CQV Engineer - Immediate Start

Arcadis; Dublin; On-site; EUR 70,000 - 95,000; Full time

Job summary

Arcadis DPS is seeking an immediately available CQV Engineer for the greater Dublin area. The role focuses on commissioning, qualification and validation of process equipment, facilities and utilities on site, with oversight of vendors and adherence to regulatory standards.

Applicants should have at least three years’ CQV experience in a pharmaceutical setting and demonstrate experience writing validation plans, requirements gathering, design documentation and IQ/OQ/OS testing.

Qualifications

• At least three years CQV experience within a pharmaceutical setting.
• Experience writing validation plans, requirements gathering, design documentation, system configuration, system testing and troubleshooting.

Responsibilities

• Support the commissioning, qualification and validation of process equipment, facilities and utilities on site.
• Review vendor documents to support commissioning and qualification requirements.
• Complete development, review and execution of validation plans, URSs/DQ/FATs/SATs/IQ/OQ protocols/reports.
• Ensure validation non-conformances or deviations are minimized during execution of CQV activities; close out issues promptly.
• Supervise vendors/contractors on site during commissioning activities.
• Ensure compliance with current industry regulations and guidelines relating to qualification and validation.

Skills

CQV experience

Job description

Arcadis DPS now require a CQV Engineer who is immediately available in the greater Dublin area.

About Arcadis

Arcadis is the world’s leading company in sustainable design, engineering, and consultancy for natural and built assets. With over 36,000 professionals across 70+ countries, we are united in our mission to improve quality of life and solve the world’s most complex challenges.

Be part of something meaningful – join us!

Responsibilities:

• Support the commissioning, qualification and validation of process equipment, facilities and utilities on site.
• Review vendor documents to support commissioning and qualification requirements.
• Complete the development, review and execution of validation plans, URSs/DQ/FATs/SATs/IQ/OQ protocols/reports.
• Ensures validation non-conformances or deviations are minimized during execution of CQV activities. For issues that do arise ensure they are closed out in a timely manner.
• Supervise vendors/ contractors on site during commissioning activities.
• Ensure compliance with current industry regulations and guidelines relating to qualification and validation.

Requirements:

• At least three years CQV experience within a pharmaceutical setting.
• Experience of writing validation plans, requirements gathering, design documentation, system configuration, system testing and troubleshooting

Why Join Arcadis?

At Arcadis, we empower individuals to excel because your contributions matter. Taking a skills-based approach, we provide opportunities for you to shape your career, maximize your impact, and grow professionally.

By joining us, you’ll engage in meaningful work that drives sustainable solutions for a better planet while leaving a lasting legacy.

Our Commitment to Equality, Diversity, and Inclusion

We are dedicated to creating an environment where everyone can thrive. Through our six ED&I workstreams—Age, Disability, Faith, Gender, LGBT+, and Race—we foster innovation by bringing together diverse perspectives. Together, we strive to improve quality of life while building a more inclusive future