Pablo Ojeda is a Senior Regulatory Affairs Specialist at RegDesk since February 2023, with extensive experience in regulatory affairs and quality management within the medical devices industry. Previous positions include Product Engineering Manager, Quality Management Specialist, and Product Manager at CORMEDIC S.A. | SVELTIA from August 2017 to January 2023, and Operations Manager at LATECBA from July 2011 to July 2017, focusing on production planning and ISO 13485:2003 compliance. Earlier roles include Technical Director & RA Manager at Trust Technology, overseeing regulatory affairs for medical devices, and Project Leader at Medes Argentina SRL, specializing in quality management systems. Pablo Ojeda holds a degree in Bioengineering from Universidad Nacional de Entre Ríos and a specialization in Quality Engineering from Universidad Tecnológica Nacional.
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