Validation Specialist IS (GxP) -CDI- F/M

Your mission

R&D Pharma Pierre Fabre is hiring in Toulouse (Langlade, Oncopole) a Validation Specialist IS to be responsible for ensuring that GxP Information Systems—on premise and cloud based—are validated, compliant, and maintained in a validated state throughout their lifecycle, in line with regulatory requirements and internal Quality standards.

The role supports both RUN and CHANGE activities for R&D Pharma systems and plays a key role in modern validation approaches, including cloud environments (e.g. AWS or AZURE) and scripted / automated validation, while ensuring audit and inspection readiness.
 

Your role within a pioneering company in full expansion:

IS Validation & Compliance