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• Manage site activities for assigned clinical sites in Europe (with emphasis on Germany), including site feasibility, initiation, monitoring, and close-out visits.
• Ensure study conduct complies with the approved protocol, Good Clinical Practice (GCP), ISO 14155, and relevant national regulations.

• Preparation, review and coordination of local regulatory submissions in alignment with global submission strategy
• Provision of local regulatory strategy advice to internal clients
• Provision of project specific local SIA services and coordination of these projects

• Own and evolve JavaScript/TypeScript client libraries and SDKs ensuring high-quality APIs, backward compatibility, and an excellent developer experience
• Drive implementation of sophisticated features across our library portfolio

• Design, bring-up, characterize and troubleshoot traction inverters
• Design and industrialize high voltage PCBA and inverter assemblies including DFT, DFM
• Perform worst case analysis, functional safety analysis, thermal analysis, and control analysis

• Medical support and medical advice for clinical trials and safety evaluation
• Medical leadership to study teams
• Creation of clinical trial protocols with latest scientific information
• Contribution to site selection
• Review and approval of study protocols and amendments

• Medical leadership to study teams
• Creation of clinical trial protocols with latest scientific information
• Contribution to site selection
• Review and approval of study protocols and amendments
• Review and approval of Clinical Study Reports (CSRs)
• Review and approval of Informed Consent Forms (ICFs)

In this PhD project, you will investigate neural 3D scene representations, including neural radiance fields, Gaussian splatting, and implicit occupancy models, and adapt them to the unique challenges of in-cabin perception. Unlike exterior environments, where a moving sensor observes a largely...

• Writing system tests
• Executing system tests
• Evaluating system tests
• Writing integration tests
• Executing integration tests
• Updating integration tests
• Taking part in E2E testing
• Cooperating with teams from partner systems
• Managing regression tests
• Reviewing tests
• Writing documentation
• Log analysis

• Maintain and develop the ocean biogeochemical model code of the HAMOCC model
• Coordinate integration of new process representations developed across multiple projects
• Establish and maintain software quality standards, testing procedures, and documentation

• Develop and optimize BEOL processes including metallization, tungsten vias, dielectrics, CMP, passivation
• Define process flows across deposition, etch, clean, and planarization steps
• Perform reliability qualification in collaboration with reliability team

• Automatizált UI és end-to-end tesztek fejlesztése, karbantartása és stabilizálása webalkalmazásokhoz
• Webes tesztautomatizálási keretrendszerek használata és továbbfejlesztése (pl. Playwright, Selenium, Cypress)
• Tesztek integrálása CI/CD folyamatokba

• Perform integrative analyses combining multi-omics data with eye imaging data
• Contribute to ophthalmic data collection and processing
• Contribute to omics data processing, statistical analyses, and the preparation of manuscripts for publication in peer-reviewed journals

• Supervision of medical writers
• Short-term and long-term resource planning for project assignment
• Regular meetings with staff and updates to senior management
• Review and approval of semimonthly time sheets
• Assistance in forecasting project-related costs and timelines
• Hiring and evaluation of employees

• Build and lead the Viral Vector Operations unit
• Drive process development and GMP manufacturing for viral vector platforms (e.g. Lentivurus, MVA)
• Ensure reliable, scalable, and high-quality GMP execution
• Oversee tech transfer, scale-up, and manufacturing readiness

• Design and develop cloud-native application architectures using Microsoft 365 technologies
• Develop and maintain PowerApps applications for enterprise use cases
• Design and implement Power Automate workflows to orchestrate business logic and automate cross-platform processes

Further developing physics-based electrochemical battery models for dynamic charging and discharging applications, including impedance-capable and multi-particle model structures...

• Collaborate with business stakeholders to identify technical opportunities and gather user requirements for Polarion customizations, workflows, reports, dashboards, and integrations.
• Configure, customize, and maintain Polarion ALM solutions to support engineering, quality, and compliance processes.

Product Compliance and Sustainability Expert DECTRIS is a successful and expanding high-tech company that develops and produces X-ray and electron detectors. Our detectors are used worldwide in large-scale research facilities and in industry. Their unique properties enable scientific breakthroughs...

• Design, implement, and analyse high- and low-resolution ocean simulations based on the ICON modeling framework
• Explore parameter and structural uncertainties in the model affecting biogeochemical processes
• Develop workflows for systematic model evaluation and benchmarking

• Take technical ownership for the Systems Engineering of a novel inspection and analysis tool for semiconductor wafers
• Lead system design, requirements definition, and architecture across mechanics, optics, electronics, software, controls, sensors, and infrastructure