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What You Will Achieve The Immunogenicity Sciences Group within the Pharmacokinetics, Dynamics, and Metabolism (PDM) Department of Pfizer's Discovery and Early Development division is an industry
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interpretation, and conducting experiments to identify and address potential issues. The role requires regular monitoring and maintenance of particle analysis equipment, staying abreast of industry developments
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conducting industry standard process safety testing to fully characterize materials, processes, and side streams prior to scale-up in laboratories and manufacturing facilities. You will collaborate with and
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manufacturing specialists for API synthesis in kilo-lab and pilot plant facilities, as well as provide support for technology transfer to Pfizer manufacturing sites and third party facilities. You will
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new areas, to evaluate the chemical & physical stability, bioperformance and manufacturability of the drug product across a diverse range of therapeutic areas. As a Senior Associate scientist, you will
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Good Lab Practices cGLP and/or (Current) Good Manufacturing Practices (part of GxP) cGMP guidelines. Your significant experience of applying knowledge of principles, concepts, and practices
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for supporting mRNA production within the Vaccine Research and Development - Early Bioprocess Development group. The colleague will execute process activities required for the manufacture of DNA template, RNA drug
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, team supply and investigational purposes Support transfer of processes to manufacturing sites Represent Conjugation on cross-functional teams Independently author technical reports and draft relevant
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pertinent industry-related experience and/or post-graduate specialty/residency are desirable Demonstrates effective relationship management and customer orientation Purpose Blueprint Contributions Analyzes
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achieve new milestones and help patients across the globe. How You Will Achieve It Develop purification processes to enable manufacturability assessment of biotherapeutic candidates. Deliver highly pure