Regional Regulatory Affairs Executive - 7-Month Contract

GMP Technologies; Singapore; On-site; SGD 39,000 - 54,000; Part time

Job summary

GMP Technologies in Singapore seeks a Regulatory Affairs Executive for a 7-month contract based in Buona Vista. The role supports regulatory activities across Singapore, Malaysia, and Brunei, including dossier management and license upkeep.

You will manage dossiers, artworks, and Veeva records, and help maintain regulatory licenses to ensure uninterrupted supply during maternity cover. Bachelor’s in Pharmacy or Life Sciences is preferred; attention to detail and strong organizational skills are

Qualifications

• Bachelor's degree in Pharmacy, Life Sciences or related field.
• Knowledge in dossier preparation, artwork management, and regulatory databases is an advantage.
• Knowledge of regulatory submission and license maintenance processes in Singapore, Malaysia and/or Brunei is an advantage.
• Strong attention to detail and organizational skills.
• Candidates with no prior work experience may be considered.
• Able to commit to contract term and commence 1 Dec 2025.

Responsibilities

• Manage preparation of regulatory documents, dossiers, and applications for OHC projects.
• Support RA team to manage artworks and upkeep Veeva database for OHC portfolios including submission dates, approval dates and submission dossier.
• Assist RA manager to apply and/or maintain all relevant licenses.
• Ensure supply continuity during Maternity Cover period including requesting approval from RA lead and relevant Health Authorities for supply exemption (if required).
• Review and approve local repacking application form in Veeva system.

Skills

Regulatory Affairs

Attention to detail

Organizational skills

Dossier management

Education

Bachelor's degree in Pharmacy, Life Sciences or related field

Tools

Veeva

Regulatory databases

Regulatory submission platforms

Job description

GMP Technologies in Singapore seeks a Regulatory Affairs Executive for a 7-month contract based in Buona Vista. The role supports regulatory activities across Singapore, Malaysia, and Brunei, including dossier management and license upkeep.

You will manage dossiers, artworks, and Veeva records, and help maintain regulatory licenses to ensure uninterrupted supply during maternity cover. Bachelor’s in Pharmacy or Life Sciences is preferred; attention to detail and strong organizational skills are