职位描述

职位描述： 实施对原辅材料、中间体产品、成品、半成品等的相关检验，并对检验原始数据负责To perform analytical and instrumental test of raw materials, intermediate, finished products and inner package material. And to be responsible for the original analysis result.洁净区环境监测及人员监测Be responsible for the environment monitoring and personnel monitoring.负责培养基、淋洗液的配制; 培养基灵敏度实验的实施，确保培养基的有效性。To be responsible for the preparation of media and . And to be responsible for the validity of the media.微生物方法验证，实施稳定性考察To perform method validation and product stability study.细菌鉴定，菌种的使用和保藏Bacterial identification, the use and preservation of bacteria实施对工厂水系统、压缩气体等的取样监测To perform method validation and product stability study.对实验室相关SOP、检验方法的起草及维护，组织制备有关产品质量或微生物检验的技术文件，负责原始记录等的管理和归档Be responsible for initial and maintenances the related SOP, test method and assist in preparation of product quality and microbial test technical document. And to be responsible for organizing the preparation of technical documents related to quality or chemical test and the management and filing of those documents.新员工的培训Train the new staff.保持实验室工作的科学性和先进性。To keep scientific advancement of lab.负责完成质量部经理或QC主管交办的其它工作。To carry out other works assigned by QO Manager or QC Supervisor.遵守公司有关EHS的政策和规定，并完成EHS相关工作Comply with EHS policy and regulation, and complete the EHS related work.最低任职要求MINIMUM REQUIREMENTS教育程度/经验Education Background/ Experience大学本科及以上学历，药学、微生物专业或相关专业或相关工作经验University degree or above, major in pharmacy, microbiology or related major or related work experience特别知识Special Knowledge掌握辉瑞质量管理系统，国家GMP政策和药政法规。Grasp Pfizer quality management system, state GMP policy and regulations技能Skills:1.具有良好的英语综合能力及计算机应用能力。Ability to speak and write and understand English and use the computer.2.具有团队合作精神，工作责任心强；Have the spirit of teamwork and strong sense of taking responsibilities3.具有一定的沟通协调能力和培训能力。Have the capability of communicating, coordinating and training. 职能类别： 药品生产/质量管理

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