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group’s research advances polymer network design to achieve high mechanical performance for the evolving demands of modern technologies. For more details, please view https://www.ntu.edu.sg/mse/research
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OR Master's degree with 2+ years experience in Health Sciences, Nursing, Healthcare Management, Design, Business, Service Design, Biomedical Engineering, Clinical Research or related disciplines with relevant
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years in the Norwegian educational system Documented experience with designing and conducting user experience studies and quantitative performance evaluation Documented experience in the system
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, robotics or other field relevant for the position Foreign completed degree (M.Sc.-level) corresponding to a minimum of four years in the Norwegian educational system Documented experience with designing and
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devices; evaluate and integrate new analytical instrumentation. Testing & Characterization: Design and execute experiments to evaluate mechanical, thermal, and chemical properties; analyze data to inform
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execute experiments to evaluate mechanical, thermal, and chemical properties; analyze data to inform design decisions. Failure Analysis: Root-cause investigation of material failures; recommend and validate
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, system sciences, systems engineering, design engineering, sociology, science communication or other relevant discipline, and/or relevant work experience. Evidence of, or demonstrated interest in
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Center for Drug Evaluation and Research (CDER) | Southern Md Facility, Maryland | United States | 4 days ago
manufacturing technologies to evolving regulatory expectations. You will gain experience in hands-on microbiological research, performing quantitative colony counting, ATP-bioluminescence data analysis with
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American Foundation for Suicide Prevention: Postdoctoral Research Fellowship Innovation Grants Eligibility: Doctoral degree (PhD, MD, etc.) awarded within the past six years; no more than three
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Center for Drug Evaluation and Research (CDER) | Southern Md Facility, Maryland | United States | about 19 hours ago
framework for selecting (primary) endpoint strategies and determining the corresponding statistical analysis plan for non-malignant hematologic diseases in confirmatory trials, starting with the use