Automation & CSV Engineer (Permanent) - West Yorkshire

Pharmaceutical Manufacturing | High-Tech GMP Environment | Career Growth Opportunity

An exciting opportunity is available for an Automation & Computer System Validation (CSV) Engineer to join a highly regulated manufacturing environment within the pharmaceutical/life sciences sector.

This role is ideal for an engineer who enjoys working at the intersection of automation, validation, digital systems, and manufacturing operations. You'll play a key role in supporting critical production systems, driving continuous improvement initiatives, and ensuring compliance across computerized and automated processes.

Key Responsibilities

• Support and maintain automation and control systems across manufacturing operations
• Troubleshoot equipment and process-related automation issues
• Participate in computerized system validation (CSV) activities within a GMP-regulated environment
• Assist with qualification, commissioning, and lifecycle management of automated systems
• Support continuous improvement and process optimization projects
• Collaborate with engineering, production, quality, and external vendors
• Maintain technical and validation documentation in line with regulatory expectations
• Contribute to data integrity and compliance initiatives
• Provide technical support and training to operational teams

Ideal Background

• Degree qualified in Automation, Electrical, Electronics, Mechatronics, or related Engineering discipline
• Experience working with PLC, HMI, SCADA, or industrial control systems
• Exposure to regulated industries such as pharmaceuticals, biotech, medical devices, or food manufacturing preferred
• Understanding of GMP and computerized system validation principles
• Strong troubleshooting and problem-solving skills
• Ability to work both independently and within cross-functional teams
• Excellent communication and technical documentation abilities

Desirable Experience

• PLC/SCADA programming or support
• System integration projects
• Equipment qualification or validation activities
• Knowledge of data integrity and regulatory compliance requirements
• Experience supporting utilities, manufacturing systems, or process equipment

What's on Offer

• Opportunity to work in a modern, highly automated manufacturing environment
• Exposure to cutting-edge pharmaceutical technologies
• Career progression within engineering and digital manufacturing
• Collaborative and technically focused culture
• Competitive salary and benefits packag

This is an excellent opportunity for an ambitious engineer looking to develop within a fast-paced and growing technical operations environment.

For a confidential discussion or to learn more, please contact Simon Fowler on

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