QMS Specialist — ISO 9001, Onsite

Vertiv Group Corporation; Letterkenny; On-site; EUR 45,000 - 65,000; Full time

Job summary

The QMS Specialist at Vertiv Group Corporation Letterkenny is responsible for the continuous improvement, maintenance, and alignment of the Quality Management System on site. You will manage QMS documentation, plan audits, and ensure certification readiness while working with production, EHS, and VOS teams.

Reporting directly to the Quality Manager, you will drive non-conformity resolution, track audit action plans, and raise QMS awareness through training and presentations to foster a culture

Qualifications

• 3 years of experience in a QMS or Quality Assurance role within a manufacturing environment.
• Certified Internal Auditor ISO 9001.
• English proficiency at 90% or higher.

Responsibilities

• Maintain, update, and control all QMS documentation (procedures, work instructions, forms).
• Plan, coordinate, and execute internal audits in accordance with ISO 9001.
• Coordinate external audits and ensure certification readiness.
• Manage Non-Conformity Reports (NCRs) and corrective actions, ensuring timely closure.
• Track and follow up on audit action plans.
• Maintain the Risk and Opportunities register on a regular basis.
• Consolidate customer quality requirements per project.
• Coordinate customer visits and quality-related site walkthroughs.
• Supervise and maintain the claim management tool.
• Raise QMS awareness across the site through training and presentations.
• Support process improvement initiatives with relevant departments.
• Collaborate with local VOS and EHS teams on integrated management system activities.
• Support FMEA activities with manufacturing teams.

Skills

Quality Assurance

Internal Auditor ISO 9001

English proficiency

Education

Certified Internal Auditor ISO 9001

Tools

Audit management systems

Document control software

Excel

Word

Job description

The QMS Specialist at Vertiv Group Corporation Letterkenny is responsible for the continuous improvement, maintenance, and alignment of the Quality Management System on site. You will manage QMS documentation, plan audits, and ensure certification readiness while working with production, EHS, and VOS teams.

Reporting directly to the Quality Manager, you will drive non-conformity resolution, track audit action plans, and raise QMS awareness through training and presentations to foster a culture