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 breakthroughs in treating some of the world's most devastating diseases, including HIV, viral hepatitis, COVID-19, and cancer. The company's innovative therapies have delivered a cure for hepatitis C, revolutionary advancements in HIV treatment and prevention, and significant progress in oncology and inflammatory diseases. Headquartered in the United States with a global presence, Gilead employs thousands of passionate professionals united by a mission to advance transformative therapies with uncompromising quality and compliance.

Gilead's commitment extends beyond drug development to ensuring equitable access to life-saving treatments worldwide. In HIV, Gilead's portfolio includes groundbreaking antiretrovirals that have transformed the disease from a death sentence to a manageable condition. In oncology, the acquisition of Kite Pharma has bolstered cell therapy innovations like Yescarta for certain lymphomas. For inflammatory diseases, Gilead continues to explore novel modalities to address unmet needs. Joining Gilead means contributing to bold ambitions that improve patient lives for generations.

Role Overview

The Director, GVP Audits position at Gilead Sciences is a pivotal leadership role within the R&D Quality Organization. Based in either Stockley Park, UK, or Cambridge, UK, this role requires a 3-day hybrid work structure in the office. Reporting to the Head of GVP Audits, you will drive audit excellence, ensure global compliance across pharmacovigilance (GVP) activities, and oversee complex audits involving R&D functions, external vendors, and critical workstreams.

This position demands strong collaboration with cross-functional stakeholders, including R&D Quality Business Partners (QBPs), Patient Safety, and the Qualified Person for Pharmacovigilance (QPPV). You will proactively identify, evaluate, and mitigate compliance risks while managing the GVP Audit Master Index and risk-based audit processes, including annual and long-range plans. Beyond audits, support regulatory inspections, inspection readiness, and quality governance to reinforce Gilead's culture of continuous improvement.

Key Responsibilities

GVP Audit Program Leadership

Accountable for the oversight and completion of GVP audit activities across affiliates, partners, vendors, and internal PV processes. Drive the strategic execution and enhancement of the risk-based audit approach. Serve as process owner for documentation, strategy materials, and risk assessments. Lead internal R&D Quality audits and continuous improvement initiatives to embed a quality mindset.

GVP Audit Operations

Act as a trusted advisor on GVP regulatory requirements and Gilead policies. Execute the annual audit plan by planning, scheduling, conducting audits, delivering reports, and ensuring CAPA closure. Collaborate with Inspection Management, QBPs, and SMEs for partner audits. Lead risk assessments and support overall inspection readiness.

Qualifications & Requirements

Ideal candidates bring extensive experience in pharmacovigilance audits within biopharma, with proven leadership in R&D Quality. Expertise in global GVP regulations, risk-based auditing, CAPA management, and digital audit systems is essential. Strong communication skills for stakeholder engagement, strategic planning abilities for audit programs, and a track record in inspection readiness are required. A degree in life sciences, pharmacy, or related field, plus relevant certifications, positions you for success. Experience in HIV, oncology, or inflammatory disease pharmacovigilance is highly valued.

Benefits & Perks

Gilead offers a comprehensive benefits package, including competitive salary estimated at £140,000 - £200,000 annually, health insurance, retirement plans, and performance bonuses. Enjoy a hybrid work model, professional development opportunities, and wellness programs. Employees benefit from inclusive leadership training, as People Leaders are key to fostering an empowering culture.

Career Growth

At Gilead, career progression is driven by bold ambitions and employee development. As Director, GVP Audits, you'll partner with the R&D Quality Extended Leadership team, positioning yourself for advancement to Head of Quality or executive roles. Gilead invests in training, mentorship, and global projects, enabling you to build expertise in emerging therapies for HIV, oncology, and inflammatory diseases.

Why Join Gilead

Join a company where your work directly impacts patients worldwide. Gilead's relentless drive against health challenges offers purpose-driven careers in a collaborative, innovative environment. With a focus on quality and compliance, this role lets you lead audits that safeguard transformative therapies. Be part of a team evolving culture, empowering employees, and creating possible together.

Role FAQs

Q: What is the work arrangement? A: 3-day hybrid structure in Stockley Park or Cambridge, UK offices.

Q: What diseases does Gilead target? A: HIV, viral hepatitis, oncology, inflammatory diseases, and more.

Q: Is prior GVP audit experience required? A: Yes, extensive leadership in pharmacovigilance audits is essential.

Q: How does this role support inspections? A: By leading readiness efforts and partnering on regulatory preparations.

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