Jobs at Gilead Sciences

Territory-based sales role promoting Gilead HCV/PBC therapies in South Georgia. Build relationships with healthcare providers, meet/exceed sales targets, deliver clinical education, develop territory business plans, collaborate with cross-functional teams, and ensure compliance with regulations and adverse event reporting.

The Senior Director will lead strategic HR communications, advising the CHRO, developing executive materials, and fostering employee engagement to support Gilead's culture and workforce initiatives.

Lead the design, startup, and operation of a new biologics manufacturing facility, ensuring compliance with GMP and coordinating across teams to optimize processes and strategies.

The role involves leading pricing and analytics across Gilead's portfolio, overseeing pricing strategy implementation, and enhancing the functionalities of PriceRight. Responsibilities include tracking price trends, developing pricing models, and providing analytical insights to support decision-making processes.

As an Associate Director in Biostatistics, you lead statistical analysis for clinical studies, provide consultation on trial design, oversee data analysis, and contribute to protocol design, ensuring regulatory compliance and statistical excellence.

Lead the design and operation of a biologics manufacturing facility, ensuring compliance with cGMP, executing processes, and improving operational efficiency.

Lead product strategy and roadmap for AI-enabled PDM and Tech Ops capabilities. Partner with senior stakeholders to identify AI opportunities, prioritize backlogs, mentor delivery teams, ensure GxP and regulatory compliance, align solutions with data platforms (Databricks, AWS), track success metrics, drive adoption, and manage vendors for AI/LLM product delivery.

Manage patient cases from referral through resolution, coordinating patients, providers, payers and internal teams; update tracking systems; handle hotline calls, documentation, appeals, site training and supply logistics to ensure timely treatment access and exceptional customer service.

The role entails managing supply chain operations, developing and implementing strategies, supervising team performance, and ensuring compliance with regulatory requirements.

The Sr IT Business Analysis Specialist will align technology with business goals in Biologics Clinical Manufacturing, managing IT solutions and stakeholder relationships while driving business value and capability development.

Lead Quality Assurance oversight for GMP manufacturing and QC at a biologics single-use facility. Ensure GMP/GLP compliance, approve investigations, CAPA, change controls, and risk assessments. Support audits and inspections, manage quality systems and documentation, mentor QA staff, and partner cross-functionally to enable compliant product disposition and continuous improvement.

Provide QA leadership and oversight for Manufacturing and QC at the Foster City biologics site. Ensure GMP/GLP compliance during design, startup, and operation of a single-use drug substance facility and QC lab. Oversee batch record review and product release, external lab oversight, method lifecycle, investigations (OOS/OOT), CAPA, change control, audits, risk assessments, and continuous improvement.

The Senior Staff Software Engineer supports and enhances Dotmatics research systems, working collaboratively with scientists and ensuring effective operational support. Responsibilities include configuring project pages, user training, troubleshooting, and managing requests using Jira.

The Director of GV&A HIV Execution leads market access strategies for HIV products in ICR markets, partnering with cross-functional teams, stakeholders, and market affiliates to optimize access and reimbursement while implementing new capabilities and monitoring KPIs.

Responsible for achieving sales targets, training team members, monitoring sales progress, managing budgets, collaborating with partners, and ensuring compliance with company policies.

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 manage quality initiatives, documentation, and cross-functional collaboration.

The Scientist in Process Development will develop chemical processes for drug manufacturing, conduct laboratory experiments, propose chemistry alternatives, and collaborate across teams for project goals.

Lead product strategy and roadmap for AI-enabled research capabilities across discovery and translational sciences. Partner with senior research leaders to identify high-impact AI opportunities, translate needs into prioritized roadmaps, align solutions with data architecture and AI platforms, oversee cross-functional delivery, and drive change management, adoption, and measurable business outcomes.

Lead product strategy and roadmap for AI-enabled clinical development capabilities. Partner with clinical leaders to identify AI opportunities, translate objectives into requirements, align solutions with data architecture and platforms, drive adoption and change management, and act as COE lead and primary IT-clinical interface to deliver scalable AI/data products for trial operations, data management, reporting, safety, and analytics.

As Senior Director of Strategy and Operations at Gilead, you'll support the GCSO Leadership Team, manage strategic projects, ensure effective communication, and drive operational efficiency across organizational functions.