Regulatory Co-op Fall 2026

AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure’s Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure’s AtriClip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure’s Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure’s cryoICE cryoSPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit AtriCure.com or follow us on Twitter @AtriCure.

We foster a culture of inclusion by embracing diverse experiences and individuals where everyone’s authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally.

POSITION SUMMARY:

The Regulatory Affairs Co-op is intended to support the Regulatory team by assisting with day-to-day tasks and regulatory submissions to the FDA. The Co-Op will be responsible for helping with the organization of documentation and other carious tasks for the deoartment. In addition to calendar management, the individual may perform duties such as coordination of meetings, filing expense reports, and working on special projects. This role may require handling of highly confidential and sensitive information.

ESSENTIAL FUNCTIONS OF THE POSITION:

• Assists with preparation of 510(k)’s, PMA’s, and other regulatory submissions

• Provides support and documentation to international partners in support of international registrations of medical devices

• Maintains internal documentation of domestic and international regulatory approvals

• Creates, edits, and develops visual presentations as needed <span data-ccp-props="{"201341983":0,"335551550":6,"335551620":6,"335557856":16777215,"335559685":540,"335559737":414,"335559738":0,"335559740&am