
Horizon Controls Group is a global digital process automation company specializing in automation consultancy, engineering design, system integration, and training services primarily for the Life…

Horizon Controls Group is a global digital process automation company specializing in automation consultancy, engineering design, system integration, and training services primarily for the Life…
Position Summary Horizon Controls Group is seeking an experienced Senior Automation Engineer with strong hands-on expertise in both Emerson DeltaV and Werum PAS-X Syncade systems to support and enhance pharmaceutical manufacturing operations in Limerick, Ireland.
The successful candidate will play a critical role in the design, implementation, validation, optimization, and lifecycle management of automation and MES platforms supporting GMP-regulated production environments. This role requires deep technical knowledge of process control systems, manufacturing execution systems, integration architecture, and pharmaceutical compliance standards.
This position is ideal for a professional who has successfully delivered automation and digital manufacturing projects within biotech or pharmaceutical manufacturing facilities and possesses strong collaboration skills across engineering, operations, quality, validation, and IT teams.
Key Responsibilities DeltaV Automation Responsibilities
Syncade MES Responsibilities
System Integration Responsibilities
Develop and maintain integrations between DeltaV and Syncade platforms.
Validation & Compliance
Requirements Required Qualifications Education
Bachelor’s or Master’s degree in:
Automation Engineering
Electrical Engineering
Computer Engineering
Chemical Engineering
Biotechnology Engineering
Other related technical discipline
Mandatory Technical Experience DeltaV (Required)
Minimum 5+ years of hands-on Emerson DeltaV experience.
Strong experience with:
DeltaV Batch
Recipe configuration
Control strategies
Syncade MES (Required)
Minimum 3+ years of hands-on Syncade MES experience.
Experience configuring and supporting:
Electronic Batch Records
Workflow management
Manufacturing execution processes
Recipe execution
Strong MES integration experience with DeltaV.
Candidates must possess strong practical experience in BOTH DeltaV and Syncade. Experience in only one platform will not meet the requirements for this role.
Preferred Qualifications
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Design, configure, implement, and maintain Emerson DeltaV DCS/PCS systems for pharmaceutical manufacturing processes.
Develop and modify:
Control modules
Equipment modules
Batch recipes
Phases and operations
Alarms and interlocks
HMI graphics
Support commissioning, startup, SAT, FAT, and qualification activities.
Troubleshoot DeltaV hardware and software issues in manufacturing environments.
Perform system upgrades, patches, migrations, and lifecycle management activities.
Configure and maintain:
DeltaV Batch
DeltaV Continuous Historian
DeltaV Live
OPC interfaces
SIS/ESD integrations where applicable
Ensure high system availability and cybersecurity compliance.
Participate in root cause investigations and CAPA implementation for automation-related deviations.
Configure and support Werum PAS-X Syncade MES applications within GMP production operations.
Develop and maintain:
Electronic Batch Records (EBR)
Workflows
Material management processes
Weigh & dispense solutions
Equipment tracking
Recipe execution flows
Collaborate with manufacturing and quality teams to optimize MES-driven workflows.
Integrate Syncade with:
DeltaV
SAP/ERP systems
LIMS
Historians and data platforms
Support electronic review-by-exception initiatives.
Drive digital manufacturing and paperless manufacturing transformation programs.
Troubleshoot MES execution issues and support manufacturing operations during production campaigns.
Support ISA-88 and ISA-95 aligned automation architectures.
Collaborate with IT/OT teams on:
Network architecture
Data integrity
Cybersecurity
System interoperability
Ensure compliant data flow between automation layers and enterprise systems.
Support serialisation, track-and-trace, and digital manufacturing initiatives where applicable.
Ensure systems comply with:
GMP/GxP requirements
FDA 21 CFR Part 11
Annex 11
Data Integrity standards
Author and review:
URS
FS/DS
IQ/OQ/PQ protocols
Risk assessments
Traceability matrices
SOPs
Participate in audits and regulatory inspections.
Maintain validated state of automation and MES systems.
Commissioning and troubleshooting
System administration
Experience in GMP pharmaceutical or biotech manufacturing environments.
Experience in sterile, biologics, API, or fill-finish manufacturing environments.
Knowledge of:
ISA-88
ISA-95
OPC/OPC UA
SQL databases
Historian systems
Industrial networking
Experience with:
Emerson Lifecycle Services
PAS-X integrations
SAP integration
Serialization systems
Digital transformation projects
Exposure to cloud manufacturing analytics platforms is advantageous.
PMP, DeltaV, or MES certifications are a plus.