Aaron Snyder
Lead Faculty | Trainer for FDA and industry personnel, 21 CRF 820 and ISO 13485:2016 SME at AAMI | Greater Boston
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Aaron Snyder serves as the Lead Faculty and Trainer at the Association for the Advancement of Medical Instrumentation (AAMI), where he plays a pivotal role in shaping the future of quality management systems (QMS) within the medical device industry. With a deep expertise in FDA regulations, particularly 21 CFR 820 and ISO 13485:2016, Aaron is recognized as a Subject Matter Expert (SME) who bridges the gap between regulatory compliance and industry best practices. His commitment to advancing knowledge is evident in his extensive experience training over 100 FDA personnel and more than 400 industry professionals, equipping them with the essential skills to navigate the complexities of quality assurance.
In his current role, Aaron leads key projects focused on enhancing understanding of Quality System Requirements and Design Controls, ensuring that both regulatory bodies and industry stakeholders are aligned in their approaches to compliance and efficiency. His innovative training methods not only cover the fundamentals of Good Manufacturing Practices (GMP) but also delve into advanced topics such as Corrective and Preventive Action (CAPA) and Design of Experiments, fostering a culture of continuous improvement and proactive problem-solving.
Aaron’s passion for learning and teaching is complemented by his proficiency in Six Sigma methodologies, which he integrates into his training programs to help organizations streamline their processes and achieve operational excellence. As a thought leader in war room management and regulatory affairs, Aaron Snyder is dedicated to empowering QA teams to implement robust QA processes that withstand regulatory scrutiny while driving innovation in the medical device sector. His contributions to AAMI and the broader industry underscore his commitment to fostering collaboration between regulators and manufacturers, ultimately enhancing patient safety and product quality.
Lead Faculty | Trainer for FDA and industry personnel, 21 CRF 820 and ISO 13485:2016 SME at AAMI in April 2015 to Present
Quality Assurance Lead Consultant at Quality Systems Explained in January 2025 to Present
Vice President Quality Assurance at Allotex in January 2023 to January 2025
Head Of Quality Assurance at Fresenius Kabi in April 2021 to May 2023
Director Global Quality Assurance | QA Executive, Strategic Planning, Change Agent at Mölnlycke in November 2018 to March 2021
Senior Quality Assurance Manager | Sr QA Leader, Strategic Planning, Change Agent, Problem Solver at Waters in June 2013 to October 2018
Quality Assurance Manager | QA Leader, Continuous Improvement, FDA Audit Management, Problem Solver at Covidien in September 2011 to June 2013
Project Manager Regulatory Compliance | QA Leader, QMS Expert, FDA Audit Management, Problem Solver at Covidien in February 2011 to August 2011
Corporate Regulatory Compliance Specialist | QMS Auditor, Team Leader, Executive Communication at Covidien in May 2009 to January 2011
Senior Quality Engineer | QMS Auditor, Team Builder, Problem Solver at Covidien in December 2006 to April 2009
Senior Quality Engineer at Cardinal Health in June 2004 to December 2006
Techical Coop at General Electric in August 2001 to August 2003
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Quality System
ISO 13485
FDA
Medical Devices
Quality Assurance
Six Sigma
Quality Auditing
CAPA
Lean Manufacturing
GMP
Validation
Design Control
Quality Management
Quality Control
Continuous Improvement
Root Cause Analysis
Value Stream Mapping
DMAIC
FMEA
Process Simulation
Project Management
Product Development
Design of Experiments
SPC
Supplier Quality
Change Control
Corrective and Preventive Action (CAPA)
Regulatory Affairs
Kaizen
Leadership
Public Speaking
Cross-functional Team Leadership
Personal Development
Teaching
21 CFR
FDA GMP
Complaint Management
Complaint Investigations
Process Validation
Part 820
Integrity
Passion for Learning
Listening
War Room Management
FDA Audit Management
Diligent
Trustworthy
Coaching & Mentoring
Biotechnology Industry
U.S. Food and Drug Administration (FDA)
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Discover more about AAMIWhat is Aaron Snyder email address?
Email Aaron Snyder at [email protected]. This email is the most updated Aaron Snyder email found in 2026.
What is Aaron Snyder phone number?
Aaron Snyder phone number is +19372581824.
How to contact Aaron Snyder?
To contact Aaron Snyder send an email to [email protected]. If you want to call Aaron Snyder try calling on +19372581824. (updated on November 04, 2024)
What company does Aaron Snyder work for?
Aaron Snyder works for AAMI
What is Aaron Snyder's role at AAMI?
Aaron Snyder is Lead Faculty | Trainer for FDA and industry personnel, 21 CRF 820 and ISO 13485:2016 SME
What industry does Aaron Snyder work in?
Aaron Snyder works in the Medical Equipment Manufacturing industry.
Aaron Snyder Email Addresses
Aaron Snyder Phone Numbers
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