12-Month QA Validation Lead — Life Sciences (GxP)

Joinimagine; Dublin; On-site; EUR 65,000 - 95,000; Part time

Job summary

DHL Supply Chain in Ireland is seeking a QA Validation Manager to oversee qualification and validation of equipment and control systems for the Life Sciences business. The role ensures GxP compliance and supports supplier qualification, with a focus on IQ/OQ/PQ and EU GMP Annex 11/15.

The position requires strong MS Office skills, a background in pharmaceutical or medical devices QA, and experience managing quality systems within a GxP framework. Applicants must have full work rights in Ireland.

Qualifications

• Previous experience in a QA Validation Manager or equivalent role within the Pharmaceutical or Medical Devices industry.
• Demonstrated knowledge of equipment qualification activities, including IQ, OQ, and PQ.
• Good understanding of EU GMP Annex 11 and Annex 15.
• Experience in the management of Quality Systems in compliance with GxP requirements.
• Computer literate (MS Office).
• Life Science logistics industry experience.

Responsibilities

• Manage the Computer System Validation process in line with GAMP 5 requirements.
• Oversee qualification and requalification schedules for GxP-critical equipment and systems.
• Complete qualification activities with mapping contractors and maintain compliant documentation.
• Monitor temperature across all facility areas.
• Lead supplier qualification, approval, and requalification of GxP-critical suppliers.
• Assist with supplier and equipment selection, approval, and implementation with stakeholders.
• Support day-to-day quality activities to ensure compliance and service continuity.

Skills

IQ/OQ/PQ qualification

GxP knowledge

MS Office

Life sciences logistics

EU GMP Annex 11/15

Job description

DHL Supply Chain in Ireland is seeking a QA Validation Manager to oversee qualification and validation of equipment and control systems for the Life Sciences business. The role ensures GxP compliance and supports supplier qualification, with a focus on IQ/OQ/PQ and EU GMP Annex 11/15.

The position requires strong MS Office skills, a background in pharmaceutical or medical devices QA, and experience managing quality systems within a GxP framework. Applicants must have full work rights in Ireland.