Assoc. Spclst., 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.…