Associate Director/Director, Clinical Quality Assurance
BridgeBio PharmaSan Francisco, California, United States • San Jose, California, United States
Posted October 9, 2025
170000 - 233000 USD year
Full Time
About the Company
BridgeBio Pharma is dedicated to developing breakthrough medicines for genetic diseases by bridging scientific advancements with commercial viability. The company focuses on treating underserved patient populations through innovative drug development and a commitment to fostering passionate, driven leaders in the field.
Job Description
BridgeBio Pharma is seeking an Associate Director/Director of Clinical Quality Assurance to support Clinical functional areas in managing Clinical Controlled Documents within a rapidly growing biopharma company. This role involves designing and implementing training programs, championing Quality System Deviation and CAPA processing, and driving process improvements. The company focuses on developing targeted treatments for FGFR-driven skeletal dysplasias, particularly Achondroplasia.
Requirements
- Own and manage Clinical Quality Assurance controlled documents
- Design and manage project-specific training programs
- Serve as the primary Clinical QA lead for Quality System Deviations and CAPA processes
- Review audit reports and provide actionable feedback
- Support mock inspections and identify potential compliance gaps
Benefits
- Market leading compensation
- 401K with 100% employer match
- Employee stock purchase program
- Pre-tax commuter benefits
- Referral program with $2,500 award
- Health & Wellbeing
- Hybrid work model
- Unlimited flexible paid time off
- Paid parental leave
- Skill Development & Career Paths
