Documentation Manager állás innen: Magyarország

2025. 07. 16. | Teljes munkaidõ | Budapest | DNV• Complete specific projects in relation to medical device procedures, processes, systems and documentation as requested by the Medical Devices Operations Manager. • If

2025. 07. 16. | Teljes munkaidõ | Budapest | UnisysWhat success looks like in this role We are seeking a highly experienced and proactive Principal Security Vulnerability Manager to join our cybersecurity team. This role is responsible for identifying and mitigating potential vulnerabilities across network, system, and application environments

2025. 07. 16. | Teljes munkaidõ | Budapest | Tech PeoplePartners to coordinate test activities. Manage and maintain test environments and staging. Ensure that all releases meet defined quality criteria before delivery. Maintain release documentation. Continuously optimize and improve release processes. Drive quality assurance and quality management topics

2025. 07. 16. | Teljes munkaidõ | Budapest | LimeFlightSystem of our platform. You’ll work closely with Product Managers, Engineers, and Marketers to craft a powerful, intuitive, and visually appealing SaaS product that delights users and supports LimeFlight’s mission of sustainable aviation. Key Responsibilities - Translate product ideas into detailed

2025. 07. 16. | Teljes munkaidõ | Budapest | DNVOf the business. • Complete specific projects in relation to medical device procedures, processes, systems and documentation as requested by the Medical Devices Operations Manager

2025. 07. 16. | Teljes munkaidõ | Budapest | ComputacenterSetting and strategic plans Accountable for overall budget/ P&L ensuring that spend is in line with budgetary limitations Contribute to business strategy (within own division/business area) and prioritise projects and objectives accordingly Engage and work with Functional & Operational Managers to ensure

2025. 07. 16. | Teljes munkaidõ | Budapest | KOSTAL Global Business Services Center4HANA. - Creating process documentation and training materials. Assisting in the training of key users - Advising on future SAP developments and collaborating with international key users Qualifications - A university degree in computer science, business informatics or a university degree in combination

2025. 07. 16. | 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