职位描述
职位描述: 职责描述:? Responsible for regulatory submissions and act as a liaison with the authority and department concerned to facilitate timely approvals of product registration/notification, for both import and locally manufactured products.? Closely work with marketing, Labs, plants and other relevant functions to ensure the product launch on time and assist and provide technical support to solve problems on any product related issues.? Deal with external relationships with government/authorities (such as provincial FDA and local CIQ bureau etc.), test agencies and registration related units.? Lead and train team members by coach, supervise them in daily work.? Support for regulation evolution? Optimize the registration related workflows when need.任职要求:? Responsible for regulatory submissions and act as a liaison with the authority and department concerned to facilitate timely approvals of product registration/notification, for both import and locally manufactured products.? Closely work with marketing, Labs, plants and other relevant functions to ensure the product launch on time and assist and provide technical support to solve problems on any product related issues.? Deal with external relationships with government/authorities (such as provincial FDA and local CIQ bureau etc.), test agencies and registration related units.? Lead and train team members by coach, supervise them in daily work.? Support for regulation evolution? Optimize the registration related workflows when need. 职能类别: 药品注册 医疗器械注册