Quality Systems Coordinator

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Propel your career at Belden, where innovation creates possibilities—for our people, our customers, and the communities we serve. We connect people, information, and ideas to solve the world’s most complex connectivity challenges, turning curiosity into meaningful impact. Here, you’ll take on work that challenges you, supports your growth, and empowers you to shape what’s next. You’ll collaborate with global teams, gain diverse perspectives, and contribute to solutions that extend beyond our business—creating value in the world around us.

Together, we are shaping the future of digitization and paving the way for the next generation of innovation.

The Quality Systems Specialist is responsible for maintaining, improving, and ensuring the effectiveness of the Quality Management System (QMS) on a site focussed on Research & Development. The role drives compliance with ISO 9001 requirements throughout the electronics product development lifecycle, including contract manufacturing, by ensuring that documented processes are implemented, monitored, and continually improved.

Working closely with Engineering, Project Management, and Supply Chain teams, the Quality Systems Specialist promotes a quality-focused culture that enables the development of innovative, reliable, and manufacturable electronic products while meeting customer, regulatory, and business requirements.

This role is a remote-hybrid position with up to 50% travel.

• Maintain and continuously improve the ISO 9001 Quality Management.
• Develop, review, and maintain quality procedures, work instructions, templates, and process documentation.
• Support Management Review by preparing quality performance reports and improvement recommendations.

• Ensure quality requirements are integrated throughout the product development lifecycle, including:
• Support lessons learned and knowledge capture following development projects.

• Maintain controlled procedures, specifications, standards, design templates, and quality records.
• Ensure document revisions are properly reviewed, approved, distributed, and archived.
• Support engineering change management processes and document change control activities.

• Plan, coordinate, and conduct internal audits.
• Coordinate external certification audits and customer quality audits.
• Track audit findings through to effective closure.

• Coordinate the CAPA process.
• Facilitate root cause investigations using structured problem-solving techniques such as:
• 5 Why, Fishbone Diagram (ISHIKAWA), A3, FMEA
• Verify effectiveness of implemented corrective actions.
• Monitor recurring issues and identify systemic improvement opportunities.

• Promote risk-based thinking throughout product development activities.
• Encourage preventive actions through proactive process improvement.

• Deliver training on Quality Management System processes and ISO 9001 requirements.
• Support onboarding of new engineering staff regarding quality procedures.
• Promote awareness of quality objectives and customer requirements throughout R&D.
• Encourage best practices in documentation, traceability, and process discipline.

• Bachelor's degree in Engineering, Electronics, or a related technical discipline.

• 3–5 years' experience in Quality Systems, Quality Assurance, or Engineering within an electronics or technology development environment.
• Experience maintaining an ISO 9001 certified Quality Management System.
• Experience supporting engineering or product development teams.
• Internal auditing experience preferred.

• ISO 9001:2015 Quality Management Systems
• Document control
• Root cause analysis
• Process mapping and process optimisation

Knowledge of the following is advantageous:

• IPC standards
• IEC standards applicable to electronic products
• Electronic document management systems (eQMS)

• Strong understanding of Quality Management Systems.
• Excellent organisational and documentation skills.
• Strong…