Senior CSV Engineer

QCS Staffing Ltd; Dublin; On-site; EUR 60,000 - 80,000; Full time

Job summary

Quanta Consultancy Services Ltd is looking for a Senior CSV Engineer for a 6-month contract in Dublin. The role involves developing project-related documentation and executing Computerised Systems Validation (CSV) while ensuring compliance with current GMP requirements.

The ideal candidate will have extensive experience in the pharmaceutical industry, strong knowledge of automation, and project management skills. Join their dynamic team and contribute to groundbreaking projects in a leading organization.

Qualifications

• Extensive professional experience in the pharmaceutical industry.
• Strong knowledge of automation and computer system validation.
• Demonstrated project management and leadership capabilities.

Responsibilities

• Develop and execute project-related documentation for Computerised Systems Validation.
• Lead risk analysis for equipment, systems, and processes.
• Issue commissioning and qualification plans and support technical knowledge.

Skills

Project management knowledge

Leadership capabilities

Knowledge in automation

Computer system validation

Job description

Senior CSV Engineer – OEM / SCADA – 6 Months Initial Contract

Our client is a global leader in pharmaceutical innovation, specialising in the development and manufacture of cutting‑edge drugs.

As they continue to grow, they’re seeking an experienced Senior CSV Engineer to join their dynamic team and drive forward groundbreaking projects in Dublin.

Responsibilities

• Develop, review and execute project‑related documentation against current GMP requirements such as (but not limited to): planning and execution of Computerised Systems Validation (CSV) in cooperation with IT and Process Automation.
• Lead and participate in risk analysis of equipment, systems and processes.
• Issue formal commissioning and qualification plans, protocols and reports and support different Equipment and Systems owners by providing technical knowledge.

Qualifications

• Extensive professional experience in the pharmaceutical industry.
• Knowledge in automation and computer system validation.
• Project management knowledge and leadership capabilities with respect to quality topics.

If this role is of interest to you, please apply now.