Scott Rettig
With over 25 years of experience across regulated industries, Scott Rettig brings deep expertise in global compliance, quality management, and scientific operations to Cadoret Global. His work spans the Biotech, Pharmaceutical, and Life Sciences sectors, encompassing GMP Manufacturing, GLP Pre-Clinical Development, and GxP Scientific Compliance.
Scott specializes in aligning complex quality systems with evolving international regulations including GCP, GLP, GMP, ISO, QS, and USDA standards. He has led cross-functional teams on major quality system remediations, implemented document, learning, and validation management systems, and driven efficiency through innovative digital solutions.
Throughout his career, Scott has held senior leadership and consulting roles, including serving as interim Head of QA for CMC-related quality and co-developing a certified CLIA lab compliance program for COVID-19 testing in Illinois. He also led the expansion and streamlining of a global GxP Scientific Compliance group, reducing operational burdens while improving compliance visibility through a validated global GLP communication and issue management system.
Scott is known for fostering collaboration across scientific, operational, and regulatory teams to deliver practical, sustainable compliance outcomes.
Specialties:
Global GxP Compliance, GMP/GLP Operations, and Regulatory Leadership
Quality System Remediation, Document & Validation Management
Process Optimization and Digital Quality Tool Implementation
