職位描述:Job title:Regulatory Affairs SpecialistReports to: Regulatory Affairs ManagerBand: PBResponsibilities1. Responsible for premarket GE products registration at CFDA, including document preparation, testing, submission until final approval.2. Implement labeling procedure to ensure final product shipment to China.3. Provide regulatory assistance for GE business needs.4. Help manager to maintain and develop current regulatory knowledge of domestic and internationals, guidelines, and standards and supply appropriate implementation strategies.Qualifications1. Around 3 years Regulatory Affairs experiences in Medical Device industry in China.2. Bachelor's degree, major in medical science orrelated field from an accredited college or university is preferred.3. Good communication skills, both oral and written in Chinese and English.4. Ability to focus on details and accuracy.