We’re currently recruiting for an exciting opportunity with an award-winning Medical Device organization based in Galway.


This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.


Duties


At our Manufacturing Engineering Department, we focus on providing Stable, Flexible and Cost Effective Manufacturing processes that produce the highest quality products through innovative engineering services and solutions. Manufacturing Engineers are directly involved in maintaining and continuously improving the manufacturing processes to the highest standards.

Responsibilities may include the following and other duties may be assigned.
You will be responsible for product family (processes, equipment and documentation to meet quality, service and cost objectives for AOP targets). You will be responsible for manufacturing line/cell products, processes, equipment, and documentation to meet quality, service and cost objectives for AOP targets. Knowledge of MDR and Project Management principles desirable.

Responsible for the installation, calibration and preventative maintenance of process equipment.
You will lead process improvement projects, Lean Sigma initiatives and demonstrate ability to identify and project lead continuous process improvement/cost saving opportunities. You will guide the conceptualization of new methodologies, materials, machines, processes or products. You will have the ability to lead cross site engineering projects to harness corporate wide best practice. You will have experience in validation of manufacturing processes and associated equipment and understand failure points and take appropriate steps to address same. You will liaise with other sites regarding technical issues.




Education & Experience


We are looking for a qualified person to a minimum of level 8 BSc/BEng Degree in Engineering or Science. Minimum 5 years of related experience. You will have a proven record of successful project and people management experience. You will have experience of working in a changing environment within the medical devices sector, preferably with familiarity of ISO and FDA regulations. You will have strong technical engineering knowledge with problem solving experience using DMAIC methodology.• Project management
• Demonstration of previous Continuous improvement projects/initiatives
• Familiar with applicable cGMP and other business compliance regulations
• Demonstrate capabilities in strategic thinking
• Customer focus and results and performance driven
• Sense of Urgency
• Ability to work well within team structures and provide leadership.