Margriet Tate is an experienced pharmaceutical professional with over 20 years in developing, implementing, validating, and leading production and quality systems across various regulatory markets. Currently serving as the Quality Systems & Regulatory Compliance Manager at Abbott since 2025, Margriet's expertise includes small- and large-volume parenterals and oral solid dosage forms for diverse product types. Margriet has held numerous roles in the pharmaceutical industry, including Operations Manager at Curium Pharma and Quality Assurance Manager at Catalent Pharma Solutions, showcasing a strong background in quality and regulatory compliance. They earned a B.S. in Management and an A.S. in Business from Indiana Wesleyan University.
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