Author állás innen: Budapest

2026. 01. 31. | Teljes munkaidõ | Budapest | HiflylabsRequirements into technical specifications. - Automation & Optimization Identify opportunities to automate manual processes and optimize CI/CD pipelines for faster, more reliable releases. - Quality Assurance Review and test code authored by team members, providing detailed analysis and ensuring high-quality

2026. 01. 30. | Teljes munkaidõ | Budapest | Ceva Santé AnimaleTeam is responsible for preparing regulatory dossiers, responding to authority inquiries, and ensuring compliance with regulatory requirements throughout product development and lifecycle management. They collaborate closely with R&D, industrial functions, and project teams to address scientific

2026. 01. 29. | Teljes munkaidõ | Budapest | GSI Electronics IncInformed. Process and review credit applications for new dealers/customers, and track/apply sales managers’ discretionary spend balances to accounts as needed. Returns & Adjustments Process return rebills and adjustments promptly, handle Return Material Authorizations (RMAs), and ensure proper

2026. 01. 29. | Teljes munkaidõ | Budapest | Learning Technologies GroupSpecific development according to prioritization set by R&D management. Experience working with agile development and cross functional teams is required. Areas of responsibility include Advising Engineers without formal authority. Communicating with multiple levels of management. Providing customer facing

2026. 01. 29. | Teljes munkaidõ | Budapest | ParexelSubmission content to ensure alignment with regulatory requirements, specifically related to variations and questions from health authorities. Manage projects within all Regulatory Information Management systems, ensuring the maintenance of worldwide submissions. Identify, escalate, and mitigate risks

2026. 01. 29. | Teljes munkaidõ | Budapest | AGCOCustomers informed. Process and review credit applications for new dealers/customers, and track/apply sales managers’ discretionary spend balances to accounts as needed. - Returns & Adjustments Process return rebills and adjustments promptly, handle Return Material Authorizations (RMAs), and ensure proper

2026. 01. 29. | Teljes munkaidõ | Budapest | IQVIARisk evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to responses to questions from health authorities, reviewing and contributing to periodic aggregate reports, contributing to safety review of study protocols, investigators brochure and other

2026. 01. 28. | Teljes munkaidõ | Budapest | Hilti GroupSupplies, and refreshments, Organizing and facilitating online meetings (. all-staff meetings), Welcoming international visitors and preparing for their arrival, Supporting the management team with administrative and operational tasks, Managing the company’s signing and authorization processes. What You’ll