Sr Director, Process Development

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About the role

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. Job Description At Kite, we are united by one goal: curing cancer. Join us in connecting that purpose to our work every day. Kite is seeking a highly accomplished Senior Director, Manufacturing Science & Technology (MSAT) , for its commercial cell therapy manufacturing facility in Amsterdam. Reporting to the VP, TCF04 Site Head, this role leads the site MSAT organization and serves on the Site Leadership Team. As the site’s senior technical authority and process steward, the Senior Director ensures robust, compliant, and reliable commercial operations. The role sets MSAT strategy and leads manufacturing support, technology transfer, lifecycle and validation activities, laboratory operations, process and data science, and operational automation. Success requires deep cell therapy or biologics expertise, strong knowledge of global GMP requirements, and the ability to lead leaders and influence across a matrix network. Key Responsibilities • Define and execute the site MSAT strategy, operating plan, budget, workforce model, governance, capabilities, and performance measures in alignment with site and global network priorities. • Build and develop an inclusive, high-performing organization of managers and senior technical leaders, strengthening succession, technical depth, accountability, and ownership. • Lead technical governance, escalation, and risk-based decisions for manufacturing support, process performance, validation, and other high-impact issues affecting patients, quality, supply, or compliance. • Oversee shop-floor support, major and critical investigations, root-cause analysis, CAPAs, laboratory studies, and process improvements. • Lead technology transfer and lifecycle management, including facility fit, risk assessment, control strategy, comparability, qualification, PPQ readiness, training, and sustained post-transfer performance. • Govern the validation lifecycle and use process knowledge, statistics, digital capabilities, and data science to improve robustness, yield, cycle time, and proactive risk management. • Set direction for MSAT laboratories and operational automation, ensuring capable, reliable, validated systems, data integrity, and effective manufacturing integration. • Lead technical content and readiness for regulatory submissions, health-authority questions, inspections, and commitments. • Represent site priorities in global forums and partner across Manufacturing, Quality, Supply Chain, Facilities & Engineering, Product Development, Regulatory Affairs, and global MSAT to deliver lifecycle, capacity, cost, reliability, and continuity objectives. • Sponsor cross-site initiatives that advance operational excellence, technology modernization, and long-term site and network competitiveness. Basic Requirements • PhD/MS degree in relevant Science or Engineering with relevant experience of biopharmaceutical manufacturing, technology transfer or process development OR • BA/B

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