Jobs at Gilead Sciences

Lead global MES strategy and roadmap, govern MES/EBR standards, partner with Manufacturing/Quality/IT for MES delivery, ensure GxP compliance and data integrity, drive integrations, deployments, and operational value across multi-site regulated manufacturing.

Perform various manufacturing operations in compliance with SOPs, conduct equipment maintenance, ensure documentation accuracy, and support team performance while adhering to cGMP in a cleanroom environment.

The Senior Manager will lead New Product Introduction efforts, manage cross-functional teams, ensure compliance with industry standards, and report to senior management on project statuses.

The Senior Director, Supply Chain at Gilead provides leadership for supply chain planning and materials management, ensuring compliance with international regulations, managing staff development, and executing strategic plans to meet corporate objectives.

The Senior Quality Assurance Specialist manages batch record reviews, assesses risks, ensures compliance with GMPs, and leads internal audits while supporting quality issue resolution and continuous improvement initiatives.

The QA Specialist III will support SAP QM solutions, manage incidents, drive quality process optimization, and ensure compliance with regulatory requirements.

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

Support end-to-end supply chain operations for a pharmaceutical company by analyzing data, executing ERP and GMP-compliant processes, driving continuous improvement across logistics and distribution, developing documentation and SOPs, managing projects, supervising junior staff, and supporting inventory and planning initiatives.

Lead site Quality Control for small molecule and biologics at La Verne, providing strategic oversight for GMP compliance, inspection readiness, analytical support for manufacturing/PPQ, capability building, Lean lab adoption, global harmonization, and cross-functional partnership to ensure reliable product supply and continuous improvement.

Lead US Liver commercial learning strategy and execution: design and deliver disease, product, onboarding, launch, and selling skills training; manage and develop the L&D team; partner cross-functionally for compliant programs; leverage AI and multiple modalities; measure training impact; manage vendors, budgets, and talent development to strengthen field capability and manager effectiveness.

Lead design and execution of US Oncology commercial learning strategies, managing a team to deliver compliant, scalable, AI-enabled instructional programs for launch readiness, field effectiveness, manager development, and cross-functional alignment across Sales, Medical, Marketing, and Regulatory.

The role involves overseeing clinical trials, managing relationships with investigator sites, ensuring compliance with regulations, and supporting patient advocacy groups to enhance product development based on patient perspectives.