David Doyel is a seasoned Sr Validation Engineer specializing in Pharmaceuticals and Medical Device Manufacturing, with 17 years of experience in FDA-regulated industries. They hold a Bachelor's of Science in Biotechnology from California State Polytechnic University-Pomona. David has successfully completed numerous projects focused on Equipment and Process Validation, including writing and executing validation protocols and generating quality documentation. Currently, David works as a Senior Staff Validation Engineer at Flex and previously provided consulting services through Doyel Quality Consulting, LLC.
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