PLC/SCADA Automation Engineer

PLC/SCADA Automation Engineer

Posted 4 days ago by 1756284359

Negotiable
Undetermined
Undetermined
Ireland, Dublin

Summary: The PLC/SCADA Automation Engineer role in Dublin involves managing and executing automation projects, including installations and upgrades of vendor package equipment systems. The position requires compliance with site standards and collaboration with vendors under the direction of the Automation Manager. Candidates should possess a strong background in engineering and automation systems, particularly in a GMP environment. This is a 12-month contract opportunity with a leading company in the industry.

Key Responsibilities:

  • Maintain compliance at all times with Site standards and procedures.
  • Manage/execute the installation of Obsolescence Upgrades to Automation Elements on Vendor Package Equipment systems.
  • Manage Vendor activities on Obsolescence and upgrade projects under direction of Automation Manager.
  • Manage/execute the installation, commissioning and qualification of new Vendor Package Equipment systems.
  • Support Commissioning activities.
  • Witness or perform FAT & SAT execution.
  • Draft, review and approve Automation Change Packs to support all system remediation, optimisations at various stages of the project.
  • Author Validation plans and pre and post approve executed FAT/SAT protocols.
  • Develop, review, and approve VPE SOPs.
  • Prepare Permit to work, SPAs etc for work on active projects as required.

Key Skills:

  • Bachelor's Degree (or equivalent) in Engineering, Science or a related field.
  • In-depth knowledge of Rockwell Automation Control-Logix, Studio 5000 and FT View essential.
  • Knowledge of Siemens S7, Win CC and TIA Portal an advantage.
  • Basic knowledge of DCS Systems Delta V / Honeywell an advantage.
  • Knowledge of Clean/Grey Utilities systems.
  • Knowledge of Process systems; Centrifuge, Parts Washers, Autoclaves.
  • An understanding of applicable regulations such as Annex 11, GAMP and 21 CFR Part 11.
  • 7+ years’ experience in a GMP environment, preferably Pharma/Biopharma.
  • Strong problem solving skills.
  • Ability to work as part of a wider team and to Lead project upon direction of Manager.

Salary (Rate): undetermined

City: Dublin

Country: Ireland

Working Arrangements: undetermined

IR35 Status: undetermined

Seniority Level: undetermined

Industry: Other

Detailed Description From Employer:

PLC/SCADA Automation Engineer - Dublin - 12 month contract

Do you want to work with an exciting company who are an established market leader within their niche field? We have a fantastic opportunity for a PLC/SCADA Automation Engineer to join one of our industry leafing clients in Ireland.

Responsibilities

  • Maintain compliance at all times with Site standards and procedures.
  • Manage/execute the installation of Obsolescence Upgrades to Automation Elements on Vendor Package Equipment systems.
  • Manage Vendor activities on Obsolescence and upgrade projects under direction of Automation Manager.
  • Manage/execute the installation, commissioning and qualification of new Vendor Package Equipment systems
  • Support Commissioning activities
  • Witness or perform FAT & SAT execution
  • Draft, review and approve Automation Change Packs to support all system remediation, optimisations at various stages of the project
  • Author Validation plans and pre and post approve executed FAT/SAT protocols.
  • Develop, review, and approve VPE SOPs
  • Prepare Permit to work, SPAs etc for work on active projects as required

Qualifications
  • Bachelor's Degree (or equivalent) in Engineering, Science or a related field
  • In-depth knowledge of Rockwell Automation Control-Logix, Studio 5000 and FT View essential
  • Knowledge of Siemens S7, Win CC and TIA Portal an advantage
  • Basic knowledge of DCS Systems Delta V / Honeywell an advantage
  • Knowledge of Clean/Grey Utilities systems;
  • Knowledge of Process systems; Centrifuge, Parts Washers, Autoclaves
  • An understanding of applicable regulations such as Annex 11, GAMP and 21 CFR Part 11
  • 7+ years’ experience in a GMP environment, preferably Pharma/Biopharma
  • Strong problem solving skills
  • Ability to work as part of a wider team and to Lead project upon direction of Manager

If this role is of interest to you, please apply now!

#LI-BP1