Overview
Planet 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.
Responsibilities
Lead the design and development of the
delivery system
for an aortic stent graft, from concept through to commercialization
Manage and mentor a team of engineers
Drive structured project execution across design, verification, validation, and regulatory milestones
Collaborate with clinical, regulatory, and manufacturing teams to ensure alignment with FDA Class III device requirements and PMA strategy
Support clinical trial preparation and execution, including design transfer and documentation
Ensure robust design control, risk management, and compliance with ISO 13485 and FDA 21 CFR Part 820
Foster innovation and technical excellence while maintaining a disciplined, milestone-driven approach
Required Qualifications
Bachelor's or Master's degree in
Biomedical Engineering
,
Mechanical Engineering
, or
Materials Science
Minimum
5 years' experience
in medical device engineering, specifically Class III implantable devices
Proven expertise in
vascular technologies
, ideally with
aortic stent grafts
, or alternatively in
coronary stents/stent grafts
Demonstrated
leadership experience
, with ability to delegate, motivate, and guide teams through full product lifecycle
Strong organizational skills and a structured approach to problem-solving and project management
What You'll Gain
A chance to shape a next-generation vascular device with global impact
Exposure to clinical and regulatory strategy for PMA and international markets
A collaborative, mission-driven culture focused on improving patient outcomes
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