岗位职责:
Job purpose
职位目标
? Manage and train subordinate team, optimize production process, improve production quality and efficiency.
管理并培养下属团队，优化生产流程，提高生产质量和效率。
Main Responsibilities, Activities, Duties and Tasks
主要工作职责，活动和任务
? Arrange and adjust staff schedule of production basing on approved production schedule.
根据批准的生产计划负责生产部人员的排班和调整；
? Manage EHS activities and safety check .
管理和安排安全活动及安全检查；
? Responsible for monthly report to production management.
负责将每月月报发至生产经理；
? Initiate and follow-up Deviation .
发起和追踪相应偏差；
? Ensure site work e.g. dispensing, pooling, filling, sterilization process, visual inspection, packaging compliant with effective SOPs and PMF.
确保生产现场，原辅料称量、配料、灌封、灭菌、灯检和包装符合现行SOP和工艺规程；
? Participate in validation or qualification activities from production department according to validation protocal.
作为生产部门，根据验证方案要求参与验证和确认活动;
? Aware of and comply with the corporate and local Quality/EHS Manual, Quality/EHS Management System, Quality/EHS Management Policy, Quality/EHS Goals, and applicable laws and regulations as they apply to this job type/position.
关注和遵守公司要求的质量、环境健康手册、管理体系和管理政策、目标和该职位的相关的法规要求。
? Other work assigned by superior.
上级领导交代的其他工作。
任职要求:
Education
教育背景
? University graduate or above, (Chemistry/Pharmacy is preferred).
本科或以上学历（化学、制药专业优先）;
Professional Experience, Knowledge & Technical Skills
工作经验，知识和硬性技能
? Above 3 years related working experience in pharmaceutical industry, familiar with GMP and pharmaceutical affairs law and regulation.
三年以上制药企业工作经验，熟悉GMP及药政法规;
? Candidates with working experience in injections are preferred.
有注射剂工作经验的候选者优先考虑;
? English, basic listening, speaking, reading, and writing.
英语，基本听说读写。