John Levy
About John Levy
John Levy serves as the Quality Manager at RayBiotech, Inc. in Norcross, GA, where he ensures compliance with regulatory standards and oversees internal audits related to Good Laboratory Practice and Good Manufacturing Practice.
Work at RayBiotech
John Levy has served as the Quality Manager at RayBiotech, Inc. since 2016. In this role, he conducts internal audits that focus on compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) standards. His responsibilities include overseeing adherence to ISO 17025 and ISO 13485 standards, ensuring that the company meets regulatory requirements. He also plays a key role in training new staff on quality system requirements and regularly collaborates with Senior Management to address any nonconforming processes or products.
Previous Experience at Le Jacobs Capital Inc
Before joining RayBiotech, John Levy was the Owner of Le Jacobs Capital Inc for a period of 11 months in 2015. This role provided him with experience in managing business operations, which contributed to his expertise in quality management and compliance.
Education and Expertise
John Levy studied at American Intercontinental University, where he earned a Bachelor of Science in Business Administration with a focus on Operation Management. His studies spanned from 2009 to 2011, equipping him with foundational knowledge in business operations that supports his current role in quality management.
Compliance Oversight and Training
In his capacity as Quality Manager, John Levy is responsible for ensuring compliance with both ISO and regulatory requirements, including ISO 17025 and ISO 13485. He guides external auditors through the compliance process and addresses regulatory inquiries related to ISO and Code of Federal Regulations (CFR) requirements. Additionally, he oversees the training of new staff in quality system requirements, ensuring that all team members are well-versed in compliance protocols.