Regional Regulatory Affairs Lead – Asia

3 days ago

Singapur, Singapore Charterhouse Pte Ltd Full time

Coverage: Asia Region

Industry: Biologics / Specialty Pharmaceuticals

Our client is a leading multinational company in the biologics sector, committed to improving patients’ lives through high-quality, innovative therapies. With a strong global footprint and a pipeline of specialty products, they are now seeking a Regional Regulatory Affairs Lead to join their growing team.

In this regional role, you will play a pivotal part in shaping regulatory strategies and ensuring successful product registrations across the Asia region. You’ll act as the key link between global regulatory affairs, local partners, and health authorities - helping to bring life-changing products to market efficiently and compliantly.

Key Responsibilities:

  • Lead and support regulatory submissions across the Asia region, ensuring full compliance with local and country-specific requirements

  • Serve as the primary liaison between global regulatory affairs, in-country partners, and health authorities

  • Monitor regulatory changes in the region and provide timely updates to global teams

  • Collaborate closely with internal cross-functional teams including country managers, QA, and medical affairs

  • Support product lifecycle management and contribute to strategic regulatory planning

  • Maintain and update internal regulatory databases and systems

  • Facilitate effective communication and alignment with local agents and authorities

Travel Requirements:

  • Occasional travel to meet with health authorities, local regulatory partners, or attend key international regulatory events and conferences

What We’re Looking For:

  • Advanced degree in life sciences, regulatory affairs, pharmacy, or a related field

  • Minimum 6 years of experience in regulatory affairs roles, with proven multi-market coverage in Asia

  • Strong knowledge of country-specific regulatory requirements for biologics or pharmaceuticals

  • Familiarity with electronic regulatory systems and databases

  • Excellent written and verbal communication skills in English

  • Strong project management capabilities and a collaborative, solution-oriented mindset

This is a high-impact role ideal for someone who thrives in a global matrix setting, is passionate about regulatory science, and wants to contribute to meaningful healthcare outcomes across diverse markets.

Please email your resume to Mervin Chai at for a confidential discussion.

EA License no: 16S8066 | Reg no.: R

Only successful candidates will be notified.

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