Perform the principal duties of the Packaging Engineer position: 包装工程师履行的主要职责：

• In collaboration with Production and Quality, develop and maintain all packaging and labeling processes for all products groups和生产质量部门一起，开发和维护所有产品的包装和标签工艺
• 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 Manufacturing Engineers to maintain the item master, product routings and bills of material in the SAP system支持制造工程师维护SAP中主数据，产品流程和物料清单
• Responsible for compiling all manufacturing procedures for packaging and labeling processes负责编写所有包装和标签的工艺文件
• Deliver necessary training for workshop employees给现场的员工做必要的培训
• In collaboration with the maintenance team, develop and implement Maintenance Excellence program和设备维护团队合作，开发和执行维护项目
• Propose, develop or participate in continuous improvement initiatives, such as projects to improve quality, cost, delivery and efficiency建议，开发，参与持续改善，例如一些提高质量和效率，降低成本
• Use methodology to improve processes and reduce non-value added waste and activities. (Including process FMEA, Predictive Indicator and use of statistical techniques使用一些方法论提供工艺和降低没有附加值的浪费（包含PEMEA和一些数理统计的技术方法）
• Participate to identify capital spend and budget requirements识别资本花费和预算需求
• Support capacity planning/ management, identify needs of new equipment or processes支持产能计划和管理，识别新设备或新工艺需求
• Participate or lead the layout design / implementation for facility and equipment参与或指导设备设施的布局设计
• Support R& D on new products development支持研发新产品的开发
• 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
• Responsible for creating and maintain manufacturing documentation for equipment and processes负责工艺过程中设备和工艺的流程文件的创建和维护
• Develop and implement process validation plans开发和执行过程验证计划
• Responsible for compiling the validation/verification protocols and completing studies by creating finished reports负责执行验证/确认方案，完成报告
• Understand special processes requirements such as Sterilization, Cleaning, Packaging, FPI etc.理解特殊工艺需求，如灭菌，清洗，包装，荧光探伤等
• Understand computer software validation requirements理解计算机软件验证需求
• Participate / conduct internal and supplier quality audits if required必要时候，参与执行供应商内部审核
• 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 packaging and labeling related audits (internal, Corporate, External, for Quality, H& S, Environment, etc.) 负责所有包装和标签相关的审核（内部，公司层面，外部，质量，环境健康相关）