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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 ..
... system to treat cancer. The Senior Scientist/Prinicpal Scientist will be the analytical lead ... modalities including lentiviral vector. The Senior Scientist/Prinicpal Scientist will lead the post-commercial strategy ... documents..
... looking for a dynamic Principal Scientist to join our dedicated team ... excellence in their work.nThe Principal Scientist reports to the Senior Director of Laboratory Operations and ... compliance..
Research Scientist Growing technology company seeks Research Scientist for an immediate opening! PhD in CE/EE/CS Design, implementation of medical imaging and robotics Software engineering background in C/C ; Python, Pytorch, Tensor ..
Gennao Bio is a privately held genetic medicines company developing first-in-class targeted nucleic acid therapeutics utilizing a proprietary gene monoclonal antibody (GMAB) platform technology. GMAB is an adaptive technology that uses ..
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 ..
... has an opening for a Senior Principal Scientist, Nonclinical Disposition and Bioanalysis in ... GastroPlus) is a plus. The Senior Principal Scientist will represent Nonclinical Disposition and ... ADME..
Job Information Bristol Myers Squibb Scientist, Viral Vector Process Development in ... us and make a difference. Scientist, Viral Vector Process Development Bristol-Myers ... and transformative business results. The Scientist..
Job Information Bristol Myers Squibb Senior Scientist, Viral Vector Process Development in ... us and make a difference. Senior Scientist, Viral Vector Process Development Bristol-Myers ... and transformative business results...
This position involves coordinating filing activities, compiling information from scientists, and authoring the CMC sections of regulatory documents (e.g., IND, CTA, NDA/BLA) to support the timely submissions of both investigational and ..