Jobs at Horizon Controls Group

Support integration, commissioning, optimisation, and ongoing support of OEM equipment and automated systems in a GMP pharmaceutical manufacturing environment. Perform PLC programming, HMI/SCADA development, automation troubleshooting, and collaborate with engineering, validation, and operations teams.

Coordinate site-level MES implementation and post-go-live support. Serve as primary liaison among site users, Global MES, IT, vendors, and offshore teams. Manage MES lifecycle activities, track actions/risks, support testing, training, compliance/CSV inputs, documentation, L2/L3 support, and continuous improvement to keep MES aligned with site operations.

Coordinate site-level MES implementation and post-go-live support, acting as liaison between site users, Global MES, IT, vendors, and offshore teams. Manage MES lifecycle activities (requirements, testing, training, go-live, hypercare), track issues/risks, support site readiness (infrastructure, devices, connectivity), maintain documentation and governance, and drive continuous improvement to prevent MES-related bottlenecks.

Provide engineering support for Emerson DeltaV DCS in a GMP pharma site: design, configure, test, and maintain control strategies, batch logic, graphics, historian and alarms. Support validation, commissioning, process optimization, projects, change control, CAPAs, and on-call support while ensuring GMP and quality compliance.

Provide hands-on support for PLC, SCADA and DCS automation systems in a GMP pharmaceutical environment. Troubleshoot control systems, assist with system configuration, validation (IQ/OQ/PQ), documentation, and small automation projects. Collaborate with operations, maintenance, quality and IT on continuous improvement, digitalisation, and compliance activities while developing technical skills through structured training.

Design, configure, implement, and support Emerson DeltaV control systems in a GMP pharmaceutical environment. Develop control strategies, batch logic, alarms, and HMI graphics; support commissioning, qualification, and validation (FAT/SAT/IQ/OQ/PQ); ensure compliance with GMP/GAMP5/21 CFR Part 11; troubleshoot systems; produce technical and validation documentation; support upgrades, continuous improvement, and vendor/integrator collaboration.

Lead and execute CSV activities for automation and control systems in a GMP environment. Develop and run validation documentation (URS, FRS, IQ/OQ/PQ), validate DCS/PLC/SCADA, support FAT/SAT, perform risk assessments, manage change control and lifecycle documentation, and support audits/inspections (FDA/EMA/HPRA).

Plan, develop, execute, and document CSV activities for GxP computer systems. Author and review validation deliverables (URS, IQ/OQ/PQ, protocols, reports), ensure compliance with 21 CFR Part 11, EU Annex 11 and GAMP5, support audits, manage change control and re-validation, participate in system implementations/upgrades, and provide CSV training and guidance.

Lead CSV Engineer responsible for computer system validation across automation and IT systems. Develop and approve validation deliverables (QAPs, test plans, RTMs), ensure vendor compliance with MSD/GAMP5 standards, provide FAT oversight, create SDLC templates, liaise with stakeholders, and support delivery of validated systems.

Lead automation engineering role to design, configure and deliver DeltaV-based process control systems for bioprocess facilities. Duties include creating automation standards, developing control strategies (Batch and Continuous), configuring DeltaV/DeltaV SIS/AMS, mentoring teams, managing project execution, startup support, S88 batch architecture consulting, and ensuring CSV and safety instrumented system coordination.

Support automation activities in a GMP pharmaceutical manufacturing site including configuring, testing, and troubleshooting PLC/SCADA/DCS systems, participating in commissioning/qualification (IQ/OQ/PQ), supporting validation and change controls, performing routine system checks, and assisting documentation and continuous improvement under senior engineer guidance.

Design, configure, validate, and support Werum PAS-X Core 3 MES solutions in GMP-regulated pharmaceutical/biotech manufacturing. Implement MBRs/EBRs, workflows, materials/resource management, and process integrations. Lead testing (FAT/SAT/IQ/OQ), commissioning, troubleshooting, and documentation while ensuring compliance with GAMP5 and 21 CFR Part 11 and collaborating with QA, Validation, Automation, and IT.

Provide independent DDQ/CSV oversight for shopfloor automation implementations and changes, review and approve lifecycle documentation, manage qualifications, changes, deviations and investigations, and collaborate with technical and business teams to ensure regulatory, SDLC, cyber security and data integrity compliance.

Design, program, commission, and maintain PLC control systems for GMP-regulated pharmaceutical manufacturing. Integrate PLCs with SCADA/HMI, support FAT/SAT and start-up, perform troubleshooting, participate in CSV/IQ-OQ testing and change control, and ensure compliance with GMP and data integrity standards while collaborating with engineering, QA, maintenance, IT, and vendors.

Provide senior technical leadership and hands-on support for ABB MOD300 and 800xA DCS in pharmaceutical manufacturing, leading upgrades, commissioning, troubleshooting, qualifications (FAT/SAT/IQ/OQ), compliance with GMP/GAMP5/ISA standards, documentation, vendor coordination, and mentoring junior engineers.

Lead design, implementation, validation, and lifecycle management of Emerson DeltaV DCS and Werum PAS‑X/Syncade MES for GMP pharmaceutical manufacturing. Configure control and batch recipes, develop MES EBRs and workflows, integrate DeltaV with enterprise systems, support commissioning/qualification, troubleshoot production issues, ensure compliance with FDA/Annex 11, and drive digital/paperless manufacturing initiatives.

Lead design and development of Rockwell PLC automation architectures and PLC code for regulated pharmaceutical manufacturing. Collaborate with process, CQV, MES, and digital teams to ensure compliant, scalable automation, support testing/commissioning/qualification, integrate PLCs with enterprise systems, produce technical documentation, and mentor junior engineers.

Lead design, implementation, validation, and lifecycle management of PLC/SCADA/DCS automation systems for regulated manufacturing. Manage projects from concept through commissioning, ensure GMP/data integrity/compliance (GAMP5/CSV), develop URS/FDS and FAT/IQ/OQ tests, coordinate vendors, provide technical support and troubleshooting, and mentor junior staff.