Global QMS Auditor – Job Description
The Integral QMS Auditor is responsible for conducting independent, risk‐based assessments of global Quality Management System (QMS) processes to ensure compliance, identify systemic risks, and drive sustained process effectiveness.
This role supports standardization, continuous improvement, and governance visibility across the enterprise by validating that processes are defined, deployed, executed, and effective in protecting product quality, regulatory compliance, and customer experience.
Responsibilities
Plan and execute risk-based internal audits across global sites, functions, and processes to assess compliance and effectiveness.
Evaluate process effectiveness and maturity, ensuring controls are preventive and consistently executed.
Identify systemic risks and gaps across core QMS business processes, differentiating between localized issues and enterprise-level weaknesses.
Document and communicate audit findings with clear evidence‐based observations, findings, and risk prioritization.
Drive and verify corrective actions (RCCA/CAPA), ensuring true root cause identification and sustainable resolution.
Validate effectiveness of corrective actions through data, follow-up audits, and performance trends.
Monitor and report audit performance and systemic trends to Global Quality leadership, supporting governance and management review.
Ensure compliance with applicable quality standards and requirements, including ISO ****, regulatory, and customer‐specific quality systems requirements.
Provide auditor training to site and functional resources to ensure consistent application of audit methodologies and QMS requirements.
Provide support and guidance for external quality systems audits,



ensuring audit readiness, effective execution, and timely, sustainable responses to findings.
Minimum Job Qualifications
3+ years of experience in a QMS role.
Certified Internal Auditor.
Working knowledge of ISO **** standard requirements.
Demonstrated experience conducting process‐based internal audits in a global, multifunctional environment.
Proven ability to drive sustainable corrective actions (RCCA/CAPA) and verify effectiveness.
Effective written and verbal communication skills, including the ability to document clear, objective audit findings.
Proven analytical skills with the ability to identify, assess, and prioritize systemic global process risks.
Strong proficiency in spoken and written English.
Preferred Qualifications
ISO **** Lead Auditor Certification.
Demonstrated capability in auditor training, coaching, and QMS capability development across site and functional quality teams.
Experience in a global, multi‐site industrial manufacturing environment.
Strong working knowledge of DFMEA, PFMEA, Control Plans, and advanced risk‐based quality methodologies.
IAFTA and VDA 6.3 certifications.
Education and Certifications
Bachelor's degree.
Certified Internal Auditor.
Travel
Travel time required: 60%.
Work Authorization
Only individuals legally authorized to work in the United States are eligible for this position.
No sponsorship will be provided.
Equal Opportunity Employer
Vertiv promotes equal opportunities for all with respect to hiring, terms of employment, mobility, training, compensation, and occupational health, without discrimination as to age, race, color, religion, creed, sex, pregnancy status, marital status, sexual orientation, gender identity, or disability.
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📌 Quality Qms Auditor (Mexicali)
🏢 Vertiv
📍 Mexicali