A quality professional with proven results and an outstanding contribution to both quality and compliance throughout 22 years of dedicated service in the automotive and medical device industries.Thrive in complex environments. Able to drive multiple projects and achieve planned results in the shortest time possible. Experienced in ISO 13485 and ISO 9001, in addition to FDA CFR 820 requirements which provides a complete quality package along with the common quality tools such as SPC, Gage R&R, Capability studies, Process validation, Fault tree analysis and Fish Bone techniques relying on team approach and cross functional collaboration involving customers, design and manufacturing engineering, purchasing, suppliers and service