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Software Product Manager

10 hours, 14 minutes ago
United States
Freelance
Mid Level
Product Manager
Software Development
Agile Cybersecurity UI Design UX Design Wireframing
Apply Now
SI-BONE

SI-BONE

SI BONE develops the iFuse Implant System for minimally invasive treatment of sacroiliac joint disorders, advancing diagnostic understanding and providing innovative solutions in orthopedics.

Health Care Providers & Services
201-500
Founded 2008
$225M raised
View All Jobs 2

Description

  • Collaborate with product development and engineering teams on software product development.
  • Lead UX/UI and software application design strategy.
  • Define, author, and maintain user requirements, product requirements, user stories, backlogs, and release scope.
  • Plan and conduct voice-of-customer, usability, and design-surgeon activities; translate findings into design inputs and workflow decisions.
  • Partner with engineering, Regulatory, Quality, and design surgeons to develop and launch products.
  • Support software risk analysis, intended-use and indications statements, and submission documentation.
  • Review software verification and validation protocols, results, and human-factors validation from a user-needs perspective.
  • Identify market opportunities, partnerships, and growth initiatives; conduct market research and support business cases and go-to-market planning.
  • Establish repeatable software product-management templates, review cadences, and decision records for internal teams.
  • Support the SI-BONE Quality System and comply with applicable regulatory and quality requirements.

Requirements

  • Bachelor’s degree with 2–4 years of experience, or a master’s degree.
  • 2+ years of software product management, product marketing, or sales support experience; medical device experience is preferred.
  • Experience in medical devices, healthcare, or another regulated industry; spine experience is a plus.
  • Hands-on experience with pre-operative planning, surgical navigation, or 3D image-based software, including DICOM workflows, CT/MRI segmentation, and implant templating or measurement tools.
  • Working knowledge of Software as a Medical Device development, including IEC 62304, IEC 62366, ISO 14971, and FDA premarket software and cybersecurity guidance.
  • Experience with software verification and validation in a design-controlled environment, including traceability, protocol review, defect triage, and design-history-file documentation.
  • Experience supporting software regulatory strategy, including 510(k), De Novo, clinical decision support, and AI/ML device considerations.
  • Ability to work in agile development while meeting design-control and documentation requirements.
  • Experience managing external software development or contract engineering partners.
  • Experience translating surgeon and operating-room workflows into user needs, requirements, and wireframes; conducting customer interviews and usability studies.
  • Strong written communication skills and proficiency with Microsoft Word, PowerPoint, and Excel.
  • Ability to work independently in a fast-paced environment, influence cross-functional stakeholders, travel 1–4 times annually, and occasionally lift up to 22 pounds.

Benefits

  • Part-time independent contractor arrangement.
  • Remote work within the United States.
  • Compensation of $200–$280 per hour, based on location, experience, education, training, certifications, and other factors.

Interested in this position?

Apply directly on the company website

Apply Now

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