Regulatory Affairs Associate

About the role

Join a fast‑growing regional pharmaceutical company operating across ASEAN. The Regulatory Affairs Associate will support both regulatory affairs and pharmacovigilance activities for the Philippines and other ASEAN markets, reporting from Ortigas Center, Pasig City.

Key responsibilities

• Support regional pharmacovigilance by maintaining the Quality Management System, handling adverse event reports, product complaints, medical information enquiries, monthly reconciliations and literature screening.
• Conduct training on Good Distribution Practice (GDP), Good Storage Practice (GSP) and Pharmacovigilance (PV) requirements and keep training records up to date.
• Assist in investigating quality‑related issues, manage quality agreements with partners, and provide QA support for technical enquiries.
• Prepare and maintain regulatory dossiers, track registrations, renewals and variations across ASEAN, and compile regulatory reports.
• Monitor regulatory changes, ensure compliance with local and regional requirements, and provide local regulatory support in the Philippines as needed.
• Support internal and external audits, including CAPA management and documentation.

Required profile

• Bachelor’s degree in Pharmacy with a valid professional license.
• 2–3 years of experience in pharmacovigilance.
• Highly organized, analytical and detail‑oriented.
• Willingness to travel across ASEAN countries.
• Based in Ortigas Center, Pasig City.

What we offer

• Regional ASEAN exposure and the chance to work on both PV and RA functions.
• Opportunity to collaborate with regional teams and international partners.
• Career growth within a dynamic and expanding healthcare business.
• Being part of a growing pharmaceutical company with a regional footprint.