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MS in Chemistry, Chemical Engineering or related field, 2-5 years experience working in formulations lab and performing quality testing procedures. Project management experience is preferred. Must have
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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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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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or her accomplishments and abilities. Promotion on this track will be based on achievement of goals. Minimum Qualifications PhD in physics, engineering, medical physics, or biomedical imaging strongly
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development for degenerative retinal disease. We employ multidisciplinary approaches, including engineered mice, human pluripotent stem cells, organoids, CUT&RUN, CRISPR gene editing, bulk and single-cell RNA
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to relevant Standard Operating Procedure (SOP) guidelines and Good Lab Practices cGLP and/or (Current) Good Manufacturing Practices (part of GxP) cGMP guidelines. Your significant experience