ABOUT INSPIRE MEDICAL SYSTEMS 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. WHY JOIN OUR FAST-GROWING TEAM 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.

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! The Senior Regulatory Affairs Specialist will lead and execute regulatory strategy for an implantable neurostimulation therapy for the treatment of obstructive sleep apnea.

This role supports global regulatory activities with primary focus on the United States and European Union. Working independently under the direction of Regulatory Affairs Management, this position owns regulatory impact assessments and develops compliant, risk‐based regulatory strategies across product development and lifecycle activities.

Requirements

Experience supporting software-enabled or software-driven medical devices is strongly preferred.

and risks. Independently assess regulatory impact for new product development and post-market product changes, including design, manufacturing, labeling, and supplier changes. Develop and communicate regulatory pathway options and recommendations aligned with business objectives and global regulatory expectations.

S. for PMA, IDE, supplements, and amendments, and EU for MDR Class III Technical Documentation, design change, notified body responses. Collaborate with subject matter experts to prepare accurate, timely, and professional responses to regulatory authority questions.

Review and approve product development, operations, labeling, clinical, and software documentation to ensure regulatory compliance and submission readiness. Maintain accurate regulatory files, submissions, and tracking systems across the product lifecycle. Manage multiple projects simultaneously, maintaining high attention to detail, accountability, and execution quality.

Identify opportunities for continuous improvement in regulatory processes, tools, and documentation practices.

: Bachelor’s degree in engineering, life sciences, or related scientific discipline (or equivalent experience) Required Experience: 5+ years of experience in a regulated industry with transferable skills to medical devices. Strong technical writing, communication, and stakeholder‐management skills. Demonstrated ability to work independently on regulatory assessments and submissions.

RESPONSIBILITIES

Serve as a strategic regulatory partner to product development, operations, quality, clinical, manufacturing, and marketing teams, providing clear guidance on regulatory

. Comply with applicable Quality System procedures and regulatory

QUALIFICATIONS

Educational