Summary
Process Engineer to provide technical process design support for Bioprocess systems on new Process Area CAPEX project.
Essential Duties and Responsibilities
* Generation User Requirement Specification (URS) for assigned systems.
* Reviews and approves Basis of Design (BOD) and detail design of assigned systems i.e. PFDs, P&IDs, etc.
* Ensures procurement packages (bill of materials (BOM), datasheets, cutsheets, etc.) meet company equipment specifications.
* Tracks HAZOP action items and ensures action items are incorporated into system design.
* Attends 30%, 60% and 90% model reviews ensuring systems meet operational, safety and ergonomic requirements.
* Reviews and approves system lifecycle documentation (FS, SDS, IO lists, etc.) and ensures they meet company requirements.
* Attends factory acceptance test (FAT) of associated equipment if required.
* Attends automation software bench FAT if required.
* Supervises and executes Site Acceptance Testing (SAT) and commissioning activities.
* Generates FAT, SAT and commissioning protocols for assigned equipment and ensures protocols meet specifications.
* Ensures Vendor Document Requirements (VDR) meet requirements.
* Builds Preventative Maintenance (PM) tasks and spare parts lists on Computerised Maintenance Management System (CMMS).
Education and Experience
* Requires BS/BEng in Chemical, Process or Mechanical engineering with 3–5 years related experience.
* Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.
* Experience with design and commissioning within biopharmaceutical sector would be desirable.
* Experience with DeltaV would be desirable.
Please click the link below to apply or alternatively send an up-to-date CV to howie.leahy@peglobal.net
Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland.
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