Our client, a major multinational based here in Galway, are seeking a Supplier Quality Engineer II to join their team.
There are two roles available, one perm and one FTC
The Role:
As the Supplier Quality Engineer, you will work with suppliers in one or more commodities and also have the opportunity to be involved in supplier-related projects both at the site and across the global supplier quality management network.
The role will require an element of travel as part of supporting and working with our suppliers.
Responsibilities:
Technical team member on teams comprising representatives from Purchasing, Supplier Quality, and Business Units responsible for all aspects of Supplier Management.
Demonstrates technical skills in commodity management.
Responsible for supporting objectives of the team in terms of Quality, Cost, and Service.
Supports continuous improvement of Quality & Quality Systems, Service Capability, and Total Cost of Ownership throughout the Supply Chain.
Supports investigation of Material Quality issues as they arise.
Works with Quality, Procurement & Business Units to resolve issues and disposition product.
Promotes the Quality System within the supply base.
Works with Procurement, Supplier Quality Engineering, Receiving Inspection & Business Units to ensure that components meet established requirements.
Ensures that adequate corrective actions are identified, implemented, and controlled by Suppliers.
Provides guidance to other functional areas in applying Supplier Management system requirements.
Contributes to the development, maintenance, and improvement of Supplier Management policies and procedures.
Communicates effectively with all internal & external stakeholders.
Develops new supply sources with the Procurement Team.
Assesses and approves supplier-requested process changes.
Identifies, supports, and leads material value improvement projects (VIPs) throughout the Supply Chain.
Requirements:
Bachelor of Science Degree (level 8) in Engineering/Technology.4+ years experience in a manufacturing environment or equivalent with direct experience in a QA environment (preferably GMP regulated).Experience in the medical device industry is an advantage.
Experience on an automated/high volume line is an advantage.
For more information and a confidential discussion on the role, please contact Michelle Mc Inerney.
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