Assistant/Regulatory Manager, Therapeutic Products Branch
Singapore Economic Development Board
- Singapore
- Permanent
- Full-time
- Screen Applications: Verify that required documentations for new drug applications and generic drug applications meet the submission requirements for evaluation.
- Process Variation Applications: Process applications for post-approval changes to registered therapeutic product as part of product lifecycle management.
- Develop Procedures: Collaborate with the team to establish procedures for new services or enhance existing services related to therapeutic product registration.
- Case Management: Coordinate the submission, manage application and track key milestones for international collaboration projects on evaluation of drug applications.
- Handle Procurement Matters: Work with Corporate Service teams on procurement matters.
- Develop Automation and Data Analytics: Develop automation and data analytic tools to analyse databases and generate insightful reports.
- Manage Enquiries: Manage enquiries related to regulatory requirements and procedures for therapeutic product submissions from industry and healthcare stakeholders, as well as general enquiries from members of public.
- Possess Knowledge in Pharmaceutical Science, Biomedical Science, Biotechnology or related disciplines.
- Prior experience with data analytics, automation and python coding is an advantage.
- Prior work experience is not a requirement.