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CREGG

Manufacturing Engineer

CREGG

Galway, County Galway, Ireland (Hybrid) · Tempo pieno

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Esperienza
2+ yrs
Stipendio
Aperture
1
Pubblicato
2 ore fa
Work mode
Ibrido
Istruzione
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

Descrizione del lavoro

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 garykeane@cregg.ie.

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