Project Engineer

  • Contract
  • Cork

Website TPM05432

Our client is a pharmaceutical company based in East Cork, looking for a Support the site Capital Projects Engineer to deliver a key strategic site project for a New GDP Warehouse & Upgrade to Site Facilities.


  • Manage design, procurement, construction, commissioning and qualification phases of the project.
  • Generate technical documentation for the project systems in line with the project validation plan and company standards (HVAC systems, coldroom, freezer, building management system, environmental monitoring system, product sampling booths, etc.)
  • Generate site change controls on the client electronic change management system.
  • Manage project changes and ensure all are captured, documented and assessed.
  • Technical review of design deliverables produced by the appointed design consultant.
  • Management and technical review of vendor deliverables to the agreed timelines for specialist systems.
  • Manage & complete on-site construction quality reviews of systems installation.
  • Work closely with all department’s QA/Supply Chain/Validation/Engineering/H&S & Environmental to deliver projects successfully.
  • Ensure there is a strong safety culture and performance in the execution of capital projects.
  • Project Validation execution.
  • Assist project manager with cost, schedule & quality management tasks on the project.

Qualifications & Experience:

  • Degree in a relevant science / engineering discipline.
  • 8 to 10 years (minimum) of project management/engineering experience across the project life-cycle within a Pharmaceutical environment.
  • Experience in working in client-side Capital Projects execution role.
  • Experience in client electronic change management systems & full end-to-end Project Life-cycle.
  • Experience in working within cross functional project teams, delivering complex Manufacturing Facility projects, in a GMP Manufacturing Environment.
  • Understanding of Environmental, Health and Safety requirements of the Pharmaceutical industry.
  • Strong understanding of the principles of current Good Manufacturing Practices (cGMP).
  • Strong experience in GMP Utilities Systems Validation.
  • Understands the project management process; programming, scope development, design development, implementation, and project closeout.

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