Project Engineer Consultant

Harmonics Recruitment; Limerick; On-site; EUR 65,000 - 90,000; Full time

Job summary

Harmonics Recruitment seeks a Project Engineer Consultant for a major CAPEX project in the biopharma sector. You will drive delivery of new process systems, ensuring design, installation and commissioning meet stringent regulatory and operational standards.

Key duties include writing URS, reviewing BOD/PDs, managing BOMs, tracking HAZOP actions, leading FAT/SAT, and creating PM tasks in CMMS. DeltaV experience is desirable; 3–5 years of relevant experience preferred.

Qualifications

• Generates URS for assigned systems
• Reviews Basis of Design (BOD) and P&IDs
• Ensures BOM, datasheets and cutsheets meet specs
• Tracks HAZOP actions and incorporates into design
• Participates in 30%, 60% and 90% model reviews
• Reviews lifecycle docs (FS, SDS, IO lists) for compliance
• May attend FAT and leads SAT/commissioning
• Develops FAT/SAT/commissioning protocols
• Ensures Vendor Document Requirements (VDR) are met
• Creates PM tasks and spare parts in CMMS

Responsibilities

• Generate URS for assigned systems.
• Review BOD and detailed design (P&IDs).
• Ensure procurement packages meet equipment specs.
• Track HAZOP items and integrate into design.
• Attend key design reviews and ensure safety/ergonomics.
• Approve system lifecycle docs.
• Attend FAT when required; supervise SAT/commissioning.
• Create commissioning protocols and PM tasks.
• Ensure VDR compliance.
• Maintain CMMS spare parts lists.

Skills

Project Engineering

CAPEX Delivery

Commissioning

Validation

Regulatory & GMP

Education

BS/BEng in Chemical, Process or Mechanical engineering

Tools

DeltaV

Job description

About the job Project Engineer Consultant

Our client, a global leader in the biopharma sector, is seeking a Project Engineer Consultant to support a major CAPEX project. This role will focus on the delivery of new process systems, ensuring design, installation, and commissioning meet the highest operational and regulatory standards.

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. P&IDs, etc.
• Ensures procurement packages (bill of materials (BOM), datasheets, cutsheets etc) meet the companys 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.
• Supervises and executes Site Acceptance Testing (SAT) and commissioning activities.
• Generates FAT, SAT and commissioning protocols for assigned equipment and ensures protocols meet company specifications.
• Ensures Vendor Document Requirements (VDR) meet company requirements.
• Builds Preventative Maintenance (PM) tasks and spare parts lists on Regeneron 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

Skills:
Project Engineering & CAPEX Delivery, Commissioning & validation expertise & Regulatory & GMP compliance knowledge