Responsible for maintaining, optimizing, and improving manufacturing automation systems within a GMP-regulated environment, ensuring system performance, compliance, and reliability.SectorsPharmaceuticals, Biotechnology, ManufacturingCompany Size & TypeLarge multinational pharmaceutical manufacturerNon-Negotiable RequirementsDegree in Engineering (Automation, Robotics, Computer Science or related) or equivalentMinimum 5 years of Experience in GMP manufacturing environmentsExperience with industrial automation systemsExperience with at least one of: Siemens, Omron, Mitsubishi automation platformsKnowledge of GxP/QA requirementsKnowledge of 21 CFR Part 11 and/or Annex 11Experience in pharmaceutical manufacturingKnowledge of GAMP or ANSI/ISA standardsFamiliarity with ISPE standardsExperience with data analysisExperience contributing to automation strategy or roadmapExperience mentoring or training othersResponsibilitiesMaintain and optimise automation systems to ensure uptime and performanceManage user access, backups, and system restoresImplement corrective actions and liaise with vendor technical supportSupport capital projects, including planning, execution, and documentationEnsure compliance with site and corporate quality systemsCreate and maintain engineering documentation and test scriptsDevelop and implement automation standardisation strategiesDeliver automation solutions for manufacturing processesDrive automation projects to meet cost, schedule, and technical targets
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