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throughout the labeling review and approval process through notification to stakeholders in order to ensure that these documents are produced in a timely manner according to internal SOPs and external
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Sciences group by way of process improvement. Develop expertise navigating Pfizer compliance systems, registries (e.g. GDMS, pTMF, Clinical Trial Registries, etc.) and other study systems related
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cutting edge design and process development capabilities to accelerate and bring the best - in - class medicines to patients around the world. What You Will Achieve In your role, you will be at the center
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operation of fermentation equipment (i.e. benchtop to large scale bioreactors, centrifuges, etc.) · Setup and operation of freeze-dryers · Accountable for cross-functional work in multiple platforms/process
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) 3+ years of management/supervisory experience Experience managing projects PHYSICAL/MENTAL REQUIREMENTS This position/role works in an office where physical requirements are consistent with typical
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set-up. Proactively coordinate with Clinical Scientists and Lead Clinician to assure understanding and agreement on deliverables throughout the process Provide input for the design of the Statistical
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The R&D Manufacturing Process Development team is looking for a Senior Biologics Development Manager. The ideal candidate has a passion for bringing innovative products to the market and understands
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. POSITION SUMMARY You will represent Biostatistics on cross
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cutting edge design and process development capabilities to accelerate and bring the best - in - class medicines to patients around the world. What You Will Achieve The Vaccine Asset Planner (Manager
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development process, related to monitoring clinical trials, GCP, FDA, or country-specific regulatory environment Demonstrated success in prior scientific/technical/administrative roles Demonstrated experience