◆ Responsible for all regulation affairs and post-market surveillance for all Zimmer Dental implant products. ◆ Preparing product specification, tracking the whole testing and registration process, timely handling and coordinating all issues during testing and approval. ◆ Response for China clinical trial. Communicate with CRO company, global RA and Clinical research team, other related team and NMPA reviewer to make sure clinical trial goes smoothly as planned.◆ Based on China team’s registration inquiry, make an evaluation about timeline and cost for high level reference so that high level could final the registration strategy.◆ Responsible for the integration of local China on QA/RA related things.◆ Responsible for China’s quality system is compliance with global subsidiary procedures and compliance with NMPA regulations. ◆ Receive customer complaints from distributors and feedback to global customer service team. ◆ Responsible for the compliance of post-market IFUs and labelling. ◆ Responsible for the handling of adverse events and recall. ◆ Maintain and update current regulations and standards database. ◆ Establish and maintain good relationship with NMPA, government, testing center, etc.◆ Work closely with marketing, sales and global teams to better understand regulatory environment, requirements and business impact.

◆Be responsible for the registration of importer medical equipments which mainly include Class II and Class III.◆According to different registration requirements of different countries, track with foreign manufacturers for reference documents. Draft product standard, track the whole testing process and solve the question during testing process in time.◆Be responsible for the collecting, translation and managing for submission documents, ensure all the submission documents meet the requirement of NMPA regulation.◆Track the registration process, coordinate the questions with NMPA and ensure the technical review goes smoothly. ◆Be responsible for the assignment of internal work, track the whole progress, adjust the timeline in time. ◆Cooperate marketing to evaluate new projects so that marketing can make reasonable quotation. ◆Be responsible for the coordination and communion among every department.Origanze underling to communicate each other for registration experience. Study and update the newest regulation.

◆Deal with hotline for maintaince and provide technical support. According to actual status, arrange the field service.◆Be responsible for telephone report and the feedback of customer's complaint. Issue survey report every month.◆Be responsible for the technical review of sales contract.To ensure no any question in technical.◆Be responsible for checking the expense of internal dept. Make the budget and the statistic monthly.◆Assist department manager to hold internal meeting and plan activities.◆Be responsible for coordination with other departments.

◆Be responsible for the management for the storage of reagents. Checking the product quantity, sending out and ordering goods. Double checking the storage with accountant.◆According to the plan for selling, make the plan for ording the raw material of reagents and arrange the manufacturing plan. Solve the urgent things and coordinate goods with distributers and offices. ◆Be responsible for the management for accessories of diagnostic equipments. Send out accessories based on engineer's application and contact with Japanese engineers.