Richard Reeves

Biography

Richard Reeves brings 40 years of experience in the Biotech, Medical Device, Biologics and Pharma industries in Regulatory Affairs and Quality Assurance. He earned a BSc in Physical Chemistry and MBA from the University of California Berkeley and has held roles in R&D, Marketing, Finance, Program Management, Regulatory Affairs and Quality Assurance. He has more than 20 years of experience at the VP level for Quality and Regulatory for Fortune 500 medical device companies and Joint Ventures. He has also built numerous medical device and biologics GMP quality systems from the ground up and lead corporate teams in more than 100 audits by FDA, Notified Bodies and Competent Authorities at sites all over the world.

Mr. Reeves has extensive experience training in regulatory submissions and quality systems including Design Control, Medical Device Software development, Production and Process control, Verification and Validation, Sterilization and Risk Management. He retired from industry in 2014 and has been providing consulting services to device, biologics and pharma companies all over the world. In addition, Mr. Reeves is a long-time member of RAPS and is chair emeritus of the San Francisco Bay Area chapter.