Carlo Capati, Cls
About Carlo Capati, Cls
Carlo Capati is the Head of Lab at Qvin in Menlo Park, California, where he has worked since 2021. He has extensive experience in clinical and research applications, particularly in GMP and GLP environments, and has held various roles in the healthcare diagnostics field since 2001.
Work at Qvin
Carlo Capati has been serving as the Head of Lab at Qvin since 2021. In this role, he oversees laboratory operations and ensures compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). His responsibilities include performing studies for clinical and research applications, demonstrating his expertise in managing complex laboratory environments. His leadership contributes to the overall efficiency and effectiveness of the lab's operations in Menlo Park, California.
Previous Experience in Healthcare Diagnostics
Prior to his current position, Carlo Capati worked at Siemens Healthcare Diagnostics, Inc. as a Biochemist from 2004 to 2009. He also held the role of Clinical Laboratory Scientist/Assay Development Specialist at LGC Labs for one year, from 2020 to 2021. Additionally, he served as a Senior Clinical Laboratory Scientist at InSource Diagnostics for six years, from 2014 to 2020. His diverse experience in various laboratory roles has equipped him with a comprehensive understanding of clinical diagnostics.
Education and Expertise
Carlo Capati earned a Bachelor of Science in Medical Technology from the University of Santo Tomas, completing his studies from 1994 to 1998. His educational background has provided him with a strong foundation in healthcare sciences. He possesses expertise in method optimization and validation of analytical test methods, contributing significantly to laboratory practices and the development of Standard Operating Procedures.
Background in Quality Control and Clinical Science
Carlo Capati began his career as a Quality Control Associate at Diagnostic Product Corporation, where he worked from 2001 to 2004. He has a proven track record of resolving complex clinical and instrument problems in laboratory settings. His extensive background in clinical laboratory science and quality control has enhanced his skills in managing and analyzing routine and clinical data for the release of immunoassay products.