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. Assisting in test procedure development and non-routine analyses relating to root cause investigations.
* Co-ordination of 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 the 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 is desirable.
* Strong interpersonal, communication, and organizational skills.
* Practical working knowledge of statistical data analysis, problem solving, and quality improvement tools and techniques is preferable.
* Technical writing skills.
* Ability to multi-task and take initiative is essential.
* Builds and maintains positive relationships with others; shows respect and consideration for others.
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