Registration and certification commissioner 3000-5000

Responsibilities:
1. Responsible for the registration of the company's related medical devices, and wrote the related declaration documents according to the products;
2. Responsible for product inspection and follow-up inspection;
3. Maintain good communication with relevant government departments, solve problems in the product registration process, and ensure the smooth progress of the registration process;
4. Follow up the update of relevant national policies and regulations;
5. Timely feed back the comparison information between the declared varieties and the similar varieties in the market;
6. Assisted in following up the r&d process and provided legal and regulatory consultation;
7. Regularly report work progress and assist leaders to carry out other work.
Personnel requirements:
1. Proficient in word, excel and other office software;
2. Have strong language expression ability and writing organization ability;
3. Proactive, stable, good at expressing my own opinions and team spirit;
4. Experience in class ii aseptic medical device registration is preferred.

5. Bachelor degree or above, majored in biomedical engineering, machinery, electromechanical and other related majors.

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