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candidate will play an essential role in support of large-scale non-GMP transient protein lead production across Pfizer's diverse biotherapeutics discovery portfolio to enable Pfizer's research units and
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Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based
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Medical Information (MI) is a global customer-focused group that provides a scientific service for responding to unsolicited medical inquiries regarding Pfizer products. Key expectations
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tasked with leading characterization activities for pharmaceutical drug substances, intermediates and drug products, creation of methods and authoring sections of regulatory submissions. This role supports
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compound concentration, detect the presence of anti-drug antibody and neutralizing anti-product antibody activity utilizing various platforms in a regulated (GLP, GCP) environment against challenging
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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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form of active pharmaceutical ingredient (API) and drug product formulations from discovery to commercial launch. You will be able to leverage your existing scientific knowledge, as well as develop in
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GLP requirements. The individual is expected to contribute and participate in general laboratory maintenance activities (such as maintenance of equipment, managing laboratory waste). Qualifications Must
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using commercial clinical data management systems and/or EDC products (Oracle RDC / Inform preferred) Experience using relational databases (e.g. MS SQL Server, MS Access, or Oracle) and data
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using commercial clinical data management systems and/or EDC products (Oracle RDC / Inform preferred) Experience using relational databases (e.g. MS SQL Server, MS Access, or Oracle) and data