About Gilead Sciences

Gilead Sciences is a leading biopharmaceutical company dedicated to creating a healthier world for all people. For over 35 years, Gilead has pioneered therapies for some of the world's most challenging diseases, including HIV, viral hepatitis, COVID-19, and cancer. With a relentless focus on virology, oncology, and inflammation, Gilead's innovative medicines have transformed lives and expanded access to treatment globally. Headquartered in Foster City, California, the company fosters a culture of collaboration, determination, and scientific excellence, where every team member contributes to groundbreaking discoveries.

Role Overview

The VP, R&D Quality role at Gilead Sciences in Foster City, California, reports directly to the SVP of Global Regulatory Affairs, Patient Safety and Quality. This executive position shapes the worldwide R&D and Medical Affairs quality strategy for investigational and marketed products across Gilead’s key therapeutic areas: virology, oncology, and inflammation. As a strategic leader, you will build and manage a global team, ensuring independent, objective quality oversight in a dynamic, cross-functional environment. This is a pivotal opportunity to drive compliance, innovation, and excellence at the forefront of biopharmaceutical R&D.

Key Responsibilities

In this high-impact role, you will provide visionary leadership to the global R&D Quality & Medical Governance organization. Key duties include strategic oversight of clinical compliance, pharmacovigilance, electronic systems, laboratory compliance, and quality documents. You will promote a culture of GxP quality with unwavering integrity, represent Gilead in regulatory meetings worldwide, and implement robust quality measures aligned with global laws and guidance.

Strategic and Operational Leadership

Lead the development of process capabilities like a Global Process Owner network and end-to-end R&D visualization. Oversee compliance in operations, manage quality issues with CAPAs, transaction monitoring, and data privacy collaborations. Drive risk assessments, vendor engagement, employee training on GxP policies, and audit programs to mitigate organizational risks.

Inspection and Continuous Improvement

Ensure preparedness for regulatory inspections and internal audits globally. Provide strategic vision for inspection management, optimize procedural documents and training, and lead R&D Quality management reviews. Serve on the Enterprise Quality Council to enable integrated GxP oversight with executive management.

Qualifications & Requirements

To succeed as VP, R&D Quality at Gilead, candidates need 15+ years of comprehensive regulatory compliance leadership in the pharmaceutical industry. A Bachelor’s degree is required, with preference for advanced degrees such as a Master’s, PhD, MD, or PharmD. Demonstrated expertise in leading global teams, influencing cross-functionally, and mastering quality programs under health authority rules is essential. Your deep knowledge of industry guidance will position Gilead at the cutting edge of compliance.

Benefits & Perks

Gilead Sciences offers an exceptional compensation package tailored for executive talent, including a competitive base salary estimated between $450,000 and $650,000 annually, performance bonuses, and equity opportunities. Employees enjoy comprehensive health coverage, retirement plans, generous paid time off, and wellness programs. As a people leader, you'll benefit from leadership development resources, fostering an inclusive environment where every voice drives innovation.

Career Growth

Joining Gilead means investing in your professional future. This VP role positions you as a key decision-maker in a rapidly evolving biopharma leader, with opportunities to influence global strategy. Gilead's commitment to employee development includes mentorship, training, and pathways to C-suite advancement. Collaborate with top scientists and regulators, advancing your expertise in virology, oncology, and inflammation while shaping the future of healthcare.

Why Join Gilead

Gilead Sciences stands out for its mission-driven culture and tangible impact on global health. By tackling HIV, oncology, and inflammatory diseases, you'll contribute to therapies that save lives and improve access worldwide. In Foster City, California, enjoy a collaborative, multi-cultural workplace that values integrity, innovation, and bold ambitions. As a VP, R&D Quality, you'll empower teams to exceed standards, ensuring Gilead remains a compliance leader in biopharma.

Role FAQs

What is the reporting structure for this role?

This position reports to the SVP of Global Regulatory Affairs, Patient Safety and Quality, with close collaboration across R&D, Medical Affairs, and executive leadership.

What therapeutic areas does this role cover?

The role oversees quality for virology, oncology, and inflammation portfolios, including investigational and marketed products.

Is relocation support available?

Gilead offers competitive relocation assistance for qualified candidates relocating to Foster City, California.

What makes this role unique at Gilead?

It's an independent function driving global quality strategy, with direct stakeholder engagement and regulatory representation in a fast-paced innovation environment.

This VP, R&D Quality position at Gilead Sciences is more than a job—it's a chance to lead transformative quality initiatives in biopharma. Apply now to make a difference in HIV treatments, cancer therapies, and beyond.