John A. Dziuba

John A. Dziuba has extensive experience in quality systems management and regulatory compliance within the life sciences and pharmaceutical sectors. Currently serving as the Sr Quality Systems Manager for ISO 13485 Medical Devices at Fortis Life Sciences, John oversees regulatory 510K submissions. Previously, John held the role of Corporate cGMP Quality Assurance Manager at Amcor, focusing on FDA compliance and ISO 13485 implementation. Prior to that, John worked at Amway as a Senior Quality Engineer, spearheading supplier quality development and leading numerous audits. With experience at Eli Lilly and Pfizer, John has a strong background in quality assurance, compliance management, and technical regulatory affairs. John holds a Bachelor of Arts in Chemistry from Southern Illinois University Edwardsville and is certified as a Lead Auditor in ISO 9001 and HACCP.