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development and execution of control plans Utilize operational performance data to characterize state of control, improvement opportunities and drive process and system optimization Deliver effective business
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of new risks and evolving existing risks in relevant Quality Risk Management (QRM) tools. Provide feedback to QRM Business Process Owner (BPO) to continuously improve Integrated Quality Management Plan
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requires understanding of GCP and GMP to support the regulatory requirements and needs of different study types, quality management, inspection readiness, audit/inspection process, clinical trial processes
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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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This posting covers two available positions (I&I and Rare Disease). Therapy area responsibility will be determined through the selection process. ROLE SUMMARY Specialty Care (SC) Medical Affairs
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This posting covers two available positions (I&I and Rare Disease). Therapy area responsibility will be determined through the selection process. ROLE SUMMARY Specialty Care (SC) Medical Affairs
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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 Senior Scientist, you will be
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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