Project Engineer

QCS Staffing Ltd; The Municipal District of Dundalk; On-site; EUR 60,000 - 80,000; Full time

Job summary

QCS Staffing Ltd is seeking a Project Engineer for an initial 9-month contract in Ireland, supporting a global life sciences client in Dublin. The role focuses on engineering, commissioning, and qualification activities for pharmaceutical/biotech projects.

The position requires extensive experience in commissioning and qualification management, with a strong grasp of GMP/safety and regulatory requirements.

Qualifications

• Engineering or commissioning and qualification management experience.
• Engineering qualification at third level or equivalent.
• Extensive knowledge of commissioning activities.
• Qualification for Pharmaceutical/Biotech projects preferred.
• Knowledge of safety, GMP and environmental regulatory requirements.

Responsibilities

• Prepare User Requirement Specifications (URS).
• Develop test planning and test strategies including Single Test Approach and OneCQV.
• Execute Design Qualification (DQ).
• Perform component-level impact assessments.
• Manage project change control.
• Support Factory Acceptance Testing (FAT) and supplier-site testing activities.

Skills

Engineering experience

Commissioning management

Qualification management

GMP knowledge

Regulatory knowledge

Education

Engineering degree

Job description

Project Engineer – Ireland – Initial 9-Month Contract – Life Sciences

Our client is a global leader in pharmaceutical innovation, specializing in the development and manufacture of cutting-edge drugs. As they continue to grow, they’re seeking an experienced Project Engineer to support their dynamic team and drive forward groundbreaking projects in Dublin.

What you’ll deliver:

• User Requirement Specifications (URS)
• Test planning and test strategies, including Single Test Approach and OneCQV (combined equipment and automation testing)
• Design Qualification (DQ)
• Component Level Impact Assessments
• Project Change Control
• Factory Acceptance Testing (FAT), including support and participation in supplier-site testing activities

What you’ll need:

• Extensive experience in Engineering or Commissioning and Qualification Management
• Technical qualification at third level or equivalent in Engineering.
• Extensive knowledge and demonstrated experience managing Commissioning activities
• Qualification for Pharmaceutical / Biotechnology projects preferred
• Knowledge of safety, GMP and environmental regulatory requirements.