Managing the site Quality Management System (QMS) documentation structure to ensure compliance with industry standards and regulations. Managing organizational documentation through the document life cycle, including review, approval, and distribution. Ensuring the security, accessibility, and proper distribution of organizational documents. Distributing/notifying of document releases, changes and obsolescence. Conducting internal audits and preparing reports by collecting, analyzing, and summarizing information. Supporting regulatory and third-party audits, investigations, and inquiries regarding the control and assessment of product design and manufacturing quality. Assisting, as needed, with certified operator audits to monitor adherence to policies and procedures. Montioring the performance of the QMS by gathering relevant data and producing reports to identify areas for improvement in quality processes. Assisting with the generation and updating of processes, procedures, standard works, and audit checklists. Associates degree with a technical discipline OR High School Diploma/GED equivalent and 5 years experience in manufacturing, quality, industrial or mechanical role within a manufacturing environment. 3 year of auditing experience or AS9100 Lead Auditor Certified and 1 year of auditing experience. Within 50 miles of Orchard Park, NY This position requires use of information or access to hardware which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee AS9100, Federal Aviation Administration (FAA) European Union Aviation Safety Agency (EASA) Communication Teamwork Problem Solving Data Analysis
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