Jobs at Gilead Sciences

Leads trial equity and optimization initiatives focused on improving diverse patient awareness, recruitment, enrollment, participation, and retention. Designs data-driven digital campaigns, partners with clinical and external stakeholders, monitors recruitment performance, and develops scalable patient enrollment practices. The role serves as a digital marketing and patient enrollment subject matter expert while supporting representativeness across global clinical trials.

Leads administration, support, maintenance, compliance, validation, and technical governance for the LabVantage-based KLIMS platform. Responsibilities include incident response, troubleshooting, upgrades, integrations, documentation, audit support, project delivery, infrastructure coordination, and stakeholder training. The role serves as the regional technical lead and partners with quality, manufacturing, validation, infrastructure, and business teams to maintain reliable, compliant laboratory operations.

Performs aseptic pharmaceutical manufacturing activities in cleanrooms, including equipment setup, operation, cleaning, sterilization, filling, formulation, hydration, dispensing, and lyophilization. Follows SOPs, batch records, and cGMP requirements; documents production data; troubleshoots processes; manages MES and Oracle transactions; maintains inventory records; supports audits; and trains others across multiple manufacturing processes.

Performs pharmaceutical manufacturing activities in cGMP cleanroom environments, including aseptic processing, dispensing, formulation, hydration, equipment operation, sterilization, filtration, vial filling, and product handling. Follows SOPs and batch records, documents production data, troubleshoots processes, resolves inventory discrepancies using Oracle and MES, maintains equipment and areas, supports audits, and trains others. Requires cross-training in at least two manufacturing processes and work under minimal supervision.

Performs routine and complex pharmaceutical manufacturing activities in cGMP cleanroom environments, including aseptic processing, dispensing, formulation, hydration, equipment operation, sterilization, cleaning, sterile filtration, and product handling. Maintains batch records, logbooks, inventory transactions, and manufacturing documentation. Troubleshoots processes, reports line issues, supports audits, creates consumable purchase orders, and trains others across multiple manufacturing processes.

Leads pharmaceutical sales planning, analytics, field-force effectiveness, territory optimization, incentive compensation, performance reporting, and dashboard development. Analyzes complex commercial data to identify opportunities, support targeting and account planning, measure marketing effectiveness, and improve sales execution. Coordinates cross-functional projects, data quality, user testing, training, and continuous improvement initiatives, including AI applications. The role also manages stakeholders and presents insights to senior leadership.

Manages commercial pharmaceutical labeling projects from initiation through implementation, coordinating Regulatory Affairs, Quality, Supply Chain, Manufacturing, Packaging Engineering, and vendors. Leads artwork development, review, approval, and implementation; manages timelines, risks, documentation, change controls, and controlled records. Reviews packaging and printer proofs for compliance, resolves labeling issues, supports labeling systems, and drives workflow improvements.

Leads regulatory product strategies and submissions for clinical trials and marketing applications across the product lifecycle. Provides regulatory guidance, risk assessment, compliance oversight, health authority interaction, and responses to agency requests. Serves as US Regulatory Lead, monitors regulatory intelligence, coordinates briefing materials and meetings, and mentors regulatory personnel. Requires extensive experience with global regulations, investigational and marketed products, cross-functional project teams, and regulatory submissions.

Leads US Commercial business strategy and operations, partnering with the General Manager on strategic planning, financial and resource planning, executive decision support, governance, performance management, organizational effectiveness, communications, and product launch readiness. Coordinates cross-functional initiatives, operating cadences, leadership meetings, and enterprise planning while driving accountability, transformation, and execution across a complex biopharmaceutical organization.

Leads global forecasting and market research for CAR-T cell therapy commercialization. Builds evidence-based forecasting models, conducts scenario analyses, manages qualitative and quantitative research with physicians, patients, and payers, and integrates competitive intelligence into strategic recommendations. Partners cross-functionally with commercial, marketing, R&D, finance, and business development stakeholders to inform product strategy, lifecycle management, demand planning, brand planning, and opportunity assessments.

