Oversee and lead the NC process. Responsible for the confirmation of non-conforming products identified by warehouse staff. Documented with written signatures on the confirmation of non-conforming products.监督和指导不合格品流程的实施。负责对仓库发现的不合格产品的确认，对不合格品的确认给出书面的意见和签字；Come up with mitigation strategies to reduce NC of imported products by communication with oversea product manufacturer and tracking the progress.与海外产品制造商沟通不合格情况，制定降低进口产品不合格的策略，并跟踪进展。Responsible for working with oversea manufacturer on developing, reviewing and approving the rework instruction for specific product.负责和海外制造商针对特定产品制定、审核和批准返工作业指导书；Responsible for supervising the handling of non-conforming products identified in the Zeiss Shanghai warehouse, including rework, repairment, concession, scrapping, and etc.负责监督蔡司上海仓库发现的不合格品的处理，包括返工、返修、让步接收、报废等；Responsible for summarizing the disposal information of non-conforming products in Zeiss Shanghai warehouse and monthly reporting to the quality manager.负责每个月汇总蔡司上海仓库发现的不合格产品处置信息，并向质量经理汇报；Being responsible for supervising the investigation, processing and reporting of quality complaints related to the warehouse.负责督导与仓库相关的质量投诉的调查、处理及报告；To be responsible for cooperating with the management of medical device recalls.负责配合医疗器械召回的管理；Support the qualification with medical device third party logistics enterprises, performing on-site audits and Supplier Corrective Action Request (SCAR).参与对医疗器械第三方物流企业的质量保障能力进行现场审核和提出供应商整改要求；Responsible for organizing quality management training for warehouse personnel负责组织对仓库人员开展质量管理培训Perform other tasks as assigned by the Quality Manager质量经理指派的其他工作

Education

Bachelor or above with major in Medical equipment, Machanical, Electronics, Biology, Chemistry, Medicine, Pharmacy, Chemical industry, Computer Science.

Experience

1-2 years or more professional working experience in quality area for GSP compliance.Familiar with relevant NMPA regulations, the knowledge of ISO9001, ISO13485 is a plus.