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Manage new product launch projects and cross-functional teams within Global Supply Chain, ensuring compliance with cGMP and regulatory standards.

The Associate Director, Connect Process at Gilead supports process analysis and documentation for Clinical Operations, managing projects and improving processes while ensuring compliance with regulatory standards and best practices.

The Director of Marketing Sciences will lead market research initiatives to inform strategy and growth, communicate insights, and collaborate with various stakeholders to drive success in the biotechnology sector.

The Associate Director leads global regulatory strategy for Biologics, ensuring CMC submissions meet requirements and regulations, and maintains communication with Health Authorities.

As a Senior Data & AI Platform Integration Architect, you will integrate data governance controls into the enterprise Data and AI platform, ensuring trusted and secure data access for analytics and AI workloads. You will lead the operationalization of governance policies across cloud data platforms.

The Senior Director will lead US contracting and pricing strategy for virology products, shaping pricing, rebate investments, and ensuring market alignment with long-term goals, while overseeing a small team and managing key relationships with payers.

The Director, Total Rewards will advise on compensation programs to attract and retain talent, collaborate across business units, and implement total rewards initiatives.

The Manager of Regulatory Operations at Gilead leads regulatory documentation publishing processes, manages vendor relationships, and oversees the execution of regulatory submissions to health authorities. Responsibilities include optimizing workflows, mentoring staff, and ensuring compliance with regulatory standards.

The Sr. Risk and Audit Data Analyst will enable data-driven auditing and continuous risk monitoring, partnering with audit teams to translate risks into actionable analytics and reporting solutions.

The Senior Therapeutic Specialist II is responsible for achieving sales targets, conducting training, managing budgets, collaborating with internal teams, and ensuring compliance with regulations while promoting pharmaceutical products.