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Principal Electrical Engineer

MicroTransponder
Minneapolis, United Statesfull_timeVerifiedPosted 23 Oct 2025
💰 $160,000/yr($110,000/yr$160,000/yr)

About the role

About MicroTransponder

MicroTransponder, Inc. is dedicated to transforming the lives of stroke survivors through its innovative neurostimulation technology. The company's flagship product, the FDA-approved Vivistim® Paired VNS™ System, enhances stroke rehabilitation by pairing vagus nerve stimulation (VNS) with physical and occupational therapy. This approach leverages the brain's neuroplasticity to improve upper limb function, offering new hope to those with chronic arm and hand impairments following an ischemic stroke.

By integrating this therapy into rehabilitation programs, MicroTransponder aims to help stroke survivors regain independence in daily activities and enhance their quality of life. The company's commitment to advancing stroke recovery is evident in its ongoing research and collaboration with healthcare providers to make this therapy accessible to more patients.

About the role


The Principal Electrical Engineer’s primary responsibility is to support the electrical development
and maintenance of MicroTransponder’s products and systems including the Vivistim Paired
VNS Therapy system. This role includes development for new products, continuation activities
to maintain existing products, and support for manufacturing processes.
The successful candidate will work closely with in-house teams (Quality, Operations,
Regulatory, Marketing, Clinical, and Sales), external contract design partners, and clinicians to
ensure products are developed, supported, and meet customer needs while adhering to design
controls, applicable standards, and regulations.

What you'll do

  • Support product development projects through the full lifecycle, concept to production
    transfer, as dictated by design controls. This may include deliverables such as: concept
    generation, schedule generation, identifying resource requirements, developing design
    requirements, verifying and validating design requirements, and transfer to production.
  • Manage and execute continuation activities for internal and contract manufacturer
    changes and projects. This may include managing a project and/or being an individual
    contributor as required by the task.
  • Support maintenance of existing devices and systems through technical evaluation of
    field returns, feedback, and complaints.
  • Executes as technical lead on projects and/or deliverables not requiring a larger project
    team. This may include identifying requirements, tasks, schedule, budget and
    completing these deliverables and documentation with minimal external support.
  • Ensure compliance to electrical safety standards IEC60601-1 and IEC 60601-1-2, and to
    other product specific international standards including ISO 14708-3.
  • Develop and perform, or guide development and performance of bench-top testing and
    verification / validation activities per applicable standards and product requirements. This
    includes documentation of test protocols and results to meet design control and quality
    system requirements.
  • Participate in Design Assurance activities including risk assessment and FMEA.
  • Provide technical support for product manufacturing including development and
    validation of manufacturing and test processes.
  • Support analysis of product and clinical data through direct analysis and development of
    automated systems to process data.
  • Apply engineering knowledge and knowledge of medical device industry to proactively
    assist company in developing strategic plans for development of new products and
    enhancements to existing products.
  • Generate and leverage existing and new intellectual property for new therapy and/or clinical use.
  • Provide technical supervision and mentorship to lower-level electrical engineers and
    direction to other technical personnel including external contractors as required.

Qualifications

  • BS in Electrical engineering from an accredited university.
  • 8+ years of experience in medical device development; or equivalent combination of
    relevant experience and education. Active implantable medical device experience
    preferred.
  • Pr

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Company

MicroTransponder

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