Medical Device Quality Technician - GMP/QA Focus

PE Global (UK); Sligo; On-site; EUR 32,000 - 42,000; Full time

Job summary

PE Global are currently recruiting a Quality Technician for our Medical Device client site in Sligo on a 12-month initial contract. You will join the Quality Assurance team to support GMP-compliant operations.

The role focuses on daily quality system tasks, product testing, documentation control, and continuous improvements to ensure compliance with cGMP and ISO/FDA regulations. Attention to detail, consistency, and teamwork are essential as you will generate metrics for management review and

Qualifications

• Experience working in a GMP-regulated environment is desirable.
• Experience with quality systems and documentation control is desirable.
• Attention to detail and ability to adapt to new processes.

Responsibilities

• Work as part of the Quality Team to meet quality goals.
• Ensure actions comply with current GMP.
• Operate within QC/IQA and Metrology areas as required.
• Perform incoming product testing per approved specs.
• Perform in-process and final release testing per specs.
• Keep Management informed of Quality Events.
• Ensure quality system documents are complete and compliant.
• Audit the quality system with other personnel when required.
• Support Change Management including document review.
• Provide metrics for management review and monthly reports.
• Ensure training requirements are maintained.
• Participate in continuous improvement programs.
• Generate batch records as needed to support manufacturing orders.
• Complete disposition decisions for incoming materials.

Skills

Attention to detail

Regulated GMP experience

Quality mindset

Education

Third-level qualification

Job description

PE Global are currently recruiting a Quality Technician for our Medical Device client site in Sligo on a 12-month initial contract. You will join the Quality Assurance team to support GMP-compliant operations.

The role focuses on daily quality system tasks, product testing, documentation control, and continuous improvements to ensure compliance with cGMP and ISO/FDA regulations. Attention to detail, consistency, and teamwork are essential as you will generate metrics for management review and