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Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and controls (CMC) regulatory strategies for small and/or large molecules to meet global regulatory requirements
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Team to develop and maintain Core Data Sheets (CDS), United States Package Inserts (USPI), Summary of Product Characteristics (SPC) for products registered in the EU via the Centralized, Mutual
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processes and maintain compliance with applicable policies. Provide project management oversight of designated vendors on system design projects and other enhancement projects or initiatives. Develop
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Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and controls (CMC) regulatory strategies for small and/or large molecules to meet global regulatory requirements
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independently on project teams, although, may need instruction on more complex or unusual study challenges and/or tasks. Serve as technical support for clinical issues raised by internal and external
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Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and control (CMC) regulatory strategies for large molecules and antibody-drug conjugates to meet global regulatory
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able to operate independently on project teams, although, may need instruction on more complex or unusual study challenges and/or tasks. Serve as technical support for clinical issues raised by internal
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boards, as well as advisor identification and engagement. Provide high-quality scientific/clinical input and review of educational grant requests, and publications as needed. Provide scientifically
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. Interface with study teams to develop shipping schedules. Assist study managers with completing courier questionnaire and provide guidance to study managers on regional sample management requirements
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. What You Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and control (CMC) regulatory strategies for small and large molecule pharmaceuticals and devices to meet global