Overview
An
Automation Engineer
is required to support the day-to-day operation and continuous improvement of
complex automated manufacturing systems
within a
large-scale, GMP-regulated aseptic production facility
.
The role supports automated systems across
drug product manufacturing operations
, including formulation, aseptic filling, lyophilisation, inspection, and packaging.
You will work as part of a multidisciplinary engineering team, ensuring automation systems remain compliant, reliable, and fit for purpose, while also contributing to ongoing improvement and technology upgrades.
The environment promotes
continuous improvement, innovation, and operational excellence
, with a strong focus on patient safety and supply continuity.
Key Responsibilities
Safety & Compliance
Promote a safe working environment by adhering to all
EHS, GMP, and regulatory requirements
.
Ensure automation systems operate and are maintained in a
validated state
.
Automation System Ownership
Act as
System Owner
for assigned automation platforms within a regulated manufacturing environment.
Support the lifecycle management of automation systems, including upgrades, changes, and obsolescence management.
Lead and support
incident investigations and troubleshooting
related to manufacturing automation systems.
Provide technical input to deviation investigations and root cause analyses.
Implement
corrective and preventive actions (CAPAs)
, including software changes, configuration updates, and documentation revisions.
Update
design documentation, system descriptions, and SOPs
as required.
Engineering & Innovation
Review existing automation architectures and recommend improvements aligned with
current technology and regulatory standards
.
Support the introduction of
new products, processes, and technologies
, including engineering assessments, system modifications, and engineering trial runs.
Qualifications & Experience
Bachelor's degree in
Electrical Engineering, Automation, Computer Science, Chemical Engineering, Biotechnology
, or a related engineering discipline.
5+ years' experience
supporting automation systems in an
operational manufacturing environment
.
Strong background in
automation design, programming, commissioning, and lifecycle support
.
Experience working within
GMP-regulated environments
, including system validation and change management.
Proven ability to troubleshoot
PLC, HMI, SCADA, serialisation, and vision systems
.
Automation Technologies (experience in some or all):
HMIs:
Siemens and Rockwell-based systems
SCADA:
iFix, InTouch, Zenon, PCSS7, FactoryTalk View
Fieldbus & Networks:
ControlNet, DeviceNet, Profibus, Profinet, AS-i, BACnet
Manufacturing Exposure (advantageous):
Biopharmaceutical
formulation and fill/finish
Aseptic processing and lyophilisation
Inspection and packaging systems
Regulatory & Standards Knowledge
Understanding of
GAMP 5
, automation software development lifecycle
Familiarity with
ANSI/ISA-88 (Batch)
and
ANSI/ISA-95 (Manufacturing Integration)
standards
Experience supporting validated systems in line with regulatory expectations
What's on Offer
Long-term role supporting
critical manufacturing operations
Exposure to
complex, high-availability automation systems
Opportunity to contribute to
technology upgrades and continuous improvement
Collaborative engineering environment with strong technical ownership
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