Director, GLP Quality Assurance

Director, GLP QA leads GLP compliance for Revolution Medicines and external vendors, developing audit plans, conducting vendor audits, reviewing study protocols and reports for compliance, maintaining vendor approvals in systems like Veeva, and providing QA guidance across GLP-related regulations. Responsibilities include QA oversight of CRO studies, advising on compliance for test and control articles, coordinating with GLP vendor QA departments, delivering GLP training, participating in cross-functional meetings, and developing SOP content for GLP audits. Requires 12+ years of global GLP QA experience; Bachelor’s or Master’s degree; strong regulatory knowledge including 21 CFR Part 58, Part 11, OECD standards, and ICH E6 guidelines; ability to manage multiple projects and communicate effectively with senior leadership. Onsite role at headquarters in Redwood City, CA.