Joe Paparella
Quality Assurance and Regulatory Affairs Leader with experience in the Medical Device and Aerospace industries in the capacity of manager, project leader, and individual contributor.
- Role
- Director of Quality Assurance and Regulatory Affairs at Marizyme Inc
- Location
- West Palm Beach, FL, US
- LinkedIn followers
- 500 followers
About Joe Paparella
Quality Assurance Leader with over 20 years of experience in the Medical Device and Aerospace industries in the capacity of manager, project leader, individual contributor, developer and implementor of strategies, processes, and procedures in compliance with regulatory requirements, mission, and vision of organizations. Wealth of knowledge and expertise in quality system management and regulatory compliance to cGMP, FDA regulations 21 CFR 820, ISO 13485, ISO 14971, MDD, EU MDR, AS9100, DO-178C.
Experience
Director of Quality Assurance and Regulatory Affairs
Oct 2023 — Present · West Palm Beach, FL, US
Education
Miami-Dade Community College
Associate in Arts
1992
DeVry University
Bachelor of Science, Biomedical Engineering Technology
2009
Florida International University
Master of Science, Engineering Management
2011 — 2011
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