Mary D Villalona is an experienced quality assurance professional with a strong background in compliance and quality systems within the pharmaceutical and medical device industries. Currently serving as the Director of Quality at Pocket Naloxone Corp. and a Quality Assurance Auditor at The FDA Group, LLC, Mary has conducted extensive audits and refined quality processes to meet FDA, EU, and ISO standards. Previous roles include Quality Assurance Consultant at Oxford Global Resources, Executive Director Quality/Compliance at EEC & Associates, and Director of Quality at Granules Pharmaceuticals, where Mary managed vendor qualification programs and developed training initiatives. Mary holds an MBA in Pharmaceutical Management from Fairleigh Dickinson University and a Bachelor of Science in Biology from Seton Hall University.
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