Regulatory Affairs Specialist

Atri Cure, 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 Atri Cure technologies for the treatment of Afib and reduction of Afib related complications. Atri Cure’s Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib.

Atri Cure’s Atri Clip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. Atri Cure’s Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. Atri Cure’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  or follow us on Twitter @Atri Cure.

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.

This position will originate appropriate documents to obtain and maintain marketing privileges consistent with applicable government requirements where Atri Cure conducts business. This position will also maintain internal documentation of such approvals and handle requests for documentation from our international distributors and customers. This position is responsible for practicing Quality System Manual procedures and complying with its requirements, and carrying out responsibilities as outlined in safety, health and environmental policies.

• Support global regulatory pre-market applications for geographies included but not limited to:
  Taiwan, Singapore, Australia, Brazil, Korea, UAE, EU, UK, U.S, Japan, and Canada. Submission support may include but is not limited to: IDEs, PMA submissions and supplements or 510k for US, EU Technical Documentation, and/or Japan Shonin.
• Support global regulatory post-market activities for the responsible geographies above, such as updating 510(k) letters to file, Technical Files and Design Dossiers on an annual basis, preparing and submitting product renewals, and annual/post-approval reports.
• Support product marketing in additional geographies, as necessary, with international regulatory submissions, product renewals, tender bids, and fulfilling custom requirements.
• Request Certificates to Foreign government and Free Sale Certificates as new products are approved
• Obtain notarization and legalization of documents as required
• Maintain, update and track open regulatory requests. Provide periodic status updates on open and closed requests
• Review of product and manufacturing changes for compliance with applicable regulations (Change Control)
• Work with Regulatory Affairs staff, engineers and technical experts to resolve potential regulatory issues, deficiencies and questions from regulatory agencies
• Maintain submission correspondence files and other regulatory files in a complete manner
• Maintain regulatory files for product compliance
• Perform other related duties as assigned in support of regulatory activities
• Assist in interacting with reviewers from regulatory agencies on specific projects
• Provide support during internal and external audits
• Maintain current knowledge of worldwide regulatory requirements

• Regular and predictable work performance
• Ability to work under fast-paced conditions
• Ability to make decisions and use good judgement
• Ability to prioritize various duties and multitask as required
• Ability to successfully work with others
• Additional duties as assigned
• Hybrid environment (with remote possibilities)
• Travel responsibilities to Atri Cure facilities for team functions and activities when needed

• Bachelor’s degree in a technical/scientific/life science discipline required or 3+ years of Regulatory experience in the medical device industry
• Profic…