Leads US payer and value marketing strategy across Kite’s cell therapy portfolio. Oversees payer-facing value stories, economic resources, budget impact models, access tools, and educational materials. Partners with HEOR, Medical Affairs, Brand, Pricing, Contracting, Legal, Regulatory, and field teams to translate evidence into compliant access strategies. Monitors payer dynamics, establishes performance metrics, manages budgets and agencies, and leads a team supporting portfolio and product-specific initiatives.

Designs, evaluates, and implements secure enterprise technology solutions across Windows, Linux, databases, cloud, containers, and infrastructure platforms. Partners with business stakeholders, IT teams, security groups, and vendors to translate requirements into scalable architectures. Creates architecture and data-flow documentation, supports hybrid cloud and production transitions, evaluates resiliency and disaster recovery, and contributes to automation, troubleshooting, standardization, and operational excellence in complex manufacturing and quality environments.

Provides clinical oversight and medical monitoring for clinical trials in neurology and autoimmune disease. Supports study design, protocol development, safety review, regulatory submissions, investigator engagement, data interpretation, and clinical development planning. Partners cross-functionally with Regulatory Affairs, Clinical Operations, Safety, Biometrics, Medical Writing, and other teams. The role may also contribute to publications, scientific presentations, advisory boards, due diligence, and external stakeholder engagement.

Leads clinical operations for Phase I–IV studies, managing teams, budgets, timelines, resources, CROs, vendors, regulatory documentation, risk mitigation, and cross-functional study teams. Oversees study execution from startup through closeout, ensures compliance with FDA, EMA, ICH, GCP, SOPs, and local regulations, and supports organizational initiatives, process improvement, and talent development.

Leads business strategy, operational excellence, organizational change, and cross-functional execution for Gilead’s La Verne manufacturing site. Advises the VP of Operations and site leadership, translates enterprise priorities into actionable plans, oversees governance and KPI systems, manages budgets and talent development, and drives continuous improvement. The role leads Lean Six Sigma initiatives, process optimization, cost reduction, change adoption, communication, and compliance with SOPs and GMP standards.

Leads global insights and analytics supporting CAR-T commercialization, lifecycle management, and product strategy. Builds patient-based forecasting models, conducts scenario analysis, and supports demand planning. Independently manages qualitative and quantitative market research with physicians, patients, and payers across global markets. Integrates research, competitive intelligence, and secondary analytics into actionable recommendations, manages vendors, and presents forecast assumptions and strategic insights to senior stakeholders.

Leads MSAT operations and automation technology for clinical cell therapy manufacturing. Supports GMP equipment, automation systems, technology transfers, new product introductions, troubleshooting, investigations, change controls, validation, data integrity, and continuous improvement. Partners with manufacturing, engineering, quality, IT, process development, and vendors to improve equipment reliability, operational readiness, scalability, and manufacturing performance. Manages technical initiatives and develops manufacturing technology capabilities.

Leads strategic account management and market access for Gilead’s long-acting injectable products. Builds relationships with healthcare systems, hospitals, clinics, pharmacy leaders, P&T committees, and other decision-makers to secure formulary inclusion, EMR placement, pathway access, and contract pull-through. Coordinates cross-functional teams across sales, medical, market access, contracting, marketing, and reimbursement. Develops account strategies, supports product launches, delivers stakeholder education, and manages onsite account engagement.

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

Leads end-to-end Quality Control operations at Gilead’s La Verne facility across small-molecule and biologics products. The role owns QC strategy, GMP compliance, inspection readiness, analytical and microbiology programs, manufacturing and product lifecycle support, and regulatory inspection representation. It also strengthens technical capabilities, develops QC talent, drives global harmonization, and implements Lean Laboratory principles, digitalization, automation, performance metrics, and continuous improvement across cross-functional and global teams.