
QA Specialist
- Dún Laoghaire, Co Dublin
- Contract
- Full-time
- Oversight and continuous improvement of key site quality systems, including Change Control, Deviation/CAPA, and Documentation Management.
- Provide expert input and guidance during Change Control and Deviation Review Boards.
- Management of Quality Risk Management (QRM) processes, including integration of QRM principles within quality frameworks.
- Maintain and enhance the Quality Management Review process and ensure alignment with corporate policies.
- Ownership of trending programs related to quality systems and the ability to interpret data to inform optimisation strategies.
- Monitor regulatory updates and ensure that the site quality systems remain compliant and inspection-ready.
- Drive sustained compliance initiatives, including self-inspections, internal audits, and continuous improvement activities.
- Develop and manage Quality Agreements relevant to the specialist area.
- Degree in Science, Engineering, or related discipline.
- 8+ years' experience in QA roles within the pharmaceutical or biotechnology industry.
- Strong written and verbal communication skills.
- Experience with root cause analysis, investigations, and problem-solving.
- Excellent understanding of regulatory expectations and inspection readiness.
- Experience in aseptic operations, protein formulation, vial, and syringe filling is highly advantageous.
- Proven ability to manage cross-functional collaboration and influence stakeholders.