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repository Finalize documents post QC Manage the document status in document management system and notify internal stakeholders of the availability of labeling documents. Create and QC SPL (xml) for USPIs
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Maintain, update, and support Pre & Post deal analytics, Formulary tracking, Market Dynamics, and Op Planning BASIC QUALIFICATIONS Candidate demonstrates a breadth of diverse leadership experiences and
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, e.g., GDMS. Finalize documents post QC (including update of GDMS document properties such as entry of PfLEET2 number, update of document title, update CDS cover page etc.). Manage the document status in
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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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, and support Pre & Post deal analytics, Formulary tracking, Market Dynamics, and Op Planning BASIC QUALIFICATIONS Candidate demonstrates a breadth of diverse leadership experiences and capabilities
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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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Pfizer processes and systems. The GLL also interfaces with Hub Labeling Managers and Pfizer Country Office (PCO) colleagues to support timely and quality submissions globally. The GLL will support the use
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have the medicines they need, when they need them. What You Will Achieve Working with Pfizer's dynamic engineering team, you will play a critical role in automation development and testing on projects
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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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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