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    Automation Engineer REF: 214MQ - Dublin, Ireland - Headcount

    Headcount
    Headcount Dublin, Ireland

    1 week ago

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    Description

    Headcount Solutions is recruiting an Automation Engineer (Utility Systems) for projects at a multination client's facility in Dublin. 12-Month Minimum

    Reporting to the Associate Director Automation Systems this person will support Utility Automation Control systems such as the Waste Water Treatment plant PLC/SCADA system, Utility Automation OEM systems, Electrical Automation System and Building Automation System.

    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.

    · Creating and carrying out test procedures and automation change controls.

    · Liaising with installation/project engineers.

    · Writing reports, documentation, and work instructions.

    · Training maintenance and operative staff where appropriate.

    · 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.

    · Minimum 5 years' experience providing automation system solutions and support to manufacturing organisations in the biotechnology or pharmaceutical industry or similar is required.

    · 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.

    · 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.

    For further information, please contact Mick on (phone number removed) or forward details in confidence to

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