Quality Coordinator

Spirax Group plc

La Vergne, TN

JOB DETAILS
SKILLS
Auditing, Best Practices, Business Analysis, Business Writing, Coaching, Computer Software, Continuous Improvement, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Detail Oriented, Documentation, Establish Priorities, External Audit, Government Regulations, ISO (International Organization for Standardization), ISO 9001, Improvement Metrics, Internal Audit, International Electro-Technical Commission (IEC), Lean Manufacturing, Lean Six Sigma, Maintain Compliance, Management of Information Systems/Technology (MIS), Manufacturing, Microsoft Excel, Microsoft Office, Microsoft PowerPoint, Organizational Skills, Performance Metrics, Presentation/Verbal Skills, Problem Solving Skills, Process Improvement, Proofreading, Quality Management, Quality Metrics, Regulations, Regulatory Compliance, Regulatory Requirements, Reporting Skills, Root Cause Analysis, Staff Training, Standard Operating Procedures (SOP), Supply Chain, Team Player, Time Management, Typing
LOCATION
La Vergne, TN
POSTED
30+ days ago

The Role:

Reporting to our Quality Manager, the Quality Coordinator will manage and strengthen our ISO quality management system (QMS), ensuring compliance with standards like ISO and IEC through documentation control, internal audits, CAPA management, and staff training, which are crucial for our ongoing quality excellence.

Within this role, the Quality Coordinator will partner closely with several teams -Process Improvement, Plant Quality, Operations, Engineering, and Supply Chain-highlighting the collaborative effort needed to ensure we meet the organization''s compliance expectations.

Your Responsibilities:

You will help maintain, update, and manage revision tracking for quality manuals, Standard Operating Procedures (SOPs), and Manufacturing Instructions (MIs).

You will train and coach employees on quality procedures, best practices, and regulatory requirements, helping them feel valued and confident in their contributions.

You will lead, coordinate, and participate in internal and external audits, ensuring all records are audit-ready and compliant with regulatory regulations (e.g., ISO, ATEX, Customer Requirements, etc.)

You will monitor Corrective and Preventive Actions (CAPA) and actively contribute to root cause analysis for quality nonconformances, emphasizing the team''s role in continuous improvement.

You will track trending quality systems data and quality performance metrics, identify improvement opportunities, and follow up on action items.

Our Requirements:

At least 3+ years of working experience with Quality Management Systems in an ISO 9001-certified manufacturing environment.

A Bachelor's degree in Business or a related field; a combination of relevant education and work experience is also preferred.

An ISO 9001:2015 Lead Auditor certification is preferred, not required.

Working experience and knowledge of Six Sigma, lean manufacturing, continuous improvement, problem solving and corrective action implementation is preferred, not required.

Working experience analyzing general business periodicals, professional journals, technical procedures, or governmental regulations.

Working experience writing reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the public.

Experience and knowledge of a variety of computer software applications, preferably Microsoft Office, Excel, and PowerPoint.

An immense attention to detail in composing, typing and proofing materials, establishing priorities, and meeting deadlines.

About the Company

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Spirax Group plc