Defibtech
Erika Benlisa is a Senior Validation Engineer at Defibtech, LLC since June 2019, previously serving as a Validation Engineer at the same company. Prior experience includes a role as a Process Development Engineer at Cirtec Medical from August 2016 to June 2019, and an internship at FloDesign Sonics focused on R&D in acoustic technology. Erika also worked as a Peer Tutor at Western New England University, providing support in Physics I and II, and served as an Undergraduate Researcher at North Carolina A&T State University, investigating microfluidics and magnesium-based alloys for cardiovascular applications. Earlier experience includes a position as a File Clerk at GEICO. Erika holds a Bachelor’s Degree in Biomedical/Medical Engineering from Western New England University (2012-2016).
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Defibtech
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Defibtech, LLC, is a leader and innovator in the design and manufacture of automated external defibrillators (AEDs) and other lifesaving resuscitation products such as the new automated chest compression device Lifeline ARM. By using advanced design and manufacturing techniques, Defibtech provides value-oriented, easy-to-use solutions with high quality and reliability. Defibtech devices include the Lifeline™ and ReviveR™ families of AEDs and related accessories. With more than 450,000 defibrillators shipped worldwide in various language configurations, Defibtech has drawn accolades and won numerous awards for innovative product design, growth, quality, and services. Defibtech’s products are sold exclusively through their network of distribution partners in the United States and in more than 50 countries around the world. With headquarters in Guilford, Conn., Defibtech designs and manufactures its products in the United States according to current Good Manufacturing Practices in state-of-the-art ISO compliant facilities.