Summary
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
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
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Accessibility and accommodation
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
