QA Resources is looking for a Process Engineer for a client based in Limerick.
Role and requirements:
The Process Engineer will provide technical process design support for Bioprocess systems on new Process Area CAPEX project.
* 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 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 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
Interested candidates should submit an updated CV to