Who We Are FTI Consulting is the leading global expert firm for organizations facing crisis and transformation. We work with many of the world’s top multinational corporations, law firms, banks and private equity firms on their
MÉDICOS SIN FRONTERAS busca para su oficina en Buenos Aires, Argentina COORDINADOR ZONAL (PART TIME) – CAMPAÑA DIÁLOGO DIRECTO para el Departamento de RECAUDACIÓN DE FONDOS CONTEXTO GENERAL Médicos Sin Fronteras (MSF) es una organización médico-humanitaria de carácter
We currently have an outstanding opportunity to join our Corporate Business Development (CBD) team as an Associate Director or Director, Search & Assessment, to support the development of Lundbeck’s pipeline through identifying and accessing new innovative
We currently have an outstanding opportunity to join our Corporate Business Development (CBD) team as an Associate Director or Director, Search & Assessment, to support the development of Lundbeck’s pipeline through identifying and accessing new innovative
Job descriptions may display in multiple languages based on your language selection. What we offer: At Magna, you can expect an engaging and dynamic environment where you can help to develop industry-leading automotive technologies. We invest
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。
Job Overview 综述 The selected candidate will lead the execution of various strategic initiatives, including raw material qualifications (RM Qualifications) and the transfer of production activities within Celanese’s global manufacturing network (PTR). In this role, the
CEVA Logistics provides global supply chain solutions to connect people, products, and providers all around the world. Present in 170+ countries and with more than 110,000 employees spread over 1,500 sites, we are proud to be
At ABB, we help industries outrun - leaner and cleaner. Here, progress is an expectation - for you, your team, and the world. As a global market leader, we’ll give you what you need to make
HSBC Qianhai HSBC Qianhai Securities Limited (HSBC Qianhai), a joint venture securities company, was incorporated on 28 August 2017, pursuant to Supplementary Agreement X to the Closer Economic Partnership Arrangements (CEPA) between the mainland and Hong
About Us Centric Brands is a leading lifestyle brand collective that designs, sources, markets, and sells high-quality products in the kids, men’s and women’s apparel, accessories, beauty, and entertainment categories. The Company’s portfolio includes licenses for
Company Description H&M Group is a global company of strong fashion brands and ventures. Our goal is to prove that there is no compromise between exceptional design, affordable prices, and sustainable solutions. We want to liberate
About impact.com impact.com is the world’s leading commerce partnership marketing platform, transforming the way businesses grow by enabling them to discover, manage, and scale partnerships across the entire customer journey. From affiliates and influencers to content
Locations: Beijing, China Categories: Site Activation & Maintenance Req ID: 12990 Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager in Beijing or Shanghai to join our Clinical
Locations: Shanghai, China Categories: Site Activation & Maintenance Req ID: 12991 Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager in Beijing or Shanghai to join our Clinical
Company Description H&M Group is a global company of strong fashion brands and ventures. Our goal is to prove that there is no compromise between exceptional design, affordable prices, and sustainable solutions. We want to liberate
About Flexport: At Flexport, we believe global trade can move the human race forward. That’s why it’s our mission to make global commerce so easy there will be more of it. We’re shaping the future of
We are looking for the right people — people who want to innovate, achieve, grow and lead. We attract and retain the best talent by investing in our employees and empowering them to develop themselves and
Whether you’re at the start of your career or looking to discover your next adventure, your story begins here. At Citi, you’ll have the opportunity to expand your skills and make a difference at one of
Its more than a job As a member of the Freight Forwarding team Kuehne+Nagel, you will play a key role in transporting goods, optimising processes, and fulfilling our customers promises. And by transporting medicines, toys and