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Corinne Miller, CQA, has extensive experience in quality management and regulatory compliance within the medical device industry. Currently serving as the Director of Production Quality at Omnicell, Corinne is responsible for ensuring compliance with 21 CFR 820 and ISO 13485:2016 standards. Previous roles at Omnicell include Sr. Manager of Production Quality and Lead Quality and Regulatory Engineer, where responsibilities encompassed managing quality system processes, conducting audits, and mentoring team members. Corinne's background also includes significant experience at Cohera Medical, where oversight of laboratory operations and quality systems was performed in adherence to regulatory guidelines. Additionally, Corinne has held various roles in fitness instruction and served on the board for Zachary's Mission. Corinne holds a Bachelor of Science degree in Biochemistry from the University of Dayton.