Job duties:
1、Gathering, compiling, and preparing the materials needed for registration and submission to regulatory agencies.
2、Communicate, Coordinate, with regulatory agencies, prepare, or review regulatory submissions for products.
3、Being the contact point for colleagues within the company in terms of all questions concerning the technical documentation and the approval of medical devices.

Job Requirements:
1、1 year training in ITALY after entry.
2、Bachelor’s degree or above from an accredited university.
3、A major in medical engineering or similar is preferred.
4、Excellent written and verbal presentation skills in English.
5、Strong leadership and interpersonal skills、Superb attention to detail, A positive attitude and willingness to learn.