Quality Systems Engineer
Listed on 2026-11-04
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Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, Production QC/QA
Our client is an established manufacturing organization committed to producing high-quality products and maintaining strong customer relationships. The company emphasizes quality, operational excellence, continuous improvement, and customer satisfaction.
About the RoleOur client is seeking an experienced Quality Systems Engineer to manage, maintain, and continuously improve the quality management system at an established industrial manufacturing facility in Fort Wayne, Indiana. This is an excellent opportunity for a quality professional with a strong background in ISO 9001, IATF 16949, quality system compliance, audit leadership, and document control.
The Quality Systems Engineer will help ensure that manufacturing processes and quality systems meet internal standards, customer requirements, and applicable certification requirements. This individual will lead and support quality audits, maintain controlled documentation, manage corrective action processes, and work with cross-functional teams to strengthen the organization's overall quality management system.
If you're an organized, detail-oriented quality professional who enjoys improving systems, leading audits, strengthening compliance, and helping teams maintain consistent quality standards, we'd like to hear from you.
The Quality Systems Engineer will play an important role in maintaining certification readiness, improving quality management processes, and ensuring that quality procedures and documentation are consistently followed throughout the organization.
As a Quality Systems Engineer, you'll oversee key elements of the quality management system and collaborate with customers, engineering, operations, and production teams to maintain compliance and drive continuous improvement.
Responsibilities- Relocation Assistance:
Available - Your responsibilities will include:
- Manage, maintain, and improve the Quality Management System (QMS) to ensure products and processes meet company standards and applicable customer requirements.
- Support the maintenance of ISO 9001 and IATF 16949 certifications and ensure ongoing compliance with applicable quality management system requirements.
- Lead, maintain, and improve internal and external audit programs, including certification and surveillance audit preparation, coordination, and follow-up.
- Lead customer audits and coordinate responses to audit findings, including opportunities for improvement (OFIs) and required corrective actions.
- Investigate and support the resolution of customer complaints, product returns, nonconformances, and internal quality issues.
- Lead or participate in structured problem-solving activities using appropriate quality tools to develop, implement, and sustain corrective and preventive actions.
- Support the management of the corrective action database to ensure actions are assigned, tracked, completed on time, and verified for effectiveness before closure.
- Apply Failure Mode and Effects Analysis (FMEA) methodology and associated Control Plans to evaluate product and process risks and support risk-reduction initiatives.
- Support customer quality requirements, including the preparation, review, and maintenance of PPAP, APQP, and other required quality documentation.
- Assist with customer plant visits, as needed, to evaluate product rejects and support quality issue resolution.
- Support continuous improvement activities designed to strengthen the QMS, improve process consistency, reduce variation, and enhance customer satisfaction.
- Support Measurement Systems Analysis (MSA), including Gage R&R studies, to help validate the reliability of measurement systems and quality data.
- Review, maintain, and improve document control processes to ensure documents remain accurate, current, accessible, and compliant with IATF requirements and internal procedures.
- Maintain and administer the SharePoint file management system for quality documentation and controlled records.
- Maintain awareness of internal calibration procedures, records, and documentation requirements, providing support as needed.
- Develop, maintain, and improve quality procedures, work instructions, forms, and other controlled documentation.
- Train team members on quality standards, document control requirements, and proper process documentation practices.
- Serve as a technical resource for quality-related questions and mentor supervisors, process engineers, technicians, and production employees on quality standards and improvement techniques.
- Identify opportunities to improve audit…
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