HISTOSONICS INC

Senior Software Systems Analyst

HISTOSONICS INC Ann Arbor, Michigan, United States · $135K–$160K/yr

Medical Equipment Manufacturing · 201-500 employees

6 h ago
system-analyst Senior (5-10 yrs) Full-time United States
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About the role

Gather, analyze, and document software requirements, translating stakeholder needs into specifications and supporting development teams in implementing them. Analyze system and subsystem interactions, collaborate with cross-functional teams on testing and risk traceability, and help ensure software meets product goals and medical device quality and regulatory requirements.

What they look for

Software Requirements Analysis Requirements Documentation User Stories Use Cases Business Process Analysis Stakeholder Communication Hardware-Software Integration Medical Device Development Software Development Methodologies Cross-Functional Collaboration Quality Assurance Risk Management Design Controls IEC 62304 ISO 14971 ISO 13485

Requirements

Requires a bachelor’s degree in a relevant engineering or computer science discipline and at least five years of experience in a regulated industry or medical device development. Candidates should have strong communication and requirements-writing skills, expertise in medical device hardware-software integration, knowledge of software development methodologies and tools such as Microsoft DevOps, and familiarity with relevant regulatory standards.

Benefits

Health Insurance Dental Insurance Vision Insurance Life Insurance Short-Term Disability Insurance Long-Term Disability Insurance 401(k) Paid Time Off

Full description

HistoSonics is a commercial-stage medtech company advancing the Edison® System, a novel non-invasive sonic beam therapy based on histotripsy. Since receiving FDA De Novo grant for the non-invasive destruction of liver tumors in 2023, the company has progressed beyond initial market entry into commercial expansion, reimbursement momentum, and ongoing clinical and pipeline development. In addition to its current liver tumor indication, HistoSonics is pursuing future indications across multiple applications including kidney, pancreas, prostate, neuro, women’s health, and other significant underserved human health areas, to realize the broader potential histotripsy across multiple disease states and medical specialties.

We offer an exciting work culture where cutting-edge science meets real-world application, and each team member’s contribution is important to our success in ensuring our physicians and their patients get what they need most.

Location: Plymouth, MN or Ann Arbor, MI - Hybrid

Travel Expectation: Approximately 10%

Position Summary (Why this role matters):

Sr. Software Systems Analyst position involves acting as a liaison between stakeholders and development teams to gather, analyze, and document software requirements. The role requires translating business needs into clear technical specifications for developers, ensuring the final product meets user needs and business objectives.

Key Responsibilities (What you’ll do):

  • Create detailed specifications, user stories, functional requirements, and use cases in clear, readable documents for both technical and non-technical audiences.
  • Analyze business needs and processes, identify gaps, and determine feasibility of potential solutions.
  • Serve as a bridge between business stakeholders and development teams to ensure clear understanding of requirements.
  • Support developers by ensuring requirements are understood and correctly implemented in the software.
  • Develop a deep understanding of the HistoSonics system, understand the interactions between all the subsystems and understand how the Edison software interacts with each of the subsystems.
  • Ensure the software development efforts align with the overall product vision and company goals.
  • Conduct in-depth analysis of existing software systems, identifying areas for improvement, optimization, and integration of new features.
  • Collaborate closely with cross-functional teams including R&D, Quality, Manufacturing, Field Service, and Regulatory Affairs.
  • Collaborate with quality assurance teams to design test cases, scenarios, and test plans based on documented requirements.
  • Collaborate with risk management to help identify, document and trace risks to requirements and implementation.
  • Participate in the quality assurance process by reviewing and validating software functionality against specified requirements.
  • Stay up to date with industry trends, best practices, and emerging technologies to suggest process improvements and innovative solutions.
  • Maintain awareness of relevant medical device standards (e.g., IEC 62304, ISO 14971) and design control requirements.

Qualifications and Skills:

  • Bachelor’s degree in Computer Science, Systems Engineering, Biomedical Engineering, Mechanical Engineering, Electrical Engineering or related discipline.
  • 5+ years of experience in regulated industry or medical device development.
  • Excellent verbal and written communication skills with the ability to translate technical information to non-technical stakeholders.
  • Proficiency in creating clear and concise software requirement documents, use cases, and user stories.
  • Ability to work effectively in cross-functional teams, bridging the gap between technical and non-technical team members.
  • Expertise in hardware-software integration for medical device.
  • Strong understanding of software development methodologies.
  • Familiarity with software development tools (e.g. Microsoft DevOps).
  • Solid knowledge of medical device regulatory frameworks, including ISO 13485 and ISO 14971.

Benefits: We offer a comprehensive benefits package for full-time employees. This includes health, dental, and vision insurance, life, short-term and long-term disability insurance, 401(k), paid time off, and more.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

U.S. Work Authorization & Sponsorship: Employer will not sponsor visas for position.

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