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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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, working knowledge of US health care system and healthcare economics and its impact on medical decision making Understanding of quality measures which inform healthcare decision making in the healthcare
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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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ROLE SUMMARY: Lead as a player/coach the group of Asset Quality Leaders and accountable for the management and oversight of GCP performance and quality systems within the oncology portfolio. Responsible for ensuring Level 1 GCP quality for clinical development programs within Pfizer Oncology R&D...