Process Engineer

Summary: Process Engineer to provide technical process design support for Bioprocess systems on new Process Area CAPEX project.

Essential Duties and Responsibilities include, but are not limited to, the following:

• 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

• 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***