The Project Manager QC is responsible for leading several critical projects within the QC (Quality Control) department, mainly related to laboratory equipment replacement, obsolescence management, and the closure of analytical projects.
More precisely, you will :
* Lead the execution of multiple QC equipment replacement and upgrade initiatives.
* Manage full project lifecycle: planning, budgeting, risk management, and reporting.
* Coordinate all GMP-related activities, including validation (IQ/OQ/PQ), QA reviews, change controls, and required documentation.
* Oversee logistical operations for laboratory equipment: ordering, reception, deinstallation, relocation, installation, and retirement.
* Supervise the completion and closure of ongoing analytical equipment activities, ensuring compliance and timely delivery.
* Support the preparation and structuring of future investment projects, including feasibility assessment and scope definition.
* Maintain dashboards, KPIs, and governance routines; prepare project committees and ensure proactive communication.
What are we looking for?
For this role, we are looking for :
* A medior profile with a scientific or engineering background (biochemistry, pharmacy, chemical engineering, biotechnology...).
* Experience in a GMP pharmaceutical environment.
* Competence in validation, change control, and good understanding of QC laboratory activities.
* Previous experience in project support or project management.
* Knowledge of MS Project is an asset.
* Strong written and verbal communication skills.
* Fluent in French and capable of exchanging in English (written and spoken).