Role at a glance
- Job function
-
Manufacturing & Skilled Trades Manufacturing & Production
- Salary
- Not Disclosed
- Location
- China, Wuxi
- Work arrangement
- On-site
- Employment
- Full-time
- Experience
- 3 years of management working experience related pharmaceutical industry
- Education
- University graduate or above
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Role Summary
This role supports pharmaceutical production and process management while coordinating project delivery across facility and process design, supplier selection, qualification, handover, and related activities. The role also supports compliance, team development, continuous improvement, digital tool adoption, and alignment between production capacity and assets.
What You'll Do
- Coordinate delivery of project streams, including facility and process design, supplier selection, FAT, SAT, qualification, and handover.
- Work with stakeholders and stream leaders on project targets, reporting, escalation, communication, and change management.
- Conduct project execution progress communications across client teams and perform risk-based impact assessments for change controls as...
- Ensure production meets targets for timing, cost, and quality, and solve problems by identifying underlying causes using resources and data.
- Issue and update work instructions and reports, and review production records for compliance.
- Lead continuous improvement and digital tool initiatives, including coaching and training others in digital tools.
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Pharmaceutical-related background with a good understanding of GMP; people management, leadership, communication, problem-solving, investigation, and continuous improvement capabilities; good English reading, writing, and speaking skills; good MS Office skills.
Required
- Pharmaceutical-related background
- Good understanding of GMP
- People management skill
- Proven leadership and communication skills
- Problem-solving, investigation, and continuous improvement capability
- Good English in reading, writing, speaking
- Good MS Office skill
- 3 years of management working experience related pharmaceutical industry
Original job description
Content provided by the employer
Original job description
Content provided by the employer
Typical Accountabilities
主要职责
Project Management
项目管理
• Enable the streams deliverables to plan, incl., facility/process design, supplier selection, FAT, SAT, qualification, handover, etc.
确保相关业务模块成果按计划交付,包括厂房/工艺设计、供应商选择、FAT、SAT、确认、移交等。
• Work with all stakeholders to achieve the defined project targets.
紧密与所有利益相关者合作,设计和交付项目目标。
• Support stream leaders to ensure the project management under AZ PMF framework, incl., reporting, escalating, communication, change management, etc.
支持相关业务模块负责人确保AZ PMF 框架下的项目管理,包括报告、升级、沟通、变更管理等。
• Conduct communications across client teams to share the progress of the project execution.
与用户团队进行沟通,分享项目实施的进展情况。
• Be as the production representative to do the impact assessment for each change control via risk-based approach.
作为生产代表,对每个变化在考虑风险的基础上进行影响性评估。
People management and teambuilding
人员管理及团队建设
• Ensures compliance of self and others to internal and external regulations, policies and principles.
确保自己和他人遵守内外部法规,政策,原则。
• Ensure Compliance of self and others to current GMP, SHE requirements.
确保自己和他人遵守现行GMP,安全等的规定。
• Ensure team are following company culture and maintain healthy team
climate.
确保团队符合公司文化及打造健康的团队氛围
Production and process management
生产任务及流程管理
• Ensure production adherence meet target with reasonable cost and high quality standard.
确保生产任务在合理的成本下按时完成,并产出高质量的产品。
• Solves problems quickly by addressing the right underlying causes, leveraging resources and data.
熟练使用数据资源,快速识别根因并解决问题
Documentation
文件
• Issue and update the relative WIs and reports to supervise the production activity.
撰写/维护生产相关的文件,例如操作指导、报告等。
• Ensure production record are executed per requirement through review.
经过审核确保批生产记录按照要求执行。
Project, continuous improvement initiatives management
项目及持续性改进计划的开展
• Ensure project to be extended timely and continuous improvement to
be executed to deliver high performance.
确保项目的有效开展,并能积极开展持续性改善项目来提高绩
效。
• Identifies and proposes approaches to improve efficiencies within area through adoption of digital tools.
负责所在区域数字化应用,针对效率提升提出改善建议
• Proactively supports and engages with digital learning by coaching/training others in use of digital tools.
积极参与并支持团队内部的数字化能力建设,主动辅导/培训团队数字化工具的使用
Assets management
固定资产的管理
• Ensure the matching rate of production capacity and the asset.
确保生产设备等固定资产配额和产能的评估及管理。
Production and process management
生产任务及流程管理
• Ensure production adherence meet target with reasonable cost and high
quality standard.
确保生产任务在合理的成本下按时完成,并产出高质量的产品。
• Solves problems quickly by addressing the right underlying causes, leveraging resources and data.
熟练使用数据资源,快速识别根因并解决问题
Education, Qualifications, Experience and Capabilities 教育、资质、经验和能力
Education, Qualification, Experience
教育、资质、经验
Education-教育
University graduate or above 大学本科以上
• Qualifications-资质
Pharmaceutical related background, good understanding of GMP
药学背景熟悉GMP
Technical / skill training
技术/技能训练
Good manufacturing Practice
生产规范知识
People management skill
人员管理技能
• Experience-经验
3 years of management working experience
related pharmaceutical industry
三年制药相关行业管理经验
• People management skill
人员管理技能
Capabilities
能力
• Proven leadership, communication skills
领导力和沟通能力
• Problem solving, investigation, and continuous improvement capability
问题解决、调查和持续改进能力
• Good English in reading, writing, speaking
较好英语读,写,说能力
• Good MS-office skill
良好的MS 办公软件应用技能
Date Posted
14-Sep-2026Closing Date
30-Dec-2026AstraZeneca 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.
About the company
AstraZeneca
Large Enterprise
AstraZeneca is a global biopharmaceutical company dedicated to the research, development, and commercialization of innovative medicines. Headquartered in Cambridge, UK, the company focuses on areas such as oncology, cardiovascular, renal, metabolism, and respiratory diseases, striving to deliver life-changing treatments to patients. With a strong commitment to scientific excellence and collaboration, AstraZeneca invests in cutting-edge technologies and partnerships to drive advancements in healthcare. The company is also committed to sustainability and corporate responsibility, aiming to make a positive impact on communities worldwide.