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, sealants and functional coatings. With our trusted brands, our cutting-edge technologies and our disruptive solutions, you will have countless opportunities to explore new paths and develop your skills. Grow
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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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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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Labeling reviewers and Regulatory Authorities. Prepare comparison tables for labeling team discussions. Edit and format labeling documents- Ensure the document complies with the appropriate template (e.g
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in accordance with agreed upon timelines. Contribute to the training of colleagues on quality standards and processes. Develop and sustain constructive relationships within other Pfizer lines including
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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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nonclinical safety studies. Provide critical experimental design input for in vivo and in vitro studies. Develop automated statistical solutions to increase the efficiency of DSRD study conduct and reporting
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statistical deliverables on assigned projects, including timeliness and quality of deliverables according to project plans. Develop effective collaborations with others within clinical teams, partner lines
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channels, driving improved education, clinical/business decision making, and impactful patient outcomes globally. Through innovative technologies and medical insights, the team will optimize existing
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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