General Description: We have an exciting opportunity within our Regulatory Affairs CMC team for an intern who will be responsible for public affairs and documentation activity to the growing Regulatory CMC team. Essential Functions of the job: 1. Plan and support team activities like portfolio review meeting and group meeting etc. 2. Support the project development and registration by request 3. Coordinate the translation vendor and proofread CMC related documents after translation (EN/CN) 4. The other documentation activities and archive internal and external documents 5. Other daily support work within the group Core Competencies, Knowledge and Skill Requirements: Have a high passion in innovative drug development.An ability to balance multiple tasks to achieve goals and to meet deadlines and customers’ expectations.Have an accountable attitudeBe a good team playerCurious with learning agilityGood at communicationOperationally excellent Language and computer skill requirements: Be skilled in oral or written EnglishStrong PC literacy required; MSOffice skills (Outlook, Word, Excel, PowerPoint)