Regulatory Affairs Specialist

Regulatory Affairs Specialist, Thailand

Join a leading global medical device organization renowned for its innovation, quality, and patient-focused solutions.

I am representing an innovative medical device company to hire a Regulatory Affairs Specialist to lead product registrations, lifecycle maintenance, and regulatory compliance activities in Thailand.

This role will act as the key liaison with the Thai FDA, driving submissions, change management, and regulatory strategy for a diverse portfolio of medical technologies.

Key Requirements:

• More than 3 years of Regulatory Affairs experience within medical devices.

• Hands-on experience with product registrations and regulatory submissions in Thailand.

• Strong stakeholder management and authority engagement skills.

• Fluent in both Thai and English.

Why Consider This Opportunity

• Global multinational environment with strong regulatory exposure.

• Opportunity to work closely with international manufacturing and cross-functional teams.

• Hybrid working arrangement (3 days in office).

• High-impact role with visibility across the regional business.

If you are looking to advance your regulatory career within a respected global healthcare organization, I would be delighted to speak with you.

CEI: R2090154 | Licence No.: 22S1313