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. Analyze operational process problems and recommend appropriate corrective and preventative actions. Manage change control authoring and execution. Participate in the site and network wide teams to provide
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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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Sciences group by way of process improvement. Develop expertise navigating Pfizer compliance systems, registries (e.g. GDMS, pTMF, Clinical Trial Registries, etc.) and other study systems related
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cutting edge design and process development capabilities to accelerate and bring the best - in - class medicines to patients around the world. What You Will Achieve In your role, you will be at the center
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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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training slides and detailed information contained in the site Study Reference Manual. Provide support for queries and resolve issues from global study teams on the sample management process, including
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. ROLE RESPONSIBILITIES Responsible for creating financial modeling, presentations, and market analysis to support contract decisions and Internal governance process: Run internal net cost models from both
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throughout the labeling review and approval process through notification to stakeholders in order to ensure that these documents are produced in a timely manner according to internal SOPs and external
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on deliverables throughout the process Provide input for the design of the Statistical Analysis Plan (SAP) and the clinical data output Responsible for review of patient level data across a study and for