職缺描述
1.Responsible for product registration, managing the product portfolio, and preparing regulatory documentation. 2.Handle drug substance registrations with health authorities worldwide. 3.Communicate effectively with regulatory authorities and overseas partners. 4.Manage license extensions for existing products and coordinate SMF (Site Master File) renewals. 5.Monitor and implement product-related changes in compliance with updated health authority regulations. 6. Provide regulatory support and customer service as needed.
收合內容