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Senior Systems Engineer

Job in Pleasanton, Alameda County, California, 94566, USA
Listing for: Calyxo, Inc.
Full Time position
Listed on 2025-12-20
Job specializations:
  • Engineering
    Systems Engineer
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

Job Overview

Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year. Our team is led by executives and investors with a proven track record of commercializing paradigm-shifting devices to meet unmet needs within urology.

Are you ready to change the future of kidney stone treatment? We are seeking high achievers who want to be part of a dynamic team working in a fun, diverse atmosphere.

Summary

We are seeking a highly capable Senior Systems Engineer to drive system-level requirements, architecture, and interface definition across a complex multi-product medical device ecosystem. This role is central to shaping next-generation endoscopic platforms, capital equipment, embedded software, and multiple disposables. You will own the creation, decomposition, and validation of requirements across hardware, software, and disposables. You will play a critical role in defining system architecture, managing interfaces between subsystems, guiding design teams, and ensuring external development partners deliver against clear, testable, and appropriately flexible requirements.

This is a deeply cross‑functional role that directly impacts the company’s 4‑year product pipeline and the future of clinically impactful technologies in the kidney stone space.

In This Role, You Will Requirements Development & Ownership
  • Own the development of system-level and subsystem-level requirements
    , including:
    • performance requirements (fluidics, vision, disposables, embedded systems),
    • interface requirements,
    • regulatory compliance requirements,
  • Lead decomposition of user needs into clear, measurable system and subsystem requirements
  • Ensure traceability is complete across the full lifecycle of the system
System Architecture & Interface Leadership
  • Serve as a key contributor to the multi-product system architecture across capital equipment, endoscopes, disposables, and embedded software.
  • Own interface definition and control
    , including mechanical, electrical, software API, fluidic, and system-level behavioral interactions.
  • Challenge design decisions and drive bench‑top and animal trade studies to ensure architectural alignment with requirements.
Cross-Functional & External Collaboration
  • Partner closely with mechanical, electrical, firmware, software, clinical, quality, and product teams to ensure alignment and understanding of system needs.
  • Lead and facilitate formal requirements reviews
    , design discussions, and architecture workshops.
  • Work directly with external contract design firms by:
    • providing clear system/subsystem requirements,
    • reviewing design concepts,
    • ensuring interface consistency,
    • aligning deliverables with internal architecture and verification needs.
Risk & Systems Engineering Processes
  • Develop and maintain dFMEAs for system-level features and interactions.
  • Ensure requirements link to risks, mitigations, and verification.
  • Support test teams by ensuring all requirements are objectively verifiable and aligned with test method needs.
Who You Will Report To
  • Sr. Manager, Sr. Manager, Systems and Test Engineering
Requirements
  • Bachelors degree in Mechanical or Biomedical Engineering, Masters or PhD preferred.
  • 7+ year’s experience.
  • Strong expertise in fluidics (irrigation, vacuum, pressure/flow systems).
  • Experience with vision/imaging systems and their system-level behavior.
  • Proven experience owning system architecture and interface control documents (ICDs).
  • Hands‑on experience with disposables and capital equipment integration.
  • Proficiency with Jama, FMEAs, and fault-tree analysis.
  • Deep knowledge of major U.S. medical device standards (14971, 62304, 60601‑x, etc.).
  • Skilled in writing clear, testable, non-prescriptive requirements across hardware and software.
  • Strong communicator, fast-moving, decisive, and comfortable driving alignment among diverse teams.
  • Strong problem‑solving skills and experience working as part of multifunctional technical project teams through all development lifecycle phases.
  • Experience in requirements…
Position Requirements
10+ Years work experience
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