Quality Engineer II

Gi Group; Limerick; On-site; EUR 55,000 - 75,000; Full time

Benefits offered by this job

4 day work week

Job summary

Gi Group Recruitment in Limerick is seeking a Quality Engineer II on a 12‑month fixed term contract. The role focuses on supporting manufacturing operations in a medical device environment, driving CAPA, RCA, and complaints investigations, and collaborating with cross‑functional teams to improve yield and process performance.

The candidate will analyse data, implement validation activities (IQ/OQ/PQ), and contribute to risk management and continuous improvement initiatives across Quality, R&D,

Qualifications

• Strong analytical capability and problem‑solving skills.
• Proven experience driving CAPA, RCA, and complaints investigations in a highly regulated medical device environment.

Responsibilities

• Provide direct line support by responding to manufacturing issues, troubleshooting problems, and ensuring production continuity.
• Lead and support Root Cause Analysis (RCA) using structured methodologies (5‑Why, Fishbone, Fault Tree, DMAIC etc.).
• Drive CAPA ownership, ensuring investigations are thorough, data‑driven, and closed with effective long‑term solutions.
• Conduct and support complaints investigations, linking field performance to manufacturing processes and risk documentation.
• Partner with Engineers to implement line improvements focused on yield, throughput, cycle time, and defect reduction.
• Support rollout of new fixtures, equipment, and process changes by executing validation activities (IQ/OQ/PQ).
• Analyse data using statistical tools to identify trends, validate hypotheses, and support decision‑making.

Skills

CAPA

RCA

Problem solving

Data analysis

Cross-functional collaboration

Job description

Title: Quality Engineer II

Location: Limerick

Contract: 12 Month Fixed Term

Summary: Gi Group Recruitment are seeking a highly skilled Quality Engineer II to support our client based in Limerick City on a contract basis. Our client is a global leader in life‑saving medical technologies. Engineers here work in a mission‑driven environment where every improvement directly impacts patient outcomes. They are renowned for their world‑class facilities, strong career development, and the opportunity to contribute to innovative products used in hospitals worldwide. This role is ideal for a quality professional with strong analytical capability, exceptional problem‑solving skills, and proven experience driving CAPA, RCA, and complaints investigations in a highly regulated medical device environment. This position offers significant cross‑functional exposure and the opportunity to influence product and process performance at a high level.

Why Join Us?

• Join a mission‑driven organisation where your work directly improves and saves patient lives.
• Work in a world‑class manufacturing facility with cutting‑edge technologies and global engineering standards.
• Collaborate with highly skilled cross‑functional teams across Quality, R&D, Manufacturing, and Operations.
• Gain exposure to complex investigations, advanced quality tools, and high‑impact engineering projects.
• Build your expertise in risk, validation, continuous improvement, and problem solving.
• Strong opportunities for career progression into senior, technical specialist, or leadership roles.
• Extremely competitive remuneration package
• Possibility of a 4 day work week promoting a strong and healthy work/life balance

Responsibilities

• Provide direct line support by responding to manufacturing issues, troubleshooting problems, and ensuring production continuity.
• Lead and support Root Cause Analysis (RCA) using structured methodologies (5‑Why, Fishbone, Fault Tree, DMAIC etc.).
• Drive CAPA ownership, ensuring investigations are thorough, data‑driven, and closed with effective long‑term solutions.
• Conduct and support complaints investigations, linking field performance to manufacturing processes and risk documentation.
• Partner with Engineers to implement line improvements focused on yield, throughput, cycle time, and defect reduction.
• Support rollout of new fixtures, equipment, and process changes by executing validation activities (IQ/OQ/PQ).
• Analyse data using statistical tools to identify trends, validate hypotheses, and support decision‑making.
• Collab…