This role sits within the Commissioning, Qualification and Validation (CQV) and automation function at a large-scale pharmaceutical manufacturing site, operating within a strict GMP (Good Manufacturing Practice) environment. The successful candidate will provide hands-on 800xA Batch Automation Engineer, working closely with the site's C&I and automation teams to maintain, configure and troubleshoot the batch control system.
Work basis: On-site presence required
Rotation: Participation in rotation work, including weekends, is required