Professional Overview
Matthew Gombos is a seasoned Quality & Regulatory Specialist currently based in New York, New York, United States. In his current role, he leverages his expertise in quality management, regulatory compliance, and documentation to drive business growth and ensure industry standards are met. His key expertise areas include quality assurance, regulatory affairs, and documentation management, with a focus on the medical device and pet food industries.
Experience Summary
Current Role
As a Quality & Regulatory Specialist at MediView XR, Inc., Matthew is responsible for managing quality systems, ensuring regulatory compliance, and coordinating documentation efforts. Notable achievements include the implementation of quality control processes and the development of regulatory strategies. His work has significant industry impact, contributing to the advancement of medical device technology and pet food safety.
Career Progression
Matthew's career trajectory showcases notable previous roles, including Associate Supplier Quality Engineer at Medtronic and Documentation Specialist at Canidae Pet Food. These positions demonstrate his growth in quality management, regulatory compliance, and documentation. Key achievements include the development of supplier quality programs and the implementation of documentation management systems.
Areas of Expertise
Matthew's expertise spans industry-specific skills, such as quality management and regulatory compliance, technical competencies, including documentation management and quality control, and leadership and management capabilities, with a focus on team collaboration and process improvement.
Professional Impact
Notable projects and initiatives include the implementation of quality control processes and the development of regulatory strategies. These contributions have had a significant impact on the medical device and pet food industries, ensuring safety and compliance.
Conclusion
Matthew Gombos' professional trajectory demonstrates a commitment to quality management, regulatory compliance, and documentation. His current focus on the medical device industry and recent experience in quality assurance and regulatory affairs position him as a valuable asset to organizations seeking expertise in these areas. His value proposition lies in his ability to drive business growth, ensure industry standards, and contribute to the advancement of medical device technology and pet food safety.
