Validation Engineer

Cpl • Cork, County Cork • Posted June 11, 2026
About the Role

Validation Engineer
Summary
The Validation Engineer is responsible for owning and supporting validation activities within a regulated Medical Device manufacturing environment. The role focuses on ensuring compliant qualification and validation of processes, equipment, facilities, utilities, software, and computer systems while maintaining adherence to GMP and regulatory requirements.
Responsibilities
Own and support validation activities within a Medical Device regulated environment.
Execute and support Process, Equipment, Facility, Utility, Software, and Computer System Validation activities as assigned.
Generate Validation Plans, Protocols, Reports, and associated documentation to support validation projects.
Investigate and resolve issues encountered during validation and qualification activities.
Ensure a consistent validation and qualification approach across systems, equipment, and projects.
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