Quality Assurance Engineer

About the Role:Our client, a specialist cleanroom fit-out contractor working exclusively in the pharmaceutical sector, is seeking an experienced Quality Assurance Engineer to support the delivery of cleanroom fit-out projects in Limerick. This is a hands-on, site-based role focused on quality management throughout the fit-out phase, from installation through to final handover. You will work on GMP-compliant cleanroom environments in a fast-paced construction setting.Key Responsibilities:Manage quality documentation and compliance throughout the fit-out phase using Procore or similar project management platformsSet up and manage Inspection Test Plans (ITPs), ensuring all quality procedures and documentation are completeCollate and organize turnover packages/handover packs for client delivery, ensuring all documentation is audit-readyLead snagging walkdowns and coordinate defect resolution with site teams and subcontractors for client handoverConduct site inspections and quality audits on cleanroom installations, partitioning, finishes, and associated fit-out worksWork closely with construction teams, subcontractors, and the client to resolve quality issues on-siteEnsure all work is completed to specification, on schedule, and meets regulatory requirementsProvide technical support and problem-solving throughout the project lifecycleEssential Requirements:Proven experience as a Quality Assurance Engineer on construction or fit-out projectsStrong background in quality management within pharma, cleanroom, or GMP-regulated environmentsHands-on experience setting up Inspection Test Plans (ITPs) and quality documentationExperience with snagging processes, defect management, and final handover proceduresProficiency using Procore or equivalent construction management softwareExcellent communication and coordination skills with ability to liaise effectively with clients and site teamsAbility to work independently on fast-paced construction sitesDesirable Skills:Experience with pharma cleanroom or controlled environment fit-out projectsKnowledge of GMP requirements and pharma construction quality standardsFamiliarity with cleanroom classifications and associated compliance requirementsApply here or email your CV directly to m.firnett@x4lifesciences.com