Junior QA / Validation Test Lead – Life Sciences / LIMSLocation: Beerse, BelgiumWork Mode: HybridContract: 1-year, renewable (long-term project)Rate: €425 per day (market-aligned for junior/mid-level)Role SummaryWe are looking for a Junior QA / Validation Test Lead to support laboratory information systems (LIMS) implementations, upgrades, and sustainment programs within regulated Life Sciences environments. The role focuses on hands-on testing, validation support, and compliance activities, working closely with senior QA and validation teams.This is an excellent opportunity for candidates with 2–5 years of Life Sciences validation experience, who want to grow into a Test Lead role while working with LIMS, MES, DeltaV, and regulated systems.Key Responsibilities1. Testing & Validation SupportExecute testing and validation of LIMS modules: sample lifecycle, stability management, lab workflows, and reportingPerform instrument integration testing and API validation (as applicable)Execute functional, regression, and compliance testing under CSV protocolsSupport FAT / SAT, IQ / OQ / PQ activities and system qualification2. CSV & Regulatory ComplianceSupport Computer System Validation (CSV) lifecycle documentation: URS, FS, RA, IQ/OQ/PQ, Traceability MatrixEnsure adherence to GxP standards, FDA 21 CFR Part 11, EU Annex 11, and ALCOA+ data integrity principlesAssist in internal and external audits, documentation review, and validation approval processes3. Tools & ReportingUse test management tools such as JIRA, Xray, ALM, or similar for test execution, defect logging, and reportingAssist in reporting quality metrics, defect dashboards, and release readiness status4. Stakeholder CollaborationCollaborate with laboratory SMEs, QA teams, regulatory teams, and vendorsSupport multi-vendor coordination and defect triage forums under guidance5. Optional / Nice-to-HaveExposure to test automation, AI-based defect prediction, or regression optimization is a plusMandatory Skills / Experience2–5 years of QA / Validation experience in Life Sciences / Pharma environmentHands-on LIMS experience (LabWare, LabVantage, Sample Manager, aLIMS, rLIMS, or similar)Experience with CSV / validation documentation (IQ/OQ/PQ, VMP, Traceability Matrix, URS)Knowledge of GxP, FDA 21 CFR Part 11, EU Annex 11, ALCOA+Experience with test management tools (JIRA, Xray, ALM, Confluence)Strong stakeholder communication skills and ability to work in hybrid team setupsEnglish fluency (spoken & written)Preferred / Nice-to-Have SkillsExposure to test automation (writing or reviewing automated scripts, API testing)Experience in data migration validationMulti-vendor testing coordination experiencePharma regulatory audit support experienceCandidate ProfileMid-level QA / Validation professional aiming to take on a Test Lead roleStrong interest in LIMS and Life Sciences systemsHands-on experience in validation testing, documentation, and regulatory complianceWilling to work in hybrid mode in Beerse, BelgiumWhy Join UsHands-on experience with LIMS, MES, DeltaV, and regulated lab systemsOpportunity to work under experienced senior QA / Validation leadershipHybrid work mode with long-term project stabilityCompetitive day rate (€425/day) for junior/mid-level Life Sciences QA / Validation talent