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Imperative Care

Stroke-care medical devices and trials

Staff R&D Engineer - Devices

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeCampbell, CA, USA

About the Job

Requirements

  • A bachelor's degree in engineering or a related discipline and at least 8 years of related experience driving innovation in the development of flexible medical device instruments, or an equivalent combination of education and work experience in a related regulated industry.
  • Strong background in intravascular medical device design, development, prototyping, design verification, test method validation, and manufacturing methods and controls, with a focus on guidewires, stents, stent delivery devices, catheters, or similar devices.
  • Familiarity with special-purpose machine design, automation, precision machining, including centerless grinding, CNC Swiss machining, and laser micromachining; equipment and manufacturing methods used for device fabrication; and process development and validation within a regulated manufacturing environment.
  • Experience with advanced materials such as polymers, stainless steel, platinum, hydrophilic coatings, and nitinol, and related precision fabrication and processing techniques, including tube drawing, coil winding, braiding, laser processing, grinding, electrical discharge machining, and CNC.
  • Ability to travel domestically and internationally as necessary.

Responsibilities

  • Lead technical innovation, design, development, manufacturability, and testing, verification, and validation of new medical devices, including specialty devices for interventional neurovascular and vascular markets, from early stage through commercial release and transfer to manufacturing according to established Design Control procedures.
  • Work with Marketing, Clinical Engineering, and physician partners to define product requirements, create designs using computer-aided design software (SolidWorks), and lead prototyping, bench and other preclinical testing, and experiments to ensure product performance, reliability, and safety.
  • Collaborate with Process Development, Quality, Regulatory, Marketing, and Manufacturing/Operations teams and contract manufacturers to ensure new product manufacturability, robust process control, and alignment with design specifications, quality systems, operational capabilities, and cost targets.
  • Optimize and scale existing processes to improve efficiency, yield, and product quality, working with outside partners as needed.
  • Support and collaborate with contract manufacturing partners to design, implement, and validate manufacturing equipment and processes for scalable, high-accuracy medical device production.

About the Company

Imperative Care

Stroke-care medical devices and trials

Imperative Care develops medical technologies for stroke and vascular diseases, delivering devices and solutions to healthcare providers to improve patient care. Its approach centers on rapid development and testing, guided by clinical evidence and feedback from physicians, including large multicenter trials like the Imperative Trial. The company moves from concept to market by conducting clinical research and refining products through physician input, with revenue generated from selling devices to hospitals and clinicians. Its differentiator is the combination of evidence-based development, physician-driven insights, and an agile response to the evolving needs of stroke care. The overarching goal is to improve outcomes for stroke patients by providing practical, clinically validated tools that healthcare teams can adopt quickly and effectively.

Company size
201-500
Company stage
N/A
Total funding
$598M
Headquarters
Campbell, CA
Founded
2015

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