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Michael Nketiah, MBA, RAC

Senior Vice President Regulatory, Clinical & Quality Affairs at Nexalin Technology

Michael Nketiah, MBA, RAC has extensive experience in regulatory affairs, clinical affairs, quality assurance, and operations. Michael is currently serving as the Senior Vice President of Regulatory, Clinical & Quality Affairs at Nexalin Technology since November 2022. Prior to this, they held the position of Vice President of Regulatory Affairs at InterVenn Biosciences from November 2021 to October 2022. From April 2019 to December 2021, they served as the VP of Quality and Regulatory Affairs at Tivic Health System, Inc. Before that, they worked as a Consultant, VP of Clinical Affairs, Quality, and Regulatory Affairs at ClearPath Surgical, Inc. from January 2017 to June 2021 and as a Consultant VP of Quality, Regulatory Affairs, and Operations at SIRIS MEDICAL from November 2015 to June 2021. Other roles include VP Quality Assurance & Regulatory Affairs at Previvo Genetics, Inc. in 2018, Sr. Director of Quality and Regulatory Affairs at PROCEPT BioRobotics from August 2014 to March 2018, and Quality and Regulatory Affairs Consultant at Altura Medical Inc in 2014. Michael also served as the Director of Quality Systems at Biomimedica Inc from January 2013 to February 2014 and at Crux Biomedical from November 2009 to January 2013. During their time at Crux Biomedical, they also held the position of Quality Assurance Manager from November 2009 to July 2012.

Michael Nketiah, MBA, RAC, obtained their Master of Business Administration (M.B.A.) degree from Saint Mary's College of California in 2015. Prior to that, they completed their Bachelor of Science (BS) degree in Mechanical Engineering at San Jose State University from 2002 to 2008. In 1994, they earned another Bachelor of Science (BS) degree, this time in Chemistry, from Midwestern State University, which they completed in 1998.

In addition to their academic achievements, Michael Nketiah has also obtained certifications in regulatory affairs. Michael received the RAC-DEVICES certification from the Regulatory Affairs Certification Program in September 2020, and the RAC-US certification in June 2016, also from the same institution.

Links

Previous companies

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Timeline

  • Senior Vice President Regulatory, Clinical & Quality Affairs

    November, 2022 - present

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