Teams at Pfizer

Supports global and regional pharmaceutical regulatory strategy, lifecycle maintenance submissions, CMC Module 1 preparation, labeling updates, safety reporting, and Health Authority responses. Coordinates submission components, performs quality checks, maintains regulatory trackers, and collaborates with global, regional, country, clinical, safety, quality, supply, and commercial teams. Contributes to process improvement, automation, and standardized regulatory workflows while ensuring timely, accurate, and compliant deliverables.