675 West Kendall Street Cambridge, MA 02142 US
Formulation and process development, characterization of drug product in vials and in prefilled syringes. Responsibilities include initiating projects, literature review, experimental design, execution, data analysis, and report writing in support of early and late stage manufacture and process characterization activities
Support In-house and external drug product production of non-clinical, developmental and clinical material. Design, manage and execute in-house lab activities Author and review of technical protocols and reports in support of manufacturing process characterization activities
Skills: 1-3 years of hands-on experience in parenteral formulation and/or process development Hands-on experience in parenteral drug product formulation process development and aseptic operation Hands-on experience in analytical and characterization methods for drug products and processes UPLC/HPLC, UV/vis spectroscopy, viscosity, density, titration and compendia assays, particle analysis Demonstrated in-depth understanding of formulation and process of designing experiments and interpreting results
Education: Bachelor's degree in chemical engineering, biochemical engineering, or pharmaceutical sciences
?( Target pay: 33-35/hr)
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