与我们携手施展你的超能力！ 探索未知、打破壁垒、勇于发现，你准备好了吗？你有宏图大志正待实现，我们同样雄心勃勃。我们遍布全球的员工热爱科技创新，以医药健康、生命科学和电子科技领域的解决方案，切实改善人类生活。我们怀揣远大梦想，热忱关爱员工、客户、患者和人类居住的这颗星球。因此我们一直在寻找永葆好奇心的你，与我们一路同行、敢想敢做，把不可能变为可能！ 职位描述： 职位目标： PIS 操作员的主要职责是参与 PIS 工厂的建设、调试、IOQ，向 PIS 主管报告执行性能鉴定并加速以正确的质量、数量和正确的时间交付成品。从调试到提升阶段，PIS 运营商应满足所有合规性、EHS、内部和外部质量要求。生产稳定后，进一步确保所有日常运营符合质量、EHS、合规要求。 主要职责： 与工程团队一起参与PIS装置的建设、调试、安装资质、运行资质。在现场专家、技术转让团队和供应链生产计划的支持下，向 PIS 主管报告执行 PIS 工厂的性能确认和工艺验证。 确保遵守所有集团和中国当局的 EHS 要求和法规。了解、遵循和促进公司的安全实践。坚持每一次事故都是可以预防的理念，不断增强安全意识并提高工厂在 EHS 方面的有效性。 通过培训和自学，学习公司的生产流程、操作规程，确保遵循既定的生产程序和说明。 确保符合质量和安全标准。确保工作区域干净、安全且维护良好。 如果生产政策和程序需要更新，及时向主管反馈。在 PIS 主管的指导下完成所有必要的文书工作和报告。 在主管的密切指导下执行任务。 这项工作可能包括，卸料/装料，操作阀门，泵，装袋机，内务等。 ISO9001 发布后遵循其要求。 支持PIS生产主管在PIS生产范围内进行现场应急演练 指导和提高 PIS 新操作员的技能水平。 积极参与工厂的质量文化建设和质量相关活动 主动汇报质量相关事件，积极参与工厂的质量持续改进的活动 任职要求： 职业/高中及以上学历 3年以上工作经验，GMP或化工厂工作者优先 良好的安全知识和意识。 了解基本的自动过程控制理论。 愿意轮班工作，对轮班工作保持精力充沛 能够使用Windows、Words和Excel。 清晰有效的口头沟通技巧。 目标明确、结果导向、协作。
• Supports country SSU strategy in close collaboration with the SSO Study Start-Up Team Lead and the SSO Study Start-Up Managers to ensure SSU timelines and deliverables are met according to country commitments • Accountable for
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Company Description Renesas is one of the top global semiconductor companies in the world. We strive to develop a safer, healthier, greener, and smarter world, and our goal is to make every endpoint intelligent by offering
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in accordance with
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in accordance with
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in accordance with
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in accordance with
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in accordance with
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in accordance with
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in accordance with
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in accordance with
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in accordance with
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in accordance with
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in accordance with
Assisting PI to administer the clinical trials in accordance with the SOP, ensuring the clinical trials are conducted in accordance with GCP guidelines and quality. About the role Assisting PI to administer the clinical trials in accordance with
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
液化空气集团早在1916年就进入中国，70年代开始向中国提供空分设备，经过多年的稳步发展，目前在中国设有近120家工厂，遍布40多个城市，拥有约5000名员工。集团在华主要经营范围包括工业及医用气体的运营，家庭健康服务，工程与制造业务，以及全球市场与技术和上海创新园从事的创新业务。公司业务已覆盖中国主要的沿海工业区域，并继续向中部、南部和西部地区拓展。 液化空气通过创造卓越绩效和履行责任追求盈利性增长和长期可持续发展，并保持在中国的行业领先地位。依托于集团的长期战略与全球资源，公司聚焦能源、环境、高科技和健康等领域，以迎接挑战并创造新的市场机遇。凭借专业团队的全力支持，公司致力于为客户提供可信赖的服务与高附加值解决方案，同时履行企业社会责任。The Data Compliance Manager provides vital operational and strategic support to ensure the company’s data compliance framework adheres to the Cybersecurity Law (CSL), Data Security Law (DSL), Personal Information Protection Law (PIPL), and other data