Regulatory Affairs Executive

Lives Group; Singapore; On-site; SGD 50,000 - 80,000; Full time

Job summary

Labgistics Asia Pte Ltd in Singapore seeks a Regulatory Affairs Executive to manage permit and licenses, oversee product registrations, renewals and amendments, and address regulatory issues affecting sales and distribution.

You will review records for movement and traceability, ensure SOP compliance, prepare dossiers for submissions, and track submissions and license filings, supporting regulatory compliance across the portfolio.

Responsibilities

• Permit and Licenses application and maintenance
• Product registration, renewals and amendments for all new and existing products and ensure compliance to regulatory authorities’ requirements
• Attend to regulatory issues relating to the sales and distribution of regulated products
• Review records for movement and traceability of the products
• Compliance with standard operating procedures (SOPs), Local Regulations & GDP standards
• Review and prepare product dossiers for submission, including variations (therapeutic products, medical device etc.)
• Track registration and notification submissions and completions
• Maintenance and filing of current product licenses and registration documents
• Submission of Reports of all transaction of the controlled drugs when required by respective authorities

Job description

1 - 5 Years

Contract

Job Description

Group Company: Labgistics Asia Pte Ltd

Designation: Regulatory Affairs Executive

Primary Responsibilities:

• Permit and Licenses application and maintenance
• Product registration, renewals and amendments for all new and existing products and ensure compliance to regulatory authorities’ requirements
• Attend to regulatory issues relating to the sales and distribution of regulated products
• Review records for movement and traceability of the products
• Compliance with standard operating procedures (SOPs), Local Regulations & GDP standards
• Review and prepare product dossiers for submission, including variations (therapeutic products, medical device etc.)
• Track registration and notification submissions and completions
• Maintenance and filing of current product licenses and registration documents
• Submission of Reports of all transaction of the controlled drugs when required by respective authorities

Job Snapshot

Updated Date

21-10-2026

Job ID

LIVESGROUP_309

Department

Quality & Regulatory Affairs

Location