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... for the development of the CMC regulatory strategy for submissions. These ... functions to prepare and review CMC submission documents, registration dossiers, and ... for the regulatory evaluation of..
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 ... provides regulatory expertise related to CMC activities through all stages of ... the organization develop global regulatory..
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... from scientists, and authoring the CMC sections of regulatory documents (e.g., ... global Health Authorities on the CMC sections of regulatory documents. These ... Evaluation, and Global Regulatory Sciences..
... for the development of the CMC regulatory strategy for submissions. These ... regulatory agencies and represent Regulatory CMC at regulatory agency meetings. Prepare ... for the regulatory evaluation of..
... and transformative business results. The CMC Team Lead is responsible for ... and clinical material space. The CMC Team Lead is accountable for ... implementation of strategic and tactical..
... OF POSITION: The Cell Therapy CMC Business Development lead will possess ... of technologies, scientific approaches and CMC strategies in cell therapy. A ... understanding of the drug discovery,..
Job Information Bristol Myers Squibb Procedural Document Assoc Manager in New Brunswick New Jersey Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver ..
... transformative business results. Summary The CMC Regulatory Associate Director is responsible ... submissions. In this role, the GRS-CMC Associate Director will serve as ... Global Product Supply (GPS). The..
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 ..
... from scientists, and authoring the CMC sections of regulatory documents (e.g., ... global Health Authorities on the CMC sections of regulatory documents. This ... drug product and/or drug substance..
