Jeffrey Berman Asq
About Jeffrey Berman Asq
Jeffrey Berman is a Quality Engineer with extensive experience in customer support for medical devices, focusing on FDA compliance. He has worked in various roles in quality management and engineering since the mid-1980s and is currently employed at Plexus Corp.
Work at Plexus
Currently, Jeffrey Berman serves as a Quality Engineer at Plexus Corp., a role he has held since 2016. In this position, he focuses on providing customer support specifically for medical devices, ensuring that products comply with FDA requirements. His responsibilities include conducting internal audits to maintain quality standards and acting as a product safety specialist for UL, CSA, and notified body certifications. Additionally, he is involved in the implementation of Unique Device Identification (UDI) and SAP product labels to meet regulatory standards.
Education and Expertise
Jeffrey Berman has pursued extensive education in quality management and related fields. He has been studying at the Quality Management Institute Ltd (QMI) since 1993. He also attended the College of Lake County, focusing on Management since 1991. His technical background includes an Associate's degree in Electronics from Harper College, where he studied from 1985 to 1992. Furthermore, he has been studying at UL University since 2007, enhancing his knowledge in quality engineering.
Background
Jeffrey Berman has a significant history in the quality engineering field, with over three decades of experience. He worked at Domino Amjet, Inc. as a Group Leader from 1985 to 1992, followed by a 28-year tenure at UL as a Field Specialist II, retiring in 2015. His career has been primarily based in Illinois, with his current role at Plexus Corp. located in Neenah, Wisconsin. He completed his secondary education at Wheeling High School.
Achievements
Throughout his career, Jeffrey Berman has specialized in the development of Assembly Build Instructions (ABI's) and process Failure Mode and Effects Analysis (pFMEA) for production processes. His work has contributed to the implementation of regulatory standards in the medical device industry. He has played a key role in ensuring compliance with safety and quality standards, which are critical in the field of medical devices.