MES QA Specialist — GMP & Quality Systems Lead

CareerWise Recruitment; Limerick; On-site; EUR 60,000 - 90,000; Full time

Job summary

CareerWise Recruitment seeks a QA Specialist (MES) for our Limerick-based pharma client. You will lead QA governance for MES systems, investigate issues, and ensure GMP compliance across documents and change controls.

You will support audits, participate in quality meetings, and drive the site quality program. A strong MES background and GMP knowledge are essential for success in this role.

Qualifications

• 5 years experience in a MES/QMS role.
• BSc/MSc/PhD in Chemistry, Engineering, or related discipline.
• Solid understanding of GMP requirements and regulatory guidelines.
• Experience with quality systems, change controls, deviations, and investigations.

Responsibilities

• Provide QA leadership, direction, and governance for MES and MES-related systems.
• Investigate and troubleshoot MES-related issues.
• Manage quality matters specific to the area of responsibility.
• Approve quality-related documents and ensure GMP requirements are met.
• Promote safe practices and escalate safety concerns.
• Support audits from an MES perspective and assist cross-functional teams.

Skills

Quality leadership

GMP knowledge

QA systems

Audit support

Education

BSc/MSc/PhD in Chemistry or Engineering

Job description

CareerWise Recruitment seeks a QA Specialist (MES) for our Limerick-based pharma client. You will lead QA governance for MES systems, investigate issues, and ensure GMP compliance across documents and change controls.

You will support audits, participate in quality meetings, and drive the site quality program. A strong MES background and GMP knowledge are essential for success in this role.