- Foster City, California, United States
- Senior
- $182K–$236K per year
- 5+ years
Lead strategic oversight and operational execution of cGMP analytical testing for commercial small molecule programs, ensuring compliance, data integrity, and regulatory readiness.
Compensation
The salary range for this position is: $182,070.00 - $235,620.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package.
Responsibilities
- Define, implement, and continuously improve QC strategy for commercial small molecule programs
- Serve as point of contact for QC activities including method validation, transfer, reference materials, specifications, cGMP release testing, stability strategy and testing
- Manage and approve specifications, collaborating cross-functionally to establish scientifically sound, phase-appropriate specifications
- Represent QC on cross-functional product development teams, providing technical input and direction
- Identify and drive opportunities for improvement in QC testing, workflows, data management, and compliance processes
Requirements
- Bachelor's degree
- Master's degree
- PhD or PharmD