Ingénieur fiabilité sr page is loaded## Ingénieur fiabilité srremote type: Sur sitelocations: Galway, County Galway, Irelandtime type: Temps pleinposted on: Offre publiée hiertime left to apply: Date de fin : 30 avril 2026 (Il reste 7 jour(s) pour postuler)job requisition id: R63814Chez Medtronic, vous pouvez entamer une longue carrière d’exploration et d’innovation tout en aidant à soutenir l’accès aux soins de santé et l’équité pour tous. Vous dirigerez avec détermination en surmontant les obstacles à l’innovation dans un monde davantage connecté et compatissant.**Journée type****Medtronic**At Medtronic, we value what makes you unique. Be part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.**Our Purpose** Peripheral Vascular Health offers a diverse portfolio of devices and therapies to restore the right blood flow to the right patient.Peripheral Vascular Health therapies treat patients with Peripheral and Carotid Artery Disease, End-Stage Renal Disease, Superficial and Deep Venous Diseases, and a variety of conditions treated with Peripheral Embolization. The operating unit leads the way in the Superficial Venous, Deep Venous Stenting, and Drug- Coated Balloon markets, caring for nearly 1 million patients globally with lifesaving and life-enhancing therapies.***Come for a job, stay for a career!*****A Day in The Life Of:**Responsibilities may include the following and other duties may be assigned.* You will act as an extended team member on a PDP Project, representing the Design Assurance function and reporting indirectly to the quality lead on the project.* You will lead strategies for risk management, test method validations, design verification and shelf-life protocols / reports.* You will be responsible for keeping abreast of industry best practice with respect to product design.* You will maintain expert, up to date knowledge of developments in regulatory compliance requirements for product design, development, transfer and commercialisation activities.* You will collaborate with various departments both internally and externally to build strong partnerships.* You will be required to provide Quality input into new product development, process improvements and change control.* As required, you will support cross functional teams to design protocols to ensure that new products/ product changes are adequately evaluated/tested with respect to standard requirements.**Key Skills & Experience*** We are seeking a qualified individual with an NFQ Level 8 degree and minimum of 4 years of relevant experience OR Master's degree with a minimum of 2 years relevant experience OR PhD with 0 years relevant experience.* The candidate should be an established and productive individual contributor who works independently with general supervision on larger, moderately complex projects and assignments.* The candidate should have a practical knowledge of project management.* The candidate should be a dynamic team player and leader who can work effectively and proactively on cross-functional teams.* The candidate should have competent experience in medical device product design.* Excellent communication skills and the ability to influence are critical for this role.* Fluency in English, both written and spoken, is required.* Flexibility to travel