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This job expired on 26/07/2026. It no longer accepts applications.
QA Compliance Specialist
AbbVie · Sligo
Job description
About the role
AbbVie is seeking a QA Compliance Specialist to join its Ballytivnan site. Reporting to the Quality Systems Manager, you will help build and maintain a robust quality system that meets all regulatory and AbbVie requirements.
Key responsibilities
- Coordinate the quality system and ensure full compliance across all personnel.
- Manage Product Quality Reviews, Technical Agreements, Track‑and‑Trend activities, and site‑wide QRM initiatives.
- Facilitate RCS and FMEA activities, conduct internal audits, and support change management processes.
- Investigate customer complaints, implement corrective and preventive actions (CAPA), and verify their effectiveness.
- Liaise with Global Quality Assurance, FDA, HPRA and other regulatory bodies.
- Oversee the supplier program, perform vendor audits, and maintain commodity specifications.
- Support inspection readiness, including preparation, logistics, and documentation management.
Required profile
- Third‑level qualification in a science, quality or engineering discipline.
- Minimum 3 years of experience in a similar QA/compliance role within the pharmaceutical industry.
Required skills
- Quality Management System (QMS) coordination
- CAPA implementation and verification
- Regulatory compliance (FDA, HPRA)
- Internal audit execution
- Change management and control
- Supplier and vendor audit management
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AbbVie
Sligo