trends and equipment issues, supporting CAPA activities. Assist with installation, commissioning, qualification and validation activities, including IQ/OQ/PQ. Ensure compliance with GMP, GxP and ALCOA+ data integrity requirements. Analyse data from serialisation, automation and production systems to identify opportunities for performance improvement. Support and maintain PLCs, HMIs … related discipline Experience supporting serialisation, automation or packaging line systems within a manufacturing environment. Strong fault‐finding and troubleshooting capabilities Experience working within GMP, pharmaceutical, medical device or other highly regulated environments. Understanding of packaging machinery, automation systems and data integrity requirements. Working knowledge of PLCs, HMIs, vision systems, scanners ...