Baxter seeks a Validations Engineer to lead qualification and startup of new production equipment and lines at its expanding Sabiñánigo facility. The role involves managing validation protocols, coordinating cross-functional teams, and ensuring compliance with GMP and quality standards during industrial transformation projects.
Responsibilities
Manage validation and commissioning of new machines and production lines
Coordinate resources across teams to ensure timely project execution
Develop and maintain technical documentation for standardized operations
Create validation protocols and reports for equipment and process qualification
Monitor project milestones, deadlines, and deliverables to ensure expected outcomes
Requirements
Engineering degree (any specialty)
Prior experience in process or project engineering with validation projects
Background in pharmaceutical sector preferred
Experience in industrial or manufacturing environments
Analytical mindset with focus on continuous improvement
Strong organizational and priority management skills
Professional-level English proficiency