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Daniel M. currently serves as Associate Director of Device and Combination Product Compliance at Catalent Pharma Solutions since July 2024. Prior experience includes roles such as Director of Quality Assurance at Proliant Health and Biologicals, Quality Engineering Manager at OriGen Biomedical, and Quality Manager at Quest Diagnostics. Daniel has also worked in QA/QC in Bio-Production at Raybiotech and as a Process Engineer in Validation at the Atlanta VA Medical Center. Academic credentials include positions at the Massachusetts Institute of Technology as a Community Manager and at Emory University School of Medicine and Georgia Institute of Technology as Lead Research Specialist, focusing on various biomedical research areas.