Jobs at Horizon Controls Group

Leads computer system validation activities for pharmaceutical manufacturing, laboratory, automation, engineering, and business systems. Develops and approves validation documentation, applies GAMP 5 and risk-based methodologies, ensures GMP and data integrity compliance, executes testing, manages deviations and vendor deliverables, and supports audits and inspections. Partners with Quality, Engineering, Automation, IT, Operations, laboratories, and vendors while mentoring junior validation professionals and improving CSV processes.

Provides Computer System Validation leadership for pharmaceutical capital projects. Develops, reviews, and approves validation, qualification, SDLC, testing, and requirements documentation; coordinates with Automation, IT, Quality, Engineering, vendors, and system integrators; ensures GAMP5, GMP, data integrity, and regulatory compliance; supports FAT, audits, inspections, project planning, stakeholder communication, validation execution, and project closeout.

Supports commissioning and qualification of DeltaV DCS systems in a GMP environment, including loop testing, onsite commissioning, site testing, and OQ execution. Manages automation change requests, stakeholders, risk assessments, issue resolution, and validation documentation. Partners with CSV, Digital Data Quality, vendors, and internal Digital teams to ensure compliant, secure implementation. Produces commissioning plans, execution records, qualification evidence, completion reports, and audit support documentation.

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 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 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 automation engineer responsible for designing, implementing, and overseeing DeltaV-based process control systems for a bioprocess facility. Duties include developing control strategies, configuring DeltaV (including SIS and AMS), creating design documentation, applying S88 batch concepts, mentoring teams, managing project execution, and ensuring CSV and startup of large automation projects.

Lead development, design, and implementation of process control systems (DeltaV) for bioprocess projects. Provide engineering leadership, create automation standards/specs, develop control strategies, mentor teams, manage project execution, support startups, and consult on S88/batch architectures and CSV for large capital projects.

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.