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    Process Engineer

    LimerickContractCompetitive
    Back to job search
    2 hours ago
    JN -102025-1989706
    New

    Process Engineer

    Limerick Contract Competitive

    Process Engineer

    About the job

    We are seeking a Process Engineer to provide specialist technical support for bioprocess systems as part of a major capital investment project. This role is focused on process design, system implementation, and lifecycle support to ensure operational readiness, safety, and compliance with industry standards.

    Key Responsibilities:

    • Develop User Requirement Specifications (URS) for designated systems.
    • Review and sign off on Basis of Design (BOD), detailed engineering deliverables, and key process documentation such as PFDs and P&IDs.
    • Ensure all procurement documentation (e.g., BOMs, datasheets, technical cut-sheets) aligns with internal equipment standards.
    • Monitor and close out HAZOP-related actions, integrating outcomes into design deliverables.
    • Participate in design model reviews (30%, 60%, 90%) to validate that systems are safe, practical, and fit for purpose.
    • Approve and maintain system lifecycle documentation, including Functional Specifications (FS), Software Design Specifications (SDS), and IO lists.
    • Support and attend Factory Acceptance Testing (FAT) and software bench testing when required.
    • Lead and oversee Site Acceptance Testing (SAT), commissioning, and qualification activities.
    • Draft and execute FAT, SAT, and commissioning protocols, ensuring adherence to internal specifications.
    • Validate and maintain vendor documentation to meet internal standards.
    • Create Preventive Maintenance (PM) plans and establish spare parts requirements using the Computerized Maintenance Management System (CMMS).

    Qualifications and Experience:

    • Bachelor's degree in Chemical, Process, or Mechanical Engineering (or equivalent) with 3-5 years of relevant industry experience. Equivalent practical experience may be considered in lieu of formal education.
    • Previous exposure to biopharmaceutical manufacturing or process equipment is strongly preferred.
    • Background in process design, commissioning, and validation within regulated industries is highly desirable.
    • Familiarity with DeltaV distributed control systems is a plus.

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