Scientist, AAV Analytical Development
Employment Type: Full-Time
Job Description: Lead the successful design, execution, analysis and documentation of experiments to develop analytical methods for AAV vectors Oversee the qualification of vector analytical methods Author, review and approve technical documents including standard operating procedures, test methods, and technical reports Present findings on method development provide interpretation related to vector product quality to cross-functional teams Participate in program teams to design and execute CMC activities to support cell therapy product development Contribute to the development of novel technologies for gene and cell therapy
Basic Qualifications: M.S. degree in virology, analytical sciences, or related field with 8+ years of relevant experience or Ph.D. in relevant field with 2+ years of experience Proven track record in method development, including experimental design, execution and evaluation Knowledge of and experience with viral vectors (lentiviral and AAV) Experience with ddPCR as well as qPCR, nucleic acid isolation, cell culture, ELISAs, and viral transduction Ability to work in a fast-paced environment, meet deadlines, and prioritize work on multiple projects Strong communication skills in technical writing and oral presentation
Preferred Qualifications: Track record of participation in cross-functional teams Familiarity with gene editing technologies Experience authoring technical and regulatory documents Experience interfacing with research organizations and GMP test laboratories
Bristol-Myers Squibb (BMS) is developing novel cellular immunotherapies based on two distinct and complementary platforms – Chimeric Antigen Receptors (CARs) and T Cell Receptors (TCRs) technologies. Our goal is to revolutionize medicine by re-engaging the body’s immune system to treat cancer.
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