Medical Device Manufacturing Technician — Lean & Quality

haemonetics; Galway; On-site; EUR 37,000 - 50,000; Full time

Job summary

Haemonetics is seeking a Manufacturing Technician to support day-to-day production in a regulated medical device environment. You will perform equipment set-ups, maintenance, troubleshooting, and ensure GMP-compliant documentation.

Working with cross-functional teams, you will implement process improvements, maintain batch records, and participate in line validations and product transfers. The role requires 2–5 years of hands-on medical device experience and knowledge of ISO 13485, MDR and FDA

Qualifications

• Third level qualification in a relevant technical field is required.
• Knowledge of ISO 13485, MDR, and FDA requirements is advantageous.
• Good documentation practices (GDP) expected.

Responsibilities

• Provide day-to-day technical support to the manufacturing line to ensure consistent and efficient operations.
• Respond promptly to line stoppages or anomalies to minimise downtime.
• Troubleshoot and resolve equipment, tooling, process, or material issues.
• Perform line set-ups and operate equipment with proper use and functionality.
• Carry out routine and preventative maintenance on production equipment.
• Identify and implement process improvements to enhance quality and efficiency.
• Support process development activities for new and existing products.
• Maintain accurate batch records and logs in compliance with GMP.

Skills

Communication

Teamwork

Autonomy

Documentation (GDP)

Organisational skills

Education

Third level qualification in a relevant technical field

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

Haemonetics is seeking a Manufacturing Technician to support day-to-day production in a regulated medical device environment. You will perform equipment set-ups, maintenance, troubleshooting, and ensure GMP-compliant documentation.

Working with cross-functional teams, you will implement process improvements, maintain batch records, and participate in line validations and product transfers. The role requires 2–5 years of hands-on medical device experience and knowledge of ISO 13485, MDR and FDA