Juliana Arias has extensive experience in regulatory affairs within the medical device industry, currently serving as Global Regulatory Affairs II at Nipro Diagnostics since December 2015. Prior to this role, Juliana held the position of Regulatory Affairs Specialist at Nipro Diagnostics from April 2012. Juliana's earlier experience includes working as a Regulatory Affairs Specialist at Biomet 3i from September 2010 to April 2012, and as a Regulatory Affairs Associate and Quality Control professional at Biomet 3i from April 2003 to 2010.
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