Lorna L.

Lorna L. has a diverse work experience in the medical device industry. Lorna started their career at Boston Scientific in 1999 as a Manufacturing Operator. Lorna then moved on to Medtronic where they held various roles, including Laboratory Assistant and Production Operator, where they were responsible for manufacturing and inspecting stent components and ensuring compliance with quality standards. Lorna then joined Creganna Tactx Medical as a Product Builder before transitioning to Vivasure Medical. At Vivasure Medical, they held multiple roles, including Associate Engineer, Senior Quality Engineer, and currently serves as the Principal RA/QA Specialist.

Lorna L. completed their Bachelor's of Science degree in Biomedical Science (Hons) with a specialization in Pharmacology from the University of Galway between the years 2006 and 2010. Lorna then pursued a Certificate in Science, specializing in Quality and Regulatory Affairs, from Galway-Mayo Institute of Technology from 2013 to 2014. Most recently, Lorna L. is working towards obtaining a Master's degree in Medical Technology & Regulatory Affairs from the Institute of Technology, Sligo, from the years 2020 to 2022.

In addition to their formal education, Lorna L. has also acquired certifications to enhance their skills and knowledge. In 2015, they obtained the Six Sigma Green Belt Certification from ASQ. Furthermore, in 2019, they acquired the QMS Auditor/Lead Auditor (ISO 13485:2016) certification from the Kelmac Group (CQI/IRCA).