At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.
Position Summary
The Director, Analytical Science and Technology Cell Therapy Critical Reagent provides strategic and technical leadership for the commercial critical reagent program across the Cell Therapy manufacturing network. This role is accountable for the global strategy, governance, lifecycle management, testing oversight, and supply continuity of critical reagents supporting GMP Quality Control operations.
The Director leads a team of technical professionals and partners across Quality, Supply Chain, Procurement, Regulatory, and External Partners to ensure availability, comparability, compliance, and sustainability throughout the product lifecycle. As a recognized technical leader, the Director drives network harmonization, innovation, risk management, and enterprise-wide initiatives that support reliable patient supply and commercial growth.
Duties Responsibilities
Define and execute the network strategy, governance model, and operation framework critical reagents supporting commercial Cell Therapy manufacturing and testing.
Establish standards for critical reagent qualification, characterization, performance monitoring, lifecycle management, and replacement strategies.
Serve as the enterprise owner for critical reagent governance across the Cell Therapy network.
Establish long-term plans to ensure reagent availability, sustainability, and business continuity
Provide oversight of the lifecycle management of commercial critical reagents including qualification, implementation, monitoring, change management, retirement, and replacement.
Lead reagent comparability assessments and bridging strategies required to support manufacturing continuity.
Establish proactive reagent refresh and replacement strategies to mitigate supply risks.
Drive network harmonization of critical reagent specifications, testing requirements, and performance monitoring programs.
Provide governance for critical reagent supplier qualification, performance monitoring, and risk assessments.
Lead technical evaluations for supplier changes, reagent discontinuations, and supply interruptions.
Develop mitigation strategies for sole-source reagents and high-risk materials.
Support implementation of new commercial manufacturing technologies and product launches.
Evaluate emerging technologies and next-generation reagent platforms to strengthen manufacturing reliability and scalability.
Identify opportunities to improve reagent robustness, simplify testing approaches, and increase supply resilience.
Translate industry trends and scientific advances into future-state reagent strategies.
Develop and implement long-term strategies that ensure critical reagent quality, supply reliability, compliance, and operational scalability.
Serve as the ASAT representative and technical authority for critical reagent strategies and testing programs across the Cell Therapy network.
Serve as a recognized subject matter expert for Critical Reagent for Cell Therapy.
Drive scientific innovation and continuous improvement initiatives that advance testing capabilities, efficiency, and quality.
Provide strategic oversight of investigations, deviations, CAPAs, change controls, and risk assessments affecting critical reagent testing programs.
Lead inspection readiness activities related to critical reagents and represent the organization during regulatory inspections and audits.
Foster a culture of accountability, inclusion, collaboration,…