manufacturing initiatives including MES, electronic batch records, paperless production, laboratory digitisation, analytics, AI, integration, cloud, and edge technologies. Ensure architecture decisions align with GMP, GxP, CSV/CSA, data integrity, cybersecurity, validation, and operational resilience requirements. Develop and maintain architecture artefacts including capability maps, data flows, system landscapes, integration diagrams … Strong understanding of pharmaceutical manufacturing technologies and processes. Proven experience defining architecture roadmaps, standards, governance frameworks, integration strategies, and platform lifecycle plans. Experience supporting GxP-regulated environments, including validation, data integrity, change control, audit readiness, and inspection support. Knowledge of manufacturing systems including: ERP MES LIMS ...