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Automation Engineer

4 months ago

Hertfordshire, United Kingdom Cpl Full time

CPL Life Sciences are partnered with a pharmaceutical manufacturing organisation based out of Hertfordshire in their search for an Automation Engineer. 


⢠This role will perform automation engineering activities and manage aligned prioritised projects.

⢠Lifecycle management of automation systems integrated with manufacturing / packaging equipment. 

⢠Lifecycle management of serialisation and vision systems integrated within packaging equipment including interfaces with enterprise systems. 

⢠Responsible for providing cGMP compliant control systems as per GAMP5 and EU GMP Annex 11.


Duties are performed to ensure:

⢠A safe working environment is maintained for self and other employees, ensuring all near miss incidents and accidents are reported in accordance with procedures.

⢠The Quality of products manufactured and released is assured through adherence to all procedures.

⢠Opportunities to improve operations and reduce cost are identified and progressed through the continuous improvement and demand innovation initiatives.

⢠All stakeholder and customer expectations are understood and met through communication. 

⢠Performance is in line with personal and company objectives with demonstrated behaviours and competencies.


⢠Contribute to the development and implementation of the automation transformation strategy.

⢠Support the successful implementation of the supervisory control and data acquisition (SCADA) and manufacturing execution system (MES) within the production facility.

⢠Management of the design, development, maintenance and troubleshooting of automated systems, ensuring they are compliant as per GAMP5 and EU GMP Annex 11.

⢠Successful delivery of automation projects to meet strategic business objectives.

⢠Execute or facilitate automation design solutions in accordance with stakeholder requirements and business processes. 

⢠Responsible that all project documentation has been compiled and approved at gate reviews.

⢠Responsible that Good Engineering Practices (GEP) are employed in the design, installation and commissioning of assets.

⢠Responsible that Good Manufacturing Practices (GMP) are employed, including activities determined from user requirement specifications (URS) through to qualification.

⢠Coordination of specialist contractors undertaking work packages, ensuring safe systems of work are adopted throughout implementation phases.

⢠Support for commissioning, qualification and validation activities.

⢠Review and approval of GxP documentation, including technical specifications, user requirements, design / code reviews, qualification protocols and site acceptance testing.

⢠Lead quality and engineering change controls to maintain the validated state of the automated systems.

⢠System support in the areas of asset management, critical spares, preventative maintenance, training programs and data integrity.

⢠Provide coaching and development opportunities for the wider engineering / automation teams.


For further information please contact jamie.keith@cpl.com