Assoc. Spclst., Regulatory Affairs

Job Description

Support activities related to specific short-term projects.

Responsibilities

• Contribute to the planning and execution of registration strategies for medicinal products in Singapore and Brunei to ensure timely and successful registration outcomes.
• Assist with variation submissions and follow through with regulatory agencies in Singapore and Brunei until approval.
• Create artworks for variation submissions and commercialization after regulatory agency approval in accordance with Singapore and Brunei regulations and internal procedures.
• Maintain and update internal regulatory affairs databases and systems.
• Support the regulatory team with other administrative tasks, including document archival and clean-up of archival documents where necessary.
• Support product listing reviews for Zuellig and PV.
• Support tender and renewal requirements by providing information and document support.
• Support invoicing processing and SOP reviews.
• Contribute to digital initiatives.

Required Skills

• Adverse Event Report
• Art Creation
• Audits Compliance
• Commercial Regulatory
• Data Quality Assurance
• Document Control Systems
• Electronic Common Technical Document (eCTD)
• Employee Training Programs
• Pharmaceutical Manufacturing
• Pharmaceutical Processing
• Policy Implementation
• Project Management
• Records Retention Management
• Regulatory Affairs Compliance
• Regulatory Affairs Management
• Regulatory Applications
• Regulatory Communications
• Regulatory Compliance
• Regulatory Compliance Audits
• Regulatory Management
• Regulatory Strategy Development

Employee Status

Intern/Co-op (Fixed Term)

Flexible Work Arrangements

Hybrid

Job Posting End Date

07/23/2026