Regulatory Affairs Specialist

About OrganoX

Organ Ox is a commercial stage organ technology company dedicated to developing technologies to improve outcomes for patients with acute or chronic organ failure. The company was established as a spin out of the University of Oxford in 2008 and is now part of the Terumo Group. Organ Ox is a pioneer in normothermic machine perfusion (NMP). It's flagship platform, the metra®, is available for use in the U.S., Europe, Canada, and Australia.

It has been utilized in over 7,000 liver transplants to date to keep donor livers in a metabolically active state outside the body enabling longer preservation times and functional assessment of the organ prior to transplant, leading to an increased number of organs available for transplant. Founded in 1921, Terumo Corporation (TSE:4543) strives to fulfill its mission of "Contributing to Society through Healthcare" by providing a comprehensive range of solutions in the fields of therapeutic procedures, hospital operations, and life sciences in more than 160 countries and regions.

The Regulatory Affairs Specialist supports global regulatory submissions, registrations, and product lifecycle activities for Organ Ox products, with a focus on regulatory information management and coordination across the Regulatory Affairs function.

The role works closely with Regulatory Affairs team members responsible for software, hardware, disposable products, labelling, and other regulatory disciplines to support submission activities, maintain accurate regulatory records, and ensure alignment across product areas and markets.

This role will report directly to the Director, Regulatory Affairs and works collaboratively with Regulatory Affairs colleagues and cross-functional partners throughout the organization.

This is a hybrid position in Madison, NJ, with approximately 2 days per week in office. The role may require up to 5% additional travel to Organ Ox and/or supplier locations.

• Support the preparation, compilation, review, and submission of regulatory filings for Organ Ox products in the United States, European Union, Canada, Australia, and other markets
• Work collaboratively across the Regulatory Affairs function, including software, retained unit, disposable set, labelling, and regulatory systems, to coordinate regulatory deliverables and maintain alignment across product areas
• Support regulatory authority and Notified Body interactions associated with assigned submissions and regulatory activities
• Create, maintain, and periodically reconcile regulatory records to ensure accurate representation of product registrations, submissions, approvals, certificates, licenses, regulatory commitments, market status, and other regulatory information
• Support configuration, process improvements, reporting, and implementation of new functionality within Rimsys
• Maintain alignment between regulatory records, change-control activities, approved product configurations, and other applicable business systems
• Support maintenance of regulatory registrations, renewals, annual reports, and other recurring regulatory obligations
• Collaborate with Regulatory Affairs and cross-functional stakeholders to support assigned regulatory activities and ensure regulatory requirements and deliverables are appropriately communicated and completed
• Adhere to the letter and spirit of Organ Ox's Code of Conduct and all other company policies

• Working knowledge of medical device regulatory requirements and FDA regulatory processes
• Ability to prepare clear and well-organized regulatory documentation and submissions
• Working knowledge of medical device regulatory requirements in one or more international markets such as the European Union, Canada, and…