Director of Quality, MedRes US
Stephanie has 17 years in the medical device industry, with recognized strength for enabling and managing change, empowering teams and managing metrics.
Stephanie Fossat-Dominguez is currently the Director of Quality at MedRes International in Carlsbad, CA where she is responsible for the overall effectiveness and integrity of MedRes US Quality system. She has worked for 17 years in various quality positions in the medical device industry in both large and small company environments. Stephanie was VP of Quality and VP of Operations for CeloNova BioSciences, a Class II and III medical device manufacturer, where her team obtained PMA, ANVISA and EU MDR approvals. She led her organization into the Voluntary Improvement Program as part of the FDA Case for Quality, and is involved in various Case for Quality working groups with MDIC, MITRE and industry stakeholders. She thrives on finding a balance between regulations and activities that will benefit both patients and customers. Before joining the medical device field, Stephanie gained broad experience in the semiconductor industry where she worked for 11 years for International Rectifier (now Infineon, Vishay). There she made impactful contributions in manufacturing line transfers, as well as production, process and supplier optimizations, in Italy, the US and Mexico.
Stephanie holds a MS in Engineering in Material Science from Institute National des Science Appliqués (INSA) of Toulouse, France and is ASQ CQE certified since 2007.
