# M&S - MQC Analyst I at Sanofi

Sanofi is hiring an M&S - MQC Analyst I in Beijing, China. Level rates it Little AI ●○○○; you can [apply on Sanofi](https://jobsbylevel.com/go/ede6ff31-620a-46a0-93a2-b471f190606e?utm_medium=ai-agent).

AI Level 1, AI centrality 0 out of 100. Beijing.

## Details

- Company: [Sanofi](https://jobsbylevel.com/companies/sanofi)
- AI level: AI Level 1 (score 0 out of 100)
- Location: Beijing
- Posted: November 12, 2026
- Apply: https://jobsbylevel.com/go/ede6ff31-620a-46a0-93a2-b471f190606e?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=m-s-mqc-analyst-i-at-sanofi-e976b6

## Prepare for this job

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## Description

Our Team/ Overview 我们的团队 The Site Quality department plays a critical role in ensuring that Sanofi's manufacturing sites produce safe, effective, and high-quality products that meet all regulatory requirements and patient needs. Their mission is to maintain the highest quality standards throughout the manufacturing and testing process while supporting continuous improvement and operational excellence. 工厂质量部门在确保赛诺菲生产基地生产安全、有效和高质量的产品方面发挥着至关重要的作用，这些产品需满足所有法规要求和患者需求。其使命是在整个生产和检测过程中保持最高质量标准，同时支持持续改进和卓越运营。 Main Accountabilities 主要职责 •Is responsible of the delivery the microbiology quality control lab aspects of the project, within the allocated budget, schedule and the expected objectives, performances, HSE, Quality. Ensure the project is performed according to the Sanofi Standard and Good Practices. 负责在预算、进度及预期目标、绩效、HSE和质量范围内交付项目的微生物质量控制实验室相关工作。 确保项目按照赛诺菲标准和良好实践执行 • Participation in the establishment, qualification and commissioning of the Microbiology QC laboratory in IFB. 参与IFB微生物质量控制实验室的建立、确认和调试。 • Implementation of microbiology tests as part of the DS, incoming material, in-process controls, clean utility monitoring and cleaning validation of insulin drug substance manufacturing. 对原液、进厂物料、中间产品、公用系统及胰岛素药物制造的清洁验证实施微生物检测。 • Implementation of environment monitoring and gas monitoring for the InsuLINK Facility. 实施胰岛素项目设施的环境监测和气体监测。 • Support of microbiology method transfers and verification/validation activities. 支持微生物学方法转移及验证/确认活动。 • Executing microbiology testing and data review in a timely manner, ensuring adherence to the committed scheduled plans. 及时执行微生物检测和数据审查，确保遵守承诺的计划 • Performing the microbiology data review of executed tests in a timely manner, ensuring adherence to the committed scheduled plans. 及时对已执行检测进行微生物学数据审查，确保遵守承诺的计划。 • Conscientious documentation of all measurement results, raw data and calculations according to cGMP and data integrity requirements. 根据cGMP和数据完整性要求，认真记录所有测量结果、原始数据和计算。 • Participation in the preparation and review of laboratory specifications, methods, procedures, templates, protocols and reports. 参与实验室质量标准、方法、程序、模板、协议和报告的起草与审核。 • Implementation of equipment (re-)qualifications under supervision. 在监督下实施设备确认与再确认。 • Calibration and maintenance of the assigned equipment or coordination of it, e.g. by external service providers, including the associated documentation. 协助校准与维护指定设备的，例如：由外部服务提供商提供，包括相关文档。 • Ensuring that he/she is trained and qualified to the assigned microbiology testing that requires to be qualified. 确保接受适当的培训并具备相应的微生物检测资格。 • Assist in troubleshooting and investigating microbiology issues. 协助排查和调查微生物学问题。 • Receiving, storing, documenting, handling, and disposing of reagents, biological indicators, culture media, strains, and lysates, while managing their stocks and other testing-related consumables to ensure adequate supply; including inactivation of material with growth. 接收、储存、记录、处理和处置试剂、生物指示剂、培养基、菌株和鲎试剂，同时管理其库存及其他检测相关消耗品，以确保充足供应，包括活菌类物质灭活。 • Maintenance of documents, e.g. form sheets, test instructions, SOPs, SOP attachments, Logbooks. 文件维护，例如：表格、测试指导、标准作业程序（SOP）、作业程序附件、日志本。 • Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks. 按照cGMP和HSE要求执行其任务，并遵守与这些任务相关的指示、程序和记录 • Informing his/her manager of any quality (change control, deviations, LI) or HSE event in a timely manner to ensure investigation and impact assessment are performed appropriately. 及时通知其经理任何质量事件（变更控制、偏差、LI）或HSE事件，以确保调查和影响评估得到妥善执行。 • Executing assigned CAPAs related to remediation plans, continuous improvements. 执行与整改计划、持续改进相关的指定CAPA。 • Execute other works which is assigned by the line manager. 执行由直属经理分配的其他工作。 Additional Accountabilities 额外的职责 1. Quality Department HSE Responsibilities ➤ Responsible for following the company’s HSE policy and integrated all requires into daily job. ➤Incorporate HSE work into the work plan ➤ Organize the implementation of HSE management target plan of this department, implement HSE rules

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