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Regulatory Affairs Manager - Global Supplement Company

Bangkok Province Permanent THB80,000 - THB100,000 per month (THB960,000 - THB1,200,000 per year) View Job Description
The Regulatory Affairs Manager will oversee the preparation, submission, and maintenance of regulatory filings to ensure compliance with industry standards. This role requires an expert understanding of regulatory frameworks within the life sciences sector.
  • Work with a leading healthcare company expanding across global markets.
  • Lead impactful regulatory strategies in a fast-growing pharma business.

About Our Client

The organisation is a well-established entity within the life sciences industry, recognised for its focus on innovation and adherence to regulatory excellence. Operating at scale, it serves a diverse range of clients and stakeholders, consistently meeting high standards.

Job Description

  • Manage the end-to-end process of product registration for pharmaceutical, OTC, herbal, and related product categories.
  • Review and evaluate product dossiers and coordinate with relevant teams to obtain additional documentation, clarifications, or samples when required.
  • Ensure all submissions and approvals fully comply with Thai regulations, guidelines, and regulatory practices.
  • Communicate approved product information and any regulatory updates to internal and external stakeholders.
  • Build and maintain strong relationships with regulatory authorities to support government affairs and regulatory advocacy.
  • Monitor regulatory changes and proactively adapt strategies to address evolving legal and compliance requirements.
  • Identify potential regulatory and quality risks and develop preventive and corrective action plans.
  • Maintain up-to-date regulatory intelligence on laws, guidelines, and industry developments relevant to product registration.
  • Oversee pharmacovigilance activities to ensure compliance with Thai FDA requirements.
  • Ensure proper documentation and record keeping for all registered products.
  • Lead, coach, and develop team members to achieve performance goals and professional growth.
  • Drive team performance to deliver key priorities on time and with high quality standards.

The Successful Applicant

  • Hold a bachelor's or master's degree in Pharmacy.
  • Possess a valid pharmacist license.
  • Have a minimum of 5 years of management experience in regulatory affairs or pharmaceutical industry.
  • Demonstrate experience in product registration across pharmaceutical, biologics, OTC, or related product categories, which is an advantage.
  • Show strong networking and stakeholder management skills with a results-driven mindset.
  • Be proficient in Microsoft Office applications.
  • Demonstrate fluency in English across speaking, reading, and writing.
  • Possess the ability to manage multiple tasks and projects simultaneously.
  • Have strong working relationships with Thai FDA and proven experience in regulatory negotiations.
  • Good command in English.

What's on Offer

  • Work with a leading healthcare company expanding across global markets.
  • Lead impactful regulatory strategies in a fast-growing pharma business.
Contact
Nantipat Pongsirikun
Quote job ref
JN-072026-7053039
Phone number
+6620125001

Job summary

Sector
Healthcare & Life Sciences
Specialisation
Regulatory Affairs
What is your area of specialisation?
Healthcare / Pharmaceutical
Location
Bangkok Province
Contract Type
Permanent
Consultant name
Nantipat Pongsirikun
Consultant phone
+6620125001
Job Reference
JN-072026-7053039

Diversity & Inclusion at Michael Page

We don't just accept difference - we celebrate it. We encourage applicants from all backgrounds to apply for this role and are committed to building inclusive, diverse workplaces where everyone can thrive. If you require any support or reasonable adjustments during the recruitment process, please let us know.