Our client is a world leading medical device company based in the West of Ireland. Due to expansion at its production facility, the company are seeking a skilled Quality Engineer to join their team.

The Role

The Quality Engineer, working with Engineering, Manufacturing, Supply Chain and Product Development is responsible for:

• Completion of equipment and process validation through DV, FAT, IQ, OQ, PQ protocol development, implementation and review and approval of subsequent report.
• Supporting quality improvement and compliance activities as needed.
• Reviewing and approving statistical analysis per Quality System requirements.
• PFMEA execution through cross-functional input.
• Providing assistance on CAPA investigation, as required.

The Person

In order to undertake their duties effectively, the Quality Engineer must have:

• A degree in Science or Engineering and have a Quality Engineering qualification or equivalent.
• At least 5 years' experience working in Med Device or similar manufacturing environment.
• Technical knowledge of statistical analysis, ISO 13485 and FDA 21 CFR regulations.

The Benefits

• Salary (DOE)
• Family healthcare
• Performance bonus
• 23 days leave
• DC pension scheme

To discover more about this opportunity, apply now or contact Aidan Toner at HRM on 091 782110 for a confidential discussion.