CSV Engineer — Global Pharma Validation

Job OverviewAs a qualification engineer you will work on projects in the life science industry. You will ensure that products, processes, systems, services, and documentation meet regional and global quality regulations and standards.ResponsibilitiesWork in a laboratory or production environment, or relate to business technologies.Perform computer system...

As a qualification engineer you will work on projects in the life science industry. You will ensure that products, processes, systems, services, and documentation meet regional and global quality regulations and standards.Activities take place in a laboratory or production environment, or can relate to business technologies.Key area(s) of work...

Job OverviewAs a qualification engineer you will work on projects in the life science industry. You will ensure that products, processes, systems, services, and documentation meet regional and global quality regulations and standards.ResponsibilitiesWork in a laboratory or production environment, or relate to business technologies.Perform computer system...

Capgemini in Belgium (Diegem) seeks a Computer System Validation (CSV) Engineer to ensure computerized systems in regulated environments meet compliance and function as intended. You will develop and execute validation strategies across cross-functional teams, aligning with ISPE GAMP5 principles.You will work on validating automated systems in pharmaceutical...

Your roleAs an Engagement Manager for MES Pharma, you will be the strategic and operational leader responsible for managing complex digital manufacturing programs within regulated pharmaceutical environments. Acting as a trusted advisor to senior client stakeholders, you will combine deep MES expertise with strong delivery leadership and business development...

Your role As Technical Lead for a PAS-X MES Roll-out Program, you will provide end-to-end technical leadership across site-level MES implementations within a complex, multi-site pharmaceutical manufacturing environment. You will be the go-to technical authority, ensuring architectural consistency, integration quality, and compliance with corporate standards...