Requirements: English
Company: Akkodis
Region: Mons , Wallonia
AKKODIS Belgium is looking for an experienced personin a pharmaceutical environment in the field of Commissioning &Qualification. Tasks Act as C&Q to provide guidance and tomanage suppliers and all C&Q activities for the systems, fromdesign 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 Controlsrelated to C&Q. Drive verification testing, protocolexecution, walk-downs, verification of system drawings andtroubleshoot as required. Responsible for the Planning, Trackingand Reporting of C&Q status and risks/issues for the selectedsystems. Conduct deviation investigation and resolution, takeappropriate corrective actions as required. Responsible for thePlanning, Tracking and Reporting of C&Q status and risks/issuesfor the selected systems. Ensure Start-up of equipment/ system iscompleted in a safe and coordinated manner. Profile Bachelor orMaster''s degree in Engineering or in Life Sciences with relevantexperience. Experience delivering Commissioning and Qualificationfor Pharmaceutical / Biotechnology projects. Knowledge of GxP. Understanding of a risk-based approach to C&Q. You are fluentin French and English. Raja BOUDAIA -Talent Aquisition OfficerAkkodis Raja.BOUDAIA@akkodis.com