Summary
• 此角色利用化学实验室技能测试和测量产品或物料, 同时确保分析按照既定的标准操作程序 （SOP）、分析方法和当前的药典。
About the Role
Major Accountabilities
~ 样品存储和管理
~ 药品/成品/投诉/稳定性/包装材料样品（根据 GxP 标准）进行分析测试/记录
~ 测试/样品存储和管理。
~ 稳定性样本与 GxP 标准的分析文档
~ 收到后 24 小时内报告与诺华产品相关的技术投诉/不良事件/特殊情况
~ 营销样本的分发（适用）
Key Performance Indicators
• 此角色利用化学实验室技能测试和测量产品或材料, 同时确保分析按照既定的标准操作程序 （SOP）、分析方法和当前的编年。
Work Experience
~具备制药/化学分析/QC/同等的技术和科学知识
~在制药行业的实验室环境中的工作经验
Skills
~实验室设备
~质量控制 （QC） 测试
~质量控制抽样
~全面质量管理
~Gxp（吉特普）
~行业标准
~实验室卓越
~决策能力
~处理歧义
~自我意识
~持续学习
~技术专长
Language
中文
英语
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
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Division
Operations
Business Unit
Innovative Medicines
Location
China
Site
Changping County (Beijing)
Company / Legal Entity
CN06 (FCRS = CN006) Beijing Novartis Pharma Co., Ltd
Functional Area
Quality
Job Type
Full time
Employment Type
正式
Shift Work
No