The role provides critical regulatory support for international country teams across the full product lifecycle from initial registration to withdrawal
Job Summary
The role provides critical regulatory support for international country teams across the full product lifecycle from initial registration to withdrawal.
Success is measured by the timeliness, quality, compliance, and efficient delivery of critical on-the-job deliverables while implementing portfolio execution efficiencies.
Pfizer fosters a patient-centric culture guided by values of courage, joy, equity, and excellence with a focus on digital transformation.
Matching Summary
The role provides critical regulatory support for international country teams across the full product lifecycle from initial 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
Experience with pharma organizational structures
Understanding of country regulatory trends
Self-initiated problem solving in ambiguous situations
Familiarity with digital transformation strategies
Key Requirements
B.S./B.Sc. in Pharmacy, Life Sciences, Business, or IT