Senior R&D Engineer, Transcatheter Heart Valves

Jenavalve Technology Inc

Irvine (CA)

On-site

USD 86,000 - 117,000

Full time

14 days+
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Benefits offered by this job

Health insurance

Job summary

Jenavalve Technology Inc. in Irvine, CA is seeking a Senior Engineer, Research and Development to contribute to subsystems and components for transcatheter heart valves and delivery systems.

This role requires collaboration across engineering, quality, and manufacturing to ensure robust designs and compliant documentation. The successful candidate will design, document, procure, and validate components, supervise Technicians, and lead risk analysis and verification activities within a medical

Qualifications

  • BS degree in Mechanical or Biomedical Engineering or equivalent.
  • 3–5+ years in R&D, level I–III DOE.
  • Knowledge of medical device product development and quality systems.
  • Ability to work with cross-functional teams.
  • Strong documentation and communication skills.

Responsibilities

  • Develop components or subsystems for transcatheter heart valves and delivery systems.
  • Design and document components and subsystems.
  • Procure components.
  • Develop assembly procedures.
  • Conduct engineering analysis and feasibility testing of components of subsystems.
  • Partner with Quality to conduct risk analysis and design verification.
  • Partner with Manufacturing to develop procedures and transfer to external manufacturing houses.
  • Supervise Technicians.

Skills

Cross-functional teamwork
Documentation
Verbal & written communication
Hands-on work
Attention to detail

Education

Bachelor of Science in Mechanical or Biomedical Engineering

Job description

Jenavalve Technology Inc. in Irvine, CA is seeking a Senior Engineer, Research and Development to contribute to subsystems and components for transcatheter heart valves and delivery systems.

This role requires collaboration across engineering, quality, and manufacturing to ensure robust designs and compliant documentation. The successful candidate will design, document, procure, and validate components, supervise Technicians, and lead risk analysis and verification activities within a medical

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