Freelance Validation SpecialistAbout the OpportunityTo support ongoing expansion, we are seeking experienced freelance validation professionals to collaborate on projects within the pharmaceutical and life sciences sector.Role OverviewAs an independent validation specialist, you will reinforce project teams at client sites. Your focus will be on planning, executing, and documenting qualification and validation activities in compliance with current GMP and GxP requirements.Assignments may vary in duration (short- or long-term) depending on project scope, your expertise, and availability. Engagements are primarily located across Belgium and the Netherlands.Key ResponsibilitiesDepending on your background and strengths, responsibilities may include:Qualification of laboratory equipmentCommissioning and qualification of facilities and utility systemsProcess validation and/or cleaning validationComputerized System Validation (CSV)Preparation and review of validation documentationEnsuring compliance with applicable regulatory standardsProfile3–5+ years of hands-on experience in validation within a regulated environmentSolid understanding of GMP, GxP, and life sciences regulatory frameworksAble to work autonomously with a structured and methodical approachStrong communication skills and comfortable interacting with clients and stakeholdersFluent in Dutch and English