GMP QC Compliance Lead for Gene Therapy

MeiraGTx; Shannon; On-site; EUR 65,000 - 90,000; Full time

Job summary

MeiraGTx in Ireland is seeking a QC Senior Compliance specialist to ensure GMP-compliant activities within QC supporting the manufacture of gene therapy products. You will review and approve QC documentation to support batch release and drive quality metrics.

The role requires a scientific degree and at least 4 years in a QC/QA GMP environment, with strong documentation and data integrity focus. You will manage audits, CAPA, change controls and continuous improvement efforts.

Qualifications

• Degree in a scientific discipline.
• 4+ years in a QC or QA GMP environment.
• Experience with quality documentation review and approval (QC/Manufacturing batch records).
• Proficiency in Microsoft Office (Word, Excel, PowerPoint).

Responsibilities

• GMP Compliance activities.
• Management of audit schedule.
• Quality record KPI tracking and reporting.

Skills

Quality management

Attention to detail

Problem solving

Leadership

Planning/organizing

Professionalism

Innovation

Oral communication

Written communication

Education

Degree in scientific discipline

Job description

MeiraGTx in Ireland is seeking a QC Senior Compliance specialist to ensure GMP-compliant activities within QC supporting the manufacture of gene therapy products. You will review and approve QC documentation to support batch release and drive quality metrics.

The role requires a scientific degree and at least 4 years in a QC/QA GMP environment, with strong documentation and data integrity focus. You will manage audits, CAPA, change controls and continuous improvement efforts.