Search the 29 jobs at Gilead Sciences, Inc

The Senior Market Access Manager will lead initiatives to secure national and local access for Gilead's Virology/Liver portfolio, develop pricing and reimbursement strategies, and create value propositions for payers while collaborating with cross-functional teams and engaging external stakeholders.

The Sr. QA Specialist will collaborate with cross-functional teams to ensure compliance of QC testing with Quality and Regulatory requirements. This involves reviewing and approving test methods, lab investigations, and analytical data while managing audit readiness and continuous improvement initiatives.

The Quality Control Specialist III role involves executing Molecular Bioassay techniques, analyzing data for Biologic Products, troubleshooting instrumentation, leading investigations, and supporting quality control functions. The position requires technical leadership in analytical method validation and coordination of continuous improvement efforts in a laboratory setting.

The Senior Manager, Quality for Combination Products at Gilead is responsible for managing compliance and ensuring that the Quality Management System (QMS) meets global regulations for combination products. This role involves monitoring industry standards, participating in audits and inspections, engaging with various stakeholders, and leading improvements in QMS processes to support the development and market advancement of combination products.

The Sr Manager, IT Systems Engineering will maintain and enhance middleware solutions, leading technical discussions and ensuring seamless integration across systems. They are responsible for system performance, disaster recovery planning, and compliance with security regulations. The role involves collaboration with various teams to establish system roadmaps and enhance overall business user satisfaction with IT solutions.

The Therapeutic Specialist will drive growth for Gilead's Liver and Invasive Antifungal Infections treatments in designated regions. Responsibilities include promoting products to healthcare professionals, preparing account plans, achieving sales targets, and building relationships with key customers while ensuring compliance with regulations.

Responsible for achieving sales targets and coverage in assigned territory, collaborating with team members, and contributing to regional training while documenting and measuring performance.

The Therapeutic Specialist I is responsible for achieving sales targets in their territory, providing training, monitoring sales progress, and collaborating with external partners. The role requires strong interpersonal skills, a working knowledge of relevant therapeutic areas, and the ability to analyze complex issues and present recommendations.

The Senior Research Associate I will support small and large-molecule drug discovery by planning and conducting protein production experiments, performing protein expression and purification, troubleshooting challenges, and communicating results with project teams.

The Manager of Quality Systems is responsible for enhancing and integrating Quality Systems, documenting QA projects, managing stakeholder relationships, and ensuring project performance and risk management throughout the project lifecycle. The role includes guiding junior staff and staying updated on industry trends to improve QA processes.

The Senior Research Associate II will play a key role in drug discovery for Virology, Oncology, and Inflammation by engineering, expressing, purifying, and characterizing proteins. They will handle protein quality assessments using biophysical analytics and collaborate with cross-functional teams to present results.

The Quality Assurance Operations Specialist II interacts with contract manufacturers to resolve quality issues and ensures compliance with regulatory requirements. They participate in developing SOPs, maintain quality programs, review production documents, and lead investigations related to quality control. This role requires strong knowledge of quality systems and an ability to work independently and collaboratively within teams.

The Sr. Manager, Biostatistics will lead biostatistical analysis for clinical studies, provide statistical consultation, and support NDA submissions. Responsibilities include overseeing statistical activities, participating in clinical development planning, and contributing to trial design discussions.

The Associate Scientist will work in a laboratory setting to optimize large molecule therapeutics through biophysical, biochemical, and functional assays. Responsibilities include the engineering of antibody binding domains, evaluating binding properties of biologics, and collaborating with cross-functional teams to develop novel biologics for clinical use.

The Senior Research Associate II will conduct analytical and biophysical characterization of early-stage biologics candidates, interpreting large datasets and presenting data to project teams. Responsibilities include optimizing analytical methods, documenting experiments, maintaining instruments, and staying current with scientific literature.

The Manager, Supply Chain oversees API procurement operations, including the issuance of purchase orders and inventory management. They collaborate with finance on cash flow estimates and support internal audits, driving improvements in financial and business reporting while ensuring timely material delivery with global supply chain functions.

The People Analytics Insight Partner will leverage global data to analyze and drive insights on employee engagement and turnover. Responsibilities include designing data connection methods, uncovering hidden patterns, and presenting findings to various audiences, including C-Suite executives, to influence company decisions and initiatives.

The Sr Associate Scientist role focuses on managing Biologics Quality Control operations, developing Quality Control strategies, overseeing commercial project teams, and ensuring compliance with regulatory standards.

The Senior Research Associate will be responsible for executing high throughput antibody production workflows and optimizing automated workflows for protein expression and purification. They will independently design experiments, collaborate on new automation solutions, and maintain scientific literature familiarity to support biologics discovery and lead optimization.

Exciting opportunity for a Senior Quality Engineer to support new combination products in the commercial stage at Gilead. Key responsibilities include providing Quality oversight, creating and revising SOPs, evaluating design changes, ensuring compliance with regulatory requirements, conducting training, and resolving technical issues with stakeholders and manufacturers.