PHARMAFull-time
Execution Hub Associate
MAKATI CITY (PH)HYBRIDPOSTED: 8/11/2026
PHARMAFull-time
HIRING ORGANIZATIONPFIZERBiopharmaceutical / Healthcare
ROLE DEFINITION & RESPONSIBILITIES
Provide regulatory dossier management support for international country and cluster Regulatory teams across the product lifecycle.
Author and review Module 1 local submission components, cover letters, variations, MA applications, and local translations.
Assist with simple health authority query responses, tender support, out-of-stock reporting, Annual Product Quality Reviews, and launch planning coordination.
Perform quality review and approval of submission dossiers prepared by Hub Submission/Dossier Managers to maintain regional compliance.
REQUIRED VERIFIED SKILLS
Regulatory Affairs
Module 1 Dossier Preparation
Health Authority Responses
Regulatory Compliance
Technical Aptitude
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
ORGANIZATION CONTEXT & CULTURE
Pfizer Inc. is an American multinational pharmaceutical and biotechnology corporation. It is dedicated to the discovery, development, manufacturing, marketing, and sale of medicines and vaccines worldwide. The company focuses on breakthrough science to deliver innovative treatments across various therapeutic areas to improve health outcomes.
TEAM SIZE: 80,000+ employees
INDUSTRY: Biopharmaceutical / Healthcare
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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