Jobs at PACIV

Support design, programming, testing, and commissioning of PLC/HMI/SCADA automation systems. Assist with wiring diagrams, troubleshooting, validation, equipment startup, documentation, and cross-disciplinary collaboration. Participate in onsite installations and travel up to 15%. Receive mentorship and develop industrial automation expertise.

Manage and maintain engineering drawings and project documentation for pharmaceutical capital projects. Coordinate revision and approval workflows, support drafting and document control, use client document management systems, ensure compliance with standards and training, and collaborate with engineering, construction, and client teams to deliver accurate, timely documentation.

Build, wire, test, and troubleshoot industrial control panels from electrical schematics. Install and terminate components, perform testing and diagnostics, collaborate with engineers and project managers, maintain safety and documentation, and recommend process improvements to ensure reliable automation solutions.

Deliver end-to-end GxP and non-GxP control system upgrades and installations for a GMP manufacturing site. Responsibilities include concept studies, costing, change management, scheduling, stakeholder/vendor coordination, URS and IT scope definition, system integrator engagement, FAT/SAT/IOQ oversight, and maintaining lifecycle validation documentation in Kneat. Act as SME for automation validation, hardware/software environments, and client standards.

Lead planning and execution of site integration and utility tie-in projects for operating pharmaceutical facilities, coordinating scope, budget, schedule, contractors, and change control while minimizing GMP production impacts and ensuring safety and compliance.

Coordinate design-construction interface for pharmaceutical capital projects: manage drawings, IFC packages, RFIs, design changes, schedules, constructability reviews, BIM/document control, vendor inputs, and track impacts on scope, cost, and schedule.

Lead delivery of a pharmaceutical construction package managing scope, budget, schedule, safety, quality, contracts, contractor performance, change control, and system turnover while coordinating design, construction, equipment, and C&Q teams to ensure GMP-compliant completion.

Design, develop, configure and support DeltaV control systems (including Batch) for biopharma projects. Produce design and lifecycle documentation (GAMP), modify control modules and phases, attend team meetings, lead project tasks, and ensure regulatory compliance and validation in a regulated environment.

Provide hands-on commissioning, startup, troubleshooting, and validation of Siemens PLC/HMI automation systems in regulated manufacturing. Support C&Q activities, MQTT and edge device integration, packaged skid integration, vendor collaboration, and create audit-ready documentation for Industry 4.0 initiatives.

Lead engineering design and verification for pharmaceutical capital projects, ensuring compliance with standards and regulations, coordinating cross-functional teams, managing design reviews, verification plans, risk assessments, and driving value engineering and constructability for on-time, on-budget delivery.

Lead full-lifecycle industrial automation projects from design through commissioning. Architect and program PLC, HMI, SCADA, and DCS solutions, manage integration, perform FAT/SAT/startup, troubleshoot control systems, and act as primary technical client contact while ensuring compliance with safety and industry standards.