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
086-1030418 or [email protected]
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.
For more info: contact Gary
086-1030418 or [email protected]
INDCRG
