Henry Tillman, MSHS, CQA, currently serves as a Senior Regulatory Affairs Specialist at HealthFirst, where responsibilities include preparing and submitting critical product registration documents such as FDA listings and managing global regulatory affairs projects. Previous experience includes roles at Azenta Life Sciences as a Senior Regulatory Licensing Analyst managing pharmaceutical distribution licenses, and at TRIMEDX as a Quality & Regulatory Specialist II. Earlier positions also include serving as a Quality/Regulatory Engineer at Cork Medical, LLC, where quality management systems were overseen, and as a Quality Assurance Specialist I and Coordinator II at LifeScience Logistics, contributing to compliance and quality assurance efforts. Henry's career began at Stericycle, where experiences included auditing pharmaceuticals and managing quality oversight. Henry holds a Bachelor's degree from Indiana State University, an Associate's degree from Kaplan University, a Master's degree in Health Services from Trident University International, and is currently pursuing a PhD in Health Services from the same institution.
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