Automation Engineer - Pharmaceutical

Automation and CSV Engineer (Permanent) - West YorkshirePharmaceutical Manufacturing High-Tech GMP Environment Career Growth OpportunityAn exciting opportunity is available for an Automation and Computer System Validation (CSV) Engineer to join a highly regulated manufacturing environment within the pharmaceutical/life sciences sector.This role is ideal for an engineer who enjoys working at the intersection of automation, validation, digital systems, and manufacturing operations. You''ll play a key role in supporting critical production systems, driving continuous improvement initiatives, and ensuring compliance across computerized and automated processes.Key ResponsibilitiesSupport and maintain automation and control systems across manufacturing operationsTroubleshoot equipment and process-related automation issuesParticipate in computerized system validation (CSV) activities within a GMP-regulated environmentAssist with qualification, commissioning, and lifecycle management of automated systemsSupport continuous improvement and process optimization projectsCollaborate with engineering, production, quality, and external vendorsMaintain technical and validation documentation in line with regulatory expectationsContribute to data integrity and compliance initiativesProvide technical support and training to operational teamsIdeal BackgroundDegree qualified in Automation, Electrical, Electronics, Mechatronics, or related Engineering disciplineExperience working with PLC, HMI, ..... full job details .....