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Engineer: Sr. Electrical Design Engineer

Nanobiosym

Cambridge (MA)

On-site

USD 95,000 - 130,000

Full time

2 days ago
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Job summary

Nanobiosym, an innovative company at the intersection of physics, nanotechnology and biomedicine, is seeking a Senior Electrical Design Engineer. In this hands-on role, you will lead the design and development of advanced PCB systems, ensuring compliance with industry standards while delivering impactful products.

Qualifications

  • 5-10+ years hands-on experience in product development.
  • Strong understanding of FDA and ISO 13485 compliance standards.
  • Proven track record of delivering production-quality PCBs.

Responsibilities

  • Own full hardware development lifecycle from specification to manufacturing.
  • Lead PCB design projects focusing on scalability and performance.
  • Create test fixtures for hardware validation and functional testing.

Skills

Hardware design
Compliance standards
Embedded hardware programming
C programming
Assembly programming

Education

Master's Degree in Electrical Engineering

Tools

Altium
Autodesk Eagle
LabVIEW

Job description

Nanobiosym is an innovative, high-tech company that is developing novel technologies at the nexus of physics, nanotechnology, and biomedicine. Founded by MIT/Harvard alum and located in Cambridge, Massachusetts, Nanobiosym was awarded the first X-Prize to be given for healthcare.

Position Overview:
We are expanding our development team and seeking an exceptional Senior Electrical Design Engineer with a strong background in hardware design, design for manufacturing (DFM), and full product realization. You will be a key player in designing advanced PCB systems, driving embedded hardware development, and delivering high-quality products to market.
This is a hands-on, technical leadership role for someone passionate about innovation, quality, and building real-world products that make an impact.
Key Responsibilities:
    Own full hardware development lifecycle: Specification, architecture, circuit design, simulation, schematic capture, prototyping, validation, and release to manufacturing.
    Lead PCB design and enhancement projects, ensuring scalability, manufacturability, and performance.
    Translate early-stage concept layouts into robust, production-ready circuit designs.
    Review layout and routing concepts to finalize the electrical scope of products.
    Design systems including MPUs, memory, and FPGAs (preferred but not required), ensuring low-level integration with embedded software.
    Implement control systems in compact, single-board designs with tight constraints.
    Create and maintain thorough documentation including design requirements, component selection rationale, calculations, and power/thermal budgets.
    Collaborate with cross-functional teams to define, evaluate, and refine hardware and driver requirements.
    Design and build test fixtures for hardware validation and functional testing.
    Support regulatory and quality processes with a focus on FDA and ISO 13485 compliance.
Minimum Qualifications:
    Master's Degree in Electrical Engineering
    5-10+ years of hands-on electrical engineering experience in product development environments.
    Strong understanding of compliance standards in regulated industries (e.g., FDA, ISO 13485).
    Proven track record of delivering production-quality PCBs-from prototype through DFM and volume manufacturing.
    Deep experience with Altium, Autodesk Eagle, or comparable CAD tools (5+ years).
    Strong embedded hardware skills including C and Assembly programming for low-level systems.
    Experience with Verilog, FPGA, or ASIC design (preferred but not required).
    Familiarity with LabVIEW for test automation and instrumentation (3-5 years' experience preferred but not required).
    Java programming skills (preferred but not required).
Preferred Qualifications:
    PhD or MS/ME in EECS or related fields/experiences
    LabVIEW development experience in automated testing environments.
    National Instruments Certification (CLD or CLA).
    End-to-end experience developing and launching medical devices or similarly regulated products.
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