The position is affiliated with the Zempel Lab (Dr. Dr. Hans Zempel) at the Institute of Human Genetics at the University Hospital Cologne. The Zempel Lab investigates the molecular and cellular mechanisms underlying neurodegenerative and neurodevelopmental disorders, with a special focus on tauopathies, mitochondrial dysfunction, and rare genetic diseases. Using a combination of iPSC-derived neuronal models, CRISPR/Cas9 gene editing, live-cell imaging, and transcriptomic/proteomic profiling, we aim to unravel disease pathways and identify novel therapeutic targets. We value diversity and welcome applications from all qualified candidates, regardless of gender, background, or disability status.