The role
0301Configure and implement the MES product portfolio, including intake files, master data, recipes, workflows, and test work orders, to support a smooth production go-live and enable connected manufacturing, real-time data visibility, advanced analytics, and predictive, adaptive processes.
02Support the transition from BabtecQ CAQ to Critical Manufacturing CAQ and contribute to related system and process changes.
03Support master data preparation, cleansing, migration, and verification activities related to MES, CAQ.
04Provide MES shopfloor and post-go-live support, including hypercare, user guidance, issue escalation, operator feedback follow-up and production coordination.
05Maintain compliance and business continuity by troubleshooting CM MES issues and deviations, performing root cause analysis, supporting system recovery, defining workarounds, and escalating when needed.
06Drive MES-related procedure updates and support user engagement through training materials, hands-on coaching, knowledge transfer, and competency assessments.
07Collaborate with Engineering, Quality, Operations, Planning, and IT to align MES activities with production and business needs.
08Use MES, Industry 4.0 solutions, and data-driven methods to monitor, analyze, and improve medical device manufacturing and production processes.
09Identify continuous improvement opportunities, implement new digital technologies, and acquire data from manufacturing systems such as CNC machines, finishing equipment, and heat treatment systems.
10Support engineering projects by planning and executing activities, tracking progress and costs, preparing status reports, maintaining documentation, and meeting agreed goals and timelines.
