CQV Engineer – Pharmaceutical Validation (Dublin)

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 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.