Kinkade Analytical

Background combines strong academic preparation with a record of creativity, initiative, and performance excellence in highly visible, increasingly responsible roles in the healthcare industry. Record includes significant experience and achievement in both corporate and entrepreneurial organizational environments. A majority of his career has been spent working under cGMP and cGLP compliance standards, such as 21CFR Part 58, and 21CFR Parts 210 & 211, applied to pharmaceutical R&D, pharmaceutical manufacturing, and medical gas systems.