Quality Manager

CREGG; Limerick; Vor Ort; Confidential; Vollzeit

Zusammenfassung

CREGG in Ireland is seeking a Quality Manager to lead Receiving Inspection, Engineering and Inspection Operations, ensuring components meet specifications and regulatory requirements. You will be accountable for engineering and inspector performance, compliance, capability, capacity and continuous improvement.

You will define metrics for safety, quality, service and productivity, drive nonconforming material containment, and partner with Operations, Supply Chain, and Engineering to resolve

Qualifikationen

• Bachelor’s degree in Science, Engineering or related field.
• Experience in quality management and people management.
• Experience supporting internal audits and medical-device inspections.
• Familiarity with GD&T, measurement systems and specs.
• Lean Six Sigma and data-driven process improvements.

Aufgaben

• Define and monitor metrics for safety, quality, and productivity.
• Oversee receiving inspection and inspection operations.
• Lead continuous improvement projects to reduce cycle time.
• Ensure audit readiness and regulatory compliance.
• Collaborate with Operations, Supply Chain, and Engineering.
• Ensure records, materials handling, and traceability meet specs.
• Manage performance and development of the inspection team.

Kenntnisse

Quality management

People management

Audits & regulatory inspections

GD&T knowledge

Lean Six Sigma

Communication

Ausbildung

Bachelor’s degree in Science, Engineering or related technical field

Tools

JDE or equivalent ERP

Jobbeschreibung

Excellent opportunity for an excellent Quality Manager to join a thriving company in Co. Limerick

The Quality Manager will lead Receiving Inspection Engineering and Inspection Operations to ensure incoming components and devices meet approved specifications, regulatory requirements and company quality standards. The Quality Manager with have overall accountability for Engineers and inspector performance, compliance, capability, capacity and continuous improvement.

Key Responsibilities:

• Define and review metrics for safety, quality, compliance, service, capacity, productivity, ageing and right-first-time performance.
• Ensure nonconforming incoming material is identified, contained, documented, assessed and escalated in a timely, risk-based manner.
• Provide oversight of inspection methods, measurement systems, equipment, validation and technical problem-solving.
• Maintain audit readiness and ensure effective implementation of changes involving new products, suppliers, components or inspection methods.
• Ensure inspection records, system transactions, material identification, segregation, storage and movement meet approved requirements.
• Lead projects and continuous-improvement initiatives that strengthen compliance, improve material flow and reduce inspection cycle time.
• Partner with Operations, Supply Chain, Supplier Quality, Engineering and Quality Systems to resolve issues and support business priorities.

Key Requirements:

• Bachelor’s degree in Science, Engineering or a related technical field, with relevant quality engineering, manufacturing quality or receiving inspection experience.
• Previous experience in Quality Management & People Management essential
• Experience supporting internal audits and external regulatory inspections in a medical-device
• Experience with inspection operations, measurement systems, technical drawings and specifications, including GD&T.
• Demonstrated delivery of cross-functional projects and operational improvements.
• Excellent communication, negotiation, problem-solving and stakeholder-management skills.
• Ability to use performance metrics, Lean and Six Sigma methods to improve compliance, service, flow and productivity.
• Proficiency with Microsoft Office and relevant quality or manufacturing systems, such as JDE or equivalent.