CQV Engineer: DeltaV & GMP Validation Expert

Blackfield Associates; Leinster; On-site; EUR 60,000 - 90,000; Full time

Job summary

Blackfield Associates are supporting a leading pharmaceutical manufacturer in their search for a CQV Engineer to join their site in Dublin. This role focuses on commissioning, qualification and validation of process equipment and control systems in a highly automated GMP environment.

You will execute CQV activities for process equipment, utilities and automated manufacturing systems, develop IQ/OQ/PQ protocols, and collaborate across Automation, Engineering and Quality teams to ensure regulatory

Qualifications

• CQV, validation lifecycle knowledge.
• Experience in pharma/biotech environment.
• DeltaV commissioning, testing and qualification experience.
• GMP regulations and regulatory lifecycle understanding.

Responsibilities

• Execute CQV activities for process equipment, utilities and automated manufacturing systems within GMP.
• Support testing, commissioning and qualification of Emerson DeltaV systems and integration.
• Develop, execute and review IQ, OQ and PQ protocols to meet requirements.
• Collaborate with Automation, Engineering, Manufacturing and Quality to resolve issues and support delivery.

Skills

CQV experience

Automation engineering

GMP knowledge

DeltaV expertise

Validation lifecycle

Education

Bachelor's degree in Engineering

Tools

Emerson DeltaV

Job description

Blackfield Associates are supporting a leading pharmaceutical manufacturer in their search for a CQV Engineer to join their site in Dublin. This role focuses on commissioning, qualification and validation of process equipment and control systems in a highly automated GMP environment.

You will execute CQV activities for process equipment, utilities and automated manufacturing systems, develop IQ/OQ/PQ protocols, and collaborate across Automation, Engineering and Quality teams to ensure regulatory