Daniel Recuset has 20+ years of quality systems design / remediation / improvements, project management, product development, process validation, and strategic/tactical planning experience in the medical device industry. He has been responsible for leading numerous successful projects directed toward quality systems remediation, continuous improvement, lean manufacturing, productivity improvements, and cost reductions. As an educated engineer he held various positions in engineering, development, quality compliance before he became Director Global Compliance of a global Medical Device Company. Daniel Recuset is experienced a in multiple site FDA Warning Letters remediation program, conceptualized and managed a total redesign of a Quality System for multiple global sites and constructed/ mentored Six Sigma Project teams.