Michelle Garner has a diverse work experience in the field of biomedical engineering and regulatory and quality engineering. Michelle started their career as a Lab Assistant at Johns Hopkins University in 2010 and later worked as a Research Assistant at Tulane University. From 2012 to 2015, they served as a Jr. Biomedical Engineer at Pfizer, where they gained experience in lab testing, product development, and human factors studies. Garner then progressed to the role of Associate Biomedical Engineer, where they furthered their expertise in project planning, design control, and business development. Michelle later became a Senior Associate Biomedical Engineer at Pfizer, focusing on product development and human factors of auto-injector products. In 2019, Garner joined Regulatory and Quality Solutions LLC as a Regulatory & Quality Engineer Consultant, contributing their expertise in regulatory and quality engineering. Michelle is currently the Director of Quality at CoapTech, contributing to the quality management of the organization.
Michelle Garner earned a Bachelor of Science in Biomedical Engineering from Tulane University in 2012. In 2018, they completed a Master of Engineering Management in Applied Biomedical Engineering and Management from Johns Hopkins Engineering for Professionals.
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