Senior R&D Engineer – Aortic ProgramLocation: Limerick, Ireland
Sector: Medical Devices – Vascular Division
Be at the Cutting Edge of Aortic Endovascular Innovation Our client, a global leader in the medical device industry, is seeking a Senior R&D Engineer to play a pivotal role in the development of a groundbreaking Aortic Endovascular Repair (EVAR) device.
Based in their advanced facility in Limerick, Ireland, this role focuses on the design and development of a covered stent system aimed at treating aortic aneurysms and dissections.
This is an opportunity to lead within the Aortic Program of the Vascular Division, shaping the future of minimally invasive vascular treatments.
Role SummaryThe Senior R&D Engineer will lead the design, development, and optimisation of innovative Class III medical devices, including encapsulated stents and advanced delivery systems.
With a focus on the integration of coverings like PTFE and FEP, this role requires a deep understanding of stent encapsulation techniques and advanced forming and shaping processes.
The successful candidate will collaborate with cross-functional teams and contribute to the program's mission to transform patient care.
Key ResponsibilitiesDesign & Development: Lead the design and development of covered stent systems and associated delivery mechanisms within the Aortic Program.Material Expertise: Apply advanced knowledge of coverings such as PTFE, FEP, and electrospun PTFE in the development of encapsulated stents.Shaping & Forming: Develop and optimise processes for shaping and forming covers onto stents to meet stringent performance requirements.Team Leadership: Guide and mentor a team of engineers, fostering innovation and collaboration to achieve project milestones.Technical Problem-Solving: Address technical challenges in design, material selection, and manufacturing, ensuring the delivery of high-quality solutions.Collaboration: Work closely with cross-functional teams, including Quality, Regulatory, and Manufacturing, to drive projects from concept through to commercialisation.Regulatory Compliance: Ensure all designs meet regulatory standards for Class III medical devices.Continuous Improvement: Identify and implement process improvements to enhance efficiency and product performance.Qualifications and ExperienceEducation: Bachelor's or Master's degree in Biomedical Engineering, Mechanical Engineering, or a related field.Experience: At least 5 years of experience in the design and development of Class III medical devices, preferably in the vascular or aortic space.Specialised Expertise:Strong knowledge of stent systems, stent grafts, and delivery systems.Hands-on experience with stent coverings, including PTFE, FEP, and electrospun PTFE.Proficiency in shaping, forming, and encapsulating coverings onto stents.Leadership Skills: Proven experience leading a team of engineers and managing design projects.Problem-Solving Skills: Demonstrated ability to address complex technical challenges in design and development.Communication Skills: Excellent written and verbal communication skills for engaging with internal teams and external stakeholders.Why Join This Team?Contribute to the development of life-saving technologies that transform patient outcomes in aortic care.Be part of a global organisation renowned for its commitment to innovation and quality.Enjoy professional growth in a collaborative, cutting-edge environment.Experience the charm and culture of Limerick, one of Ireland's most vibrant cities, offering an exceptional quality of life.
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