Documentation Manager állás innen: Magyarország

2025. 07. 13. | Teljes munkaidõ | Tatabánya | AptivCommunication, visits customers and represents the organization's quality manager ensures and supervises the feedback given on the customer complaints in terms of quality and timely fulfillment ensures that the appropriate analytical tools are used to reliably solve and eliminate the problem (8D, 5Why, Ishikawa

2025. 07. 13. | Teljes munkaidõ | Budapest | foodoraDevelopment, documentation, or a related support role. - Strong ability to manage multiple tasks, maintain content repositories, and ensure version control

2025. 07. 13. | Teljes munkaidõ | Budapest | Delivery HeroJob Description The Content Specialist will support the development, maintenance, and organization of content materials (Learning/Training content, Knowledge base content & Macro content) that empower agents to succeed in our Service Operations function. Reporting to the Content Manager, this role

2025. 07. 13. | Teljes munkaidõ | Budapest | Global BlueWhat you will do. A glimpse in your role As an Associate Product Manager, you will play a critical role in ensuring the accuracy and efficiency of Global Blue’s data reconciliation platform and fraud prevention system. You will work closely with the Product Manager, development teams, and business

2025. 07. 13. | Teljes munkaidõ | Budapest | emarsysProper testing, debugging, and maintenance of new and existing code Create technical documentation for reference and reporting Find the best technical solution to complex business problems Actively participate in the full product lifecycle, from idea through design and development until maintenance

2025. 07. 13. | Teljes munkaidõ | Dunaföldvár | Saur EuropeOf materials - Preparation and ongoing management of construction documentation Requirements - Proven experience in site management or construction coordination, ideally in industrial or infrastructure projects - Ability to manage multidisciplinary teams and construction logistics - Familiarity with technical

2025. 07. 12. | Teljes munkaidõ | Budapest | IQVIAFor clinical trials with medical devices (e.g. ICH-GCP, ISO 141552020, MDR, FDA 21 CFR) under supervision of the Regulatory & Start-up Manager. Main responsibilities Search and verifies NCA/EC/IRB submission requirements. Drafts NCA/EC/RIB submission documents (e.g. application form, ICF, …). Prepares NCA/EC

2025. 07. 12. | Teljes munkaidõ | Budapest | AccentureTechnical support and troubleshooting for BMC Helix/Remedy applications, ensuring timely resolution of issues and minimal disruption to business operations. Documentation Create and maintain detailed technical documentation, including design specifications, testing plans, and user guides. Collaboration