CQV Engineer

Blackfield Associates are supporting a leading pharmaceutical manufacturer in their search for a CQV Engineer to join their site in Dublin. This is an excellent opportunity to work in a highly automated GMP manufacturing environment, supporting the commissioning, qualification and validation of process equipment and control systems.

Job Description

• Execute Commissioning, Qualification and Validation (CQV) activities for process equipment, utilities and automated manufacturing systems within a GMP-regulated pharmaceutical or biotechnology environment.
• Support the testing, commissioning and qualification of Emerson DeltaV systems, including functional verification, loop checks, alarm testing and control system integration.
• Develop, execute and review IQ, OQ and PQ protocols to ensure equipment and systems meet operational, quality and regulatory requirements.
• Collaborate with Automation, Engineering, Manufacturing and Quality teams to resolve technical issues, investigate deviations and support project delivery.
• Participate in FAT, SAT and start-up activities for new equipment and automation projects, ensuring systems are ready for qualification and routine operation.
• Maintain clear and compliant validation documentation in accordance with GMP, GAMP 5 and site quality standards.

Qualifications

• Bachelor's degree in Engineering, Automation, Biotechnology, Pharmaceutical Sciences or a related technical discipline.
• Minimum 4 years' experience in CQV, Validation, Automation Engineering or a related technical role within the pharmaceutical, biotechnology or life sciences sector.
• Hands-on experience with Emerson DeltaV is required, including commissioning, testing, qualification or operational support activities.
• Strong understanding of GMP regulations, GAMP 5 and the validation lifecycle (IQ/OQ/PQ).