31 lug - Lazio
Experteer Italy
ppIn this Automation Engineer role at Novo Nordisk Anagni, you design, implement and optimise automation across the full lifecycle to boost production performance, compliance and patient delivery.
You work within the Automation Engineering team to connect manufacturing equipment, OT and digital systems, enabling scalable, high-quality operations.
You will lead multi-disciplinary automation activities from design to commissioning and validation, driving efficient, compliant GMP manufacturing.
This hands-on project role offers cross-functional collaboration with vendors, sites and stakeholders to deliver robust automation solutions with measurable impact.
/pullicontinuous learning /liliincentives and benefits package /lilicross-functional exposure /lilicompetitive salary range /liliLead automation integration for manufacturing systems across aseptic formulation, filling equipment, facilities and utilities /liliCoordinate installation, commissioning, testing and validation activities (FAT, SAT, IQ, OQ) for automation and OT systems /liliSupport lifecycle of automation hardware, software and OT infrastructure including backup, monitoring and robotic automation /liliManage project timelines, budgets,
resources and stakeholder communication to meet objectives /liliTroubleshoot automation-related issues during start-up and ensure regulatory and technical compliance /liliIdentify opportunities to replace manual processes with automation to improve efficiency and scalability /liliCollaborate with cross-functional teams, vendors and international project stakeholders to align automation with site and business priorities /liliMaster in Automation Engineering, Electrical Engineering, Electronic Engineering, Industrial Engineering or related field /lili8+ years of automation experience in pharmaceutical, biotech or aseptic manufacturing /liliStrong knowledge of PLC, SCADA, DCS, industrial automation protocols and OT architecture /liliExperience with MES and integration between MES, OT and SCADA /liliKnowledge of validation processes (FAT, IQ/OQ, PQ) and GMP, FDA 21 CFR Part 11 and GAMP 5 /liliProject management experience including timelines, budgets, resources and stakeholder coordination /liliAnalytical, problem-solving and communication skills across departments and suppliers /liliExperience with robotic automation, advanced programming, automation infrastructure, backup or monitoring is advantageous /li /ul /p #J-*****-Ljbffr
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