Shane Spellman
About Shane Spellman
Shane Spellman is a Manufacturing Engineer at Boston Scientific in County Galway, Ireland, with a background in biomedical science and sports and exercise sciences.
Current Position at Boston Scientific
Shane Spellman holds the position of Manufacturing Engineer at Boston Scientific in County Galway, Ireland. He has been with the company since 2018. His role includes responsibilities in component qualifications and active involvement in Corrective and Preventive Actions (CAPA) projects. These initiatives focus on eliminating product risks within the SES production unit, thereby enhancing product quality and reliability.
Previous Role at DePuy Synthes Companies
Before his current role, Shane Spellman was a Manufacturing Project Engineer at DePuy Synthes Companies in County Cork, Ireland. His tenure lasted 11 months, from 2017 to 2018. During this period, he gained significant project engineering experience and contributed to various manufacturing processes.
Educational Background
Shane Spellman earned a Master of Science (MSc) in Biomedical Science from the National University of Ireland, Galway, where he studied Biomedical Sciences, General from 2015 to 2016. Prior to that, he completed a Bachelor of Science (BSc) in Sport and Exercise Sciences at the University of Limerick, studying from 2012 to 2015. His educational background has equipped him with a broad range of skills critical to his engineering roles.
Industry Experience at Boston Scientific
Shane Spellman has had multiple roles at Boston Scientific, starting as an R&D Intern (MSc Thesis) in 2016, working for 5 months in County Galway, Ireland. He later took on the role of Supplier Engineer in 2017 for a period of 7 months, also in County Galway. These positions provided him with extensive experience in research and development as well as supplier management.
Significant Projects and Compliance Work
Shane Spellman led the implementation of a sterilisation site transfer project that resulted in a significant cost saving of $800,000. Furthermore, he has actively participated in the review and preparation of EU Medical Device Regulation (MDR) documents to ensure compliance with European regulations. These projects underscore his expertise in both project management and regulatory compliance.