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materials (i.e. the US review committee (RC)) Within RC, partner with legal, regulatory, and marketing colleagues to ensure compliant, accurate and high-quality content of promotional and non-promotional
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Why Patients Need You Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure
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advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply
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, process improvements, technology or specific work processes for the use of AI within the pharmacovigilance system. Provide strategic leadership to the delivery of PVQO services, policies and works across
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management as it relates to driving labeling process in regulated industry MS Office Suite; expert formatting skills (Word, XML) Bachelor's degree (in science or life sciences preferred) Attributes: Knowledge
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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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advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply
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. QUALIFICATIONS Advanced degree (MS, Ph.D., MD) in relevant biology, biochemistry or related discipline preferred. 10+ years of biotechnology experience with vaccine/drug development expertise. Sustained and proven
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to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and