Quality Systems Specialist — GMP/GLP Compliance

Walker Cole International; Dublin; On-site; EUR 42,000 - 68,000; Full time

Job summary

Walker Cole International is recruiting a Quality Specialist to join the expanding Quality team for a leading pharmaceutical organisation in Ireland. The role covers quality systems, project activities and laboratory operations to sustain high compliance from R&D through clinical manufacturing.

You will review documentation, support GMP/GLP compliance, assist with audits and inspections, and drive continuous improvement across QA processes with cross‑functional collaboration.

Qualifications

• A degree in a scientific or engineering discipline.
• Experience in GMP/GLP-regulated pharma or CDMO environment.
• Solid understanding of quality systems and related processes.
• Strong communication and problem-solving skills.

Responsibilities

• Supporting the ongoing development and maintenance of the site's Quality Management System, ensuring quality processes remain effective and compliant.
• Providing quality guidance throughout the lifecycle of pharmaceutical development projects, reviewing documentation and resolving quality-related issues.
• Working closely with operational teams to promote GMP/GLP compliance, support audit readiness and contribute to inspection preparation.
• Identifying opportunities to improve quality processes and helping to drive a culture of continuous improvement across the business.

Skills

Quality systems

Communication

Problem solving

Education

Bachelor's degree in a scientific or engineering discipline

Tools

CAPA

Change Control

Document Management

Investigations

Job description

Walker Cole International is recruiting a Quality Specialist to join the expanding Quality team for a leading pharmaceutical organisation in Ireland. The role covers quality systems, project activities and laboratory operations to sustain high compliance from R&D through clinical manufacturing.

You will review documentation, support GMP/GLP compliance, assist with audits and inspections, and drive continuous improvement across QA processes with cross‑functional collaboration.