inflection points including submissions, audits, and early commercializationWhat We're Looking For10–15+ years of experience in Regulatory Affairs / Quality within medical devicesProven track record leading 510(k) submissions from concept through clearanceStrong experience with software-driven / SaMD / AI-enabled technologiesDeep understanding of FDA regulations, design controls, and QMS implementationPrior experience in an early-stage or startup environment (highly preferred)Demonstrated ability to operate as a hands-on leader and strategic partnerWhy This RoleOpportunity to own and build the RA/QA function from zeroWork directly with an experienced leadership team and investorsBe part of a company tackling a high-impact clinical problem with differentiated technologySignificant influence on regulatory strategy, product direction, and company trajectory
Showing 100 of 21,187 matching similar jobs in Springbrook, ND
- Sr. Quality Product Data Specialist - Remote, US
- Regulatory Affairs Specialist
- Quality Intern
- Regulatory Specialist
- Quality Specialist
- Sr Quality Assurance Auditor - Chicagoland area
- Principal Quality Assurance Auditor - Location Flexible
- R&D Specialist, Biocompatibility
- Principal Quality Assurance Auditor - Location Flexible
- Data Quality Analyst
- Associate Director, Global Patient Safety Quality and Compliance - Pharmacovigilance at Revolut[...]
- Quality & Regulatory Affairs Manager, Transfusion Medicine
- Quality Coordinator
- Sr Quality Assurance Auditor - Chicagoland area
- Quality Specialist - Kennesaw, GA
- Quality Assurance, Regulatory Assurance Compliance Specialist
- Director of Quality & Regulatory
- Global QA & Regulatory Affairs Executive
- Quality and Regulatory Analyst
- Senior Quality Specialist
- RN Quality Coordinator
- Program Quality Analyst
- Quality & Compliance Manager
- Quality Analyst
- Licensing and Credentialing Specialist
- Associate Director Quality
- Global SVP, Regulatory Affairs – Oncology
- Head of Regulatory Affairs
- Head of Regulatory Affairs & Accreditation for an Acute Care Health System
- Quality Improvement Coordinator
- Quality Improvement Coordinator
- Head of Licensing
- Head of Regulatory Affairs & Accreditation for an Acute Care Health System
- Head of Regulatory Affairs & Accreditation for an Acute Care Health System
- Senior Counsel, Global Payments & Regulatory
- Quality & Regulatory Strategy Lead
- Regulatory Affairs Director
- Global QA & Regulatory Affairs VP
- Sr Specialist Regulatory Affairs
- Regulatory Compliance / Strategic Planning Consultant - Remote