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while complying with staffing standards. Provide supervision of histology personnel. Works collaboratively with peers to develop staffing models and succession planning. Provide orientation and training
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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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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., QRD, PLR
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Achieve It Design, develop, deploy and test our automated processes, systems and equipment. Contribute substantially to the interpretation of results and the design of subsequent activities. Maintain and
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equipment. The Manager will report to the Faculty Director and carry out the following functions: Maintenance, ordering, and day-to-day upkeep of the cryo-EM Facility. Prepare samples, operate microscope, and
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responsibilities, this role will utilize and interpret data from analytic tools, in conjunction with country and regional intelligence to proactively identify risks to quality and compliance and to develop and
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documents such as Pre-INDs, INDs, BLAs, and IMPDs. Collaborate with regulatory partners to prepare Orphan Drug Designation (ODD) requests based on pre-clinical efficacy data and disease prevalence, submitting
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data sources to develop and inform financial modeling decisions Partner with key internal stakeholders to develop financial analysis supporting optimal financial investment in payer access. Utilize
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potential impact to other areas of the business. Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and
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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