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 and  Preventive 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