About AvertimAvertim is a uniquely positioned management consulting group that bridges the gap between strategy, technology, and operations. Founded in 2007 and headquartered on Brussels' iconic Avenue Louise, Avertim has grown into a European consultancy with over 350 consultants across Belgium, France, Germany, and the Netherlands.Our mission: to support leading Life Sciences companies in their digital transformation journey, helping them unlock the power of data, innovation, and compliance.Your role as a Validation EngineerAs a Validation Engineer, you are responsible for ensuring that equipment, systems and processes comply with applicable GMP and regulatory requirements. You work closely with Quality, Engineering and Operations teams and contribute to maintaining and improving validated states.You are part of the Avertim consulting team and receive guidance and support from your Business Manager.Your responsibilitiesPerform qualification and validation activities for equipment, utilities, processes and cleaningPrepare and review validation documentation such as URS, risk assessments and IQ/OQ/PQ protocols and reportsSupport CSV activities where applicableManage deviations, CAPAs and change controlsSupport internal and external audits and inspectionsEnsure compliance with GMP guidelines and quality standardsYour profileMaster's degree in a scientific or technical field (engineering, life sciences, pharmacy, chemistry, biomedicine, ...)1 to 5 years of experience in validation and/or a GMP-regulated environmentSolid understanding of GMP principlesStructured, detail-oriented and hands-onFluent in English and Dutch (French is a plus)Willing to work in a consulting environmentWhat Avertim OffersA dynamic environment where ideas and individuals matterA young, vibrant, and fast-growing teamAccess to a European network of cross-industry expertiseContinuous learning and career development opportunitiesA competitive compensation package aligned with your experience