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
To assist in the execution of the occupational therapy care plan/ treatment to patients as prescribed by the evaluating therapist and physician according to the State Practice Acts.
Lead the development and execution of an international supply chain for a proprietary specialty polymer used in next‑generation battery separator technology.
Compensation
$150,000 - $200,000 / year
Responsibilities
Develop the international supply chain
Secure raw material supply
Source and qualify vendors
Negotiate commercial terms
Manage supplier performance
Requirements
Bachelor’s degree in Chemical Engineering, Chemistry, Materials Science, Supply Chain Management, or a related field
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