Line Technician at AstraZeneca

, , China -

Full Time

Start Date

Immediate

Expiry Date

21 Jan, 26

Salary

0.0

Posted On

23 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Problem Solving, Continuous Improvement, GMP Compliance, SOP Development, Training, Lean Skills, Multi-Skill Development, Equipment Maintenance, Process Control, Team Collaboration, Communication, Quality Investigation, 5S Management, Documentation, Coaching, Resource Coordination

Industry

Pharmaceutical Manufacturing

Description

Purpose: 岗位工作地点在青岛，项目建设期间参与生产部的前期设计，建造，调试和确认等工作，作为用户代表一员支持项目组实现青岛pMDI工厂的建设。通过精益标准化和专业技能持续标准化与改善如SOP/工作指导以确保项目期间的知识，技能和经验能够传承以支持未来的商业化生产，并在项目早期就注重工艺/设备/操作等的持续改善工作。进入商业化生产期间，高质量地实现所有设定的生产目标，包括设备的操作和基本维护，生产线的清场，及技能的发展等。 This role is based in Qingdao. During project phase involved in product department Design, Construction, Commissioning and Qualification. As an end user to support Global engineering team/Project team to deliver Qingdao pMDI project. And standardize knowledge and experience during project and startup phase to prepare for Qingdao site PQ and PV and ensure following BAU smoothly in terms of daily operation including SOP/WI ready and continuously improve process/equipment/operation from project to BAU transition. Fulfill all set production objectives in respect of equipment operation & basic maintenance, line clearance, and skill development. etc. 作为最终用户参与和支持青岛工厂的项目建设 Support project team to deliver Qingdao pMDI project as end user 参与到生产部门的设计、安装、调试等工作，支持到商业化生产的能力建立。 Involved in product department design, installation, commissioning etc., BAU capability build up 学习并运用其他工厂和行业的最佳实践到新工厂 Learn and apply best practice from other sites and other experiences to Qingdao projects 通过项目期间的参与，实践为未来的商业化生产的垂直启动和成功做好充足的准备 Prepare vertical startup of BAU through expertise, lean and experience gained from project phase 良好的问题解决能力和持续改进的能力，支持项目C&Q,PQ/PV的成功 Strong PPS and CI capability to support C&Q, PQ/PV successfully 支持生产体系的搭建以支持未来的商业化生产 Support to setup manufacture system to ensure following BAU smoothly 生产和日常操作 Production and routine operator 遵守GMP和SOP的相关规定 Follow GMP & SOP 遵守公司政策 Follow AstraZeneca policy 能够独立操作各生产工段（配料、制剂、罐装、组装线、包装线）和IPC设备，明确岗位职责并考取岗位上岗证 Able to each production section (dispensing, formulation, filling, assembly lines, packaging lines)operate Assembly line machine、 Packing line machine and IPC machine ,and know the job responsibility and get the job certificate 熟知岗位中间控制职责，如果经过中间控制知识及操作技能的培训并考核合格后，承担生产过程中的中间控制职责 Familiar with in-process-control, take the IPC responsibility if finish IPC training and pass the test 及时向流程负责人/一线生产经理反馈当班过程中的人员行为和绩效，必要时对员工进行辅导 Report to process facilitator/FLM about people behavior and performance when on duty, coach employees if needed 自主解决当班过程中产线的各种问题解决，必要时升级 Facilitate problem solving when on duty and escalate if needed 参与偏差和投诉等质量事件调查 Participate in the deviation & complaint investigation 进行生产线的清洁、清场 Packing line Cleaning 积极主导现场问题的解决，并协调生产资源 Actively lead problem solving in line and coordinate line resource 具备相应的精益技能和意识，并提出改善建议，组织产线持续改进项目实施 Propose continuous improvement ideas based on lean skills and mindset, lead improve project execution 保持现场良好的5S状态 Keep good 5S status in shopfloor TPM 确保员工按照点检表要求进行点检，并不断优化点检内容 Ensure employees follow the spot check form and continuously improve the form 及时报告设备的异常，并能独立解决复杂设备问题 Report equipment abnormal in time and solve complex equipment problems 参与设备的日常保养并主导AM活动 Participate in general upkeep and lead AM activities 协助维修人员进行设备的维修和保养 Help equipment maintenance and upkeep with engineer 培训 Training 接受相关GMP和SHE的培训 Accept relative training of GMP&SHE 培训新员工和其他人员岗位操作技能 Train new staff and others’ skills 掌握多技能，并推进产线员工多技能发展 Have multi-skills and promote employees’ multi-skill development 组织培训资料的编写和操作标准的制定，并检查标准是否执行到位 Organize drafting training materials and process standard, regularly do standard confirmation 能够独立编写GMP相关文件，如SOP WI等 Can draft GMP related documents such as SOP WI GMP 要求 GMP requirements 理解业务活动中涉及GMP的相关内容及可能对产品质量产生的影响 Understand the impacts of daily work on GMP requirements and product quality 参加GMP相关培训，确保业务活动持续符合GMP要求 Attend GMP trainings and ensure that daily work is compliant to GMP consistently 严格执行本岗位的GMP相关规程 Strictly follow GMP SOPs. 向直线经理或QA沟通工作中遇到的GMP相关问题 Report to line manager or QA about GMP questions encountered in daily work 其它Other tasks 根据工作需要完成文件工作 Paper work or report upon request 提供跨部门支持 Functional support 文件工作 Documentation Requirements: 药学或理工科相关专业本科学历及以上Bachelor degree or above with pharmaceutical or Engineering related background 具备基本的英语读写能力Basic English in reading & writing 能应用微软常用办公软件Basic Microsoft office skill 个人特性Personal character ➢与团队成员真诚交流 Be honesty to communicate with each other in team ➢在高强度工作压力下具有很强的责任感 Be responsibility under high work pressure ➢团队工作精神，乐于分享 High team work spirit and be willing to share Date Posted 23-10月-2025 Closing Date 30-12月-2025 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. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company. We focus on discovering, developing and commercialising prescription medicines for some of the world’s most serious diseases. But we are more than one of the world’s leading pharmaceutical companies. At AstraZeneca, we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science, challenge convention and unleash your entrepreneurial spirit. To embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges. There is no better place to make a difference in medicine, patients, and society. An inclusive culture where you will connect different thinking to generate new and valuable opportunities. Where you will find a commitment to lifelong learning, growth and development for all. Our Inclusion & Diversity (I&D) mission is to create an inclusive and equitable environment where people belong, using the power of our diversity to push the boundaries of science to deliver life-changing medicines to patients. Inclusion and diversity are fundamental to the success of our company, because innovation requires breakthrough ideas that only come from a diverse workforce empowered to challenge conventional thinking. We’re curious about science and the advancement of knowledge. We find creative ways to approach new challenges. We’re driven to make the right choices and be accountable for our actions. As an organisation centred around what makes us human, we put a big focus on people. Across our business, we want colleagues to wake up excited about their day at the office, in the field, or in the lab. Along with our purpose to bring life-changing medicines to people across the globe, we have a promise to you: to help you realise the full breadth of your potential. Here, you’ll do work that has the potential to change your life and improve countless others. And, together with your team, you’ll shape a culture that unites and inspires us every day. This is your life at AstraZeneca.

Responsibilities

The Line Technician will support the construction and commissioning of the Qingdao pMDI project, ensuring high-quality production objectives are met. They will also facilitate continuous improvement and standardization of processes during the project and transition to business-as-usual operations.