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Automation Engineer - Pharmaceutical

CV-Library

Posted on May 11, 2026 by CV-Library
West Yorkshire, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
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 teamsIdeal 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 abilitiesDesirable 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 equipmentWhat'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 packagThis 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

+44 (phone number removed) or

Reference: 225094965

https://jobs.careeraddict.com/post/113213435
CV-Library

Automation Engineer - Pharmaceutical

CV-Library

Posted on May 11, 2026 by CV-Library

Print
West Yorkshire, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
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 teamsIdeal 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 abilitiesDesirable 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 equipmentWhat'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 packagThis 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

+44 (phone number removed) or
Print

Reference: 225094965

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