The Principal Scientist, Oral Product Development at Bristol Myers Squibb is responsible for formulation design, development, characterization, and technology transfer for small molecule drug products. This role involves collaborating with Drug Product, Analytical, API, Quality, and Regulatory functions to execute formulation/process development, strategies, and support regulatory submissions.
Qualifications include an advanced degree in a relevant scientific field with significant pharmaceutical development experience, formulation development, pharmaceutical processing, understanding of excipients, unit operations, and cGMP principles.