Manufacturing Process Specialist

Kenny-Whelan(a specialist division of the CPL group) are hiring aManufacturing Process Specialistfor the Bioprocess Supply operations Team to work on contract atJanssen Sciences in Ringaskiddy Cork Not considering Junior candidates or grads this time Desirable previous large scale CAPEX project experience and management of operations go live including handover, training technicians and management of any go live issues BU4 Manufacturing Process Specialist Location: Cork Ringaskiddy ContactJennDinanonoremail MUST ALREADY BE ELIGIBLE TO WORK ON CONTRACT IN THE REPUBLIC OF IRELAND- i.e have a valid work permit with 12 months permission + on it Job Summary Reporting to the Operations Manager, this position is responsible for BU4 Bioprocess supply operations, Supporting Capital Project Teams and supporting first line troubleshooting of the day to day activities within Operations - These activities include but are not confined to: Responsibilities Liaise with the planning group to optimize BU4 shop floor scheduling activities with a specific focus on buffer scheduling. Represent Operations on cross functional project implementation teams Monitoring and troubleshooting of the manufacturing process and equipment issues and process optimization Monitoring and reporting of process performance using statistical process control Troubleshooting of DCS (e.g Delta V) and PLC control systems Investigating and resolving issues raised within the Manufacturing Department Participate in/ Lead Cross Functional teams when required Support of Commissioning and Qualification activities Preparation and updating of Batch Records, Procedures and Work Instructions Provide process and equipment related training as required within the Manufacturing Department Completion of assigned tasks to support manufacture of quality biomedicines in accordance with cGMP and EHS requirements. Qualifications/Skills A relevant third level qualification in either Microbiology, Biochemistry, Pharmacy, Biotechnology, Science or Engineering Manufacturing experience within a GMP regulated environment. Experience of the cell culture, purification or biologics manufacturing support processes. Project / New equipment installation experience Process engineering experience Commissioning and qualification experience Postgraduate Qualification. Experience of Microsoft Word, Excel and Outlook. Experience of DCS (e.g. Delta V), SCADA and PLC systems Experience of SAP, LIMs and/or other business systems. 6-Sigma/Kepner-Tregoe or similar problem solving/decision making methodology training. Desirable previous large scale CAPEX project experience and management of operations go live including handover, training technicians and management of any go live issues MUST ALREADY BE ELIGIBLE TO WORK ON CONTRACT IN THE REPUBLIC OF IRELAND- i.e have a valid work permit with 12 months permission + on it All applications will be treated with the strictest of confidence. Contact Jenn Dinan on Skills: CAPEX projects SAP Delta V Bioprocess GMP Benefits: Staff Discounts Parking Paid Holidays