Regulatory Affairs Executive (Contract)

Pasona Singapore Pte. Ltd.; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

Pasona Singapore Pte. Ltd. is seeking a Regulatory Affairs professional to manage product lifecycle, registrations, and compliance for Singapore and Malaysia. The role involves preparing dossiers, liaising with authorities, and ensuring timely approvals.

The candidate will monitor regulatory changes, coordinate with QA, Medical, and Commercial teams, and support product launches and supply continuity within a multinational setting.

Qualifications

• Bachelor degree with at least 2 years of related RA experience in Singapore pharmaceutical market.
• Pharmacist registration will be advantageous.

Responsibilities

• Prepare, review, and submit registration dossiers to secure timely approvals and maintain licences.
• Handle new registrations, renewals, variations, and post‑approval commitments.
• Track submissions and respond to authority queries within required timelines.
• Liaise with HSA, NPRA, and other authorities on submissions and commitments.
• Monitor regulatory changes and provide intelligence to stakeholders.
• Collaborate cross‑functionally (Supply Chain, Quality, Medical, Commercial) to support product launches and supply continuity.

Skills

Regulatory affairs

Product lifecycle management

Regulatory submissions

Cross-functional collaboration

Education

Bachelor's degree in Pharmacy/Pharmaceutical Science/Life Sciences

Job description

• Basic Salary + Contract Completion Bonus

• Nearest MRT: Clarke Quay

• Multinational Organization

Job Requirements:

• Manage product lifecycle and regulatory compliance for Singapore and Malaysia.

• Prepare, review, and submit registration dossiers to secure timely approvals and maintain licences.

• Handle new registrations, renewals, variations, and post‑approval commitments.

• Review product changes and assess regulatory impact, recommending appropriate submission pathways.

• Oversee labelling, safety updates, and packaging compliance with local and global standards.

• Track submissions and respond to authority queries within required timelines.

• Liaise with HSA, NPRA, and other authorities on submissions and commitments.

• Monitor regulatory changes and provide intelligence to stakeholders.

• Collaborate cross‑functionally (Supply Chain, Quality, Medical, Commercial) to support product launches and supply continuity.

Requirements:

• Bachelor of Degree in Pharmacy, Pharmaceutical Science, Life Sciences, or a related discipline with at least 2 years of related experience in Regulatory Affairs (RA) within the Singapore Pharmaceutical market

• Pharmacist Registration will be advantage

• Eligible and willing to serve as the designated RP for Therapeutic Products Importer’s and Wholesaler’s Licenses.

We regret that only shortlisted candidates will be notified. Other applications will be updated to our database for future job opportunities.