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:

List here ideally the must-haves criteria to be successful on the role.

请列出胜任该职位所必须具备的条件。

Experience 工作经验: 不要求prior工作经验（实习生职位）/ No prior work experience required (internship position)

Soft skill 通用技能：

office software（熟练应用办公电脑软件)

Technical skill:

专业技能:

Pharmacy or related field  (药学或相关领域)

Education

教育背景:

中专及以上学历 / Technical secondary school or above

药学或相关领域专业 / Pharmacy or related field

Languages 语言要求:

流利的中文（口语和书面）/ Fluent Chinese (spoken and written)

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!