Luke Oltmans has been working in the Quality & Regulatory field since 2010. Luke began their career as a Manufacturing Engineer at Merck, where they reduced manufacturing defects by >75% and obtained a Merck Green Belt certification. In 2008, they worked as a Campus Missionary for Every Nation Ministries. In 2006, they were an Undergraduate Researcher at Clemson University CAEFF REU, where they researched rheological properties of biopolymers. In 2007, they participated in the NCSU Biomedical Engineering Department's Senior Design Course and developed a novel medical device with a pending patent. In 2016, they joined Cohera Medical, Inc. as an Engineering Project Manager and Manufacturing Engineer, where they managed complex manufacturing processes and oversaw the supply chain. In 2018, they joined Kymanox as a Sr. Quality Engineer and Team Lead and a Sr. Technical Project Manager. Most recently, in 2020, they were appointed Director of Quality & Regulatory at 410 Medical.
Luke Oltmans attended The North Carolina School of Science and Mathematics from 2002 to 2004. Luke then received a B.S. in Biomedical Engineering from North Carolina State University between 2004 and 2008. Additionally, they have obtained a LSS Green Belt certification from Merck Production Systems (MPS).
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