The role provides comprehensive regulatory support for international country teams across the entire product lifecycle from registration to withdrawal
Job Summary
The role provides comprehensive regulatory support for international country teams across the entire product lifecycle from registration to withdrawal.
Success is measured by the timeliness, quality, compliance, and efficient delivery of critical regulatory deliverables including M1 dossier components.
Pfizer offers a flexible workplace culture that encourages work-life harmony and supports digital transformation strategies to enhance patient outcomes.
Matching Summary
The role provides comprehensive regulatory support for international country teams across the entire product lifecycle from registration to withdrawal.
Skills & Requirements
Must-have
3+ years professional experience
Advanced to Fluent English language
M1 dossier component authoring
Local regulatory submission coordination
Quality review of dossier builds
Nice-to-have
Multilingual skills desirable
Familiarity with pharma organizational structures
Understanding of country regulatory trends
Experience in quality and compliance fields
Self-initiated problem solving abilities
Key Requirements
B.S./B.Sc. in Pharmacy, Life Sciences, Business, or IT