This 12month contract position is responsible for all activities required to support the successful delivery of new engineering projects with our Cork based client.ResponsibilitiesLead the delivery of Engineering projects on time, on budget & in accordance with all project & business goals.Scope new Engineering projects & secure Capital approvalLead, support and participate in commissioning and qualification activitiesTroubleshooting of process or equipment issuesCoordination of project interfaces with other projects and departmentsCoordination of and interfaces with third parties (suppliers, customers, service providers, etc.)Coordination of project documentation and or P&IDsProject Cost Management (estimation, forecasting, tracking, updating)Project Scheduling (creation, tracking & reporting)Project progress reporting & Risk ManagementConstructability & Maintainability/Operability studiesProject Resource ManagementReviewing current condition of systems (structural, E&I as well as safety, permitting and documentation)Organization & coordination of project meetingsInvestigating and resolving Deviations raised within the Engineering DepartmentProvide process and equipment related training as required.Completion of assigned tasks to support manufacture of quality medicines in accordance with cGMP and EHS requirements.Retrospective project performance review vs project goals and lessons learned.Responsible and accountable for assuring the safe accomplishment of job activities, in compliance with corporate and cGMP/EHS regulatory requirements.Carry out routine and non-routine tasks delegated by the Manager according to appropriate procedures, values and standards.Compliance with Engineering and general site procedures at all timesCompletion of all documentation in compliance with site procedures and GDPPrioritize and scheduling of activities to support business needs and to meet requirements of Master Production SchedulesGenerate and assist with generation, review and revision of Engineering documentation as necessary.Ensure that personal training requirements are completed in compliance with site procedures.Support ongoing studies by Operations, Quality Validation, MSAT, Facilities and other support functions.RequirementsThird level qualification in Engineering or Science.3+ years experience working in Pharmaceutical environmentExperience of delivering engineering projects within a GMP regulated environment, specifically Pharma.Qualification in Project Management6-Sigma or similar problem solving/decision making methodology trainingExperience of working within an Engineering team in a multinational corporate environment.
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