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• In collaboration with cross function team especially Sterility Assurance, develop and maintain all packaging and labeling processes for all products groups和各部门尤其是无菌保证部门一起， 开发和维护所有产品的清洗工艺
• ▪ Work with related functions in China and/or oversea, ensure in-time and compliant start-up of manufacturing at Suzhou site和中国以及/或国外相关部门合作， 确保苏州工厂启动项目的及时合规性
• ▪ Support to maintain the process routing, in the SAP system to make sure the product manufacturing process compliant with procedure requirement and validation result.支持维护SAP中产品流程以确保产品生产工艺符合流程要求以及验证结果。
• ▪ Responsible for compiling all manufacturing procedures related with cleaning processes负责编写所有清洗相关的工艺文件
• ▪ Deliver necessary training for shopfloor employees给现场的员工做必要的培训
• ▪ In collaboration with the maintenance team and calibration team, develop and implement Maintenance program and calibration activities. 和设备维护团队以及校准团队合作， 开发和执行维护项目以及完成校准行动项。
• ▪ Propose, lead or participate in continuous improvement initiatives, such as projects to improve quality, cost, delivery and efficiency. Predictively use methodology to improve processes and reduce non-value added waste and activities. (Including process Risk Assessment Summary, use of statistical techniques建议， 领导或参与持续改善， 例如一些提高质量和效率， 降低成本的项目。前瞻性地使用一些方法论提高工艺和降低没有附加值的浪费（ 包含pRAS和一些数理统计的技术方法）
• ▪ Financial knowledgeable participate to identify capital spend and budget requirements具备财务知识， 识别资本花费和预算需求
• ▪ Support capacity planning/ management, identify needs of new equipment or processes. Participate or lead the layout design / implementation for facility and equipment, can implement machine qualification and process validation支持产能计划和管理， 识别新设备或新工艺需求参与或指导设备设施的布局涉及， 能执行设备验证和工艺验证。
• ▪ In partnership with the Quality department, participate to the development of the quality system and its day to day implementation和质量部合作， 参与开发质量体系确保日常执行
• ▪ Understand the Quality philosophy based on FDA QSRs, ISO 9000 and CFDA requirements理解基于FSA QSRs, ISO9000和中国食品药品监督管理局要求的质量方针
• ▪ Understand, compile and control non-conformance data and product traceability理解， 符合， 控制合规以及产品的追溯性
• ▪ Understand computer software validation requirements理解计算机软件验证需求
• ▪ Perform all job duties in full accordance with: 履行所有下述职责
• - The J& J policies on Information, Assets protection, Maintain password(s) confidential, protect强生在信息技术， 资产保护， 密码的保密性
• - Critical Business Information.关键业务信息
• - All J& J policies and local regulations. 所有强生的政策和本地法规
• - The policies of the Health Care and Environmental programs. 健康护理和环境程序政策
• ▪ Propose, develop or participate in programs to improve H& S and Environment建议， 开发或参与项目以提高环境健康
• ▪ Full responsibility and ownership (like all employees on site) for all cleaning process related audits (internal, Corporate, External, for Quality, H& S, Environment, etc.) 负责所有清洗工艺相关的审核（ 内部， 公司层面， 外部， 质量， 环境健康相关）