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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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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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are committed to diversity as well as diverse faculty who will be role models for our students. Eligibility: An MD, DO, PhD, or MD/PhD (or equivalent). Be eligible for appointment as an associate or full
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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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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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Manager may be responsible to independently take on the closing out of one or more studies post database lock. Provides back up to or takes on the responsibilities of Global Study Manager as needed
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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