职位任职者将
• 提供质量支持以实现 pMDI 项目进度。
• 协助制定实验室质量控制标准和流程。
• 协助编写和维护与实验室设计和质量控制相关的文件和报告。
• 协助设计自动化数字流程以支持QC业务。
• 协助准备项目相关的质量文档，确保符合公司及法规要求。
• 与运营和质量部门的内部和外部同事进行跨职能互动，以确保完全符合 AZ 标准和当地法规。
The role incumbent will
• Provide quality support to achieve pMDI project milestones.
• Assist in the development of laboratory quality control standards and processes.
• Assist in the preparation and maintenance of documents and reports related to laboratory design and quality control.
• Assist in the design of automated digital processes to support QC operations.
• Assist in the preparation of project-related quality documentation to ensure compliance with corporate and regulatory requirements.
• Interact cross-functionally with internal and external colleagues in operations and quality to ensure full compliance with AZ standards and local regulations.
职责（包括关键结果领域、具体责任、任务等） Job Responsibilities (to include key result areas, specific accountabilities, tasks, etc.)
• 为项目和工厂提供质量专业知识支持。
• 协助 GPQS、ECMS、GVLMS 数据库的开发并提供专业知识。
• 支持和推动必要的部门流程、文档和培训。
• 支持和维护技术能力，并与工程、IT、QA、制造和技术职能部门的同行合作，在指定的项目和活动中提供质量监督。
• 支持 GMP 相关设施和设备系统的质量控制工作，以确保完全符合 GMP。
• 严格执行岗位操作规程和指南，完成日常实验。
• 参加GMP培训，严格遵守GMP与法规要求
• 发展各种工作技能并追求持续的改进
• 根据业务需要完成安排的其他工作
• Provide quality expertise support for the project and the plant.
• Support the development of GPQS, ECMS, and GVLMS databases, providing expertise.
• Support and drive necessary departmental processes, documentation, and training.
• Support and maintain technical capabilities, and collaborate with peers in engineering, IT, QA, manufacturing, and technical functions to provide quality oversight in designated projects and activities.
• Support quality control work for GMP-related facilities and equipment systems to ensure full compliance with GMP.
• Follow job operating procedures and guidelines to complete daily experiments.
• Participate in GMP training and strictly comply with GMP and regulatory requirements.
• Develop various work skills and pursue continuous improvement.
• Complete other tasks as assigned based on business needs.
Date Posted 08-7月-2026 Closing Date 30-7月-2026
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.