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in Medical Affairs experience required Knowledge and experience in Hemophilia/Hematology is preferred Basic understanding of the drug development process Basic knowledge of health care economics and
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will provide process validation leadership for one or more vaccine or biologics drug substance manufacturing processes. The position leads and/or participates in the planning, preparation, execution, and
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managementplan from a medical/safety/scientific perspective 7) Represents Vaccine Clinical Research and may participate in company-wide, global process improvement initiatives, and champions process enhancements
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documentation for several of Pfizer's multi-product, process control systems in the manufacturing of vaccines and Gene Therapy components. As a manager, your planning skills will help in preparing forecasts
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of activities supporting the site Aveva/OSI PI process data historian. It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe. How You Will
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, database, S88/S95etc) Experience with process controls equipment including PLCs, DCSs, HMIs, SCADA systems, SQL relational database systems, and Network Hubs including design and debugging skills
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Operating Unit. Provide support as needed to Quality Operations, Production and Engineering to assess product and process aseptic issues. Participate in internal and external quality assurance assessments and
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The Supervisor is accountable and responsible for leading assigned production staff to achieve targets and deliver and improve process or product consistency, quality/compliance, cost standards and customer
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of the drug development process and regional regulatory requirements Experience in the preparation/submission of regulatory documentation to support regulatory submissions Excellent oral and written
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will provide process validation leadership for one or more vaccine or biologics drug substance manufacturing processes. The position leads and/or participates in the planning, preparation, execution, and