CQV Coordinator - Life Science - M/F/X

Métier

OPERATIONS - ENGINEERING/PRODUCTION

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

[email protected]

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.

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)