QMS Auditor II

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.

This role is responsible for leading and executing Quality Management System (QMS) audits across manufacturing, quality, engineering, supply chain, and support functions to verify compliance with ISO 9001, internal procedures, customer requirements, and regulatory standards. The QMS Auditor II serves as an independent assessor of process effectiveness, ensuring documented processes are implemented as intended and are capable of consistently delivering quality products and services.

Operating with a risk‑based auditing approach, the auditor plans and conducts system, process, and compliance audits, identifies gaps and opportunities for improvement, verifies corrective action effectiveness, and supports continual improvement initiatives throughout the organization.

The role works closely with Manufacturing, Quality, Supply Chain, Engineering, Service, Document Control, and leadership teams to improve process discipline, audit readiness, and overall business performance. Success in this role means improving audit readiness, strengthening process compliance, ensuring effective corrective action implementation, and driving continual improvement across Lucid’s Quality Management System.

Develop and maintain the annual internal audit schedule using a risk‑based approach that considers process performance, customer concerns, quality metrics, organizational changes, and previous audit results. Plan and coordinate system, process, layered, and compliance audits across all business functions and manufacturing operations. Ensure audit coverage aligns with ISO 9001, customer‑specific requirements, internal procedures, and regulatory obligations.

Support management review activities by providing audit performance summaries, trends, risks, and improvement opportunities.

Conduct internal audits to evaluate compliance with documented procedures, work instructions, control plans, standards, and regulatory requirements. Gather objective evidence through interviews, process observations, documentation reviews, and sampling of records. Identify nonconformities, process gaps, risks, and opportunities for continual improvement using a fact‑based and objective approach. Document audit findings with clear supporting evidence and appropriate severity classifications.

Ensure audits assess both compliance and process effectiveness, focusing on customer impact and business risk. Issue and manage nonconformance reports. Partner with process owners to facilitate robust root‑cause analysis utilizing methodologies such as 5‑Why, Fishbone, A3, and 8D. Verify corrective and preventive actions are effectively implemented and sustained. Conduct follow‑up audits and effectiveness reviews to ensure closure of findings and prevent recurrence.

Identify systemic issues and recommend improvements to strengthen process capability and organizational performance.

Verify that documented information remains accurate, current, controlled, and aligned with operational practices. Collaborate with Document Control to maintain procedures, policies, forms, records, and process…