Commissioning & Qualification EngineerAKKODIS Belgium is looking for an experienced person in a pharmaceutical environment in the field of Commissioning & Qualification.What are your responsibilities?
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.
Who are you?
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.
What's the offer you can't refuse?As an AKKODIS Team Member, you will be:
Onboarded in your position via a buddy process
Supported in your career by your Business Manager
Actor of your training plan and your personal and professional development
Benefiting from a permanent contract
Benefiting from a competitive salary package including several extra-legal benefits
Interested? I invite you to send me your resume to the following mail adress: marie.defruit@akkodis.com
