Job Summary
The QMS Coordinator supports the implementation maintenance and continuous improvement of the Quality Management System (QMS) within a manufacturing environment. This role ensures compliance with internal procedures customer requirements and applicable quality standards while assisting with audits documentation control corrective actions and data analysis. Coordinator will support the three Pelzer facilities.
Key Responsibilities
Quality Management System (QMS) Support
Maintain and control QMS documentation including procedures work instructions forms and records
Ensure documents are current approved and properly distributed
Support compliance with applicable standards (e.g. ISO 9001 IATF 16949 AS9100 or customer-specific requirements)
Support creation of SOPs and guidelines.
Audits & Compliance
Assist with internal customer and third-party audits
Prepare audit documentation and evidence
Track audit findings and verify timely closure of corrective actions
Corrective & Preventive Actions
Support root cause analysis (e.g. 5 Whys Fishbone)
Track corrective and preventive actions (CAPA) to closure
Verify effectiveness of implemented actions
Manufacturing Quality Support
Perform in-process and final inspections as required
Review inspection records and quality data for accuracy and completeness
Support containment and investigation of nonconforming product
Data & Reporting
Maintain quality logs databases and reports
Assist in management review preparation
Training & Continuous Improvement
Assist with QMS-related training and employee awareness
Support continuous improvement initiatives and process standardization
Promote a culture of quality and compliance on the production floor
Qualifications
Required
High school diploma or equivalent (Associates degree in Quality Engineering or Manufacturing preferred)
13 years of experience in a manufacturing quality or QMS role
Working knowledge of quality management systems
Ability to read and interpret drawings specifications and procedures
Basic understanding of inspection tools and measurement techniques
Proficient in Microsoft Office (Excel Word Outlook)
Preferred
Experience with ISO 9001 IATF 16949 or AS9100
Internal auditor training or certification
Experience with CAPA document control systems and quality databases
Familiarity with statistical tools and basic SPC
Skills & Competencies
Strong attention to detail and organizational skills
Effective written and verbal communication
Problem-solving and analytical thinking
Ability to work independently and as part of a team
Time management and ability to handle multiple priorities
Working Conditions
Manufacturing floor and office environment
Exposure to noise machinery and industrial conditions
Standing walking and occasional lifting may be required
Physical Requirements
Ability to stand or walk for extended periods
Ability to lift up to 50 lbs as required
Visual acuity to perform inspections and review documentation
Required Experience:
IC
Work Authorization No calls or agencies please. Vertiv will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided. Individuals with temporary visas such as E, F-1, H-1, H-2, L, B, J, or TN or who need s ... View more