Manufacturing Engineer
Galway, County Galway, Ireland (Hybrid) · Jornada completa
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- Experiencia
- 2+ yrs
- Salario
- —
- Vacantes
- 1
- Al corriente
- hace 1 hora
- Work mode
- Híbrido
- Educación
- Degree in Engineering, Quality, or a related discipline
- Eligibility
- Applicants must hold a valid working visa for Ireland and be available for a manufacturing engineering role in Galway.
- Resume
- Required to apply
Where you'll work
Descripción del trabajo
Role overview
This opportunity is with a multinational medical device organisation in Galway for a Manufacturing Engineer to contribute to manufacturing projects. The position is a hybrid arrangement and focuses on strengthening compliance, supporting process validation, and driving new product introduction as well as continuous improvement initiatives.
Key responsibilities
- Partner with manufacturing engineers and wider engineering teams to spot compliance gaps and put corrective measures in place.
- Carry out equipment and process validation work, including IQ, OQ and PQ activities.
- Update and control quality records and technical files so the site remains ready for audits.
- Work with suppliers and vendors during new product introduction and when sourcing equipment and materials.
- Support new product introduction by validating new processes and equipment before release to the site.
- Assist in closing CAPAs and NCRs with strong, effective corrective actions.
- Create precise technical documents and SOPs for manufacturing and quality processes.
- Contribute to lean manufacturing and process improvement initiatives where applicable.
- Work closely with Manufacturing, Quality and Regulatory teams to deliver long-term, practical solutions.
Experience and skills
- A degree in Engineering, Quality, or a similar discipline is required.
- At least 2 years’ experience in medical device or pharmaceutical manufacturing is preferred, with quality engineering experience an advantage.
- Practical exposure to process or equipment validation, including IQ/OQ/PQ, and CAPA handling.
- Project management experience would be beneficial.
- Strong technical writing skills and the ability to maintain detailed documentation.
- Good understanding of GMP and regulatory expectations in the medical device environment.
- Strong troubleshooting ability and a collaborative approach to working with engineering teams.
Additional information
Candidates must already have a valid Irish work visa.
For further details, contact Gary at 086-1030418 or [email protected].