Julian-Marvin Lütten

Responsible for global complaint analysis, trend analysis, safety analysis, and process compliance. Involved in establishment of proactive post-market surveillance processes within the scope of the EU 2017/745 (MDR).

Master thesis in clinical affairs assessing the feasibility of a real-world-data-based post-market clinical follow-up study for surgical devices

Intern for Clinical Affairs: - Clinical evaluations of surgical devices - Systematic literature analyses - Real-world data research project

Working in day-to-day operations, producing diagnostic devices, supporting process & quality management, planning & conducting own projects, developing new tools for QM

Worked as part of the R&D unit and conducted a pilot study to evaluate different methods to determine metabolic thresholds - Excel work - MATLAB - Several statistic tools - Linear regression - Inter-rater reliability - Quantitative research methods

Applied skills and knowledge from the study and gathered experiences in the fields of production, 1st and 2nd level support, maintenance, process & quality management - Manual work - Remote support - Field work & maintenance - KANBAN - Excel work

Basics in using cutting techniques, connection technology, software development, CAD construction and PCB design - CNC milling - Manual works - Block diagrams - Electric layouts - C++/LabVIEW - DraftBoard Unlimited