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Stent Design Engineer Jobs (NOW HIRING)

Open Scientific

Sr. Engineer of Process Development

Sunrise, FL · On-site

$99K - $128K/yr

Design, evaluate, implement and monitor processes and operating systems for the manufacture aortic ... stent grafts * Develop and implement new mfg processes, execute process validations such as IQ, OQ ...

Barry Wehmiller Group

Controls Engineer III

Rochester, NH · On-site

$81K - $105K/yr

... design challenges. Our equipment has become the industry standard for stent crimping, balloon ... Our experienced team of engineers has been instrumental in automating manual processes that enable ...

Medtronic

Senior R&T Engineer - Onsite

Irvine, CA · On-site

$112K - $154K/yr

Through catheters, stent retrievers, flow diversion, and embolization systems, these solutions ... Electro-mechanical design, execution, and analysis of pre-clinical and cadaveric studies ...

New

Cordis

Sr R&D Engineer (Onsite)

Santa Clara, CA

$106K - $155K/yr

... stent delivery systems, and access closure devices. As an R&D engineer you will work in the design, development, and testing of Cardiovascular and Vascular Medical Devices. Engineers at Cordis work ...

Medtronic

Senior R&T Engineer - Onsite

Irvine, CA · On-site

$112K - $154K/yr

Through catheters, stent retrievers, flow diversion, and embolization systems, these solutions ... Electro-mechanical design, execution, and analysis of pre-clinical and cadaveric studies ...

New

Cordis

Sr R&D Engineer (Onsite)

Santa Clara, CA · On-site

$106K - $155K/yr

... stent delivery systems, and access closure devices. As an R&D engineer you will work in the design, development, and testing of Cardiovascular and Vascular Medical Devices. Engineers at Cordis work ...

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Stent Design Engineer information

What is the difference between Stent Design Engineer vs Interventional Cardiology Device Engineer?

AspectStent Design EngineerInterventional Cardiology Device Engineer
CredentialsBachelor's/Master's in Biomedical, Mechanical, or Materials EngineeringBachelor's/Master's in Biomedical, Mechanical, or related engineering
Work EnvironmentResearch labs, R&D departments, manufacturing facilitiesMedical device companies, hospitals, clinical settings
Industry UsageDesigning coronary and peripheral stentsDeveloping a range of interventional cardiology devices including stents

Both roles involve biomedical engineering skills and work within medical device industries. A Stent Design Engineer specializes specifically in creating stents, while an Interventional Cardiology Device Engineer may work on a broader range of devices used in cardiology procedures. The roles often overlap in skills and environment but differ in scope and focus.

What are the key skills and qualifications needed to thrive as a Stent Design Engineer, and why are they important?

To thrive as a Stent Design Engineer, you need a strong background in biomedical or mechanical engineering, with expertise in materials science and device design, typically supported by a relevant engineering degree. Familiarity with CAD software, finite element analysis (FEA) tools, and regulatory standards such as ISO 25539 is essential. Creativity, problem-solving, and effective collaboration with cross-functional teams are crucial soft skills for success in this role. These competencies ensure the development of safe, innovative stent devices that meet both clinical needs and regulatory requirements.

What does a Stent Design Engineer do?

A Stent Design Engineer is responsible for designing and developing stents, which are small mesh tubes used to treat narrowed or blocked blood vessels. They work closely with medical professionals and use specialized software and materials to create stents that meet strict safety and performance standards. Their work involves prototyping, testing, and refining stent designs to improve patient outcomes. Additionally, they ensure that their designs comply with regulatory requirements and collaborate with manufacturing teams to bring new stent products to market.

What are some common challenges faced by a Stent Design Engineer when translating design concepts into manufacturable products?

Stent Design Engineers often encounter challenges related to balancing innovative design features with manufacturability and regulatory requirements. Translating a concept into a reliable medical device requires close collaboration with manufacturing, quality assurance, and regulatory teams to ensure materials, tolerances, and design specifications meet both clinical and production standards. Additionally, engineers must consider factors like biocompatibility, durability, and ease of deployment, which can complicate the design process. Iterative prototyping, rigorous testing, and cross-functional communication are key to overcoming these obstacles and delivering safe, effective stent products.
Infographic showing various Stent Design Engineer job openings in the United States as of May 2026, with employment types broken down into 15% Internship, 15% As Needed, 15% Full Time, 39% Part Time, 8% Contract, and 8% Nights. Highlights an 98% Physical, and 2% Remote job distribution.

Sr. Engineer of Process Development

Open Scientific

Sunrise, FL

$99K - $128K/yr

Full-time

Posted 23 days ago

Job description

Company Description

Headquartered in the U.S., our client  is a division of a global company devoted to the research and development, manufacturing, and distribution of highly specialized products for Healthcare and Life Sciences worldwide.

This is a great step for someone who is looking to take a seat in a senior role and is looking to further progress down the line. If you are looking to take on a challenging role within a rapidly growing division that provides an A+ environment and excellent benefits, do not miss out on a potential opportunity to get your foot in the door. 


Job Description
  • Design, evaluate, implement and monitor processes and operating systems for the manufacture aortic stent grafts
  • Develop and implement new mfg processes, execute process validations such as IQ, OQ, PQ protocols and reports
  • Lead the design transfer phase including product development, validation planning, design for manufacturability and assembly, Design of Experiments, process capability analysis, etc.
  • Conduct risk analysis including DFMEA, PFMEA and create/maintain necessary documentation.
  • Support the conversion of small-scale processes into commercially viable large-scale operations.
  • Monitor and improve the efficiency, output and safety of manufacturing processes through observations and measurements as well as by collecting and interpreting data from other technical and operating personnel.
  • Other various responsibilities and projects, as necessary
Qualifications
  • 4 - year engineering degree or equivalent experience
  • 3+ years of experience in a technical role in the medical device industry
  • Project management experience in the medical device industry
  • Experience and understanding of quality system regulations (e.g. 21CFR820, ISO13485).
  • Project management experience in the medical device industry
  • Experience with polymers, medical grade metals and medical packaging
  • Hands-on knowledge of electronics, motion control, plastics, metallurgy, and manufacturing processes
  • Experience with polymers, medical grade metals and medical packaging

Please send suitable resumes in confidence to JPCuadra @ openscientific.com

Additional Information

All your information will be kept confidential according to EEO guidelines.

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