Jobs at PACIV

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.

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.

Designs and commissions industrial automation systems from concept through startup. Responsibilities include PLC, HMI, and SCADA development; control system architecture; electrical panel and motor control design; instrumentation and industrial networking integration; technical documentation; testing, troubleshooting, FAT, SAT, and commissioning. Serves as a technical project lead, works with customers to resolve technical issues, and supports compliance with industrial electrical and control 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.

Provide IT support and validation (CSV) for laboratory systems (Empower, SmartLab, LIMS), manage user accounts and Active Directory, troubleshoot instrument connectivity and peripherals, author and execute IQ/OQ/PQ and CSV documentation, maintain GxP-compliant records, coordinate vendor technical support, and provide on-call/off-hours support in a regulated pharmaceutical environment.

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.

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.

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.

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.