341 evolution "https:" "https:" "https:" "https:" "https:" "University of Michigan Ann Arbor" positions at CNRS in France
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Environment (UMR5300; https://crbe.cnrs.fr/en/ ) is internationally recognized for its research on the interaction between the environment and biodiversity using genetics. Numerous projects are being developed
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visit the website: https://www.is2m.uha.fr/ . The thesis will be attached to the doctoral school of physics and physical chemistry (ED182), which is co-accredited between Unistra and UHA. The doctoral
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. This primarily experimental work will also focus on analyzing the radiation at the fiber output through the development of a modal decomposition system. The main activity will be to set up an experimental system
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values foster the professional development of its staff—key contributors to collective success—as well as the growth of the laboratory itself. Where to apply Website https://emploi.cnrs.fr/Offres/CDD
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three laboratories: the Centre for Materials Development and Structural Studies (CEMES) and the Coordination Chemistry Laboratory (LCC) in Toulouse, and the Quantum Materials and Phenomena Laboratory (MPQ
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close synergy with partners. Activities: Design and synthesis of photocatalytic materials Development of semiconductor nanoparticles (sensitized or not with grafted dyes) and molecular systems
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the regulations, that the arrival of the agent be authorized by the competent authority of MESR. Where to apply Website https://emploi.cnrs.fr/Offres/CDD/UMR5026-FREBON0-276/Default.aspx Requirements Research
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the oxidation state and the electric-polarization direction in HfO2. Project included in the activities of the MEM group of CEMES, funded by the labex NanoX. Where to apply Website https
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. Where to apply Website https://emploi.cnrs.fr/Offres/CDD/UMR6457-SOPDEP-065/Default.aspx Requirements Research FieldChemistryEducation LevelPhD or equivalent Research FieldChemistryEducation LevelPhD
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the development of new bio-based production pathways. One innovative approach involves coupling furans, derived from lignocellulose, with light olefins via the Diels-Alder (DA) reaction to obtain aromatic monomers