Are you an experienced validation engineer looking for a new opportunity in Cork, Ireland? Do you have experience with automation equipment in a manufacturing environment and within the life sciences industry? Are you interested in joining a global leader in medical technologies? Don't hesitate … apply todayJob DescriptionOur client are seeking an experienced validation engineer who can provide advanced technical and engineering support for upcoming projects in their manufacturing division. This engineer will use the required engineering competencies to support their team.ResponsibilitiesResponsible for managing and delivering key project tasks assignedWork with automation vendors, engineering, and other functions in delivering key project task assignedGenerate, review, and approve project validation documentation URS, PFMEA's FAT, SAT, VP, IQ, OQ, PQ, reports, procedures, and other documents as required compliant with current Good Manufacturing Practices (GMP)Execute validation qualification test protocols documentsSupport debugging the automated system with structured problem solving and providing feedback to the project team and vendorSupport install of the automation system at the site in readiness for qualification.RequirementsLevel 8 Degree in Mechanical EngineeringProven validation experience2-4 years' experience in a manufacturing environmentExperience in an FDA regulated or regulated industry beneficialBenefitsCompetitive and attractive employee compensation packagePension contributionsHealth insurancePaid public holidaysLocation:Cork, IrelandDesired Skills and ExperienceResponsibilitiesResponsible for managing and delivering key project tasks assignedWork with automation vendors, engineering, and other functions in delivering key project task assignedGenerate, review, and approve project validation documentation URS, PFMEA's FAT, SAT, VP, IQ, OQ, PQ, reports, procedures, and other documents as required compliant with current Good Manufacturing Practices (GMP)Execute validation qualification test protocols documentsSupport debugging the automated system with structured problem solving and providing feedback to the project team and vendorSupport install of the automation system at the site in readiness for qualification.RequirementsLevel 8 Degree in Mechanical EngineeringProven validation experience2-4 years' experience in a manufacturing environmentExperience in an FDA regulated or regulated industry beneficial