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experiment design. These goals will be achieved through partnership with other disciplines including data scientists, analytical chemists, engineers, and process chemists to develop digital and robotic
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a regulated Good Laboratory Practices (GLP) setting to support Pfizer's vaccine programs according to Standard Operating Procedures. You will support the technology transfer and integration of new
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a regulated Good Laboratory Practices (GLP) setting to support Pfizer's vaccine programs according to Standard Operating Procedures. You will support the technology transfer and integration of new
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a regulated Good Laboratory Practices (GLP) setting to support Pfizer's vaccine programs according to Standard Operating Procedures. You will support the technology transfer and integration of new
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, Biochemistry, Cell Biology) or a related field (Chemistry, Chemical Engineering, Biomedical Engineering and Biological Engineering) with 3+ years or M.S with 1-2 years of relevant experience in either
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RESPONSIBILITIES Plan, execute and analyze in vivo pharmacology studies. Characterize new in vivo mouse models, including syngeneic genetically engineered and orthotopic mouse models to study biologic mechanisms and
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to scientists and management. The successful candidate must be able to endorse change to business infrastructure to ensure pipeline, legacy and technology success. Qualifications Must-Have Bachelor's degree with
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& simulation experts, project leads, biologists, and protein engineers. How You Will Achieve It Responsible for the development, qualification and implementation of transgene protein, target biomeasure and
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pharmaceutical sciences, systems pharmacology, pharmacometrics, engineering, mathematics, physics or similar disciplines where modeling and simulation is emphasized. 2+ years of pharmaceutical industry or related
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environment. The lab follows Standard Operating Procedures and cGLP (current Good Laboratory Practice) and/or cGMP (current Good Manufacturing Practices). You will be recognized as a technical expert and a