Jesús Parrilla
About Jesús Parrilla
Jesús Parrilla is a Senior Quality Engineer at Biosense Webster, where he coordinates the creation of Manufacturing Process Information documents and serves as the EU MDR Site Lead. He has extensive experience in engineering roles across various companies and holds a Bachelor's degree in Mechatronics Engineering.
Work at BioSense
Currently, Jesús Parrilla serves as a Senior Quality Engineer at Biosense Webster, a position he has held since 2019. In this role, he coordinates the creation of Manufacturing Process Information documents across various manufacturing sites in the US and Mexico. He also leads the integration of new procedures into the Biosense Webster Quality Management System and coordinates training deployment to manufacturing engineers. Prior to this, he worked as an NPI Engineer at Biosense Webster from 2013 to 2019, where he contributed to product development initiatives.
Education and Expertise
Jesús Parrilla holds a Bachelor Degree in Mechatronics Engineering from Universidad Autónoma de Ciudad Juarez, which he completed from 2009 to 2016. He also obtained a Computer Systems Technician qualification from Centro de Bachillerato Tecnologico Industrial y de Servicios No.128, where he studied from 2006 to 2009. His educational background provides a strong foundation for his expertise in quality engineering and manufacturing processes.
Background
Before joining Biosense Webster, Jesús Parrilla gained experience in various engineering roles. He worked as a Product Engineer at Federal-Mogul Motorparts for nine months in 2019 and as a Process & APQP Technician at Eagle Ottawa from 2011 to 2013. His diverse background in engineering roles has contributed to his current responsibilities in quality management and regulatory compliance.
Regulatory Affairs and Compliance
In his current role, Jesús Parrilla serves as the EU MDR Site Lead, where he translates the requirements of MDR 2017/745 into local requirements from an end-to-end perspective. He provides global support to Johnson and Johnson sites and the regulatory affairs team, assisting with product submissions and approvals. His involvement in regulatory compliance is critical for ensuring that products meet necessary standards.