Horizon Controls Group Benefits Overview

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.