摘要
~根据生产计划执行分配的生产任务和活动，使产品能够按照相关的 GMP、安全和环境准则及时生产出保质保量的产品。
~服务运营商
~根据相关的 GMP、安全和环境准则，根据生产计划执行分配的生产任务和活动。
根据生产流程和进度开展日常运营支持活动，实现产品质量和数量的及时生产
~文档专家管理员
~文档专家管理管理 GMP 制造文档和批次记录版本的修改、编辑、分发、审查和归档，以便在质量和期限内将其交付给生产。文档专家管理员确保为该单位的正常运作提供一套必要的行政任务。
About the Role
Major accountabilities:
- Equipment Operator -Participation to the manufacturing processes
- Execution of all assigned activities according to production schedule and in compliance with the valid GMP, work, operating, environmental and safety instructions and guidelines.
- Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
- Distribution of marketing samples (where applicable)
Key performance indicators:
- Deadlines: compliance with production planning, execution of tasks on time
- Quality: Amount of errors in production documents edited or updated and in batch record review
- Time management for shop floor where required
Minimum Requirements:
Work Experience:
- Operations Management and Execution
Skills:
- General HSE Knowledge
- GMP Knowledge
Languages:
- English.
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: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)
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