Lauren Troy
About Lauren Troy
Lauren Troy is a Medical Device Toxicologist II at Boston Scientific in Galway, Ireland, with a background in biomedical engineering and regulatory affairs. She holds multiple degrees, including a Master's in Regulatory Affairs and Toxicology from University College Dublin.
Title
Lauren Troy is currently employed as a Medical Device Toxicologist II at Boston Scientific, a position she has held since February 2021.
Current Company
Lauren Troy works at Boston Scientific in Galway, County Galway, Ireland. Her role as a Medical Device Toxicologist II involves focusing on biocompatibility and regulatory affairs.
Previous Experience
Lauren Troy has significant experience in the medical device industry. She served as a Regulatory Affairs Specialist at PBC BioMed in Shannon, Munster, Ireland from 2018 to 2021. In 2014, she worked as an Intern Regulatory Affairs Associate at Medtronic Vascular for five months in County Galway, Ireland. Prior to that, she was a Manual Support Operative and part of the Preventative Maintenance (PM) Team at Johnson & Johnson Vision Care-Vistakon in County Limerick, Ireland from 2013 to 2015.
Education
Lauren Troy has an extensive educational background that includes a Master of Science in Medical Device Regulatory Affairs from Institute of Technology, Carlow (completed in 2018) and a Master’s degree in Toxicology and Regulatory Affairs from University College Dublin (completed in 2020). She also holds a certificate in Lean Sigma Quality (Six Sigma Yellow Belt) from Institute of Technology, Sligo (completed in 2019). Additionally, she earned a Bachelor of Engineering in Biomedical Engineering from University of Galway in 2015.
Background in Biomedical Engineering and Regulatory Affairs
Lauren Troy combines her technical and regulatory expertise in the medical device industry through her background in biomedical engineering and regulatory affairs. This unique combination allows her to navigate complex regulatory environments while applying engineering principles to ensure medical device safety and efficacy.