Major responsibilities/主要职责: -Keep contact with inspection institute, complete homologation sample inspection work independently 保持和检测全部效交流, 自立完成样品检测工作 -Be proficient in communication with provincial and city FDA, handle problem on market surveillance actively 擅长和各地药监局交流,乐观处理市场监管中发觉的问题 -Internal quality consciousness and knowledge training 企业内部质量意识和学问培训 -Co-work with other departments, improve quality system and solve the related problem issue. 跨部门配合,推动质量改进, 解决相关质量问题 -Technical document translation (English) 技术文档翻译(英语) -Handle/ archive quality related documents and record 处理并管理质量相关文档和记录 -Complete other tasks from manager 完成上级布置的其他任务 Requirements/资历要求: -Medical device, biomedical engineering, mechanical engineering, electronic engineering, bioengineering, Chemical, Ecsomatics and so on. Associate degree and above. 医疗器械、生物医学工程、机械、电子、生物工程、化学、检验学、等专业,大专及以上 -At least two years relevant work experience,prefer medical device industry experience 2年以上相关工作阅历,有医疗器械企业相关工作阅历更佳 -Be familiar with China medical device inspection standard and related regulation 认识中国医疗器械检测标准和相关规矩 -Skilled use of office software 娴熟使用office办公软件 -Fluent English ( reading and writing ) 英语读写流利