Intern- Regulatory Affairs

Job Description Support activities related to specific short term projects. Contribute to the planning and execution of registration strategies for medicinal products in Singapore and Brunei to ensure timely and successful registration outcome. Assist with variation submissions and follow through with Regulatory Agency (Singapore and Brunei) until approval. Create artworks for variation submission and commercialization post Regulatory Agency approval in accordance with Singapore and Brunei regulations and internal procedures. Certificate of pharmaceutical product processing. Maintain and update internal regulatory affairs databases and systems. Support regulatory team with other administrative tasks. Manage document archival. Review for product listings for Zuellig and PV Support tender and renewal requirements and provide information/document support Support invoicing processing and SOP reviews. Involve in digital initiatives Clean up of archival documents, where necessary.
Require...