Senior Project Engineer - Cork

This 12month contract position is responsible for all activities required to support the successful delivery of new engineering projects with our Cork based client.

• Lead the delivery of Engineering projects on time, on budget & in accordance with all project & business goals.
• Scope new Engineering projects & secure Capital approval
• Lead, support and participate in commissioning and qualification activities
• Troubleshooting of process or equipment issues
• Coordination of project interfaces with other projects and departments
• Coordination of and interfaces with third parties (suppliers, customers, service providers, etc.)
• Coordination of project documentation and or P&IDs
• Project Cost Management (estimation, forecasting, tracking, updating)
• Project Scheduling (creation, tracking & reporting)
• Project progress reporting & Risk Management
• Constructability & Maintainability/Operability studies
• Project Resource Management
• Reviewing current condition of systems (structural, E&I as well as safety, permitting and documentation)
• Organization & coordination of project meetings
• Investigating and resolving Deviations raised within the Engineering Department
• Provide 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 times
• Completion of all documentation in compliance with site procedures and GDP
• Prioritize and scheduling of activities to support business needs and to meet requirements of Master Production Schedules
• Generate 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.

• Third level qualification in Engineering or Science.
• 3+ years experience working in Pharmaceutical environment
• Experience of delivering engineering projects within a GMP regulated environment, specifically Pharma. xcfaprz
• Qualification in Project Management
• 6-Sigma or similar problem solving/decision making methodology training
• Experience of working within an Engineering team in a multinational corporate environment.