Our client, a Galway-based multinational, is looking to hire a Quality Engineer I on an initial 12-month contract.
Responsibilities: Ability to work within a team environment and build relationships across the organisation as well as with external suppliers & regulatory agencies.Co-ordination of complaint handling analysis and investigation activities for a wide range of Medtronic products, including receipt and documentation of incoming complaint devices relating to events.Perform analysis and investigation, and laboratory duties related to the complaint analysis and investigation activities. Assist in test procedure development and non-routine analyses relating to root cause investigations.Co-ordinate cross-functional activities in the investigation of customer complaints and determination of root cause.Possess an awareness of the manufacturing process and final products, including terminology associated with product use and failure modes typically experienced by the customer.Conduct laboratory support functions, perform and coordinate instrument maintenance, calibration, and alignment checks.Communicate key information, including escalation of quality issues to management and key extended post-market quality teams & functional management to ensure full engagement & alignment.Contribute to continuous improvement activities to support the rollout of cell operating systems and principles, delivering cost-down through innovative solutions.Ensure that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.Support new product launch as part of the Product Development Process, ensuring that requirements are included in the process.Ensure compliance with all applicable department and site-wide procedures and regulations. Support internal and external audit preparation and activity, which includes application and maintenance of quality standards for all activities associated.Requirements: Minimum of a bachelor's degree (Level 8 NFQ) in a relevant technical discipline (e.g., Engineering, Science).Experience in a medical devices or related environment desirable.Strong interpersonal, communication, and organizational skills.Practical working knowledge of statistical data analysis, problem-solving, and quality improvement tools and techniques preferable.Technical writing skills.Ability to multi-task and take initiative is essential.Effective time management skills.Builds and maintains positive relationships with others; shows respect and consideration for others.For more information and a confidential discussion on the role, please contact Michelle Mc Inerney. ****** 091 706717
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