Project Engineer

QCS Staffing Ltd; Dublin; On-site; EUR 55,000 - 75,000; Full time

Job summary

QCS Staffing Ltd is seeking a Project Engineer for an Ireland, Dublin site on an initial 12-month contract in Life Sciences. The role focuses on owning syringe filling equipment from design through qualification and into commercial operation.

You will drive manufacturing readiness, support FAT/SAT, commissioning, IQ/OQ/PQ, and validation activities while ensuring GMP and regulatory compliance across the project lifecycle.

Qualifications

• Bachelor's Degree in Mechanical, Electrical, Chemical, or related Engineering discipline.
• Extensive experience in biopharmaceutical manufacturing engineering.
• Experience with aseptic syringe filling systems (high-speed lines preferred).
• Experience with single-use technologies in fill-finish environments desirable.

Responsibilities

• Act as System Owner for syringe filling equipment from design through to PQ and commercial operation.
• During equipment implementation, FAT/SAT, commissioning, qualification (IQ/OQ/PQ), and validation activities.
• Drive manufacturing readiness, start-up, and handover to operations.
• Ensure compliance with GMP, regulatory, and client standards.

Skills

Biopharmaceutical manufacturing

Aseptic syringe filling

Single-use technologies

Education

Bachelor's Degree in Mechanical, Electrical, Chemical or related Engineering

Job description

Project Engineer - Ireland, Dublin - Initial 12-Month Contract - Life Sciences

Our client, a globally recognised pioneer in Biotechnology, are recruiting for the position of Project Engineer. A leader in the industry, our client focuses on areas of high unmet medical need and leverages its expertise to stride for solutions. This is your chance to support them on their global mission to better the lives of those affected by disease and illness.

What You'll Deliver

• Act as System Owner for syringe filling equipment from design through to PQ and commercial operation.
• So during equipment implementation, FAT/SAT, commissioning, qualification (IQ/OQ/PQ), and validation activities.
• Drive manufacturing readiness, start-up, and handover to operations.
• Ensure compliance with GMP, regulatory, and client standards.

Experience required

• Bachelor's Degree in Mechanical, Electrical, Chemical, or related Engineering discipline.
• Extensive experience in biopharmaceutical manufacturing engineering.
• Proven experience in aseptic syringe filling systems (high-speed lines preferred).
• Experience with single-use technologies in fill-finish environments desirable.