[Hiring] Software Product Manager @SI-BONE, Inc

Role Description

The Software Product Manager will play a key role in the upstream development and potential commercialization efforts of a software solution for SI-BONE’s spinopelvic portfolio. This individual will engage primarily in upstream product management activities to support UX / UI, software application design, and software verification and validation.

• Collaborate with SI-BONE’s product development and engineering team to provide input on software product development.
• Lead strategy surrounding UX / UI and software application design.
• Provide input on strategy for gathering and synthesizing user requirements and inputs.
• Work cross-functionally with engineering and regulatory teams and design surgeons to develop and launch new products.
• Collaborate with commercial and strategy teams to identify new market opportunities, partnerships, and growth initiatives aligned with the product roadmap.
• Conduct market research, support business case development, and contribute to go-to-market planning for new products or enhancements.
• Support the SI-BONE Quality System.
• Author and maintain user requirements, product requirements, and user stories, and manage the backlog and release scope with engineering.
• Plan and run voice-of-customer and usability activities with surgeons and OR staff, and translate findings into design inputs and workflow decisions.
• Partner with Regulatory and Quality on software risk analysis, intended use and indications statements, and the software documentation required for submission.
• Review verification and validation protocols and results from a user-needs perspective, and support human factors validation.
• Establish and document software product management practices — templates, review cadences, and decision records.

Qualifications

• Bachelor's Degree with minimum of 2-4 years of experience; or Master’s Degree.
• 2+ years of software product management or product marketing or sales support experience, ideally in the medical device industry (a plus if in spine).
• Experience in medical device, healthcare or another regulated field strongly desired (a plus if in spine).
• 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 (SaMD) development and the standards that govern it.
• Familiarity with software verification and validation in a design-controlled environment.
• Experience contributing to regulatory strategy for software, including 510(k)/De Novo pathways.
• Ability to operate in an agile, iterative development cadence while meeting design control and documentation requirements.
• Experience managing external software development partners or contract engineering firms.
• Ability to translate surgeon and OR workflow observations into user needs, requirements, and wireframes.
• Data literacy sufficient to define analytics, telemetry, and success metrics for a clinical software product.
• Able to work in a high-performing team environment and possess a demonstrated ability to multi-task.
• Demonstrated self-starter, with ability to work independently and prioritize time and resources.
• Proven track record of success and teamwork, with a strong dedication to excellence and customer satisfaction.
• Consultative operating style: able to embed with an existing product team.
• Willingness to coach and upskill SI-BONE product managers on software-specific practices.
• Strong written deliverable discipline — product requirements documents, user requirement specifications, roadmaps, and decision memos.
• Comfortable with ambiguity; able to frame a problem and recommend a path forward.
• Credibility to influence engineering, regulatory, and commercial stakeholders without direct authority.
• Highly skilled with Microsoft Office Suite, particularly Word, PowerPoint, and Excel.
• The employee must occasionally lift and/or move up to 22 pounds.
• Knowledge and familiarity of applicable regulations/standards (e.g. ISO 13485, FDA 21 CFR 820, EU MDR 2017/745, ISO 14971).

Requirements

• Must always act and conduct company business in an honest, ethical and strictly legal manner.
• Responsible for performing all duties in compliance with all applicable worldwide regulatory requirements.

Benefits

• Salary: $200-$280/hour.