As a Validation IS Engineer within our Validation team, you will contribute to ensuring the compliance and reliability of computerized systems supporting the production of essential medicines
Job Summary
As a Validation IS Engineer within our Validation team, you will contribute to ensuring the compliance and reliability of computerized systems supporting the production of essential medicines.
You will take charge of a dedicated scope – MES or digital projects outside of MES – with real autonomy and management of external resources, within a cohesive and complementary team.
Shape the future of pharmaceutical manufacturing by contributing to strategic digital projects (MES, LIMS, ERP) that concretely transform site operations.
Matching Summary
As a Validation IS Engineer within our Validation team, you will contribute to ensuring the compliance and reliability of computerized systems supporting the production of essential medicines.
Skills & Requirements
Must-have
Validation of computerized systems
Pharmaceutical industry experience
Regulatory compliance (FDA, EMA)
Quality management processes
Risk assessment and data analysis
Nice-to-have
Continuous improvement initiatives
Cross-functional team cooperation
Scientific mindset and rigor
Open-mindedness and critical thinking
Key Requirements
5+ years of experience in computerized/automated systems validation
Experience with change management, deviations, CAPA
Experience in SI qualification and validation project management
Higher scientific degree (Bac+5) or equivalent experience