Regulatory Affairs Specialist - On-site

Regulatory Affairs Specialist role within Medtronic CST focusing on planning and delivering regulatory submissions (e.g., large marketing applications and eCTD) and maintaining regulatory documentation. Responsibilities include preparing, publishing, and performing quality control of submissions, managing regulatory systems, providing user support and training, contributing to system/process improvements, and collaborating cross-functionally (with R&D, Quality, Clinical, Marketing) to provide regulatory status updates. Minimum 2 years of relevant regulated-industry experience; strong attention to detail, organizational skills, and ability to manage multiple projects; clear written and verbal communication for leadership report-outs. U.S. work authorization sponsorship offered at Principal level and above; salary ranges provided for U.S. locations. On-site role requiring 4+ days per week in-office in Lafayette, Colorado. Benefits include comprehensive compensation, health/dental/vision, savings plans, tuition assistance, and more.