MES QA Specialist — GMP Compliance & Quality Systems

CareerWise Recruitment; Limerick; On-site; EUR 60,000 - 80,000; Full time

Job summary

CareerWise Recruitment is seeking a QA Specialist (MES) for a Limerick based pharma client. The role focuses on leading quality governance for MES systems and ensuring GMP compliance across the quality program.

You will investigate MES issues, approve GMP documents, support audits, and drive continuous improvement within a validated MES environment. A background in Chemistry or Engineering with 5 years MES experience is preferred.

Qualifications

• May hold BSc, MSc or PhD in Chemistry, Engineering, or related discipline.
• 5 years experience in previous MES role.

Responsibilities

• Provide Quality leadership, direction, and governance for MES and MES related systems.
• Investigate and troubleshoot issues relating to MES and MES related systems.
• Manage Quality-related matters specific to area (Quality system or Quality Program) of responsibility.
• Approve appropriate quality-related documents. An approval signature confirms that GMP requirements have been met.
• Carry out day-to-day activities in compliance with site safety policies and procedures.

Education

BSc

MSc

PhD

Job description

CareerWise Recruitment is seeking a QA Specialist (MES) for a Limerick based pharma client. The role focuses on leading quality governance for MES systems and ensuring GMP compliance across the quality program.

You will investigate MES issues, approve GMP documents, support audits, and drive continuous improvement within a validated MES environment. A background in Chemistry or Engineering with 5 years MES experience is preferred.