Quality Assurance Director / Sr. Director (GVP/PV)

Role: The Director / Senior Director of Quality Assurance oversees GVP quality and compliance programs at Eidos Therapeutics and other BridgeBio affiliates. Responsibilities include guiding pharmacovigilance and medical affairs teams on regulatory adherence, managing audits (including leading GVP audits and inspection readiness), reviewing quality agreements, and supporting inspection activities. The role also involves developing PV quality metrics, overseeing PV computer system validation, and collaborating to improve processes and policies. Requirements: Bachelor’s degree with 10-15+ years of GVP quality experience in biopharma or CRO settings, strong knowledge of global GVP regulations (FDA, EMA, MHRA, ICH), and excellent cross-functional engagement skills. Preferred skills include industry best practices, analytical capabilities, and business communication. High-Value: Focus on pharmacovigilance compliance in a biotech environment supporting rare diseases, genetics, and multiple therapeutic areas. The position is hybrid, based in San Francisco, with in-office collaboration. Salary range: $213,700 – $280,000 USD.