Quality Specialist - Quality Systems CoE

Join a highly regulated pharmaceutical environment where your expertise will support GMP compliance, quality systems, auditing, laboratory quality, investigations, and validation .

We're looking for a quality professional who can work across a broad range of QA activities, identify compliance gaps, support investigations, and contribute to maintaining strong quality standards across the site.

• Conduct routine audits of data, documentation, procedures, equipment, computer systems, and facilities against SOPs, GMP, and regulatory requirements.
• Prepare audit reports, communicate findings, and support remedial actions .
• Provide QA oversight of deviations, CAPAs, root-cause investigations, and quality trends .
• Support analytical and microbiological laboratory quality, including change controls and method validation, verification, and transfer .
• Provide oversight of environmental monitoring and microbiological control , including OOT/OOL investigations.
• Review equipment, utility, and facility qualification and validation documentation, including IQ/OQ/PQ.
• Coordinate Quality Agreements, Change Agreements, and Supplier Qualification activities.
• Support customer complaint investigations and material expiry/retest evaluations.
• Support SAP Master Data governance and material status and expiry updates.
• Contribute to regulatory submissions, GMP declarations, inspection readiness, and quality metrics .
• Contribute to continuous improvement across the Quality function.

• Degree or postgraduate qualification in Chemistry, Microbiology, Biology, Science, Pharmacy, Engineering, or a related technical discipline .
• Experience within the pharmaceutical or chemical industry , or a government drug-regulatory agency.
• Working knowledge of cGMP regulations .
• Pharmaceutical QA/QC experience , particularly with microbiology exposure.
• Experience with OOS/OOT investigations, environmental monitoring, analytical validation, or laboratory compliance .
• Knowledge of ICH Q2, USP/EP/JP requirements , and analytical or microbiological method validation.
• Experience with Kneat, ProCal, SAP, Quality Agreements, or Supplier Qualification .
• Exposure to Lean or Continuous Improvement methodologies.
• Strong written, verbal, interpersonal, organisational, and problem-solving skills.
• Ability to work hybrid in Ballydine, Co. Tipperary, typically 3 days onsite .

You'll play a key role in maintaining GMP compliance and quality standards while gaining broad exposure across auditing, quality systems, laboratory quality, validation, investigations, supplier activities, and continuous improvement.

This role offers the opportunity to work across a varied Quality environment , rather than focusing on a single area of QA.

All applications are treated in the strictest confidence.

Your personal data will never be shared outside our organisation without your prior written consent.

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