M&S-Technician, QC Virology-Shenzhen

Job title 职位名称: QC Analyst, Lab Virology Technician 质量控制分析员，病毒学技术员

•    Location 工作地点: Shenzhen 深圳
•    Remote working and % of travel expected 远程办公和出差的概率: 5%
•    Job type 工作类型: Full time 全职
•    Site/Unit 区域/事业部: Shenzhen site 深圳工厂

About the job 工作职责
Our Team 我们的团队:
Manufacturing & Supply consists of 3 manufacturing platforms based on global business units, as well as supporting functions of Quality, Market Supply and Strategy. We are committed to making best class medicines with excellent strategies and tools and delivering them to our patients.
制造与供应事业部包含以3个全球事业部为基础的制造平台，以及质量、供应商、精益战略等支持部门。致力于用优异的战略和工具制造优质的药品并传递到患者手中。

Main responsibilities 职责描述:
Please indicate here the main job responsibilities请列举该职位的主要工作职责。
•    Execute analytical testing(including incoming material, product, and stability testing) in a timely manner, ensuring adherence to the committed scheduled plans
按时执行分析测试（包括原料、产品和稳定性测试），确保严格遵守既定计划安排
•    Perform tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, and records
按照cGMP和HSE要求以及相关指令、程序和记录执行任务
•    Record all expected raw data, calculations, and information related to tasks, complying with cGMP and Data integrity requirements
记录所有预期的原始数据、计算和与任务相关的信息，符合cGMP和数据完整性要求
•    Ensure proper training and qualification for assigned analytical testing
确保对指定的分析测试进行适当的培训和资格认证
•    Perform QC data review of tests executed by other analysts in a timely manner
及时对其他分析员执行的测试进行质量控制数据审查
•    Inform manager of any quality or HSE events (deviations, OOx) in a timely manner
及时向经理报告任何质量或HSE事件（偏差、超标等）
•    Responsible for the perform of analytical method development, verification and validation(if applicable)
负责分析方法的开发、验证和确认的执行（如适用）
•    Participate actively in investigations where involved
积极参与相关调查
•    Execute assigned CAPAs related to remediation plans and continuous improvements
执行与整改计划和持续改进相关的指定纠正和预防措施（CAPA）
•    Participate in lab operation and optimization, which include but not limited to the material management and digitalized system management.
参与实验室运营和优化工作，包括但不限于物料管理和数字化系统管理
•    Ensure lab/facilities and instruments are maintained in a quality and safety status
确保实验室/设施和仪器保持良好的质量和安全状态
•    Other Duties: Perform additional responsibilities as assigned by supervisor.
其他职责：履行领导交办的其他职责。

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:
At least 1 years of experience in quality control within the pharmaceutical industry在制药行业质量控制领域至少1年工作经验
•    Skills 技能：
Ability to analyze complex data and laboratory results to make informed decisions and identify areas for improvement. 能够分析复杂的数据和实验室结果，做出明智的决策并识别需要改进的领域。
Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements. 对细节保持敏锐的关注，以确保测试、报告的准确性，并符合监管要求。
Proficiency in identifying issues and implementing effective solutions to resolve quality control problems. 熟练识别问题并实施有效解决方案以解决质量控制问题。
•    Education 教育背景:
college degree in Chemistry, Biology, Pharmacy, or related field
化学、生物学、药学或相关领域的大专或以上学位
•    Languages 语言要求:
Perform to have English (reading, writing, speaking) skills.
有英文（读、写、说）沟通能力者优先
•    Play to Win Behaviours 全力致胜行为:
Stretch 超越自我
Take Action 主动出击
Act for Patients & Customers 以患者和客户为本
Think One Sanofi 团结一致