Job Title: QA Officer (GMP Compliance)
Location: Cookstown, Dublin 24 (Office-Based, Monday to Friday)
Job Type: Full-Time
Annual Leave: 20 Days
Are you passionate about quality and compliance within a GMP-regulated environment? We’re currently recruiting for a QA Officer to join a fast-paced, multi-disciplinary team based in Cookstown, Dublin 24. This is an exciting opportunity to take a tactical role in shaping quality assurance processes and fostering a strong quality culture across operations.

Key Responsibilities:

• Support the design and implementation of governance processes to ensure consistent GMP compliance.
• Act as a subject matter expert on quality within facility operations.
• Promote awareness of quality requirements and deliver internal training where needed.
• Maintain and manage GMP document control processes and training records.
• Conduct internal audits/self-inspections and support corrective actions through change management.
• Monitor and coordinate completion of GxP Audit PQS records (change controls, deviations, CAPAs).
• Provide compliance support and escalate issues appropriately within the PQS framework.
• Administer and maintain the Quality Management System (QMS).
• Act as a QA Archivist ensuring secure retention and storage of quality records.
• Manage issuance, review, and archiving of SOPs, forms, and QMS documentation.
• Collaborate with all departments to maintain compliance and support GMP/GDP-related activities across the site.

Required Skills & Competencies:

• Strong communication and organisational skills.
• Good working knowledge of GMPs and GDPs.
• Proven QA experience in a GMP-regulated environment.
• Ability to manage multiple tasks with attention to detail.
• Risk-based thinking and problem-solving skills.
• Professional and proactive approach to quality and compliance.
• Team-oriented with the ability to work independently.
• Results-driven with a flexible, can-do attitude.

Education & Qualifications:

• BSc or equivalent qualification in a relevant scientific discipline.

If you’re looking to develop your career in a quality-driven environment and be part of a dedicated and supportive QA team, we’d love to hear from you.

• Support the design and implementation of governance processes to ensure consistent GMP compliance.
• Act as a subject matter expert on quality within facility operations.
• Promote awareness of quality requirements and deliver internal training where needed.
• Maintain and manage GMP document control processes and training records.
• Conduct internal audits/self-inspections and support corrective actions through change management.
• Monitor and coordinate completion of GxP Audit PQS records (change controls, deviations, CAPAs).
• Provide compliance support and escalate issues appropriately within the PQS framework.
• Administer and maintain the Quality Management System (QMS).
• Act as a QA Archivist ensuring secure retention and storage of quality records.
• Manage issuance, review, and archiving of SOPs, forms, and QMS documentation.
• Collaborate with all departments to maintain compliance and support GMP/GDP-related activities across the site