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生产流程负责人(Process Facilitator)

地点 无锡市, 江苏, 中国 职位 ID TP24382 发布日期 08/10/2026

Brief Job Description 工作描述简述

Summarizes the job’s purpose or role and why it exists in the organization

概述工作的目的或角色及其在机构内的价值

• Collaborate effectively with cross functions (GERE, global SME and stakeholders, external parties, etc) to support the high-quality and efficient deliverables of CDC stream/PP Packing stream related projects, and contribute to build a smart, green factory to achieve autonomous manufacturing and zero carbon.

积极与跨部门团队(GERE、AZ 各领域专家及外部合作方等)高效协作,支持无锡工厂CDC 生产业务模块/PP 包装业务模块相关项目的高质高效交付,助力实现自动化和零碳目标,打造智能绿色工厂。

• Introduce new equipment, new process and new technology according to project strategy and plan, to deliver formulation/packing project on time.

确保按照项目策略计划支持新设备、新工艺、新技术引入,按时按质交付制剂/包装项目。

• They carry responsibility for the day-to-day performance of defined processes in terms of adherence to plan, operational standards, cost, asset, cGMP and safety.

该岗位的职责为维护日常的生产绩效,包括制定生产的计划符合性,操作规范,成本,固定资产,现行GMP 及安全等的相关业务。

• The Process Facilitator supports the Stream Leader manage teams, they are capable leaders and coaches.

生产流程负责人协助业务模块负责人管理团队,该岗位应具备领导能力和辅导能力。


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 teamclimate.

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, 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





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 authorisation and employment eligibility verification requirements.

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优秀的文化,出色的工作任务,充满支持的管理模式。 公司内部的轮换机会。 他们重视包容性和多样性。