Gusto

Chief Engineer

Gusto$155K — $195K *
Healthcare
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's or advanced degree in Electrical Engineering, Computer Engineering, Biomedical Engineering, or related field.
  • 10+ years of experience in medical device product development, with a focus on Class II or higher electronics/software-enabled devices.
  • Deep knowledge of electronics design tools, embedded C/C++, and firmware for biosensors or wearable technologies.
  • Leadership experience in building engineering teams and navigating regulatory processes like design controls and V&V.
  • Startup mindset with versatility and a proactive approach; must be hands-on.

Responsibilities

  • Provide strategic technical leadership in electronics and software development for biosensor devices.
  • Manage and direct external contractors and partners in key development activities, ensuring quality and integration with internal efforts.
  • Oversee post-delivery operations, including sensor refurbishment, technical support, and continuous improvement initiatives.
  • Lead the full product lifecycle from initial design to manufacturing transfer and market launch.
  • Build and mentor a lean internal technical team while leveraging external resources effectively.
  • Ensure compliance with medical device regulations and support regulatory submissions and audits.
  • Collaborate cross-functionally to deliver integrated biosensor solutions and manage product strategy.

Benefits

  • Opportunity to be part of a pioneering team in the biosensor technology space.
  • Ground-floor opportunity in a startup environment focused on innovative medical devices.
  • Hands-on technical leadership role with direct impact on product development.
  • Mentorship and team-building opportunities within a collaborative setting.
  • Engagement with advanced medical technologies and regulatory practices.
Full Job Description
Chief Engineer - Electronics & Software Efferent Labs, Inc. Location: Charleston, SC (local candidates preferred)

Description

We are a Medtech company developing breakthrough biosensor technologies to transform diagnostics, monitoring, and patient care. With no product on the market yet, this is a rare ground-floor opportunity to join a mission-driven team at the forefront of implantable and wearable sensing innovation. You will play a foundational role in turning cutting-edge sensor science into reliable, regulatory-compliant medical products.

As Chief Engineer, you will provide technical leadership and hands-on ownership of sensor electronics and software development and support. This includes analog/mixed-signal circuit, low-power systems, PCB layout, wireless connectivity (e.g., BLE), embedded firmware, real-time signal processing, algorithms, and software integration for biosensors. You will be part of a tight team, working directly with senior management and the CTO to manage contract efforts provided for the company, and lead the engineering function, collaborate closely with scientific teams, and drive products through design controls, verification/validation, risk management, and manufacturing transfer.

Key Responsibilities

- Provide strategic technical leadership across electronics (analog/mixed-signal circuits, low-power design, PCB layout, wireless connectivity, sensor interfaces) and software (embedded firmware, real-time signal processing, algorithms, data analytics, and supporting application/cloud integration) for our biosensor medical devices.

- Primarily manage and direct external contractors, design partners, engineering service firms, and contract manufacturers responsible for major development activities; set technical direction, review deliverables, ensure quality standards, manage timelines, resolve technical issues, and integrate their output with internal requirements.

- Lead in-house post-delivery device operations, including oversight of sensor refurbishment programs, field performance monitoring, technical support, failure analysis, sustaining engineering, software/firmware updates, and continuous improvement of deployed devices.

- Oversee the full product lifecycle for electronic and software systems-from initial architecture and outsourced development through verification, validation, risk management, manufacturing transfer, commercialization support, and post-market surveillance.

- Build and mentor a lean in-house technical team (including refurbishment technicians and sustaining engineers) while effectively leveraging and coordinating external development resources.

- Ensure full compliance with medical device regulations and standards, including FDA 21 CFR Part 820, ISO 13485, IEC 62304, IEC 60601, ISO 14971, and cybersecurity requirements across both development and post-market activities. Support regulatory submissions and audits.

- Collaborate cross-functionally with sensor science, mechanical engineering, quality assurance, regulatory affairs, clinical, and manufacturing teams to deliver integrated, reliable biosensor solutions.

- Develop and maintain technical roadmaps, manage supplier and contractor relationships, control budgets and timelines, and contribute to intellectual property development and long-term product strategy.

- Stay current with advancements in biosensor miniaturization, low-power embedded systems, secure connectivity, post-market device management best practices, and evolving medtech regulatory expectations.

Qualifications

- Bachelor's or advanced degree in Electrical Engineering, Computer Engineering, Biomedical Engineering, or related field.

- 10+ years of progressive experience in medical device product development, with a proven track record bringing Class II (or higher) electronics/software-enabled devices to market.

- Deep expertise in electronics design tools, embedded C/C++, firmware, signal processing, and relevant software languages. Direct biosensor, wearable, or electrochemical/optical sensing experience is strongly preferred.

- Hands-on leadership building engineering teams and navigating full regulatory pathways (design controls, V&V, risk analysis, submissions).

- Startup mentality: comfortable with high ownership, resourcefulness, and wearing multiple hats.

- Eligible to work in the U.S.; must be based in or willing to relocate to the Charleston, SC area.

Salary

$155,000 - $195,000 per year

About Gusto

Gusto is a cloud-based human resources software platform that provides payroll, benefits, and HR management services to small businesses. The company was founded in 2011 and is headquartered in San Francisco, California. Gusto's platform automates many of the administrative tasks associated with HR, such as payroll processing, tax filings, and benefits administration. The company also offers a range of HR services, including compliance support, employee onboarding, and time tracking. Gusto is committed to helping small businesses succeed by providing them with the tools and resources they need to manage their HR operations more efficiently.
Learn more about Gusto
Size
1,000 employees
Industry
Founded
2012

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