Matthew Snodgrass

About Matthew Snodgrass

With over 20 years of experience in the medical device and diagnostics industry, I have developed an expert understanding of ISO 13485, FDA 21 CFR Parts 820, 803, 806, 21, MDR 2017/745, IEC standards, and other relevant regulations, standards and best practices. I have also demonstrated outstanding leadership, collaboration, and problem-solving skills in managing capital projects, implementing corrective and preventive actions (CAPA), reducing costs, and ensuring customer satisfaction. My mission is to leverage my quality assurance and regulatory expertise to deliver safe, effective, and innovative medical devices that meet the highest standards of quality and performance.

Experience

1. VP, Quality Assurance and Regulatory Compliance

   Miach Orthopaedics, Inc

   Dec 2025 — Present · Westborough, MA, US

Education

• Boston University

  Some course work completed toward MS, Manufacturing Engineering

  2003 — 2006

• Community College of Rhode Island

  AS, Electronics Engineering

  1989 — 1991

• Northeastern University

  MS, Regulatory Affairs

  2010 — 2011

• Rhode Island College

  BS, Operations Management

  1991 — 1993

Skills

• Quality Control
• Gmp
• Quality System
• Process Simulation
• Change Control
• Change Management
• Iso
• Fda
• Spc
• Cqa
• Quality Management
• Lean Manufacturing
• Root Cause Analysis
• Project Management
• Iso 13485
• Computer System Validation
• R&D
• Continuous Improvement
• 21 Cfr
• Ce Marking
• Minitab
• Testing
• Six Sigma
• Quality Auditing
• Quality Assurance
• Medical Devices
• Capa
• Iso 9000
• 21 Cfr Part 11
• Fmea
• Dmaic
• Cross-Functional Team Leadership
• Supplier Quality
• Iso 14971
• Design of Experiments
• Manufacturing
• Validation