Kevin Linde is an Illinois Professional Engineer with over 27 years of extensive experience in the pharmaceutical and FDA regulated industries. He is the CEO of cGMP Consulting, a company specializing in serving FDA-regulated industries such as pharmaceuticals, medical devices, cosmetics, biotechnology, and dietary supplements, that offers a comprehensive range of services.
Kevin has led a team of experienced engineering and quality assurance consultants that have assisted numerous industry-leading companies in identifying and remediating gaps while implementing cGMP requirements. He also offers tailored support to cosmetics companies, including facility registration, product listing, regulatory compliance, and customized GMP systems aligned with MoCRA requirements. Kevin has worked on a wide variety of Quality, Engineering and Validation projects for several clients in the US and abroad.
He has provided consulting services including audits, system design, user requirements specifications development, commissioning, qualification, and process validation.
Kevin graduated with a Bachelor of Science in Chemical Engineering from the University of Missouri – Columbia in 1996. He attained his Illinois Professional Engineer license in 2006 and has played a pivotal role in assisting numerous individuals in obtaining their licenses.