Informations générales Date de parution 09/12/2025 Métier OPERATIONS - ENGINEERING/PRODUCTION Intitulé du poste CQV Coordinator - Life Science - M/F/X Contrat CDI 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 Commissioning & Qualification. Tasks • Act as C&Q to provide guidance and to manage suppliers and all C&Q activities for the systems, from design to field execution and to summary report approval. • Draft, coordinate review and approval of C&Q documents (URS/ QRA/ SRA/ ERES/DQ/FAT/SAT/IQ/OQ/ VP). • Generate and review Change Controls related to C&Q. • Drive verification testing, protocol execution, walk-downs, verification of system drawings and troubleshoot as required. • Responsible for the Planning, Tracking and Reporting of C&Q status and risks/issues for the selected systems. • Conduct deviation investigation and resolution, take appropriate corrective actions as required. • Responsible for the Planning, Tracking and Reporting of C&Q status and risks/issues for the selected systems. • Ensure Start-up of equipment/ system is completed in a safe and coordinated manner. Raja BOUDAIA -Talent Aquisition Officer AKKODIS Raja.BOUDAIA@akkodis.com Secteur Industriel Life sciences Profil Profile • Bachelor or Master's degree in Engineering or in Life Sciences with relevant experience. • Experience delivering Commissioning and Qualification for Pharmaceutical / Biotechnology projects. • Knowledge of GxP. • Understanding of a risk-based approach to C&Q. • You are fluent in French and English. Localisation du poste Europe, Belgique, Wallonie Lieu Brabant Wallon Télétravail 1-2 jours par semaine Critères candidat Niveau d'études minimum requis 5. Bac 3 / Bac 4 Spécialisation du diplôme Bio-technologie Chimie / Biochimie / Pétrochimie Hygiène, Sécurité et Environnement (HSE) Pharmaceutique Niveau d'expérience Tous niveaux d'expérience Langues Français (4 : Expert - Bilingue) Anglais (3 : Courant - Confirmé)