QMS Auditor I

About Lucid

Lucid is creating exceptional mobility experiences through innovation to drive the world forward. Built on Lucid's proprietary technology and software-defined vehicle architecture, our award-winning vehicles redefine segments with exceptional range, performance, design, and expansive space.

Quality | Casa Grande, AZ | Full-Time

The QMS Auditor I supports the execution of Lucid’s Quality Management System (QMS) audit program across manufacturing, quality, engineering, supply chain, and support functions. This role helps evaluate compliance with ISO 9001 requirements, internal procedures, customer requirements, and regulatory standards to ensure processes are implemented effectively and consistently across the organization.

• Supports audit planning activities: Preparation of audit schedules, audit checklists, documentation reviews, and audit logistics.
• Conducts interviews, process observations, and record reviews: Gather objective evidence during audit activities.
• Evaluates compliance: Document audit observations, findings, and supporting evidence accurately and objectively.
• Supports corrective action activities: Track and manage audit findings and corrective actions, assist in verification activities, and support follow-up audits.
• Data analysis and reporting: Maintain audit tracking logs, findings databases, performance metrics, and audit records; compile audit data and generate reports.

Required

• Bachelor’s degree in Engineering, Quality Management, Manufacturing, Business Administration, or a related field.
• 0–3 years of experience in Quality, Manufacturing, Engineering, Process Improvement, Compliance, or a related technical environment.
• Basic understanding of quality management systems and process-based auditing principles.
• Familiarity with ISO 9001 requirements or a demonstrated willingness to develop expertise in quality management systems.
• Experience using standard business software including Microsoft Excel, PowerPoint, and other Microsoft Office applications.
• Strong organizational, analytical, and communication skills.
• Ability to learn quickly and apply new concepts effectively.
• Ability to work independently on assigned tasks while collaborating effectively with cross-functional teams.
• Strong attention to detail and documentation accuracy.

Prioritization

• Exposure to manufacturing, engineering, or regulated industry environments.
• Coursework or experience related to quality systems, auditing, compliance, or process improvement.
• Familiarity with document control systems and quality management software.
• Basic understanding of root cause analysis methodologies.
• Experience analyzing data and preparing reports or presentations.
• Interest in pursuing quality auditing certifications or professional development in quality management systems.