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Field
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interpretation of OMICs datasets (DNA, RNA, proteome) Supervision and technical guidance of Bachelor’s, Master’s, and PhD students, as well as technical staff within the project context Participation in teaching
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preclinical in vitro and in vivo models Supervise and mentor MSc/MD/PhD students Collaborate with national and international research partners Present your results at scientific meetings Publish your findings
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career scientist with PhD(or equivalent) in Plant Biology, Biochemistry, Molecular Biology, Analytical Chemistry, or related field interested in integrated plant metabolomics and proteomics. Hands
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of scientific publications and project reports Supervision of PhD students and other students Support in the preparation of third-party funding proposals Support in establishing the institute Your Profile: Master
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, collaborate closely with geneticists, breeders and industry partners and publish your results in high-impact journals. You supervise MSc/PhD students and contribute to new grant proposals. Your qualifications
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travel to present at scientific conferences and strengthen inter-lab cooperations Your Profile: University degree (Master) in computer science, physics or a comparable scientific field PhD in one
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finished his/her Master’s degree or PhD degree in computer science. We offer - You work in a highly innovative environment - Technical supervision at one of the leading universities of Germany - Employment
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Max Planck Institute for Heart and Lung Research, Bad Nauheim | Bad Nauheim, Hessen | Germany | about 6 hours ago
to the development and adaptation of new protocols and techniques including quality control, troubleshooting and routine upkeep. Your qualifications The qualified candidate must have a PhD and will become a member of
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• Integrated sensing and communication: fundamental limits and algorithm design (1 PhD, Mari Kobayashi, mari.kobayashi@tum.de) • Optical fiber channel modeling, receiver processing, and coding (1PhD, Gerhard
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-compatible protocols for clinical translation Assist in the preparation of regulatory documents and collaborate with clinical and regulatory teams to support the transition to first-in-human trials Profile PhD