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Construction Site Engineer – Pharmaceutical / Life Sciences Project

Location: Athlone, Co. Westmeath
Contract Type: Permanent

The Project

A major pharmaceutical development and manufacturing facility in Athlone is undergoing a large‑scale retrofit and refurbishment programme within a live, regulated environment.

The project involves extensive upgrades to existing manufacturing, development, and support buildings, delivered while maintaining strict GMP, health & safety, and quality standards. Due to the scope and complexity of the works, the project is supported by a large multi‑disciplinary construction team and a high volume of specialist subcontractors.

This is a strong opportunity to gain experience on a technically challenging, high‑profile life sciences project with long‑term delivery certainty.

The Role

We are seeking an experienced Site Engineer to join the site delivery team on this pharmaceutical retrofit project.

The successful candidate will support the day‑to‑day engineering and construction activities on site, ensuring work is delivered safely, accurately, and in accordance with drawings, specifications, programme requirements, and GMP standards.

You will work closely with Site Management, Project Engineers, M&E Coordinators, subcontractors, and the client’s engineering and CQV teams.

Key Responsibilities

Site Engineering & Setting Out

• Set out works in accordance with construction drawings and specifications
• Ensure dimensional accuracy across structural, architectural, and services interfaces
• Check and verify subcontractor setting‑out and workmanship

Quality & Technical Control

• Review drawings, specifications, and technical details
• Ensure construction activities comply with:
  • Design requirements
  • GMP standards
  • Project quality procedures
• Manage inspections, snagging, and close‑out processes
• Assist with the preparation of as‑built records and handover documentation

Health, Safety & Compliance

• Promote a strong health & safety culture on site
• Assist in the preparation and review of:
  • Risk assessments
  • Method statements
  • Permit‑to‑work documentation
• Ensure works are carried out safely within a live pharmaceutical facility

Subcontractor Coordination

• Support site management in coordinating subcontractor activities
• Monitor daily progress and resolve technical queries
• Assist with sequencing works to avoid clashes and delays

Stakeholder Interface

• Liaise with site management, consultants, and client representatives
• Support coordination with MEP, process, commissioning, and validation teams
• Maintain accurate site records and reporting

Experience & Background Required

Essential

• 2–5+ years’ experience as a Site Engineer in the construction industry
• Experience working on commercial, industrial, or regulated projects
• Strong setting‑out, QA, and technical coordination skills
• Ability to work effectively in a fast‑paced site environment

Desirable

• Experience on pharmaceutical, life sciences, cleanroom, or healthcare projects
• Experience working on live or brownfield sites
• Familiarity with GMP standards and regulated handover processes
• Exposure to MEP or services‑led construction environments

Qualifications

• Degree or Diploma in:
  • Civil Engineering
  • Construction Management
  • Structural / Building Engineering
• Degree‑qualified graduates with relevant site experience will be considered

Key Skills & Attributes

• Strong attention to detail
• Excellent communication and coordination skills
• Proactive, solutions‑focused approach
• Ability to manage multiple work fronts
• High standards for health, safety, and quality