Vikramtez Maganti
About Vikramtez Maganti
Vikramtez Maganti is a Project Lead Mechanical Engineer at Biosense Webster in Irvine, California, with a Master's degree in Mechanical Engineering from Bradley University. He has over six years of experience in the medical sciences industry, specializing in sustainable development and mechanical design verification testing.
Work at BioSense Webster
Vikramtez Maganti has been employed at BioSense Webster as a Project Lead Mechanical Engineer since 2017. In this role, he is responsible for overseeing mechanical engineering projects and ensuring their successful execution. His work is based in Irvine, California, where he contributes to the development of medical devices and technologies. With over six years of experience in the medical sciences industry, he focuses on process validation quality engineering and equipment qualification.
Education and Expertise
Vikramtez Maganti holds a Master's degree in Mechanical Engineering from Bradley University, where he studied from 2014 to 2016. Prior to this, he earned a Bachelor of Technology (B.Tech.) in Mechatronics from Vignan University, completing his studies from 2009 to 2013. His expertise includes Design for Manufacturing and Assembly (DFMA), statistical data analysis, and mechanical design verification testing. He is also skilled in computer-aided design and analysis (CAD & CAE).
Background
Before joining BioSense Webster, Vikramtez Maganti worked as an Energy Auditor at Ameren from 2015 to 2017 in Peoria, Illinois. This role involved assessing energy usage and identifying opportunities for efficiency improvements. His background in mechanical engineering and experience in energy auditing contribute to his comprehensive understanding of engineering principles and practices.
Achievements in Mechanical Engineering
Vikramtez Maganti specializes in sustainable development and cost savings within the mechanical engineering field. He has a broad-based GxP experience that supports both proprietary and generic pharmaceutical industries. His work in the medical sciences industry emphasizes process validation quality engineering, which is critical for ensuring compliance and reliability in medical device manufacturing.