Dr. David Husman, ASQ CPGP, RAC, is president and principal consultant of David Husman Consulting.
With a Ph.D. in biochemistry, David has more than 30 years of diverse international experience in quality assurance, quality control, and regulatory affairs within the pharmaceutical, biopharmaceutical, and biotech industries. He is fully versed in all quality systems and is able to effectively interact and communicate with c-suite executives, scientists, managers, directors, and team members.
David’s expertise includes compliance, quality systems, process mapping, design and implementation, auditing, validation, aseptic processing, data integrity, and information systems. He has worked with products that include both human and animal parenterals, medical devices, human tissues, blood products, biotech products, solid dosages, and vaccines.
Prior to beginning his own company, David was a principal consultant with PAREXEL Consulting for 18 years, providing both strategic and tactical guidance to companies. He also has worked in quality assurance, regulatory affairs, and in research and development.
David earned a bachelor’s degree and doctorate in biochemistry from The Ohio State University in Columbus, Ohio. He is a certified Pharmaceutical GMP Professional and has earned the Regulatory Affairs Certification.