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Myrna Thomas brings over 25 years of Quality and Manufacturing experience to Geneos. During her career, she has provided broad US and European experience in Quality Assurance, Analytical Development, Regulatory Compliance, Validation and Corporate Auditing in support of both clinical and commercial products for start-ups and large biopharmaceutical companies. She will rely on her extensive interactions with FDA during inspections and in-depth knowledge of GCP and GMP requirements to ensure the Quality and Manufacturing strategy meets regulatory expectations and supports the growth of Geneos. She will oversee implementation of the Quality Management System and collaborate with their CDMO’s.

Before joining Geneos, Myrna held senior management positions at Praxis Biologics (now Pfizer), Merck, and Isolagen (now Fibrocell Science). Myrna was the VP of QA/RA at Accupac, a CDMO, with oversight of two manufacturing facilities. Recently, she was the Site Head of Quality at Pharmedium, where she was instrumental in transitioning the company to meet cGMPs. In all of her positions Myrna has created and sustained a strong culture of quality and compliance.