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colleagues, complete review and witnessing of all experiments. Summarize and document results in process safety test reports Lead technology development and workflow initiatives to implement new capabilities
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-class process safety capabilities. Responsible for maintaining lab facilities in a neat and orderly manner complying with all local safety practices. In conjunction with the Groton, CT process safety lead
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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 Designing new medicines at Pfizer
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experiment design. These goals will be achieved through partnership with other disciplines including data scientists, analytical chemists, engineers, and process chemists to develop digital and robotic
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to support decision making in the drug development process. The General Toxicology R6 Study Director is responsible for the design, conduct, interpretation, and reporting of exploratory, mechanistic and GLP in
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and written/verbal communication skills. At Pfizer, we believe in helping people lead healthier lives from our customers to our colleagues. We offer a wide array of programs and plans that give our
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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 Drug Safety Research & Development (DSRD) is
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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 As part of the Comparative Medicine team, you
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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 Designing new medicines at Pfizer
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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 As a highly skilled and motivated Principal