Cedars-Sinai - Los Angeles, CA

posted 2 months ago

Full-time - Mid Level
Los Angeles, CA
Hospitals

About the position

The Biomedical Engineer at Cedars-Sinai's Heart Institute is responsible for the development and delivery of biomedical programs and products, focusing on the entire development lifecycle from conception to maintenance. This role involves hands-on development, mentoring junior developers, and collaborating with cross-functional teams to meet project milestones, particularly in the design and testing of medical devices such as transcatheter heart valves.

Responsibilities

  • Functions as the single point of contact to a cross-functional team.
  • Responsible for the development and delivery lifecycle during the following phases: Requirement Assessment, Development, Testing, and Delivery.
  • Works with inter-departmental teams to analyze and understand business requirements and documents new requirements.
  • Develops functionality based on requirements, following internal development standards.
  • Performs unit, regression, connectivity, and full end-to-end integration tests.
  • Collaborates with resources to migrate new or enhanced functionality from test to production.
  • Acts as a liaison with end users, research groups, and other business support areas.
  • Leads the design and development of a program/application/product.
  • Facilitates design and technical meetings and provides technical documentation.
  • Instructs, guides, and mentors junior-level staff.
  • Provides support during mission-critical upgrades/enhancements and new go-lives.
  • Develops and implements policies for security and confidentiality of program/application/product.
  • Performs other duties as assigned or required by management.
  • Responsible for the mechanical design, development, and testing of a transcatheter heart valve and related accessory components.

Requirements

  • Bachelor's degree in Biomedical Engineering or related field.
  • Experience in program/application/product development in a biomedical context.
  • Strong understanding of the development lifecycle, including design, testing, and production phases.
  • Proficiency in mechanical design and testing of biomedical devices.
  • Ability to mentor junior developers and lead cross-functional teams.

Nice-to-haves

  • Experience with regulatory submission processes for medical devices.
  • Familiarity with design verification testing methodologies.
  • Knowledge of aortic stenosis treatment options and related technologies.

Benefits

  • Competitive hourly wage between $49.92 and $79.87.
  • Health insurance coverage.
  • Retirement savings plan options.
  • Opportunities for professional development and continuing education.
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