IT Lab Engineer

Responsibilities Responsible for the specification and design of IT solutions that directly support the QC Lab within our new State of the Art Biotechnology Facility. Accountable for support and configuration of relevant Technologies ensuring that appropriate support to operations is maintained, and that all operational activities are compliant with regulatory, safety, cybersecurity, business continuity and […]

Automation Engineer

Responsibilities   Reporting to the Automation Engineering Manager, this is a key role supporting the Site Automations systems including the manufacturing process equipment, manufacturing Network, BMS/EMS, SCADA, PLCs/HMIs and Factory data systems. Manage multiple projects and tasks to address factory automation obsolescence including equipment priority, project management to meet agreed schedules. Develop regulatory compliant data […]

Automation Engineer – Laboratory Lead

Responsibilities   The site Lead Engineer for labs will be responsible for delivery of Automation and IT scope on one or more lab projects in the portfolio of capital projects. Work closely with the site teams responsible for the full Automation and IT scope and with vendors / partners with responsibility for delivery of systems. […]

Delta V Engineer

Responsibilities   Reporting to the DeltaV Lead, supporting delivery of DeltaV scope on the project. Develop and/or review System Development Life Cycle (SDLC) deliverables, compliant with site standards. Work with DeltaV vendor in development of systems architecture, specifications, controls strategies, sequence of operations through all design stages. Work closely with the Quality function to ensure […]

Automation Engineer

Responsibilities Reporting to the Automation Engineering Manager, this is a key role supporting the Site Automations systems including the manufacturing process equipment, manufacturing Network, BMS/EMS, SCADA, PLCs/HMIs and Factory data systems. Manage multiple projects and tasks to address factory automation obsolescence including equipment priority, project management to meet agreed schedules. Develop regulatory compliant data migration […]

QA Validation Specialist

Responsibilities   Quality oversight of GMP compliance for engineering and validation deliverables related to site and capital projects including requirements definition, specification, engineering design, qualification and change management. Review and approval of validation protocols, reports, procedures and other related documents to ensure compliance to internal procedures and regulatory requirements. Evaluation and approval of deviations related […]

Automation Engineer PLC SCADA

I am partnered with a global pharmaceutical company based in Dublin in their search for an experienced SCADA Engineer. The successful candidate will be responsible for the development, commissioning, and support of a plant wide SCADA project. Responsibilities: You will also be responsible for the development of the SCADA systems from design, specification, programming, simulation, […]

Senior MES Engineer

Reporting to the Project MES Lead, specifically responsible for MES Systems (Werum PasX). Required to work closely with the site teams responsible for the full Automation and IT scope and with vendors / partners with responsibility for delivery of systems.   Responsibilities   Develop and/or review System Development Life Cycle (SDLC) deliverables, compliant with site […]

QAIT Specialist Shopfloor Systems

The successful candidate will join the QA IT team to provide independent compliance oversight and support for the implementation of new shopfloor automation systems and modifications to existing site systems.  The QA IT specialist will ensure compliance with regulatory expectations and company Computer Systems Validation (CSV), System Development Lifecycle (SDLC), Cyber Security and Data Integrity […]

Quality Assurance Validation Specialist

Responsibilities   Act as Quality Assurance approver for qualification/validation lifecycle documents. Serve as a quality assurance resource for assessing validation requirements, non-conformance, impact assessments, root cause analysis and implementation of CAPA found during CQV activities. Provide Quality Assurance Validation support for Steam In Place (SIP) of buffer and media preparation systems, upstream (bioreactors) and downstream […]