Joseph Lasko

Principal Regulatory Affairs Specialist at Mozarc Medical

Joseph Lasko is a seasoned regulatory affairs professional with extensive experience in the medical device sector. Currently serving as Principal Regulatory Affairs Specialist at Mozarc Medical since April 2023, Joseph previously held roles at Medtronic from September 2014 to April 2023, including Senior Regulatory Affairs Specialist and Quality Engineer. Key contributions include compliance projects related to EU Medical Device Regulation (MDR) and facilitating international regulatory registrations. Joseph’s earlier career involved diverse roles in quality engineering and materials coordination, demonstrating a strong foundation in regulatory compliance, technical documentation review, and inventory management. Joseph holds a B.A. in Political Science with minors in Economics and American Studies from Allegheny College.

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Mozarc Medical

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Mozarc Medical leverages both companies’ leadership and expertise to develop transformative kidney health technologies. The company focuses on the development of innovative technologies that reshape kidney health with patient-centered solutions.