Senior Systems Engineer
BiomeSense
Job Description
Job Description
Senior Systems Engineer
Compensation: $100k–$125k salary + 0.1%–0.2% equity + benefits
We're looking for a versatile, hands-on engineer who thinks in systems — comfortable moving between electronics, firmware, fluidics, and mechanical interfaces, and equally at ease at a debug bench and in a requirements review. You'll be the technical connective tissue across hardware development for our next-generation GutLab instrument. What You'll Do
- Systems Integration: Liaise between electronics, firmware, fluidics, and mechanical subsystems. Define interfaces and ensure the whole instrument behaves correctly.
- Requirements & V&V: Capture and maintain system requirements, plan and execute verification, build fixtures, and own the question of "did we actually prove it works?"
- Hands-on Bench Work: Integrate, bring up, and debug electromechanical prototypes across hardware, firmware, and fluidics.
- Risk Management: Identify and track system-level risks and failure modes; drive mitigations through design and test.
- Test Automation & Documentation: Build test setups and scripts; produce clear requirements, protocols, and SOPs that keep the team moving without losing rigor.
- Bachelor's degree in Electrical, Systems, Mechanical, or Biomedical Engineering (or related), and 5+ years of hardware or instrument development experience.
- Demonstrated work across disciplines on electromechanical systems — fluent enough to connect EE, firmware, mechanical, and fluidics engineers.
- Strong hands-on instincts: bench debug, scopes, multimeters, soldering, wiring, prototype assembly.
- Experience defining requirements and tracing them through verification.
- Experience designing and executing V&V test plans on hardware or instruments.
- Familiarity with risk management practices (FMEA, hazard analysis, or similar).
- Comfort with scripting (Python or similar) for instrument control, test automation, or data analysis.
- Organized, proactive, and ready to thrive in a startup environment.
- EE/EEHW background with comfort reading schematics, working with embedded electronics, and interfacing with firmware teams.
- Experience with diagnostic instruments, lab automation, fluidic systems, or medical devices.
- Exposure to FDA design controls (21 CFR 820.30), ISO 14971, or IEC 62304.
- Background in quality engineering, validation engineering, or formal requirements management.
- Experience transitioning a product from development into design transfer and production
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