【 Medical Device Registration Engineer 】
Job responsibilities:
1. Responsible for preparing registration materials, arranging external resource testing plans and progress, and assisting product certification and registration.
2, responsible for product certification, registration regulations, related standards of consultation, collection and training.
3, responsible for checking the audit data and the regulatory compliance of the declaration process, output product certification technical documents.
4. Organize all functional departments to participate in the registration work.
Job Requirements:
1, college degree or above, medical related major.
2. Good organization and communication skills, able to integrate, check and coordinate internal and external information.
3, more than 3 years of registration work experience, at least participate in the domestic registration process of more than 2 domestic class II products, at least as the product registration person in charge of the whole process of leading the organization, participate in the domestic registration process of more than 1 domestic class II products.