QA Validation OfficerBrabant Wallon | Contracting Your Responsibilities:Review and approval of validation documentation (URS, protocols, reports) in compliance with GMP standardsSupervision and quality oversight of validation activities (IQ, OQ, PQ)Ensure proper execution and documentation of FAT (Factory Acceptance Testing) and SAT (Site Acceptance Testing)Support equipment qualification processes from installation through performance qualificationCollaborate with internal and external stakeholders to ensure validation strategy alignmentEnsure compliance with company procedures and regulatory expectations (FDA, EMA)Provide QA input during audits and inspections as a subject matter expert on validationYour Profile:Proven experience in a GMP-regulated environment, ideally at GSK or similarSolid background in equipment validation (IQ, OQ, PQ)Knowledge of validation methodologies, including FAT and SATFamiliarity with pharmaceutical manufacturing and quality systemsFluent in English and French (spoken and written)Strong attention to detail, organizational skills, and a proactive mindsetAbility to work cross-functionally and communicate effectively with technical and QA teamsOur Offer:Jefferson Wells offers you a permanent consultant contract with a competitive salary and a wide range of training opportunities. As your trusted career partner, we’ll support you every step of the way.Interested? Send your CV to jason.devillers@jeffersonwells.be