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... for the development of the CMC regulatory strategy for submissions. These submissions ... IND/CTA, NDA, CTD and MAA regulatory filings. Collaborate with other relevant ... functions to prepare and..
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas ..
... results. Functional Area Description The GRS-CMC organization provides regulatory expertise related to CMC activities through all stages of ... of the organization develop global regulatory CMC strategies and partners..
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... development strategy and all process-related CMC deliverables across multiple sites including ... implementation, platform process lifecycle strategy, regulatory submissions, and handoff to manufacturing ... with appropriate scale, GMP and..
Job Information Bristol Myers Squibb Associate Director, Parenteral ExM MS&T in New ... business results. Job Function The Associate Director MS&T External Manufacturing Parenteral Drug ... Health Authorities in support..
... transformative business results. Summary The CMC Regulatory Associate Director is responsible for content development, ... of the Quality Module for regulatory submissions to support biotechnology products ... submissions. In..
... results. Functional Area Description The GRS-CMC organization provides regulatory expertise related to CMC activities through all stages of ... of the organization develop global regulatory CMC strategies and collaborate..
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients' lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and ..