Job Description SummaryWe are seeking a Lead QA Specialist – New Product Implementation to provide Quality Assurance leadership for the introduction of new products across a global external manufacturing network. In this role, you will lead
Major responsibilities • Develop and drive robust upstream process workflows to support efficient plasmid DNA and viral vectors manufacturing. This involves designing and executing experiments, analyzing data, and providing science-based recommendations for process improvement. • Apply
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
Job Title: Senior Production Supervisor City, Country: Qingyuan, Guangdong, China We are looking for an experienced production leader to support daily manufacturing operations at our Qingyuan site. In this role, you will help ensure safe, efficient,
SummaryAt Apple, new insights have a way of becoming revolutionary products, services, and customer experiences very quickly. Bring passion and dedication to your job and theres no telling what you could accomplish. The Emerging Technologies team
SummaryAt Apple, new insights have a way of becoming revolutionary products, services, and customer experiences very quickly. Bring passion and dedication to your job and theres no telling what you could accomplish. The Emerging Technologies team
Job Description External Manufacturing Large Molecule Drug Substance Technical Lead Our Large Molecule Technical Operations Unit is seeking a highly motivated individual to fill an open Associate Director Technical Operations, to support drug substance manufacture within
Job Description 主要职责Principal accountabilities/Main tasks: 1. 确保从进料到出货阶段的所有产品能够符合客户标准和要求； Ensure that all products from the feeding to the shipping stage meet customer standards and requirements. 2. 监控过程检验稳定性及异常反馈改善跟踪； Monitoring process inspection stability and abnormal feedback improvement tracking. 3. 指出不合格和HOLD住下一制程的产品并追踪每一个区域的状况（包括HSF有害物质不合格）；
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Job Description: Responsible for the stability, security, and efficiency of the enterprise endpoint computing environment in the China region. Focuses on automated script deployment, patch management, and compliance enforcement leveraging SCCM/MECM platforms. Acts as the Tier
目的 为了安全、及时、保质保量的完成各种生产任务，在符合公司质量标准，国家药品、食品质量标准、安全及劳动法规条件下，参加各类注册产品的生产。 职责范围 一.生产运行 根据相关标准操作规程（SOP）及批生产记录的要求完成无菌生产工作。根据数据完整性要求填写岗位日志及批记录。为了满足市场对产品产量和质量的需求，充分利用各种资源，协调并参与无菌生产使之有序进行。 二.参与批记录的审核，思爱普系统（SAP）中物料的领料、退料；SOP的修改及起草; 组织协调工序内的生产活动；培训新员工以及定期对岗位员工进行岗位工作考核。 三.产品质量控制 确保生产过程中各环节符合药品生产质量管理规范（GMP）要求及公司总部辉瑞质量标准（PQS）要求，所有操作按标准操作规程执行，使产品质量得到有效保证。 四.设备维护与管理 参与并带领工序人员进行日常的设备使用、清洁、维护，使设备处于有效运行与管理之中。 五.安全与卫生 具有安全和卫生相关知识，保证生产的安全进行，保证生产现场清洁卫生，符合国家及公司要求，遵守相应的管理措施。 六.新产品、新设备与新工艺 参与并协助管理团队进行新产品试制和新设备的调试。 七.团队精神 为了完成团队共同目标，团结其它员工，达成共同目标。 八.人员培训及发展、员工纪律 协助管理人员制定培训规程及计划，并通过合适的程序保证员工得到有效的培训。 九.改进生产工艺，提高效率 提高生产效率、发挥生产能力、稳定产品质量，对工艺、设备、流程等进行不断的改进与完善，满足不断的发展需求。 十.遵守公司有关环境、健康、安全（EHS）相关政策和规定，并完成EHS相关工作进行验证及新验证项目的实施 十一.按照工厂工作制度要求，能根据排班适应早，中，夜班等特殊工时工作制的作息时间。 任职要求 1.教育程度/经验: 中专具有5-7年以上制药生产技术经验，制药/化工相关专业； 大专具有3-5年以上制药生产技术经验，制药/化工相关专业； 本科，制药/化工相关专业； 2.特别知识 制药专业知识， GMP专门知识，验证知识，其它国家药品法规，劳动法、环保法等。 3.技能： 良好的沟通能力和团队精神及分析判断能力； 良好的英语综合能力，熟练使用计算机并会操作OFFICE办公软件； 具有不断学习/接受新知识的能力； 具有同时进行并完成多种任务的能力。
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Abcam, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all
Some careers have more impact than others. If you’re looking for a career where you can make a real impression, join HSBC and discover how valued you’ll be. We are currently seeking an experienced professional to
Some careers have more impact than others. If you’re looking for a career where you can make a real impression, join HSBC and discover how valued you’ll be. We are currently seeking an experienced professional to
Job Information职位信息 Job title职位名称: QA Specialist QA专员 Location工作地点： Beijing, China 中国北京 % Remote working and % of travel expected 远程办公和出差的概率：N/A Job type工作类型: Full time全职 Site/Unit 区域/事业部：Beijing Site/ M&S China北京工厂/中国制造与供应事业部 About the job工作职责 Our Team我们的团队： The M&S
南通，中国; 珠海，中国 | 全职 | Job ID: 11669 About the role: 百欧恩泰（珠海） MAH质量保证（QA）负责人是一个领导岗位，负责监管本公司及其CDMO（合同开发与生产组织）的所有质量保证活动。该负责人将确保生物制品的生产、检测、放行及分销环节均符合监管要求、行业标准以及BioNTech内部的各项政策、标准和标准操作规程（SOP）。此外，该负责人将建立和提升百欧恩泰（珠海） MAH质量管理体系（QMS）包括监管CDMO相关活动，对CDMO实施质量监督，推动持续改进举措，与跨职能团队协作，并确保产品质量与患者安全达到高标准。该岗位负责产品放行给临床试验和商业化市场 The QA Head for BioNTech-Zhuhai MAH is a leadership role responsible for the quality assurance of the drug products manufactured by BioNTech
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
Major responsibilities Develop robust CAR-T manufacturing process with in-depth experience in multiple unit operations (e.g., viral/non‑viral gene delivery, large scale expansion, formulation). Optimize critical process parameters and workflow to improve process performance and facilitate operation efficiency,
Job Description Key Responsibilities New Process Development for Film Materials Develop, design, and implement new processes specifically for thin‑film materials (e.g., polymer films, coated substrates, flexible composites). Priority will be on implementing annealing processes including optimizing