Virginie Grondin

Virginie has been involved in quality and regulatory affairs management for medical devices for over 6 years in vital signs patient cables, endoscopy tubing kits and now in disposable water filters. She specializes in medical device regulatory compliance such as CE marking management for Europe, 510K management for USA and also has ISO 13485 “Medical devices — Quality management systems” certification. She gained experience in plastic compounds by been quality engineer for 9 years in plastic injection molding and graduated from New Jersey Institute of Technology with a bachelor of science in Mechanical engineering technology. She is concerned and motivated by patient safety and environmental protection.