Gary Saenz is an experienced professional in quality assurance and document control with a diverse background spanning over three decades. Currently, Gary serves as Quality Disposition Spec III at Matica Biotechnology, Inc. since September 2022. Previously, Gary held various roles at iBio, Inc. including QA Specialist III and Document Control Specialist III, where responsibilities included global administration of the eDMS system. Other positions include Document Control Analyst/Program Liaison at Los Alamos National Laboratory, GXP Documentation Specialist III at MedImmune, and Quality Analyst at Cobham, with a consistent focus on document management under various regulatory standards such as ISO9002 and ISO9000. Gary's earlier career featured roles as a Manufacturing Documentation Specialist at Ericsson and as a Graphic Artist at McKinley Ross Labs, alongside diverse experiences in media and building services management. Educational credentials include a BA in Communications/Video Production/Art from Liberty University and technical degrees in Electronics and Motorcycle Mechanics from specialized schools.
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