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 policies
Manage quality documentation (procedures, reports, logbooks)
Support QA training, audits, inspections, and supplier/customer approvals
Review and manage CAPA, deviations, change controls, and complaints
Gather and analyse QA data for reporting and compliance
Assist in QA projects and respond to QA queries
Work safely, follow procedures, report hazards, and use equipment correctly
Support the Quality Management System and company strategy
Maintain confidentiality, professionalism, and continuous improvement
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 policies
Manage quality documentation (procedures, reports, logbooks)
Support QA training, audits, inspections, and supplier/customer approvals
Review and manage CAPA, deviations, change controls, and complaints
Gather and analyse QA data for reporting and compliance
Assist in QA projects and respond to QA queries
Work safely, follow procedures, report hazards, and use equipment correctly
Support the Quality Management System and company strategy
Maintain confidentiality, professionalism, and continuous improvement
Requirements:
Bachelor's degree in a relevant field
QA/Technical experience in pharma
Knowledge of EU/UK pharma regulations, GMP, GDP, ICH guidelines
Strong communication, attention to detail, and multitasking skills
For more information, please contact Sinéad Cullen on ************* or ******
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