Regional Regulatory Affairs Specialist

Drive regulatory strategy across APAC as a Regional RA Specialist in a dynamic global team.

Your new company

Join our client to be part of their international team as a Regional Regulatory Affairs Specialist, where your expertise in APAC regulations and cross-functional collaboration will drive impactful healthcare solutions across diverse markets.

Your new role

You will be instrumental in managing regulatory operations across international markets. Based in Singapore, you will work closely with local affiliates and their designated Responsible Persons to ensure the timely and compliant execution of product registrations, renewals, and post-approval changes. Your role will involve preparing and overseeing regulatory documentation while ensuring alignment with evolving regional requirements. You will also maintain accurate records using electronic submission systems and tracking tools. In addition, you will collaborate with cross-functional teams such as CMC, Support & Promotion, Labelling, Business, Quality Assurance, and Pharmacovigilance to ensure regulatory alignment and contribute to strategic planning through regulatory intelligence and competitor insights.

What you'll need to succeed

  • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related discipline.
  • Minimum of 3 years of hands-on experience in regulatory affairs within the pharmaceutical industry, ideally with regional exposure across APAC markets.
  • Solid understanding of APAC regulatory frameworks, including ASEAN CTD, ICH guidelines, and country-specific requirements.
  • Proven ability to manage multiple priorities and collaborate effectively with internal teams and external partners on regulatory matters.
  • Solid interpersonal and communication abilities, with a detail-oriented and structured approach to documentation and compliance.


What you'll get in return

  • Play a key role in shaping regulatory strategies across diverse international markets, driving access to healthcare solutions globally.
  • Work closely with dynamic teams across Regulatory, Quality, Business, and Pharmacovigilance to influence strategic decisions.
  • Expand your expertise in APAC regulatory frameworks while managing end-to-end submissions and lifecycle activities in a fast-paced, multicultural environment.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

EA Reg Number: R1109288
EA License Number: 07C3924 | Company Registration No: 200609504D

Summary

Job Type
Permanent
Industry
Pharmaceuticals
Location
Singapore
Specialism
Life Sciences
Ref:
1281978

Talk to a consultant

Talk to Suriani Norahim, the specialist consultant managing this position, located in Singapore
#27-20 UOB Plaza 2, 80 Raffles Place

Telephone: 60271910

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