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Automation Engineer

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Drebbelogic Ltd 51.00 Euro . EUR Per hour

2024-04-23 03:35:02

Job location Dublin, Dublin, Ireland

Job type: contract

Job industry: Engineering

Job description

POSITION SUMMARY
The Automation Engineer (Utility Systems) will deliver upgrade projects and support Utility Automation Control systems.

KEY RESPONSIBILITIES

  • Supporting Utility Automation Control systems; Waste Water Treatment plant PLC/SCADA system, Utility Automation OEM systems, Electrical Automation System and Building Automation System.
  • Working with SCADA and PLC/HMI environments.
  • Support upgrade projects.
  • Provide troubleshooting and hands-on support to resolve technical issues.
  • Scheduling and coordinating work to tight deadlines.
  • Ensuring that equipment works to its specification.
  • Creating and carrying out test procedures and automation change controls.
  • Liaising with installation/project engineers.
  • Writing reports and documentation.
  • Writing work instructions.
  • Ensuring safe working conditions.
  • Attend Software Factory Acceptance and Site Acceptance Testing.
  • Maintaining and developing change control systems.

QUALIFICATIONS & EXPERIENCE

  • Bachelors Degree in Engineering/Computer Science, or a related engineering field or its equivalent.
  • At least 5 years experience providing automation system solutions and support to manufacturing organisations in the biotechnology or pharmaceutical industry or similar is required.
  • Experience during project delivery and operations support.
  • Experience with Rockwell and Siemens Automation Platforms. Experience of ABB PLC/SCADA platforms would be an advantage.
  • Experience of Windows Server, SQL and Active Directory would be an advantage.
  • A good understanding of computer networking, Subnets, VLANs and Firewall rules.
  • Proven success working well in a team environment with flexibility to react to changing business needs.
  • Working knowledge of GAMP software development lifecycle, ANSI/ISA-S88 industry standards.
  • Thorough knowledge of Pharmaceutical Industry Regulations (cGMP/cGLP, OSHA, EPA/EQB) required.
  • Experience of Validated and Non Validated Control System Documentation practices.
  • In addition, problem solving, critical thinking and project management ability is essential.

HOW TO APPLY
If you're interested in this role, click 'Apply Now' to forward an updated copy of your CV.

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