Jobs at Catalyx

Lead day-to-day production on-site to meet safety, quality, cost and delivery targets. Manage planning, scheduling, supervisors and cross-functional collaboration (Engineering, Quality, Procurement, HR). Drive continuous improvement, implement SOPs, reduce bottlenecks/rework, support scaling and new product introductions, and maintain audit-ready operations while developing frontline leaders and monitoring production KPIs.

Support assembly, manufacturing, and quality control of modular/prefabricated building components. Follow work instructions, maintain safety and cleanliness, operate tools after training, perform routine inspections, handle materials, and assist with deliveries and basic maintenance to meet production targets.

Support and continuously improve Large Molecule eLIMS and iLABs in a GMP-regulated QC laboratory environment. Responsibilities include resolving support tickets, troubleshooting systems, supporting deployments, investigations, CAPAs, change controls, audits, method execution, process standardization, and continuous improvement. The role partners with QC teams, SMEs, and global stakeholders to ensure effective, compliant laboratory system use.

Leads the design, development, installation, commissioning, and validation of machine vision, electrical, software, and automation solutions for regulated manufacturing customers. Supports pre-sales surveys and quotations, coordinates suppliers and multidisciplinary teams, manages scope changes, creates regulatory documentation, troubleshoots deployments, and drives continuous improvement. Requires travel throughout Ireland with rare international travel.

Integrate and support laboratory systems across applications, operating systems, data management, backups, and interfaces. Author, review, and approve system documentation; support validation and risk assessments; coordinate vendors and internal stakeholders; and manage multiple projects. Ensure laboratory systems comply with data integrity, GMP, 21 CFR Part 11, and Annex 11 requirements in a regulated manufacturing environment.

Manage full project lifecycle from requirements and sale through execution and handover for regulated-industry engineering projects. Serve as primary customer contact, plan schedules in Leanplan, coordinate cross-functional teams and suppliers, control costs/P&L, run FAT/SAT, ensure regulatory compliance, handle change management, and close projects with lessons-learned and after-sales transition.

Manage end-to-end recruitment for client accounts across Ireland and Europe, focusing on technical roles in Engineering, IT, Automation, Manufacturing and Life Sciences. Source and screen candidates, manage communications, negotiate offers, coordinate pre-employment checks and onboarding, maintain pipelines, and build relationships with hiring managers and Sales to support client growth and new opportunities.

Lead embedded operational services in a GMP-regulated pharmaceutical manufacturing environment. Oversee day-to-day delivery across manufacturing, packaging and inspection functions, ensuring compliance, safety and KPI-driven performance. Manage workforce planning, stakeholder relationships, operational governance, continuous improvement and client-facing responsibilities. Drive deviation/CAPA reduction, audit readiness, and operational excellence while coaching large operational teams and supporting strategic account growth.

Design and update PAS-X MES training using Articulate Storyline, translate MES concepts into SOPs, e-learning, and job aids; ensure GxP/FDA compliance, collaborate with MES engineers, and create role-based curricula and digital learning content for regulated manufacturing.

Provide on-site quality oversight across production stages, conduct visual and documentation inspections, support packaging and batch record reviews, manage deviations/CAPA and change control, participate in audits and quality reporting, and coach operational teams to ensure GMP and regulatory compliance.

Design, develop, and deploy custom industrial machine vision systems. Define project scope with customers, design optics and BOMs, perform POCs, oversee procurement, testing, installation, SLA support, and act as primary technical contact for vision system issues and documentation.

Provide hands-on support, maintenance, troubleshooting and lifecycle management of laboratory computer systems and IT infrastructure in GMP environments. Support Windows servers/workstations, VMware, network connectivity and instrument software; manage user access, security controls, software installs, validations (IQ/OQ/PQ), change control/CAPA, backups, audits and regulatory compliance (CSV, GAMP5, 21 CFR Part 11, Annex 11, Data Integrity).

Lead planning, coordination, and delivery of custom machine vision systems for industrial automation. Manage timelines, budgets, stakeholder communications, project documentation, billing, and cross-team collaboration. Liaise with engineering, vendors, sales, and customers across Europe to ensure solutions meet technical specifications and industry standards. Analyze procedures and support creation of design and technical documentation. Occasional travel (~10%).

Design, develop, and deploy industrial machine vision and automation systems. Define project scope, specify BOMs, design electrical/mechanical solutions, program PLCs and robots, oversee component selection, testing, installation, and SLA support. Serve as primary technical contact and improve processes and documentation.

Lead financial strategy, planning, cash flow, controls and reporting for a growing machine-vision and automation business. Manage project costing, margins, funding relationships, risk mitigation, audits, and scale the finance function while advising senior leadership and board.