CQV Engineer - Immediate Start

About the role

Arcadis is seeking a CQV Engineer to join its team in the greater Dublin area with an immediate start. The role involves supporting commissioning, qualification and validation activities for process equipment, facilities and utilities within a pharmaceutical environment.

Key responsibilities

• Support commissioning, qualification and validation of process equipment, facilities and utilities on site.
• Review vendor documentation to ensure it meets commissioning and qualification requirements.
• Develop, review and execute validation plans, URS, DQ, FAT, SAT, IQ and OQ protocols and reports.
• Minimize validation non‑conformances or deviations and ensure timely closure of any issues.
• Supervise vendors and contractors during commissioning activities.
• Ensure compliance with current industry regulations and guidelines related to qualification and validation.

Required profile

• Minimum three years of CQV experience in a pharmaceutical setting.
• Proven ability to write validation plans, gather requirements, produce design documentation, configure systems, and perform system testing and troubleshooting.

Required skills

• Commissioning, qualification and validation (CQV) processes
• Development and execution of validation protocols (URS, DQ, IQ, OQ, FAT, SAT)
• Vendor document review
• Regulatory compliance in pharmaceutical industry

What we offer

• Opportunity to work for a global leader in sustainable design and engineering.
• Supportive environment that values diversity, inclusion and professional growth.
• Engagement in meaningful projects that drive sustainable solutions.