Manufacturing Engineer (Medical Devices)

Manufacturing Engineer (Medical Devices)

Our client, a global leader in medical device industry based in Galway, is looking for skilled Quality Engineers / Manufacturing Engineers.

This is an excellent opportunity to work onsite and partner closely with manufacturing and quality teams to strengthen compliance and support process validation projects.

For more info: contact Gary

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Responsibilities

• Work alongside manufacturing owners to identify gaps and implement corrective actions to achieve compliance.
• Contribute to equipment and process validation activities (IQ/OQ/PQ).
• Revise and maintain quality system records and technical documentation to ensure audit readiness.
• Lead and support the closure of CAPAs and NCRs with robust corrective actions.
• Develop clear, accurate technical documentation and SOPs for quality and manufacturing processes.
• Collaborate with cross-functional teams, including Manufacturing, Quality, and Regulatory, to deliver sustainable solutions.

Skills & Experience Required

• Degree in Engineering, Quality, or a related discipline.
• 2-5 years of experience in medical device manufacturing, quality engineering, or remediation work.
• background in process validation (IQ/OQ/PQ) and CAPA/NCR resolution.
• Excellent technical writing and documentation abilities.
• Solid understanding of regulatory requirements. with GMP and/or med device industry
• Strong problem-solving mindset, with the ability to drive issues to fully compliant solutions.