Director, Quality Risk Management

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. Job Description   Job Description The Director, Quality Risk Management (QRM) is an enterprise Quality leader responsible for defining, governing, and advancing the global strategy for Quality Risk Management across the organization. This role actively supports the Executive Director of Risk and Proactive Quality and has direct leadership accountability for the Quality Risk Management process across PDM. This leader provides strategic direction and oversight to ensure that QRM principles, risk‑based thinking and proactive quality approaches are deeply embedded across the Pharmaceutical Quality System (PQS) and operations. The role is accountable for designing, implementing, and sustaining compliant, scalable, and efficient global processes that enable early risk identification, effective risk mitigation, and continuous improvement aligned with cGMP, ICH, and evolving global regulatory expectations. As a member of the Extended Central Quality leadership team, the Director drives cultural transformation toward a systemic, proactive, and learning‑oriented quality organization, enabling robust decision‑making, operational excellence, and sustained regulatory compliance across a complex, multinational environment. Key Accountabilities Global Business Process Responsibilities and Governance •  Define and execute the global Quality Risk Management framework, with enterprise accountability for strategy, standards, performance, and continuous improvement, enabling early risk identification, mitigation, and prevention across operations and the supply chain. •  Design, own, and approve global standards, policies, procedures and training ensuring alignment with cGMP, ICH, and applicable regulatory expectations across all markets. •  Drive the evolution of organizational risk maturity, capability, and culture, embedding proactive approach to risk and risk‑based thinking into decision‑making at all levels and across GxP processes. • Drive, implement and monitor QRM Master Plans and living Risk Assessment Portfolios across PDM. • Ensure effective integration and alignment of Risk and Change Management processes across the PQS and related business processes.   •  Ensure effective integration of Proactive HOP process and human‑centric risk mitigation approaches into quality and operational processes. •  Collaborate with the Medical Device and Combination Product (MDCP) team to support alignment and harmonization of the QRM and MDCP risk management frameworks, where applicable. •  Oversee the enterprise Quality Risk Register and development of the Operations Quality risk profile for senior leadership and management revie