工作职责 1.Establish and implement corporate regulatory policies and procedures to assure compliance with applicable international regulations and standards. 2. Work with internal regulatory resources, external distributors, and external consultants to obtain Ministry of Health agency product registration requirements. 3. Provide guidance on Ministry of Health requirements to obtain marketing approval for products in all countries in which products are to be sold. 4. Assist in training on medical device regulations. 5.Legalize documents as required for product registrations and tender bid activities 6.Prepare dossiers for international Ministry of Health product registrations/approvals. 7.Maintain documentation system to assure all Carestream associates (regulatory, sales, marketing, etc.) have access to registration, license, permit, etc. documents as required for Ministry of Health registrations, sales and marketing support. 任职资格 Knowledge: 1. A BS, or equivalent experience, in science, engineering, international business, foreign language or other relevant discipline. 2. Excellent communication both in English and Mandarin Experience 1. At least 2-3 years work experiences of product. 2. Demonstrated experience in medical product is preferred. Core Competency 1. Have good Analytical Thinking and Problem Solving skill 2. Have good communication skills 3. Deal with others in an honest and forthright manner and present views in an open and honest manner 4. Be consistent with words and actions 5. Be creative and open to suggest new ideas 6. Be customer-centric 7. Effectively prioritize tasks and goals, manage time, and stay focused on results 8. Accept responsibility for own actions and live up to commitments 9. Have team work spirit