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by manager on various GxP topics internally and externally. Drive interactions with QA colleagues at other Pfizer locations to ensure consistency in application of QA strategy and to promote
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guidance to Study Teams to answer questions related to legacy TMF systems and archive Support TMF document control efforts in preparation and participation for internal audits and external regulatory agency
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messages in a collaborative way with relevant project team subject matter experts. Ensure documents are generated in accordance with agreed internal processes and standards, are submission ready, and are
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regulatory inspections as needed Identifies and drives process improvements Delivers awareness sessions with oversight by manager on various G C P topics internally and externally Drives interactions with QA
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troubleshoot roadblocks and influence teams to achieve targets. Your ability to develop and manage plans will facilitate achieving objectives, interpreting internal and external business challenges, and
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troubleshoot roadblocks and influence teams to achieve targets. Your ability to develop and manage plans will facilitate achieving objectives, interpreting internal and external business challenges, and
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troubleshoot roadblocks and influence teams to achieve targets. Your ability to develop and manage plans will facilitate achieving objectives, interpreting internal and external business challenges, and
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. Design reviews, co-ordination with external agencies and internal customers for the approval of Architectural, Structural, Electrical and Mechanical drawings etc. Work with the team and other department
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and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the
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development timelines and solve technical challenges. You will collaborate with your internal and external network to reach business goals. You will drive programs to meet milestone deliverables by providing