QA Specialist III

Role: Quality Assurance Lead overseeing GMP compliance for clinical small molecule drug substance and oral solid dosage manufacturing at Gilead. Responsibilities: review and approve manufacturing documentation, maintain accurate quality records, support daily QA operations, lead investigations, and participate in cross-functional projects and audits. Qualifications: 5+ years in GMP environment with a BS/BA or 3+ years with MS; pharmaceutical industry experience preferred. High-Value: GMP compliance, drug substance and dosage form manufacturing, regulatory audits, investigation and root cause analysis, documentation review. WorkSetup: not specified; likely onsite with potential cross-functional collaboration.