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This role oversees the movement and compliance of clinical materials globally, optimizing transportation, managing outsourced logistics, and ensuring adherence to cGMP and company SOPs.

The Sr Director, R&D Quality at Gilead leads quality strategy implementation, manages quality risks, oversees compliance, and drives process improvements in R&D.

The Associate Director, Category Management will develop strategies for global procurement categories, enhance stakeholder engagement, and lead category innovation. Responsibilities include managing supplier relationships, implementing strategic initiatives, and collaborating with cross-functional teams to drive value in commercial services.

The Senior Director will lead global supply chain strategy and execution, ensuring reliable product availability and compliance, while managing a high-performing team.

Lead enterprise business and employee communications strategy, advising senior leaders across functions; drive executive and change communications, employee engagement, internal channels, narrative development, issue response, and team leadership to align employees with Gilead's mission and business priorities.

The Associate Director is responsible for creating and optimizing the master production schedule by aligning global demand with site operations, leading planning integration, and managing long-term production strategies.

The Associate Director will manage market research and analytics for Gilead's Lung Cancer portfolio, impacting commercial strategy and decision-making. Responsibilities include forecasting, market analysis, and partnership with stakeholders to ensure informed insights and successful launch strategies.

Lead global procurement strategies and partnerships, manage teams, and drive value creation while fostering collaboration and diversity across Gilead's Procurement operations.

Lead Quality Engineer for medical device combination product development, focusing on design controls, risk management, and lifecycle quality oversight. Ensure compliance with regulatory standards and support cross-functional collaboration for product development.

Manage outsourced manufacturing activities, including supply chain logistics, vendor relations, and compliance with pharmaceutical regulations. Oversee procurement and quality assurance processes.