1. Registration of in vitro diagnostic reagents and instruments (IVD) in the international market and related market access certification registration, mainly including product registration in the European Union, North America, Southeast Asia and Africa.
2. Document management related to the proposal, drafting and reporting of international registration and specific standard working procedures.
3. Formulate the international registration plan, and be responsible for its implementation, supervision and inspection to ensure that the plan is completed on schedule.
4, the company's product market access declaration and product export certificate declaration.
5. International declaration of trademarks and patents.
6. Track the progress of international registration of products, and handle and solve problems at any time.
7. The company's intelligence work, including the collection, research and reporting of domestic and foreign industry policies, R&D technologies, business and other information, and regularly report to the superior in writing.
Job requirements:
1, familiar with laws and regulations related to international registration of medical devices, such as CE certification, FDA5 10K registration, etc.
2. Proficient in professional English, with strong Chinese-English translation ability.
3, can bear hardships and stand hard work, proactive, serious and responsible, love work, honest and loyal.
Welcome fresh college graduates to join.