Pharma Automation Engineer — PLC/SCADA & GMP Impact

Recordati; Milano; Ibrido; EUR 39.000 - 47.000; Tempo pieno

Descrizione del lavoro

Recordati is seeking an Automation Engineer to support industrial automation across our pharmaceutical manufacturing sites in Italy. You will work on maintenance, optimization and development of plant control and supervisory systems while ensuring GMP compliance and safety.

Key tasks include PLC/SCADA improvements, FAT/SAT activities, CSV support, and cross-functional collaboration with Production, Maintenance, Quality and Engineering. Fluent Italian and strong English are required.

Competenze

• Bachelor's or Master's degree in Automation Engineering, Electronic Engineering, Mechatronics Engineering, Industrial Computer Science, or a related field.
• 2-3 years of professional experience.
• Experience with PLC/SCADA platforms and HMI/SCADA systems.
• Familiarity with GMP environments and pharmaceutical regulations is advantageous.

Mansioni

• Support maintenance and management of plant automation systems across manufacturing sites.
• Assist in implementation, modification, and enhancement of PLC and SCADA systems.
• Participate in continuous improvement and digitalization projects for manufacturing processes.
• Perform troubleshooting and failure analysis on automated systems; coordinate with suppliers and site teams as needed.
• Support CSV and qualification activities; prepare and update technical documentation and SOPs.

Conoscenze

PLC programming

HMI/SCADA

Data integrity/NIS2

Industrial networks OT

Microsoft Office

Problem solving

Teamwork

Formazione

Bachelor's or Master's in Automation/Engineering

Strumenti

Siemens S7

Rockwell

ABB

Mitsubishi

Schneider Electric

iFIX

Ignition

Profinet

Ethernet/IP

Modbus

Descrizione del lavoro

Recordati is seeking an Automation Engineer to support industrial automation across our pharmaceutical manufacturing sites in Italy. You will work on maintenance, optimization and development of plant control and supervisory systems while ensuring GMP compliance and safety.

Key tasks include PLC/SCADA improvements, FAT/SAT activities, CSV support, and cross-functional collaboration with Production, Maintenance, Quality and Engineering. Fluent Italian and strong English are required.