Director, Product Quality Leader, Biologics

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description

The Product Quality Lead (PQL) supports one or more assigned products/programs and serves as the serve as a product expert providing technical, scientific and strategic expertise and leadership to Product CMC (Chemistry Manufacturing and Controls) / Product Development and Manufacturing (PDM) Team and Product Quality Team (PQT) during clinical development through commercialization, acting as the single point of contact for product quality. The PQL will define the product Quality and Compliance strategy for the assigned products by leveraging their understanding of product development to facilitate the execution of the strategies that enable the efficient commercialization of products. The PQL is responsible for end-to-end Product Quality deliverables, including ownership, authoring, and review of GMP and regulatory documentation (including Product Quality sections of filings such as JOS), and management of product quality data such as comparability assessments, Annual Product Quality Reviews (APQRs), and product quality risk assessments. The PQL is responsible for evaluating and driving overall Product Health by proactively identifying and mitigating product risks and issues, ensuring continuous improvement throughout the product lifecycle. The role supports cross-functional Product Quality initiatives to strengthen compliance, enhance product quality, and enable robust lifecycle management. The PQL also serves as the primary Quality interface for alliance management and due diligence activities, ensuring alignment and effective collaboration with external partners.

Job Functions:

• Provide quality leadership on cross-functional teams in a matrix environment, driving alignment and decision making, performing a scientifically sound and risk-based evaluation of process and product quality data, and developing patient-oriented strategies.

• Execute/drive product strategies through strong quality and scientific knowledge related to product development, technology transfers, global regulatory filing strategies, analytical methods, stability, drug substance and drug product specifications and In-Process Controls (IPCs).

• Lead Product Quality Team (PQT) activities to align on product quality strategy, priorities, and deliverables across the product lifecycle.

• Through the product quality risk register, drive identification, assessment, and mitigation of product quality risks using a science- and risk-based approach.

• Monitor and review cross-functional process and product data to identify trends and ensure quality and compliance risks are proactively addressed and escalated, as needed.

• Lead the development of control strategies, including in-process control, starting material, drug substance and drug product specifications, stability strategy, and comparability approaches.

• Review and approve regulatory filings and support responses to health authority questions.

• Provide cross-functional guidance to align product quality strategy across development, manufacturing, analytical, and regulatory stakeholders.

• Assess product quality impact for changes, deviations, and events, and ensure appropriate implementation plans are developed.

• Support drug substance and drug product technology transfer and new product launches.

• Ensure inspection readiness, including PAI/PLI preparation through participation as a product expert.

• Apply science- and risk-based evaluation to complex issues and develop practical, patient-focused solutions that balance quality, regulatory expectations, and business needs.

• Communicate complex quality and technical information clearly to leadership, cross-functional teams, and regulatory agencies.

• Act as delegate to Commercial Product Quality Head, as needed

Knowledge, Experience and Skills:

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