质量分析员-项目周期：6个月会续签或转正

职责和责任
As production process risk management and process control coordinator, assist in maintaining risk management documents, on-site IPQA, material disposition of short expiry date, test data review and analysis, provide product COC, and other related tasks.
作为生产过程风险管理和过程控制协调员，协助维护风险管理文件、现场IPQA、短有效期物料处置、测试数据审阅分析、出具产品符合性证明等相关工作。
Assist lab equipment system administrator, address lab system user access review, lab system audit trail review and data backup.
协助实验室设备系统管理员执行实验室设备用户权限管理、审计追踪审阅和数据备份。
As quality culture coordinator, assist in routine Great Catch cases collection, disposition and feedback, and promote site quality culture and hold quality culture activities.
作为质量文化协调员，协助日常Great Catch收集、处置和反馈，以及推动工厂质量文化和举办质量文化活动。
As quality building ownership program coordinator, assist the Facility Department in handling BOP
作为质量部BOP协调员，协助设施部处理BOP。
As LMS administrator, create/maintain/assign training items, provide training data/reports based on business needs, and support the execution of training activities at the Minhang site.
作为LMS管理员，创建/维护/分配培训课程，根据业务需求提供培训数据/报告，支持闵行工厂的培训执行工作。
经验和教育
University/Bachelor’s Degree or Equivalent.
大学本科学历或同等学历。
1-2 years of experience in Quality function, in Medical Devices or Pharmaceutical industry.
1-2年在医疗器械或医药行业质量部门的经验。
Better to have knowledge of medical device regulatory requirement such as ISO13485 and China GMP is necessary, and some professional skills such as FMEA, Minitab, Power BI.
最好具有医疗器械法规要求的具体知识，比如ISO13485 和China GMP，以及专业技能，比如FMEA, Minitab, Power BI。