Vie Life Sciences Computer System Validation Engineer Belgium - 2 Years H/F - 75

Sopra Steria offers tailored, end-to-end corporate technology and software solutions to help clients make bold choices and deliver results. Successfully so ! With more than 51.000 colleagues in 30 countries, we rank as Europe's leading digital solutions provider. Some of the most successful companies in Europe rely on our technology due to our commitment to innovation, collaboration, and value in business development.

The world is how we shape IT. Let's shape IT together.Our Life Sciences department specializes in supporting pharmaceutical, biotech, and medical device companies in achieving regulatory compliance and operational excellence. We focus on the validation of GxP-critical systems across all domains (GLP, GCP, GMP, GDP, GPvP), ensuring data integrity, patient safety, and product quality. From local lab tools to global enterprise platforms, we help clients navigate complex regulatory landscapes through expert consulting, validation services, and digital transformation initiatives.

As a V.I.E. in the Life Sciences division, you will support the validation and compliance of computerized systems used in regulated environments. Your mission is to help ensure that GxP systems-ranging from lab instruments to enterprise platforms-meet regulatory standards throughout their lifecycle. You'll contribute to audits, stay informed on evolving regulations (EMA, FDA, GAMP, ISO), and work closely with Sopra Steria's validation service teams.