Manager, R&D Quality Audits, Inspections and CAPA

Manager, R&D Quality Audits, Inspections and CAPA

We're here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.

Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.

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 Kite and help create more tomorrows.

As the Manager, R&D Quality Audits, Inspections and CAPA, you will serve as a primary quality and compliance partner for assigned Kite R&D groups, studies, projects and locations. This role supports GCP and GVP quality oversight, internal and investigator site audit execution, inspection readiness, vendor audit awareness and CAPA management. You will partner cross-functionally with Kite stakeholders and Gilead RDQ teams to help ensure R&D activities remain compliant with applicable regulations, Kite's Quality Management System, internal policies and established procedures.

Key Responsibilities

• Serve as a primary quality partner for assigned R&D GCP and GVP teams, providing guidance on regulatory expectations, Kite quality requirements, internal procedures, inspection readiness and CAPA development.
• Lead or support internal R&D quality audits for assigned groups, processes, vendors or locations, including GCP-focused activities, investigator site audits, internal process audits and GVP-related audits as assigned.
• Support vendor audit awareness and compliance oversight by partnering with cross-functional teams to understand vendor qualifications, performance trends, audit needs and study-level compliance risks.
• Develop, track and support effective CAPAs in partnership with cross-functional stakeholders to address audit findings, inspection observations, deviations, quality events and other compliance risks.
• Support inspection readiness activities, including preparation, coordination, response support and follow-up actions for regulatory or compliance inspections.
• Evaluate SOPs, procedures, data, documentation and reporting for assigned R&D groups to help ensure regulatory compliance, quality oversight and alignment with business needs.
• Oversee or coordinate contract auditor activities, including auditor engagement, work direction, documentation review and audit deliverable follow-up.
• Advise teams on quality systems, processes, documentation, training and CAPA management to support consistent R&D quality practices.
• Develop and deliver GCP and GVP-focused training for assigned R&D groups and stakeholders.
• Lead or participate in continuous improvement initiatives related to R&D audits, inspections, CAPA processes, quality systems, policies, procedures and tools.
• Support quality metrics, reporting and communications related to audit plans, audit outcomes, inspection readiness, CAPA status and quality trends.
• May support task management, workload coordination or day-to-day guidance for other team members without direct people management responsibility.
• Promote a culture of quality, accountability, collaboration and inspection readiness across Kite R&D and with external partners and vendors.
• Ensure assigned work is completed in accordance with applicable regulations, established practices, policies, procedures and business processes.

Basic Qualifications

• PharmD or PhD with relevant quality and compliance experience; or
• MA, MS or MBA with 4+ years of quality and compliance experience; or
• BA or BS with 6+ years of quality and compliance experience.

Preferred Qualifications

• MA, MS or MBA with 4+ years of relevant quality and compliance experience preferred.
• Strong GCP auditing experience, including experience serving as lead auditor for investigator site…