Vice President, Head of Quality
ArriVent Biopharma
September 28, 2026
Full-time
Remote friendly (United States)
Worldwide
Operations
Role: Vice President, Head of Quality leading ArriVent’s enterprise GxP Quality functions across clinical development, manufacturing, and commercial activities for small molecule and ADC products. Responsibilities: define and implement the Quality strategy, establish governance, build and lead a high-performing Quality team, oversee GCP compliance in clinical trials, manage GMP oversight of manufacturing and supply chain, ensure inspection readiness, and maintain quality systems. Collaborate closely with Clinical, Medical, Regulatory, and Commercial teams; provide independent quality oversight and communicate risks to executive leadership. Requirements: Bachelor's in life sciences, pharmacy, or engineering; 15+ years in GxP Quality roles within pharma/biopharma, with significant leadership experience, including GCP and GMP. Preferred: experience with small molecules, ADCs, late-stage development, regulatory inspections, and external manufacturing oversight. HighValue: enterprise GxP strategy, risk-based QMS, clinical and commercial GxP oversight, inspection readiness, global GxP compliance, senior leadership engagement. WorkSetup: Not specified, but likely hybrid or onsite due to leadership scope.