Quality Specialist

Quality Specialist

Our client a global pharmaceutical services company specialising in providing access to medicines, clinical trial services, and lifecycle management are currently recruiting for a Quality Specialist to join their team.Experience with Good Distribution Practice (GDP) in the distribution of medicinal products, direct involvement in audits, and interaction with the HPRA are essential requirements for this role.

Responsibilities : Ensure compliance with GMP, GDP, SOPs, and company policiesManage quality documentation (procedures, reports, logbooks)Support QA training, audits, inspections, and supplier / customer approvalsReview and manage CAPA, deviations, change controls, and complaintsGather and analyse QA data for reporting and complianceAssist in QA projects and respond to QA queriesWork safely, follow procedures, report hazards, and use equipment correctlySupport the Quality Management System and company strategyMaintain confidentiality, professionalism, and continuous improvementQuality Specialist

Our client a global pharmaceutical services company specialising in providing access to medicines, clinical trial services, and lifecycle management are currently recruiting for a Quality Specialist to join their team.Experience with Good Distribution Practice (GDP) in the distribution of medicinal products, direct involvement in audits, and interaction with the HPRA are essential requirements for this role.

Responsibilities : Ensure compliance with GMP, GDP, SOPs, and company policiesManage quality documentation (procedures, reports, logbooks)Support QA training, audits, inspections, and supplier / customer approvalsReview and manage CAPA, deviations, change controls, and complaintsGather and analyse QA data for reporting and complianceAssist in QA projects and respond to QA queriesWork safely, follow procedures, report hazards, and use equipment correctlySupport the Quality Management System and company strategyMaintain confidentiality, professionalism, and continuous improvementRequirements : Bachelor's degree in a relevant fieldQA / Technical experience in pharmaKnowledge of EU / UK pharma regulations, GMP, GDP, ICH guidelinesStrong communication, attention to detail, and multitasking skillsFor more information, please contact Sinéad Cullen on +353879500821 or

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