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strategic regulatory expertise as Global regulatory representative to Product Team(s). As a Director, Lead and coordinate a virtual global regulatory strategy team (GRST), encompassing regional regulatory
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practices for partnered programs. You will ensure creation of strategic and operational objectives from early (lead) development through Proof of Concept and licensure of the product depending on the program
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Compliance policies and Regulatory requirements and enables monitoring of processes and standards. Lead the identification and initiation of continuous process improvements to enhance the quality of operations
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Compliance Lead with a focus on GMP principals across our Global Materials Management group. The successful candidate will ensure the highest level of quality and compliance across all aspects of GMM
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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
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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 ADC Chemistry (AC) group is seeking a
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regulations Independently conducts wide range of routine/(non-routine) complex investigator site audits (minimal to no oversight - as needed) Executes audit strategy, leads/supports process audits, and may
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and stakeholders. Lead virtual teams for process and project-related activities. Mentor and coach key PVQO staff as identified by succession plans. TECHNICAL SKILLSETS NEEDED Comprehensive knowledge
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affairs and comprehensive knowledge of other disciplines will enable you to lead complex projects across the division. While managing complex project environments, you will be able to anticipate and
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opportunities for continuous improvements and lead implementation PHYSICAL/MENTAL REQUIREMENTS Ability to work in a biological safety cabinet and perform complex data analysis Work Location Assignment:On Premise