QMS Auditor I

Lucid Motors•Casa Grande, AZ

7h•Onsite

About The Position

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.

Requirements

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.

Nice To Haves

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.

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.
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.
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.
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.
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.
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.
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.