Executive Director, Parenteral Manufacturing Science and Technology

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.

The Executive Director for Parenteral Manufacturing Science and Technology is accountable for the scientific & technical stewardship of sterile drug product (small and large molecule) manufacturing — from initial technology transfer and validation at the start of commercialization through lifecycle management — across BMS' internal and external manufacturing network. This leader has direct accountability for the Manufacturing Science & Technology organization at internal sites, including new sterile Drug Product expansions, process engineering, technical transfer, validation, and investigations activities.

This leader oversees a team of scientists and engineers responsible for ensuring process robustness, reliable supply, technical compliance, and continuous improvement across internal Parenteral manufacturing sites and the external network. The role ensures alignment with global health authority requirements (e.g. FDA, EMA, PMDA, Health Canada and other global health authorities; ICH Q7–Q12 and other guidelines and standards applicable to sterile/parenteral manufacturing) and provides strategic leadership to enable innovation, scalability, and efficient global supply of Parenteral products.

Strategic Leadership & Portfolio Ownership Define and execute the technical strategy for the global Parenteral (small and large molecule) drug product manufacturing network, from technology transfer through lifecycle management. Direct the MS&T organization for the Sterile Drug Product expansion projects, including process and facility design through commissioning, qualification, regulatory inspections, and operation. Partner with Product Development to ensure successful commercialization of the development portfolio, including filing strategies and specification setting, process design and control strategies, and PPQ strategy and execution.

Represent MS&T and commercial manufacturing operations at critical decision points in the pipeline review process, and represent MS&T internally and externally to BMS with authority on formulation, processing, and filling of Parenteral products.

Technical Stewardship & Compliance Own the end-to-end technical success of process transfers and new product launches, ensuring effective technical input on equipment and materials early in the technical transfer process. Oversee the validation programs within MS&T to assure compliance with regulatory requirements and the efficacy, repeatability, and robustness of manufacturing processes and associated equipment. Oversee Process Engineering as part of Tech Transfer/New Product launch activities and routine process support.

Lead CMC authoring activities for Drug Product manufacturing. Own data management and process monitoring activities to ensure appropriate process robustness and yields. Ensure timely completion of technical deviations and appropriate change management for Parenteral products. In collaboration with other functions, ensure effective systems and business processes are in place across the network, to assure compliance with corporate guidelines for Technology Transfer, Validation, and Raw Material Qualification.

Maintain…