目的对药品生产文件持续改进工作的开展进行初步探讨。
Objective Have a primary exploration on the continual improvement of production documentation for drug manufacturing.
负责包装区域现场管理，作持续改进工作，如5s，流程优化等。
Responsible for package work area management, make continuous improvement, such like 5s, process optimization, etc.
开展设备设施的持续改进工作，提高设备可靠性，满足生产营运的需求。
Keep continuous innovation, improve equipment reliability to meet the requirements of production improvement.
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