Automation Engineer
pfor the site Borgo San Michele LT, Italy /pWould you like to make a valuable contribution to the health of patients? And do something really meaningful on your own responsibility? Then we look forward to hearing from you! Excellence beyond manufacturing - that's what we stand for as Aenova, one of the world's leading contract manufacturers and developers for the pharmaceutical industry with 4,000 employees at 15 sites. Latina is a leading centre of excellence in sterile liquid production, with a strategic investment plan to become one of Europe's foremost hubs.ph3Automation Engineer /h3pfor the site Borgo San Michele LT, Italy /pWould you like to make a valuable contribution to the health of patients? And do something really meaningful on your own responsibility? Then we look forward to hearing from you! Excellence beyond manufacturing - that's what we stand for as Aenova, one of the world's leading contract manufacturers and developers for the pharmaceutical industry with 4,000 employees at 15 sites. Latina is a leading centre of excellence in sterile liquid production, with a strategic investment plan to become one of Europe's foremost hubs.h3Your key responsibilities /h3ulliContribute to the design, implementation and continuous improvement of automation systems and OT infrastructures, supporting automation and digitalization projects across the site. /liliManage automation projects from requirements definition through design, installation, integration and start-up, working closely with Manufacturing, Engineering, Quality, Validation and IT. /liliPrepare and review technical specifications,
system architectures, risk assessments and automation documentation. /liliCoordinate suppliers, OEMs and system integrators, ensuring effective technical execution of projects. /liliParticipate in design reviews, FAT, SAT, commissioning and qualification activities. /liliManage hardware and software modifications in accordance with site Change Control processes. /liliSupport the integration of PLC, SCADA, HMI, MES and enterprise systems. /liliContribute to automation standards, system lifecycle and obsolescence management, as well as backup, restore and disaster recovery strategies. /liliSupport compliance with GMP, Data Integrity and OT cybersecurity requirements in collaboration with Quality, Validation and IT/OT Security. /liliProvide technical expertise in troubleshooting and resolving complex automation issues. /li /ulh3Your profile /h3ulliDegree in Automation, Electronic, Electrical, Computer or Mechatronics Engineering, or a technical diploma combined with relevant professional experience. /liliAt least 3 years of experience in industrial automation. /liliWorking knowledge of PLC programming with Siemens TIA Portal and SIMATIC S7-1500.
/liliSolid knowledge of SCADA systems, particularly iFIX, including configuration, development and application troubleshooting. /liliExperience in the technical management and delivery of automation projects. /liliGood knowledge of industrial communication protocols such as Profinet, Profibus, Modbus TCP/RTU, OPC DA and OPC UA. /liliFamiliarity with Windows servers, virtualization, databases and OT infrastructures, as well as the ability to work with electrical drawings, PIDs and automation technical documentation. /liliExperience coordinating suppliers and system integrators is a plus. /liliKnowledge of Siemens HMI, Ignition SCADA, MES/historian systems and SQL databases would be a plus. /liliExperience in pharmaceutical or other regulated environments, including knowledge of GMP, Data Integrity and 21 CFR Part 11, would be highly valued. /liliKnowledge of FAT, SAT and commissioning. /liliQualifications are considered an advantage. /liliFluency in English. /liliAnalytical mindset, project orientation, autonomy and a collaborative approach when working with cross-functional and international teams. /li /ulpAnnual salary range: € 40.000 - 45.000 /ph3Your motivation /h3Are you looking for new challenges in a highly competitive environment? And you want to tackle them creativelyand on your own responsibility? Do you prefer a "get-it-done" culture and think in terms of solutions ratherthan problems? What are you waiting for? We would be happy to explain our corporate benefits in a personalconversation! /p #J-18808-Ljbffr
system architectures, risk assessments and automation documentation. /liliCoordinate suppliers, OEMs and system integrators, ensuring effective technical execution of projects. /liliParticipate in design reviews, FAT, SAT, commissioning and qualification activities. /liliManage hardware and software modifications in accordance with site Change Control processes. /liliSupport the integration of PLC, SCADA, HMI, MES and enterprise systems. /liliContribute to automation standards, system lifecycle and obsolescence management, as well as backup, restore and disaster recovery strategies. /liliSupport compliance with GMP, Data Integrity and OT cybersecurity requirements in collaboration with Quality, Validation and IT/OT Security. /liliProvide technical expertise in troubleshooting and resolving complex automation issues. /li /ulh3Your profile /h3ulliDegree in Automation, Electronic, Electrical, Computer or Mechatronics Engineering, or a technical diploma combined with relevant professional experience. /liliAt least 3 years of experience in industrial automation. /liliWorking knowledge of PLC programming with Siemens TIA Portal and SIMATIC S7-1500.
/liliSolid knowledge of SCADA systems, particularly iFIX, including configuration, development and application troubleshooting. /liliExperience in the technical management and delivery of automation projects. /liliGood knowledge of industrial communication protocols such as Profinet, Profibus, Modbus TCP/RTU, OPC DA and OPC UA. /liliFamiliarity with Windows servers, virtualization, databases and OT infrastructures, as well as the ability to work with electrical drawings, PIDs and automation technical documentation. /liliExperience coordinating suppliers and system integrators is a plus. /liliKnowledge of Siemens HMI, Ignition SCADA, MES/historian systems and SQL databases would be a plus. /liliExperience in pharmaceutical or other regulated environments, including knowledge of GMP, Data Integrity and 21 CFR Part 11, would be highly valued. /liliKnowledge of FAT, SAT and commissioning. /liliQualifications are considered an advantage. /liliFluency in English. /liliAnalytical mindset, project orientation, autonomy and a collaborative approach when working with cross-functional and international teams. /li /ulpAnnual salary range: € 40.000 - 45.000 /ph3Your motivation /h3Are you looking for new challenges in a highly competitive environment? And you want to tackle them creativelyand on your own responsibility? Do you prefer a "get-it-done" culture and think in terms of solutions ratherthan problems? What are you waiting for? We would be happy to explain our corporate benefits in a personalconversation! /p #J-18808-Ljbffr