Girish Hanchinamani, a seasoned Quality Assurance Manager at Nypro, a Jabil Company with over 20 years of experience in the manufacturing of medical devices and electronics assemblies, has directed cross-functional teams in implementing FDA 21 CFR Part 820 and ISO 13845 regulations. Girish's educational background includes a Bachelor's in Polymer Science from the University of Mysore and a Master's in Plastics Engineering from the University of Massachusetts at Lowell. His professional background is extensive, having served as a Consultant and Principal Engineer at Cameron Health, Senior Manufacturing Engineer at Hologic, Inc., and Manufacturing Engineer at VICOR corp, to name a few. In his current role, Girish manages the quality operations of a 100+ million-dollar medical device plant, leading Quality System (QSM) teams including CAPA, Customer Complaints, Internal Audits, Supplier Audits, Document Control, Training & Quality Improvement Plan (QIP). Girish interacts with regulatory bodies and customers, managing customer escalations and relationships, and has experience in global sourcing and contract manufacturing.