Senior Director, Quality Control (QC Head)

Role: Senior Director, Quality Control at Gilead, overseeing QC operations for small molecule and biologics at the La Verne site. Objectives: ensure GMP compliance, inspection readiness, and analytical support across the product lifecycle, supporting commercial manufacturing and pipeline development. Responsibilities: lead QC functions including analytical, microbiology, raw materials, in-process, drug substance, and stability programs; develop and execute site QC strategy aligned with global standards; support regulatory inspections and audits; build technical capabilities through talent development; drive continuous improvement via lean principles, digitalization, and automation; harmonize QC network practices; collaborate cross-functionally with Manufacturing, MSAT, QA, Regulatory, and Supply Chain teams. Qualifications: Bachelor’s degree in a scientific discipline with 14+ years or Master’s/PhD with 12+ years in pharma/biopharma GMP environments; proven leadership in Quality Control, analytical sciences, and regulatory inspection support (FDA, EMA, etc.); strong knowledge of GMP regulations, data integrity, and process optimization. Preferred: advanced scientific degrees. High-value specifics: experience supporting commercial manufacturing, technical transfers, and global QC initiatives across small molecules and biologics; expertise in GMP compliance, inspection readiness, and data integrity; ability to lead high-performing teams and influence at executive levels. Work setup: based at La Verne, CA; no travel specified.