Our client is a prominent and globally recognised leader in the pharmaceutical industry, with a strong commitment to developing and manufacturing life-changing medicines. The environment is a live, operational GMP facility, offering a fast-paced and technically challenging workplace where your work has a direct impact on global patient supply.
The site is embarking on a major, multi-year capital investment to modernise its core process automation systems, presenting a rare and exciting career opportunity as an
Automation Engineer
.
Responsibilities
This role is a senior technical position within the site's established Automation department, reporting directly to the Automation Manager. You will be the go-to expert on the ground, working as part of a cross-functional team that includes Process Engineers, Validation specialists, and Maintenance technicians, while also providing technical oversight to external contractors.
Your key responsibilities will include:
* Taking a lead role in the hands-on execution of a major, multi-year project to migrate the site's control system from a legacy RS3 platform to a modern Emerson DeltaV system.
* Providing expert-level daily support, troubleshooting, and maintenance for existing automation systems to ensure uninterrupted live plant production.
* Managing the full automation project lifecycle, from design and commissioning to system validation (IQ/OQ/PQ) and the creation of detailed documentation.
* Ensuring all automation activities and systems maintain full compliance with strict regulatory standards (EU & FDA GMP).
* Applying a strong, hands-on approach to a variety of tasks, including instrumentation checks, working with contractors, and developing reporting systems.
Experience
The ideal candidate will be a proactive and senior automation professional with a proven track record in a live pharmaceutical manufacturing environment.
* A degree in Engineering (Chemical, Electrical, or Automation preferred) or a relevant discipline.
* 5-10+ years of hands-on, extensive experience with Emerson DeltaV is essential.
* Demonstrable experience working on-site in a GMP-regulated pharma or biotech plant, with the ability to troubleshoot and support live operations.
* Exceptional communication skills with native-level English fluency are required for clear and effective interaction with operators, management, and contractors.
* A proven, action-oriented mindset with the ability to work independently and turn your hand to any challenge.
To discover more about this opportunity, please apply online or contact Lewis Murray at for a confidential discussion.