Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . Position Summary Working within Cell Therapy Development Organization (CTDO) the individual will become part of the Product and Analytical Sciences group, part of CTAD (Cell Therapy Analytical Development function) based in Warren, NJ. The incumbent will contribute to the IND and BLA clinical laboratory component of early and late-stage studies contributing to biological product knowledge and analytical characterization of CAR T pipeline assets. The incumbent will work with other scientists and teach junior technical staff as needed to complete pipeline development projects. Key responsibilities of this role are to lead from the bench for the laboratory support of asset programs through design and experiment execution to support mechanism of action-based studies, characterization of cellular materials, fit-for-purpose assay development, early qualification studies and investigations support. Duties/Responsibilities Under general direction, the incumbent will design/co-design and execute experiments and testing to support early and late-stage BMS cell therapy product development. Lead from the bench with assay development under strict timelines as well as routine testing requests of CAR T products as well as analysis and interpretation of characterization data to support product clinical development for Regulatory filling purposes, manufacturing investigations, life cycle management process support, and translational team requests. Lead or contribute to qualification of characterization methods to support CAR-T product CMC data packages Contribute to acquisition of deeper understanding of product biology, and support mechanism of action studies for CAR T cell programs. Present internal scientific findings and relevant literature observations within the functional area, as needed. Contribute to sample management as needed and the basic maintenance and troubleshooting of instrumentation, as needed. Individual will contribute to process/technology improvements and to scientific/technical data review and writing (e.g., regulatory documents, protocols, etc.) as required. Ensure proper operation and perform routine maintenance of laboratory equipment. Maintain a safe workplace in accordance with company and OSHA policies/procedures.
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Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees