Documentation Manager állás innen: Magyarország

2025. 07. 17. | 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. 16. | Teljes munkaidõ | Szenna | Trivium PackagingActivities. Collect and analyze data on workplace accidents and incidents. Manage and update EHS documentation. Participate in EHS audits and inspections. Organize and conduct training sessions for employees. Communicate with employees about EHS rules and procedures. Procure and maintain records

2025. 07. 16. | Teljes munkaidõ | Zalaegerszeg | Rheinmetall Hungary Zrt.Verification&Validation Manager (m/f/d) Rheinmetall Hungary Zrt. in Zalaegerszeg - Verification&Validation Manager (m/f/d) Ref.-Nr. HU00020 Schedule type Full Time Contract Type Permanent Position WHAT WE ARE LOOKING FOR Independent planning, implementation, and management of verifications

2025. 07. 16. | Teljes munkaidõ | Békéscsaba | Antal InternationalPrepare and present regular management reports. Prepare financial statements in compliance with local accounting standards and International Financial Reporting Standards (IFRS). Verify and ensure accuracy in statutory reporting. Transfer Pricing Prepare and review transfer pricing documentation

2025. 07. 16. | Teljes munkaidõ, Tréning | Budapest | SanofiMain responsibilities Creating reports and presentations, Providing day-to-day support to managers, Preparing documentation based on collected information, Participating in projects, Support Service Line Head in local project execution. Experience Ongoing studies in BSc or MSc at the fields

2025. 07. 16. | Teljes munkaidõ | Budapest | IQVIAWith the tracking and management of Case Report Forms (CRFs), queries and clinical data flow. • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. • May accompany CRAs on site visits to assist with clinical monitoring duties upon

2025. 07. 16. | Teljes munkaidõ | Miskolc | Bosch GroupAppointment booking in partner’s systems ► Claim management, addressing and resolving issues arisen during fulfillment process, documentation and reporting ► Management of related KPIs, data-analysis and reporting ► Participation in process-improvement projects to identify opportunities and reduce expenses

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