Job responsibilities:

1, responsible for the medical devices standards drafting, sample inspection and registration, integration and submit relevant materials

2, coordinate to solve problems appeared in the process of product development and regulations

3, follow up and handle product inspection and registration required for each work

4, for the company to provide timely and effective registration transaction support and related information

Job requirements:

1, master the medical device registration regulations and technical guidance, able to work independently related to medical device registration

2, understand the registration process of medical equipment, can independently complete the writing of the declaration data

3, skilled medical device registration information retrieval and analysis of research work, familiar with project management and control

4, familiar with medical device registration work content and process, and can independently accomplish the medical device reporting work