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regulations Independently conducts wide range of routine/(non-routine) complex investigator site audits (minimal to no oversight - as needed) Executes audit strategy, leads/supports process audits, and may
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of new risks and evolving existing risks in relevant Quality Risk Management (QRM) tools. Provide feedback to QRM Business Process Owner (BPO) to continuously improve Integrated Quality Management Plan
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colleagues. Ensures that all regulatory development process commitments are clearly communicated, monitored and met. Acts as the point of contact for all internal Pfizer communication regarding the status
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to develop forward thinking programs that maximize medical and commercial value. Applies extensive expertise and in-depth knowledge of the vaccine development process and project management tools to drive team
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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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collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact. PHYSICAL/MENTAL REQUIREMENTS This position/role works
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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 The ADC Chemistry (AC) group is seeking a
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, process improvements, technology or specific work processes for the use of AI within the pharmacovigilance system. Provide strategic leadership to the delivery of PVQO services, policies and works across
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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 As an Associate Scientist, you will be
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Process (AE), Six Sigma (Process Excellence) and predictive technologies etc. Evaluate CMMS work order data for repair trends and chronic issues. Qualifications Must-Have Applicant must have a High School