<p>Essential Responsibilities</p> <ul> <li>Maintain and improve the site Quality Management System in alignment with ISO 9001:2015. </li><li>Support coordination of internal audit activities (including third-party auditors) and participate in external/customer audits; assist in tracking and facilitating closure of audit findings. </li><li>Partner with the Quality Manager to lead the execution of corrective and preventive actions, including facilitating root cause analysis and verifying effectiveness of implemented actions. </li><li>Lead assigned quality improvement projects and facilitate root cause investigations across departments. </li><li>Support risk management activities, including formal risk assessments, mitigation planning, and monitoring of risks & opportunities. </li><li>Develop, review, and control quality procedures, work instructions, forms, and records. </li><li>Develop and monitor quality KPIs and provide data-driven analysis to leadership. </li><li>Support and coordinate nonconformance reporting, disposition, containment, and trend analysis. </li><li>Support supplier quality activities, including qualification, performance monitoring, and corrective action follow-up. </li><li>Support preparation of Management Review inputs, including KPI analysis, audit results, risk status, and corrective action performance. </li><li>Ensure compliance with customer specifications and contractual quality requirements. </li><li>Support training initiatives related to QMS and quality processes. </li><li>Provide leadership support to quality inspectors and cross-functional teams to promote compliance and continuous improvement. </li><li>Provide functional oversight of the Document Control function to ensure effective control of documented information in accordance with ISO 9001:2015. </li></ul> <p>Qualifications</p> <ul> <li>Bachelor's degree in Engineering, Quality, or related technical field preferred. </li><li>5+ years of experience in manufacturing quality with strong exposure to Quality Assurance systems. </li><li>Working knowledge of ISO 9001:2015 and risk-based thinking principles required. </li><li>Experience supporting audits and managing corrective action systems. </li><li>Demonstrated capability in structured problem-solving, risk assessment, and data-driven analysis to drive effective corrective actions and process improvement. </li><li>Strong proficiency in digital quality systems and data management tools. Experience with ERP systems, SharePoint, workflow automation platforms (e.g., PowerApps), and data analysis tools preferred. Ability to responsibly leverage emerging technologies (including AI-based tools) to improve efficiency, reporting, and process control is a plus. </li><li>Excellent written and verbal communication skills. </li><li>Ability to work independently and influence cross-functional teams.. </li></ul> <p>Physical Requirements</p> <p>Work is performed in both office and manufacturing environments. Regular walking through production areas is required. Must be able to lift up to 25 lbs occasionally.</p> <p>SAFETY SENSITIVE POSITION:</p> <ul> <li>This position is designated as a Safety Sensitive Position as defined by the Oklahoma Medical Marijuana and Patient Protection Act. </li></ul> <p>This job description in no way states or implies that these are the only duties to be performed by this position. The incumbent is required to perform any other duties requested by his/her supervisor.</p>