**MAIN RESPONSIBILITIES** + 管理变更控制，验证及CAPA（纠正措施及预防措施）Manage Consumable Control, Validation and CAPA (Corrective Action andPreventive Action) process + 管理日常文件 Handle routine documentation + 事件原因分析及解决 Problem solving for event + 生产车间巡视 Manufacturing site walk down + 推广质量工具（FMEA，SPC，DOE等），以提高生产工艺及设备和产品质量Spread the Quality Tools (FMEA, SPC, DOE and etc.), to improve process, equipment and product quality + 识别质量和食品安全相关的异常质量事件，运用统计分析及质量方法论，通过稳健设计方式不断提高工厂质量水平。Identify quality and food safety event, continuously improve site quality performance through robust design based on data analysis and quality methodology. + 质量推进及改善的倡导，能够激励团队践行质量卓越以完成工厂目标。The champion of quality culture improvement and optimization, engage team to continuously commit to quality excellence for achieving plant goals. **QUALIFICATIONS** + 具备五年在食品药品生产领域的经验 5 years working experience in food/pharmaceutical industry + 要求在食品药品生产领域具备良好的GMP（良好生产规范）及GDP（良好文件规范）实用知识 Good practical knowledge of GMP and GDP in food/pharmaceutical manufacturing + 了解HACCP和ISO系统知识的将优先考虑 Knowledge of HACCP and ISO systems would be preferred + 具有相关工作经历并对制造过程有所理解 Working exposure and understanding of manufacturing process + 具备相关的工作经验及/或学历 Relevant experience or equivalent combination of education and work experience + 具备团队协作能力和良好的沟通技巧 Team player with collaboration capability and good communication skills An Equal Opportunity Employer Abbot welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call 224-667-4913 or email corpjat@abbott.com