Sr Director, Patient Safety - Deputy EU-QPPV

Job Description

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Deputy EU QPPV (m/f/d) – Senior Director, Patient Safety

Help shape how we protect patients across the EEA. In this highly visible leadership role, you will partner closely with the EU QPPV and the broader Patient Safety organization to ensure our pharmacovigilance system remains robust, inspection-ready, and responsive to emerging safety needs—so patients can benefit from our medicines with confidence.

Role at a glance

As Deputy EU QPPV , you act as the designated back-up for the EU QPPV during periods of absence and provide day-to-day operational leadership within the EU QPPV Office. You will influence key safety decisions, guide cross-functional partners, and represent the EU QPPV Office in governance forums—bringing clarity, rigor, and a strong patient-first mindset.

What you will do

• Serve as Deputy EU QPPV in line with EU legislation, applicable EU regulations/directives, and GVP Modules; act as back-up to the EU QPPV as required.

• Support critical PV oversight and approvals , including aggregate reports, Risk Management Plans, risk minimisation measures/materials, PASS, responses to regulatory authorities, and the Pharmacovigilance System Master File.

• Represent the EU QPPV Office in key internal governance forums (e.g., signal detection and product safety committees) and contribute to core safety information.

• Partner across Patient Safety to drive compliance for post-marketing and clinical trial safety activities and uphold company policies and standards.

• Provide expert advice to corporate functions on drug safety requirements and best practices.

• Strengthen PV system performance through oversight of vendor/partner/distributor collaborations and support for implementation of EU GVP Modules and relevant guidance.

• Lead and coordinate responses to emerging safety issues in the EEA, including support for safety-related regulatory procedures and interaction with health authorities as needed.

• Support ATMP/cell therapy risk management needs (where applicable), including additional risk minimisation measures and registry-related work, and representation in external stakeholder discussions.

• Operate with high autonomy : set priorities, manage operational aspects of the EU QPPV Office, and provide matrix leadership to drive outcomes.

What you bring

• Advanced medico-scientific degree with significant experience leading or co-leading complex, cross-functional work in life sciences.

• Demonstrated ability to provide strategic planning, governance, and oversight across multiple large-scale, complex assignments.

• Deep understanding of EU pharmacovigilance expectations (EU legislation, EU regulations/directives, and GVP Modules) and the ability to translate requirements into pragmatic, high-quality execution.

• Strong communication and stakeholder-management skills, with confidence to represent the EU QPPV Office in internal governance and, when required, with external authorities.

• Ability to work independently, set direction, and lead through influence in a matrix environment.

• Preferred: MD with extensive PV/drug safety experience in the EU biopharma industry.

Why this role matters

This is an opportunity to make a measurable impact on patient safety at scale—helping teams navigate complex benefit–risk decisions, strengthening oversight of our pharmacovigilance system, and ensuring we meet (and exceed) expectations from regulators and stakeholders across the EEA.

Works independently with minimal input, establishes work priorities and direction, manages operational aspects of the QPPV Office, and provides matrix leadership.

Equal Employment Opportunity (EEO)

It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual’s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.

For Current Gilead Employees and Contractors:

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