A leading pharmaceutical manufacturing site has a new opportunity for an experienced DeltaV Engineer to play a key role in the delivery of a large-scale technology & infrastructure campaign.
As a highly regulated business there is a strong culture of safety, quality, and collaboration, our teams work with cutting-edge technologies to deliver reliable and sustainable manufacturing excellence.
The Position
My client is seeking a highly skilled
DeltaV Engineer
to join their Automation Project team.
In this role, you will support the design, implementation, optimisation and maintenance of Emerson DeltaV DCS systems across API and small-molecule manufacturing operations.
You will work cross-functionally with Operations, Quality, Engineering, and IT to deliver key system upgrades and implement new technologies to the expanding operations at this site.
This is a challenging position within a project environment and will require flexibility and a creative approach to problem solving.
Reporting into the Head of Automation Projects; this position sits within an established team of experts - both staff and contractors; You will work closely with this group to support the workload.
Provide day-to-day support, troubleshooting, and optimisation of DeltaV automation systems.
Design, develop, test, and commission DeltaV software changes in accordance with GMP and site change-control procedures.
Participate in automation project execution, including upgrades, system expansions, FAT/SAT, commissioning, and validation activities.
Work closely with process engineering and operations teams to translate manufacturing requirements into robust automation solutions.
Maintain system documentation, configurations, and lifecycle management activities.
Support investigations, root-cause analysis, and implementation of corrective/preventive actions.
Ensure compliance with safety, quality, and cybersecurity standards.
Contribute to continuous improvement within the Automation team and wider site operations.
The Person
All applicants must have a Degree in Engineering with a minimum of 5 years' experience within a manufacturing environment.
The right person will have experience within a highly regulated GMP manufacturing operation -Biotech or chemical sectors preferable.
Hands on experience with lifecycle management of DeltaV hardware and infrastructure with extensive understanding and background in programming and installation.
Strong understanding of batch processing, automation design, and control system troubleshooting.
Flexible approach to work and a positive attitude will be a good fit with the team dynamic.
Be collaborative and a genuine team player.
Engage cross functionally to deliver on process improvement projects in conjunction with a site-based team.
Excellent problem-solving, communication, and teamwork skills.
Knowledge of GAMP, 21 CFR Part 11, and validation principles.
Familiarity with data integrity and cybersecurity best practices.
To discover more about this opportunity, apply now or contact Aisling Clements at HRM on for a confidential discussion.