Senior CSV Engineer: Automation Validation & GMP

SimoTech seeks a CSV Engineer to support validation for a Drug Product Facility project for a biopharmaceutical client in Co. Dublin.

The candidate will author and manage C&Q plans, URS, FAT and IOQ documentation, and collaborate with SMEs, vendors and quality teams to ensure regulatory compliance and timely delivery. With 6+ years in GMP and validation, you will oversee FAT/IOQ execution, develop validation templates, and ensure traceability across cQ and automation documentation.