The Senior Design Quality Engineer will play a critical role in supporting the Interventional Therapy business by developing, implementing, and maintaining quality standards for new product development. The position requires close collaboration with engineering and manufacturing teams to ensure compliance with regulatory and internal requirements, emphasizing the inspection, testing, and evaluation of product and process quality. The successful candidate will drive design quality requirements, continuous improvement initiatives, support root cause analysis, and ensure that corrective actions are effective and thoroughly documented.
Responsibilities
Develop, modify, apply, and maintain quality standards and protocols for processing materials into partially finished or finished products.
Collaborate with engineering and manufacturing teams to establish and uphold quality standards, ensuring alignment with regulatory requirements.
Design and implement methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.
Specify inspection and testing mechanisms and equipment; conduct quality assurance tests; perform statistical analyses to assess costs and determine responsibilities for products or materials that do not meet required standards and specifications.
Ensure that corrective measures meet acceptable reliability standards and that all documentation complies with regulatory requirements.
Specialize in areas such as design quality, incoming material inspection, production control, product evaluation and reliability, inventory control, and research and development as applicable to product or process quality.
Review and approve quality documents from a regulatory standpoint to ensure compliance with industry standards.
Drive continuous improvement initiatives across processes, fostering a culture of quality and accountability.
Provide training and support to team members on quality standards and best practices.
Qualifications
Bachelor’s degree in Mechanical, Electrical Engineering, or a related field.
4 years of industry experience.
Experience in medical device quality assurance with a strong understanding of regulatory requirements.
Excellent analytical skills and the ability to work independently on moderately complex projects under limited supervision.
Preferred specialization in design quality and support for R&D and production activities within the interventional therapy space.
Strong communication and interpersonal skills, enabling effective collaboration with cross-functional teams.
Benefits & Compensation
Competitive salary with a range in Ireland: 64,640.00 EUR - 96,960.00 EUR. Eligibility for a short‑term incentive called the Medtronic Incentive Plan (MIP). Flexible benefits package available.
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