bioMérieux
Elizabeth Rohe is a skilled professional with extensive experience in quality assurance and regulatory compliance within the biotechnology and pharmaceutical industries. Currently serving as the Corporate Quality Lead Auditor and Compliance Expert at bioMérieux, Elizabeth leads audits across the company's global network and manages critical programs such as the Post Regulatory Inspection Assessment Program and the Medical Device Single Audit Program. Previous roles at bioMérieux include Director of Quality and Regulatory Compliance, where responsibilities encompassed quality management systems and facilitating compliance with FDA requirements. Elizabeth's background includes significant positions at Hospira and Talecris Plasma Resources, focusing on quality assurance, remediation strategies, and compliance management. Elizabeth holds an MBA from UNC Kenan-Flagler Business School and a BS in Chemical Engineering from Florida State University.
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