CQV Engineer

QCS Staffing; Dublin; On-site; EUR 65,000 - 90,000; Full time

Job summary

QCS Staffing in Ireland is seeking a CQV Engineer for an initial 12-month contract in Dublin. You will contribute to the development and execution of CQV testing documentation for benchtop, mobile, analytical, PAT, incubators, BSCs and TCU equipment at the Sterile Drug product facility.

This assignment offers hands-on experience with innovative equipment, large-scale operations and modern pharmaceutical technologies, helping you deliver safety, quality and regulatory-compliant commissioning

Qualifications

• Proven ability to execute CQV testing from initiation to completion.
• CQV lifecycle experience from design through C&Q to handover.
• Experience working in a diverse CQV team to deliver tasks safely, on time and within budget.
• Experience CQV of Drug Substance/Drug product small equipment with integrated automation.

Responsibilities

• Develop and execute CQV testing documentation for benchtop, mobile, analytical, PAT, incubators, BSCs, and TCU equipment.
• Meet key project deliverables for safety, CQV schedule and quality of project documentation.
• Ensure GMP equipment are tested in compliance with practices and EU & FDA regulations.
• Verify that all equipment is tested in line with commissioning standards.

Job description

CQV Engineer – Ireland, Dublin – Initial 12-Month Contract – Life Sciences

Are you a CQV Engineer looking for your next assignment in Dublin? A leading multinational in Ireland’s thriving biopharma industry requires support for their major facility development.

This project provides hands‑on experience with innovative equipment, large‑scale operations and modern pharmaceutical technologies. It’s an ideal opportunity to build your skills within one of Europe’s fastest‑growing life‑science regions.

What You’ll Do

• Development and execution of CQV testing documentation for benchtop, mobile, analytical, PAT, incubators, BSCs, and TCU equipment for the Sterile Drug product facility.
• Responsible for meeting key project deliverables for safety, CQV schedule and quality of project related documentation/electronic records for equipment, utilities assigned.
• Responsible for ensuring GMP equipment are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations.
• Responsible for ensuring that all equipment, is tested in compliance with project related standards from a commissioning perspective.

What you’ll need

• Demonstratable capacity to effectively execute the CQV testing approach for assigned from initiation to completion.
• CQV project lifecycle experience from design through to C&Q and handover.
• Demonstrable experience of performing as part of diverse team of CQV professionals/ contractors to deliver on tasks safely, with quality focus, on time and within budget.
• Experience in CQV of Drug Substance/Drug product small equipment with integrated automation.