--Responsible for research, development and implementation of capitalization strategy for A+H dual stock market of the company. Lead and participate in strategic merge and acquisition, equity and debt financing, market cap management, asset securitization, etc.--Lead strategic investment for the company's healthcare business unit, mainly including "Dikang Pharmaceuticals" and "Revotek Technology".

--Lead healthcare industry research and analysis. Develop and implement company healthcare strategy. --Lead strategic investment particularly to hospitals, healthcare clinics, retirement communities and other projects including conducting commercial due diligence, performing financial analysis, and helping developing and refining investment proposals.--Develop strategic collaboration with other industrial partners, including leading enterprises, universities, scientific research institutions, incubators, large state-owned enterprises, etc. --Execute investment and collaboration in terms of business model designing, negotiation and contracts preparing. Models Includes establishing joint ventures, strategic procurement, funding investment and other forms.

--Cooperate with global partners to provide comprehensive solutions for localization in China, including investment and financing, local industry policies, technology transfer, market access, quality system, market research and promotion, supplier search and due diligence, etc.--Responsible for developing potential customers and maintaining relationships. More than 70% are from United States, Germany, Singapore, Israel and other countries.

--Responsible for technology and manufacturing transfer between China and other countries, manage to execute 5 global transfer of imaging systems including X-ray, CT, ultrasonic products. --Develop product delivery strategy in early phase of development, complete global target market analysis, pricing strategy, financial forecast and market access solution. Manage to get the approval from China, US, EU and APAC countries.--Responsible for government communication. Lead clinical trials, support product testing, coordinate quality management system supervision, actively respond to national medical device regulatory agencies and third-party laboratory inspection.