OverviewPlanet Pharma is seeking a vascular R&D Engineer working on a transformative Class III implantable device for aortic endovascular repair. This high-impact program which will progress through clinical studies, PMA submission, and global commercialization. You’ll lead the delivery system workstream, one of three core components of the device (alongside stent and graft covering), and manage a dedicated sub-team within a broader cross-functional group.ResponsibilitiesLead the design and development of the delivery system for an aortic stent graft, from concept through to commercializationManage and mentor a team of engineersDrive structured project execution across design, verification, validation, and regulatory milestonesCollaborate with clinical, regulatory, and manufacturing teams to ensure alignment with FDA Class III device requirements and PMA strategySupport clinical trial preparation and execution, including design transfer and documentationEnsure robust design control, risk management, and compliance with ISO 13485 and FDA 21 CFR Part 820Foster innovation and technical excellence while maintaining a disciplined, milestone-driven approachRequired QualificationsBachelor’s or Master’s degree in Biomedical Engineering, Mechanical Engineering, or Materials ScienceMinimum 5 years’ experience in medical device engineering, specifically Class III implantable devicesProven expertise in vascular technologies, ideally with aortic stent grafts, or alternatively in coronary stents/stent graftsDemonstrated leadership experience, with ability to delegate, motivate, and guide teams through full product lifecycleStrong organizational skills and a structured approach to problem-solving and project managementWhat You’ll GainA chance to shape a next-generation vascular device with global impactExposure to clinical and regulatory strategy for PMA and international marketsA collaborative, mission-driven culture focused on improving patient outcomes
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