Full job descriptionAutomation & 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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