Informations générales Date de parution 19/08/2025 Métier OPERATIONS - ENGINEERING/PRODUCTION Intitulé du poste Validation Engineer - Life Sciences - M/F/X Contrat CDIC Temps de travail Temps plein Description de la mission AKKODIS Belgium is looking for an experienced person in a pharmaceutical environment in the field of validation. Your responsibilities : - Ensure the execution or review of the required pre-tests before starting the final implementation of new processes. - Coordinate all GMP documentation required for change control management (VP - TCD - VSR - QAGMP authorisation - QAGMP approval - external quota documentation, etc.). - Write or revise PQ validation protocols and reports and analyse the results during PQ runs. - Ensure the planning of validations in partnership with the C&M/QA departments and production - Ensure communication with the production team in order to have the raw materials/assemblies/ad hoc resources for the validation. - Ensure the operational management of the technicians dedicated to validations. - Ensure all deviations related to the implementation of the change. - Ensure the follow-up of QC results for each validation cycle. - Ensure timely collection/transfer of approved local documents to the RA department to ensure timely submission. - Ensure review of dossier preparation in partnership with QA prior to submission of dossier to authorities. Secteur Industriel Life sciences Profil Your profile: - You have a master's degree in industrial biology/chemistry or an industrial pharmacist title. - You have experience in project coordination in a pharmaceutical environment. A previous technical background is a plus. - You have experience and technical skills in the pharmaceutical industry. - You are fluent in French and English. Localisation du poste Europe, Belgique, Wallonie Lieu Avenue Jules Bordet 168 1140 Bruxelles Critères candidat Niveau d'études minimum requis 5. Bac 3 / Bac 4 Spécialisation du diplôme Chimie / Biochimie / Pétrochimie Hygiène, Sécurité et Environnement (HSE) Pharmaceutique Gestion de Projet Qualité et gestion des risques Niveau d'expérience 1 à 3 ans