R&D Software Project Manager at HISTOSONICS INC

Ann Arbor, Michigan, United States -

Full Time

Start Date

Immediate

Expiry Date

01 Jan, 26

Salary

0.0

Posted On

03 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Software Development, Project Management, Agile Methodology, Regulatory Compliance, Cross-Functional Collaboration, Risk Management, Documentation, FDA Regulations, IEC62304, HIPAA, GDPR, Electromechanical Systems, Matrixed Organizations, Manufacturing Transfer, Service Deployment, Post-Market Surveillance

Industry

Medical Equipment Manufacturing

Description

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: Plymouth-MN (Onsite), or Ann Arbor-MI (Onsite) Travel: Once a month or every 2 months for 2-3 days to visit our other site(s) in the Midwest. Position Summary: The Software Project Manager proactively leads the planning, coordination, and execution of medical device software development projects for the Edison system. This role is responsible for managing software projects from concept through commercialization, ensuring cross-functional alignment, regulatory compliance, and timely delivery. The Software Project Manager works with the Software Leadership team to identify resources, manage dependencies, meet schedule milestones, and adjust to complex project issues. This is a key contributor role and will be hands-on with regard to software development. Key Responsibilities * Lead the execution of software projects, including feasibility, prototyping, development, documentation, verification and validation. * Facilitate effective collaboration across program leaders, project managers, software development, test, and risk management resources. * Engages with cross-functional teams to communicate and manage dependencies * Monitor progress, oversee software configuration management, manage and produce documentation deliverables and escalate risks and impediments appropriately. * Serve as a central point of contact for internal and external stakeholders, providing regular software project updates and status reports. Qualifications * Bachelor’s degree in computer engineering, computer science, software engineering or technical related field. * 5–10+ years in medical device or regulated software development experience. * 3+ years of proven track record of managing full software development lifecycle projects, including complex electromechanical systems and software, in Agile environment. * Direct experience in product development environments with software and firmware integration. * Experience working in matrixed organizations or cross-site/global teams. * Exposure to manufacturing transfer, service deployment and post-market surveillance is a plus. * Experience with FDA medical software guidance, IEC62304, HIPAA, GDPR and other applicable regulations. * Understands phase-gate or milestone-based product development. 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. #LI-Onsite

Responsibilities

The Software Project Manager leads the planning, coordination, and execution of medical device software development projects. This includes managing projects from concept through commercialization while ensuring regulatory compliance and timely delivery.