Įžanga
~确保并支持整体GxP合规性和诺华质量管理体系的合规性。
About the Role
~ 监督所有生产和测试活动，确保符合cGxP，包括数据完整性和电子合规性
~ 支持异常调查
~ 审查和批准生产、质量控制以及 AS 和 T 记录
~ MBR审查
~ 支持运营支出改善项目
专业人员-根据注册执行批放行
~ 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
~管理责任范围内的质量方面和项目。
~确保并支持整体GxP合规性和诺华质量管理体系的合规性。
Work Experience
~在制药工业/生物技术领域从事环境监测和清洁区的QC/QA工作
~职能广度
~跨界协作
Skills
~技术智能
~QA（质量保证）
~GMP程序
~质量标准
~质量控制 （QC） 测试
~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
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.
