Mr. Pederson specializes in pharmaceutical and medical device manufacturing compliance, quality assurance, quality control systems, vendor assessments, and troubleshooting manufacturing packaging issues. He has performed hundreds of deviation investigations, and routinely assists in audits of QC labs, data integrity, sterility systems, and metrology to FDA 483 observations.

Mr. Pederson brings a holistic view of manufacturing processes and problem solving with his 22 years of experience working in the industry which also includes over 40 manufacturing sites, both domestically and internationally. At ESI, he manages and collaborates with multidisciplinary teams of scientists and engineers to solve problems with manufacturing equipment, production, and packaging.

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