Senior Software Systems Analyst

HistoSonics is a medical device company, founded in 2009, that has developed a non-invasive, sonic beam therapy platform that uses histotripsy, which is capable of destroying targeted liver tumors. Our mission and passion are to advance the novel science of histotripsy and its powerful benefits, bringing meaningful and transformational change to physicians and their patients.

Location: Ann Arbor, MI (Hybrid)

Travel Expectation: Approximately 25% to visit our other Midwest sites, Typically 1X per month for 2-3+ days.

Position Summary:

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:

• 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 and design control requirements. 

Qualifications:

• 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.

HistoSonics will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

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.

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