Opportunity Description
General Mission职责概述
Implementation for the quality assurance of production operations, including QA supervision, inspection and audit to ensure that all stages of the product complies with cGMP and Sanofi global requirement and standard requirements.
执行工厂生产运营质量保证，包括QA监督、检查和审核，确保产品所有阶段满足GMP、赛诺菲全球总部的要求和标准要求。
Activities具体职责
Collect and analyze product-related data
相关产品数据的收集和分析。
Participate in the pre-review of batch records. Should examine for: the completion of recording, whether the filling in meets the standard, whether the processing parameters fit the requirement, whether the material balancing and yielding meet the requirement.
参与批生产记录预审核，审核内容：记录完整性，填写是否规范，工艺参数是否符合要求，物料平衡和收率是否符合要求等各项。
Supervise Drug Destruction
药品销毁监销
Other tasks in case assigned by line manager.
领导安排的其他工作。
Be responsible for HSE in his/her position and job
对本岗位的职业健康安全环境工作负责
About you 任职资格:
Implementation for the quality assurance of production operations, including QA supervision, inspection and audit to ensure that all stages of the product complies with cGMP and Sanofi global requirement and standard requirements.
执行工厂生产运营质量保证，包括QA监督、检查和审核，确保产品所有阶段满足GMP、赛诺菲全球总部的要求和标准要求。
Activities具体职责
Collect and analyze product-related data
相关产品数据的收集和分析。
Participate in the pre-review of batch records. Should examine for: the completion of recording, whether the filling in meets the standard, whether the processing parameters fit the requirement, whether the material balancing and yielding meet the requirement.
参与批生产记录预审核，审核内容：记录完整性，填写是否规范，工艺参数是否符合要求，物料平衡和收率是否符合要求等各项。
Supervise Drug Destruction
药品销毁监销
Other tasks in case assigned by line manager.
领导安排的其他工作。
Be responsible for HSE in his/her position and job
对本岗位的职业健康安全环境工作负责
About you 任职资格:
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