Ann Marie Mc Donagh
About Ann Marie Mc Donagh
Ann Marie Mc Donagh is a Design Assurance Engineer II at Boston Scientific with extensive experience in quality assurance and continuous improvement within the medical device industry.
Company
Ann Marie Mc Donagh is currently employed at Boston Scientific, a prominent medical device manufacturing company. She holds the position of Design Assurance Engineer II. Prior to her current role, she has held various key positions within the company, highlighting her extensive experience in the medical device industry.
Title
Ann Marie Mc Donagh is a Design Assurance Engineer II. Her role involves ensuring that designs meet quality and regulatory standards, an essential function in the development and production of medical devices at Boston Scientific.
Education and Expertise
Ann Marie Mc Donagh has a solid educational background with a focus on quality and regulatory affairs. She completed a Level 8 qualification in Regulatory Affairs from the Institute of Technology, Sligo in 2019. She also holds a Level 8 qualification in Lean & Quality Systems from the National University of Ireland, Galway, completed in 2018. Additionally, she earned a Bachelor of Science (L7) from IT Sligo, specializing in areas crucial for quality assurance and regulatory compliance in the medical device sector.
Professional Background
Ann Marie Mc Donagh has built a robust career at Boston Scientific. She began as a Product Builder (2004-2012) and advanced through roles such as Quality Technician I, II, III (2012-2017), Supplier Quality Engineer (2017-2019), and Supplier Quality Engineer II (2019-2020). Her roles have spanned over fifteen years, demonstrating her deep-rooted experience and commitment to improving the quality of medical devices.
Skills and Certifications
Ann Marie Mc Donagh possesses expertise in DMAIC methodology, a strategy used for process improvement. Her skills include proficiency in Failure Mode and Effects Analysis (FMEA), which helps identify potential failures in processes. She has significant experience in continuous improvement practices and has worked extensively with ISO Standards, ensuring compliance and safety in the medical device industry.