QMS Auditor I

Lucid Motors; Phoenix (AZ); On-site; USD 65,000 - 80,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401(k) plan

Equity program

Job summary

Lucid Motors is seeking a QMS Auditor I to support the execution of our Quality Management System audit program across manufacturing, quality, engineering, and supply chain. The role involves evaluating compliance with ISO 9001, collecting objective evidence, and supporting corrective action activities in a dynamic manufacturing environment.

Under guidance from senior auditors and quality leadership, you will participate in system, process, and compliance audits, maintain documentation, and

Qualifications

• 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 Microsoft Excel, PowerPoint, and other Microsoft Office applications.

Responsibilities

• Participate in internal audits of manufacturing, quality, engineering, supply chain, and business processes.
• Support audit planning activities, including preparation of audit schedules, audit checklists, documentation reviews, and audit logistics.
• Conduct interviews, process observations, and record reviews to gather objective evidence during audit activities.
• Document audit observations, findings, and supporting evidence accurately and objectively.
• Assist with follow-up audits and effectiveness reviews to validate sustained process improvements.

Skills

Organizational skills

Analytical skills

Communication skills

Fast learner

Education

Bachelor’s degree in Engineering, Quality Management, Manufacturing, Business Administration, or related field

Tools

Microsoft Excel

Microsoft PowerPoint

Microsoft Office

Job description

At Lucid, we are 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 bring our “Compromise Nothing™” approach to the global automotive market. That means refusing to choose between performance and sustainability, design and engineering, ambition and integrity. In Lucid Air and Lucid Gravity, we have designed and built vehicles that have redefined their segments, combining exceptional range, performance, design, and expansive space in a single experience.

We achieve this through deep vertical integration, with design, engineering, and production happening in‑house across our global offices and manufacturing facilities. Our teams come from industries around the world, united by a shared commitment to excellence. By refusing to settle, you can help redefine what’s possible and shape the future of mobility.

The Role

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.

Working under the guidance of senior auditors and quality leadership, the QMS Auditor I participates in system, process, and compliance audits, collects and evaluates objective evidence, supports corrective action activities, and contributes to continuous improvement initiatives.

This position provides an excellent opportunity to develop expertise in quality management systems, auditing methodologies, process compliance, risk‑based thinking, and quality governance within a dynamic manufacturing environment.

Success in this role means supporting audit readiness, improving process compliance, facilitating timely corrective action closure, and contributing to continuous improvement efforts that strengthen Lucid’s Quality Management System.

What You’ll Own

Audit Support & Execution

• Participate in internal audits of manufacturing, quality, engineering, supply chain, and business processes.
• Support audit planning activities, including preparation of audit schedules, audit checklists, documentation reviews, and audit logistics.
• Conduct interviews, process observations, and record reviews to gather objective evidence during audit activities.
• Evaluate compliance with procedures, work instructions, quality standards, and established business processes.
• Document audit observations, findings, and supporting evidence accurately and objectively.
• Support senior auditors in identifying process gaps, compliance issues, and opportunities for improvement.

Corrective Action & Follow‑Up

• Support the tracking and management of audit findings and corrective actions.
• Work with process owners to collect evidence supporting corrective action implementation.
• Participate in verification activities to confirm corrective actions have been completed.
• Assist with follow‑up audits and effectiveness reviews to validate sustained process improvements.
• Maintain audit records and support timely closure of assigned audit actions.

QMS Compliance & Documentation

• Review procedures, work instructions, forms, and records for compliance with Quality Management System requirements.
• Collaborate with Document Control and process owners to ensure documented information remains current, accurate, and properly controlled.
• Support evaluation of compliance with change management and document control processes.
• Assist in monitoring training records, competency requirements, and record retention practices.
• Help identify opportunities to improve process consistency and documentation effectiveness.

Data Analysis & Reporting

• Maintain audit tracking logs, findings databases, performance metrics, and audit records.
• Compile audit data and generate routine reports related to audit completion status and corrective action progress.
• Support analysis of recurring findings, compliance trends, process risks, and improvement opportunities.
• Assist with development of audit dashboards, reporting tools, and quality performance metrics.
• Prepare summaries, reports, and presentations for senior auditors and quality leadership.

External Audit Support

• Support external certification, customer, and regulatory audits through audit preparation and evidence collection activities.
• Coordinate documentation requests and maintain audit support records.
• Participate in audit readiness reviews and preparation exercises.
• Assist with corrective action responses resulting from external audit findings.

Continuous Improvement & Professional Development

• Develop working knowledge of ISO 9001 requirements, auditing techniques, and quality management principles.
• Participate in root cause investigations and continuous improvement activities.
• Support implementation of quality system improvements identified through audits, management reviews, and business assessments.
• Complete auditor development training and certification requirements.
• Contribute to fostering a culture of quality, compliance, accountability, and continuous improvement.

What You Bring

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.

Preferred

• 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.

Work Requirement

This role requires collaboration with Manufacturing, Engineering, Supply Chain, Quality, and business support organizations. Occasional travel may be required to support audit activities, training, and business needs.

Compensation and Benefits

Lucid offers a comprehensive and competitive benefits package that includes medical, dental, vision, life and disability insurance, paid time off, and a 401(k) plan. Eligible employees may also participate in Lucid’s equity program and/or a discretionary annual incentive program, subject to the terms and conditions of those programs. Cash or equity incentive awards, if applicable, are determined by multiple factors, including individual performance and overall company results.

Equal Opportunity

At Lucid, we believe diversity strengthens everything we build. Lucid Motors is proud to be an equal opportunity employer and is committed to providing an inclusive workplace for all. We consider all qualified applicants without regard to race, color, national or ethnic origin, age, religion, disability, sexual orientation, gender, gender identity or expression, marital status, or any other characteristic protected by applicable state or federal laws and regulations.

Accessibility

Lucid Motors is committed to providing reasonable accommodations for qualified individuals with disabilities in our application and hiring process. If you need an accommodation to participate in the application process, please contact us.

Candidate Data Privacy

Bysubmitting your application, you understand and agree that your personal data will be processed in accordance with our Candidate Privacy Notice. If you are a California resident, please refer to our California Candidate Privacy Notice.