Sr. Software Design Assurance Engineer

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Inspire is the first of its kind medical device designed to make a difference in the lives of those living with Obstructive Sleep Apnea (OSA). We are revolutionizing the sleep industry with our FDA‑approved medical device, designed to reduce OSA severity for those who cannot tolerate or get consistent benefit from CPAP. Inspire Medical Systems is committed to enhancing patients’ lives through sleep innovation.

We are steadfast in our commitment to prioritize patient outcomes, act with integrity and lead with respect. With positive persistence at our core, we are committed to all those we serve.

At Inspire, we value people – your diverse experiences, backgrounds, and thoughts. We elevate voices and encourage learning opportunities to build a professional network that grows into community. We embrace a people‑first culture by offering excellent benefits, 401k matching, ESPP, flexible time off (FTO), and tuition reimbursement. If you’re passionate about making a difference in people’s lives and want to work with innovative technology, come be a part of our great team!

This position is responsible for product software quality assurance support of new product development projects and design changes. This individual will ensure design control requirements are implemented and followed, will support multiple product development projects with a primary focus on software projects. This individual will ensure that the quality objectives are met during the product development and design transfer life cycle.

This position will work with Development, Operations, Manufacturing, Regulatory, Quality and other functional areas globally to ensure work is completed accordance with Inspire procedures and geographic regulations.

• Partner with Development to generate project deliverables and conduct audits of the deliverables prior to product release.
• Ensure design history content integrity, completeness, and regulatory / standards compliance; collaborate communicating & resolving gaps with cross‑functional team members.
• Provide product software design assurance services, including planning for software design validation, design transfer, test system development and validation, including active cross‑functional root‑cause analysis investigation and resolution.
• Partner with Development on the validation of software test environments and software tools, including test methodology, test protocol and acceptance criteria development.
• Support risk management activities from product concept through commercialization.
• Product expertise and guidance on global medical device software and security standards or other specific industry standards to ensure compliance with those standards. Lead and document standard updates and compliance reviews at the prescribed frequency.
• Provide quality engineering support for design changes, sustaining engineering projects and when applicable supplier changes.
• Work within a cross‑functional team to identify and implement effective controls and support product development from concept through commercialization.
• Ensure quality system procedural requirements and development life cycle phases are followed.
• Ensure proper cyber security testing and controls are utilized and documented.
• Generate and/or approve the following: DHF deliverables, Engineering Change Orders (ECOs), Risk Management documents and Device Master Record (DMR) deliverables.
• Provide project direction, coaching, and mentoring for engineering and technical team personnel to ensure best‑in‑class Software Design Quality Engineering practices.
• Apply sound, systematic problem‑solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
• Support both internal and external audit activities.
• Support other quality projects and initiatives as assigned.

• Associate degree in a technical or scientific field.
• 5 years minimum experience…