Associate Automation Engineer — Pharma GMP Systems

Novo Nordisk A/S

Frosinone

On-site

EUR 37,000 - 60,000

Full time

2 days ago
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Job summary

Novo Nordisk A/S in Anagni, Italy, seeks an Associate Automation Engineer to support automation systems across aseptic formulation, filling, facilities and utilities. You will develop and implement automation/IT/OT work packages with external partners, ensuring reliability, compliance and readiness for production.

The role requires 1–3 years in regulated manufacturing, knowledge of PLC/SCADA, GMP, and strong English communication.

Qualifications

  • Degree in Automation, Electrical, Electronic, Industrial Engineering, Computer Science, or related field.
  • 1–3 years in pharma/biotech or regulated process manufacturing with automation/IT/OT experience.
  • Working knowledge of PLC, SCADA and process control systems.

Responsibilities

  • Plan and deliver defined automation and IT/OT activities with scope, schedules and quality criteria.
  • Support installation, configuration, integration and commissioning of systems in formulation, filling, facilities and utilities.
  • Collaborate with vendors and system integrators, tracking milestones and deliverables with the PM.
  • Assist testing and validation activities (FAT, SAT, IQ, OQ) and maintain documentation.
  • Monitor and troubleshoot automation and process control systems; resolve incidents with site teams.
  • Investigate deviations, contribute to root-cause analyses and implement improvements through change control.
  • Support operational readiness and handover of new or modified systems to production teams.

Skills

PLC
SCADA
Process control
Vendor interaction
GMP
English communication

Education

University degree in Automation/Electrical/Electronic/Industrial Engineering or Computer Science

Job description

Novo Nordisk A/S in Anagni, Italy, seeks an Associate Automation Engineer to support automation systems across aseptic formulation, filling, facilities and utilities. You will develop and implement automation/IT/OT work packages with external partners, ensuring reliability, compliance and readiness for production.

The role requires 1–3 years in regulated manufacturing, knowledge of PLC/SCADA, GMP, and strong English communication.

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