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.

Process Engineer responsible for process ownership, design, installation, commissioning, qualification, troubleshooting, and handover of F&B manufacturing systems. The role covers dry and wet processing, liquid handling, aseptic technologies, automation interfaces, CAPEX execution, vendor coordination, FAT/SAT, DQ/IQ/OQ/PQ, regulatory compliance, and operational readiness. Candidates need 5+ years of regulated process manufacturing experience, engineering qualifications, project and commissioning expertise, and valid EU work authorization with Irish residency.

Designs, implements, commissions, and supports IT/OT network infrastructure for a new F&B plant. Responsibilities include network architecture, segmentation, firewalls, virtualization, industrial Ethernet, PLC/SCADA/MES connectivity, cybersecurity controls, troubleshooting, FAT/SAT, documentation, compliance, and operational handover. The role collaborates with automation, engineering, operations, IT, vendors, and EPCM partners to ensure secure, validated, and reliable infrastructure during commissioning and startup.

Owns execution of assigned pharmaceutical capital-project work packages from field mobilization through construction, mechanical completion, commissioning, and turnover. Coordinates contractors, EPCM, design, CQV, operations, vendors, and adjacent packages while monitoring safety, quality, cost, schedule, risks, constraints, documentation, inspections, punch-list items, and readiness. Supports tie-ins, shutdowns, energization, equipment installation, system integration, and turnover activities, escalating significant execution issues to project leadership.

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.

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.