ASEAN Regulatory Specialist – Nutraceuticals

JAC Recruitment Consultant

Singapore

On-site

SGD 60,000 - 90,000

Full time

7 days ago
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Job summary

Regulatory Affairs Specialist is sought to support regulatory compliance and market access for nutraceutical ingredients across ASEAN markets, including product registrations, documentation reviews, labeling, and health claims reviews. The role collaborates with commercial, technical, and quality teams.

You will monitor regulatory developments, liaise with authorities and distributors, prepare dossiers, and ensure alignment with local requirements.

Qualifications

  • Degree in Food Science, Nutrition, Life Sciences, Pharmacy, Biotechnology, Chemistry, or a related discipline.
  • 2–8 years of Regulatory Affairs experience within relevant industry.
  • Familiarity with product registrations, regulatory documentation, compliance reviews, and labeling requirements.
  • Exposure to ASEAN regulatory frameworks is advantageous.

Responsibilities

  • Support regulatory affairs for nutraceutical ingredients and dietary supplements across ASEAN markets.
  • Prepare and maintain regulatory dossiers for registrations and renewals.
  • Ensure compliance with local regulations, ingredient requirements, labeling standards, and health claims.
  • Monitor regulatory developments across ASEAN markets and assess impact on the business.
  • Review marketing materials, product labels, and promotional claims for regulatory compliance.
  • Liaise with regulatory authorities, distributors, consultants, and external stakeholders.

Education

Degree in Food Science, Nutrition, Life Sciences, Pharmacy, Biotechnology, Chemistry, or a related discipline

Job description

Regulatory Affairs Specialist is sought to support regulatory compliance and market access for nutraceutical ingredients across ASEAN markets, including product registrations, documentation reviews, labeling, and health claims reviews. The role collaborates with commercial, technical, and quality teams.

You will monitor regulatory developments, liaise with authorities and distributors, prepare dossiers, and ensure alignment with local requirements.

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