QA Specialist: Quality Systems & GMP Leader (12-Month)

Quanta Consultancy Services Ltd; Limerick; On-site; EUR 55,000 - 75,000; Full time

Job summary

Life Sciences Ireland is seeking a QA Specialist (Quality Systems) for an initial 12-month contract in Limerick, Ireland. The role focuses on ensuring GMP compliance across manufacturing, quality systems, QC, validation, facilities and materials management.

You will review investigations, CAPAs, SOPs and change controls, lead root cause analyses, and collaborate with cross-functional teams to maintain regulatory standards in a dynamic pharmaceutical environment.

Qualifications

• QA role ensuring GMP compliance across manufacturing, quality systems, QC, validation, facilities, and materials.
• Review and approve investigations, CAPAs, SOPs, GxP records, and change controls.
• Lead investigations and root cause analysis with effective CAPAs.
• Collaborate with cross-functional teams to resolve quality issues and ensure regulatory compliance.
• Strong background in QC systems such as LIMS or Empower preferred.

Responsibilities

• Ensure site-wide quality and GMP compliance across manufacturing, quality systems, QC, validation, facilities, and materials management.
• Review and approve key quality documentation, investigations, CAPAs, SOPs, GxP records, and change controls.
• Lead investigations and root cause analysis with effective CAPA implementation.
• Collaborate with cross-functional teams to resolve quality issues and maintain regulatory compliance.

Skills

QC Testing

GMP knowledge

Quality Assurance

Regulatory compliance

Education

Degree in a Scientific Discipline

Tools

LIMS

Empower

Job description

Life Sciences Ireland is seeking a QA Specialist (Quality Systems) for an initial 12-month contract in Limerick, Ireland. The role focuses on ensuring GMP compliance across manufacturing, quality systems, QC, validation, facilities and materials management.

You will review investigations, CAPAs, SOPs and change controls, lead root cause analyses, and collaborate with cross-functional teams to maintain regulatory standards in a dynamic pharmaceutical environment.