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