Responsibility工作职责： 1. Responsible for the collection of quality management system documents, and help organizing training, implementation, and enforcement. 负责质量管理体系文件的收集，并协助组织培训、推行和落实。 2. Assist in the daily supervision and management of system operation, organize internal audits and management review. 协助体系运行的日常监督管理，协助组织实施内部审核及管理评。 3. Coordinate the third-party audit and carry out daily on-site supervision of production safety. 协调第三方审核，日常进行安全生产的现场监督。 4. Responsible for the follow-up and verification of corrective and preventive measures during the operation of the system. 负责体系运行过程中纠正预防措施的跟踪及验证。 5. Collect external documents and help to organize internal dissemination and training in the company. 收集外来文件，并协助组织在公司内部宣贯、培训。 6. Report regularly to supervisors on the operation of the company's quality management system and develop continuous improvement programs. 定期向上级领导汇报公司质量管理体系运行情况，并制订持续改进方案。 Requirement 要求： 1. Preferably majoring in Electronics, Mechanics, Medicine, with tertiary education and above. 电子、机械、医药类等理工科专业优先，大专及以上学历。 2. Have some understanding of medical device related laws and regulations, familiar with medical device production quality management standard (GMP) requirements. 对医疗器械相关法律法规、医疗器械生产质量管理规范（GMP）要求有所了解。 3. Familiar with quality management system, relevant internship or work experience is preferred. 熟悉质量管理体系，有相关的实习或工作经验优先。 4. Experience in ISO13485, ISO9001 quality management system certification is preferred. 了解ISO13485、熟悉ISO9001质量管理体系认证的工作，有相关经验优先。 5. Strong execution ability, proactive, conscientious, and responsible, with teamwork spirit. 具有较强的执行力，工作积极主动，认真负责，富有团队合作精神。 6. Strong logical thinking ability, good language communication and written expression ability. 逻辑思维能力强，有良好的语言沟通和文字表述能力。 你将获得： 独特的外企实习经验、实力外企的实习证明、全英的工作交流环境、表现优秀者可以获得转正机会。