Validation Engineer

4 days ago

Dublin, Ireland Impact Iel Full time

Impact Engineering Ltd is a trusted automation partner based in Dublin, focusing on business transformation, digitalisation, automation projects, and targeted automation training.We offer a range of services including consultancy, system upgrades, process optimization, and automation front line support.Our mission is to deliver innovative, cost-competitive, and compliant automation solutions to add value to businesses through digitalization.OverviewThis is a site based contract role for a CQV Engineer at our customer site, based in Northern Ireland.This position is a key element of a project team that will be based on site.ResponsibilitiesTake part in the planning, execution, and oversight of CQV activities to ensure that automated systems meet predefined requirements and operate within validated parameters.Create and maintain validation documentation, including protocols, test scripts, and validation reports.Ensure that all automation systems comply with industry standards, GxP guidelines, and regulatory mandates.Maintain accurate and organized documentation for all validation activities, including equipment and software specifications, validation protocols, and records.Collaborate with our client to ensure the proper documentation of automated system configurations.Qualifications & Experience5+ years working experience as CQV Engineer on Pharmaceutical or Biopharmaceutical projects or comparable experienceExperience with DeltaV is preferredOn site project experience is essential.Ability to work on site every dayAbility to interact and communicate with other engineering and business disciplines.Seniority levelMid-Senior levelEmployment typeFull-timeJob functionEngineering, Information Technology, and ManufacturingIndustriesPharmaceutical ManufacturingAutomation Machinery ManufacturingBiotechnology Research#J-*****-Ljbffr

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