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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 Associate Quality Specialist will execute and maintain Unique Device Identification (UDI) compliance activities for AtriCure products. This role is responsible for managing UDI data across global regulatory systems, supporting regulatory change assessments, and coordinating with internal teams, external regulatory agencies, and third-party partners to ensure the accuracy, completeness, and timeliness of UDI submissions. The position collaborates cross-functionally to ensure adherence to global UDI requirements and supports ongoing compliance efforts related to evolving global UDI requirements. ESSENTIAL FUNCTIONS OF THE POSITION: Collaborate cross-functionally to support global Unique Device Identification (UDI) compliance activities for AtriCure products Perform UDI data entry, verification, and ongoing maintenance within Regulatory Information Management Systems (RIMS) Manage and maintain Global Data to ensure accuracy of UDI documentation internally Evaluate and provide inputto Change Request Plan (ChRP) UDI impact assessments Interface with external regulatory agencies and third-party contractors to support external UDI data registration Manage and maintain UDI-related data within external UDI systems to ensure accuracy Support data entry and ongoing maintenance for emerging UDI requirements in new jurisdictions, including EU, Australia, Colombia, Singapore, China, Brazil, and Switzerland Support resolution of UDI-related requests and questions from internal stakeholders to reduce process bottlenecks Assess UDI activities for compliance with AtriCure Quality System requirements, applicable global regulations, and company policies and identify any gaps Participate in audit-related activities for internal and/or external audits, as necessary Support additional Quality System activities and special projects as assigned   ADDITIONAL ESSENTIAL FUNCTIONS OF THE POSITION: Demonstrate reliable, consistent, and predictable work performance Apply strong organizational and data management skills to maintain accuracy and efficiency Thrive in a fast-paced environment with the ability to adapt to changing priorities Communicate effectively, both verbal and in writing, across all levels of the organization Seeks guidance from peers or management as appropriate to resolve problems/conflicts Prioritize multiple tasks and manage competing deadlines effectively Collaborate productively with cross-functional teams and stakeholders Ability to successfully work with others Perform additional duties and responsibilities as assigned This hybrid position requires regular in-office attendance to support cross-functiona