CQV Engineer

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.

Be part of something bigger. Start your application today.

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