Jorge Esqueda López
About Jorge Esqueda López
Jorge Esqueda López is a Configuration Engineer at Plexus Corp. in Zapopan, Jalisco, Mexico, with a background in mechatronics and engineering management.
Work at Plexus
Jorge Esqueda López currently works at Plexus Corp. as a Configuration Engineer since 2021. In this role, he is responsible for managing Approved Manufacturer Lists to maintain quality standards and leads the implementation of Engineering Change Orders (ECOs) to ensure correct production processes. Prior to his current position, he served as a Configuration Engineer Intern at Plexus Corp. from 2020 to 2021, where he gained valuable experience in the field.
Education and Expertise
Jorge Esqueda López studied at Tecnológico de Monterrey, where he pursued a degree in Ingeniería electrónica, robótica y mecatrónica. He completed his studies in 2022, achieving a degree in Engineering over a five-year period from 2017 to 2022. His educational background provides him with a solid foundation in engineering principles and practices.
Background
Before joining Plexus Corp., Jorge Esqueda López held various positions that contributed to his professional development. He worked at BOHN: REFRIGERACION as a Process Engineer for six months in 2020, where he focused on process optimization. Additionally, he served as the President of the Mechatronics Student Society at Tecnológico de Monterrey from 2020 to 2021, leading initiatives within the student community.
Previous Experience
Jorge Esqueda López has diverse engineering experience. He worked as a Design Engineer at Fluxing in 2019 for four months, where he contributed to design projects. His role at BOHN: REFRIGERACION as a Process Engineer involved process engineering tasks, enhancing his skills in production processes. These experiences have equipped him with a broad skill set applicable to his current role.
Responsibilities in Medical Device Engineering
In his current role at Plexus Corp., Jorge Esqueda López builds Device Master Records (DMR) for finished medical devices, ensuring comprehensive documentation. His responsibilities include maintaining high-quality standards and ensuring that production processes align with regulatory requirements, which is critical in the medical device industry.