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Develop robust manufacturing processes for biosimilar drug products (syringes and vials), including experimental design, execution, and its documentation...

Focus on the medical applications of our ORBIS hospital information system, you will be responsible for customised configuration using our development tools (ORBIS Form Designer, ORBIS Medical Query Generator, ORBIS Experter, Jaspersoft® Studio, ORBIS U-Composer)...

• Conduct Risk Engineering surveys for the power sector (erection, commissioning and operation)
• Implementation of efficient loss prevention measures with the development of effective risk management procedures at client level
• Develop and implement HRC standards, guidelines, and risk engineering tools

• Build and develop long-term strategic relationships with leading industrial customers
• Identify innovation opportunities and translate emerging technologies into customer value
• Shape collaborations between industry partners, universities, and research institutions

• Develop both classical algorithms and modern machine learning techniques
• Implement algorithms efficiently on embedded hardware
• Optimize parameters for complex, hybrid image pipelines
• Develop innovative solutions for hardware-constrained challenges

• Lead and manage international research programs across AI, Data Science, Simulation, Processes, and Quantum Computing.
• Build and run multi-partner research consortia with world-leading universities, tech networks, and public funding agencies.

• Provide end-to-end leadership across projects within the ISP.
• For the various projects, define target application landscapes, integrations, data flows, lifecycle management, and system dependencies.

Strategy and Leadership: Define, communicate, and execute the overall Data Science roadmap and vision for the Generative AI function, ensuring alignment with N26's product and business goals....

• Define the quality requirements for power modules to achieve a reliable and durable design till manufacturing
• Represent the Quality Management for Power Modules within the development team

• Represent the Quality Management for Power Modules within the development team
• Correlate the failure mechanisms on power modules, equipped with SiC and GaN, with reliability measures to be implemented into the product quality

• Contribute to pioneering technical advances to the field of foundation models on structured data, as well as exploring world models for solving business problems.
• Define the data, training, and experimentation environment to enable scalable access to data and compute.

• Design of the vehicle mechanisms through design phases until qualification and acceptance.
• Requirements definition for vehicle mechanisms.
• Driving trade studies, manufacturing optimization and performance for mechanisms.
• Coordination partner team developments in structures and propulsion.

Conduct consulting projects in the space industry along the entire value chain ranging from satellite and launcher manufacturing to ground and service operators...

• Develop and manage the reliability test plan for GaN/SiC products and calculate extrapolated lifetime for given mission profiles
• Enable early identification and characterization of failure mechanisms and link to performance and lifetime limitations through simulation and predictive analytics

• Design and develop internal tools for R&D users
• Build user-friendly interfaces (web and desktop) for searching, entering, reviewing, visualizing, and managing complex technical data

Responsible for the whole vehicle and components design, development, and technical research of electric ride-on and electric pedestrian warehouse forklifts...

Design, plan and perform experiments with a focus on cell line development (plasmid design, cloning, transfection, pool generation, single cell cloning, cell based assays, rAAV production, analytics, gene editing etc. ) and process optimization (quality, automation, implementation of new...

• Translate and deliver key directives from the board and senior management, and serve as the clinical face of the company.
• Lead and manage all clinical development activities across the SJP portfolio
• Design Phase 2 and 3 clinical protocols and oversee CTA/IND submissions to BfArM, FDA, and EMA

• 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

• Development of APIs for electrolysis systems and analysis devices
• Implementation of autonomous process control
• Conceptualization and implementation of degradation models for electrolysis
• Studying performance and degradation of electrolysis in dependence on different operating modes