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ASE-S1-05Job PurposeResponsible for the Manufacturing of the pharmaceutical products within designated suites, accountable for the processes within an assigned manufacturing area, working closely with cross functional teams at Mundipharma. Ensuring that production KPIs are delivered whilst meeting the highest standards of cGMP and Health & Safety.Key ResponsibilitiesTo support the Cell Leads in ensuring that the Manufacturing targets are achieved within their respective area and working as a team to cover breaks and operational activities.Ensure that tasks for the oncoming shift are completed and prepared, so they are starting from a good position. E.g. parts ready for change overs, materials are readily available, 5S and workplace management is in good order.Take part in root cause analysis / problem solving as part of their development and to develop their process knowledge / understanding.Closely working alongside Engineering team and Quality team as required to overcome and resolve atypical events.Understand & support KPI delivery, including but not limited to, Changeover time targets, run speed performance and downtime or performance losses.Being involved in Continuous Improvement initiatives and projects as required such as waste reduction and yield improvements.A champion of small Kaizen projects and actively involved in Autonomous Maintenance program.Supporting any validation activities including completion of Validation Protocols and sampling requirements.Ownership for working environment, delivering work place management processes (5S delivery, GMP of area, stock levels).Managing own workload and able to resolve issues. Supporting the Co-Ordinator and Shift Manager through inputting of operational data (Downtime reporting, maximo submission).Good Manufacturing Practice (GMP)Good know