Mary Boyd
About Mary Boyd
Mary Boyd is a Quality Assurance Technician with extensive experience in the medical device and laboratory sectors, currently working at Surmodics in Ballinasloe since 2018. She has held various roles in quality assurance and laboratory operations, contributing to audit preparations and complaint investigations throughout her career.
Current Role at SurModics
Mary Boyd has been serving as a Quality Assurance Technician at SurModics since 2018. In this role, she is responsible for ensuring compliance with quality standards and regulations. She actively participates in audit preparation for both internal and external audits related to the complaints investigation site. Additionally, she chairs and records minutes for the monthly site-level Complaint Review Board (CRB) meetings, where she provides insights and feedback on customer complaint-related issues.
Previous Experience in Quality Assurance
Prior to her current position, Mary Boyd worked at several organizations in quality assurance roles. She was a Quality Technician at Boston Scientific from 2016 to 2018 and held the position of Quality Assurance Technician II Complaints at Merit Medical Systems, Inc. for 11 months in 2016. Her experience includes conducting root cause analysis using eCAPA and FMEA systems, as well as preparing and presenting monthly complaint information and trends at complaints review board meetings.
Background in Medical Laboratory and Manufacturing
Mary Boyd began her career in the medical field as a Medical Laboratory Technician at Galway Clinic, where she worked for 11 months in 2015. She also has experience as a Manufacturing Operator at Lake Region Manufacturing, Inc. for 5 months in 2014. Additionally, she worked as a Balloon Operator at Creganna Medical for 3 months in 2018. These roles provided her with a solid foundation in both laboratory and manufacturing environments.
Education and Certifications
Mary Boyd has pursued education in quality management and medical device operations. She studied Quality Management at GMIT, achieving a Certificate from 2009 to 2010. Furthermore, she completed a Level 6 Certificate in Pharmaceutical and Medical Device Operations at Innopharma Labs in 2014. Her educational background supports her expertise in quality assurance and compliance within the medical device industry.