QA Validation Officer Brabant Wallon | Contracting Your Responsibilities: Review and approval of validation documentation (URS, protocols, reports) in compliance with GMP standards Supervision 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 qualification Collaborate with internal and external stakeholders to ensure validation strategy alignment Ensure compliance with company procedures and regulatory expectations (FDA, EMA) Provide QA input during audits and inspections as a subject matter expert on validation Your Profile: Proven experience in a GMP-regulated environment, ideally at GSK or similar Solid background in equipment validation (IQ, OQ, PQ) Knowledge of validation methodologies, including FAT and SAT Familiarity with pharmaceutical manufacturing and quality systems Fluent in English and French (spoken and written) Strong attention to detail, organizational skills, and a proactive mindset Ability to work cross-functionally and communicate effectively with technical and QA teams Our 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