Regulatory Affairs Specialist
C20 Cochlear Americas (USA)
Cochlear Americas is seeking a Regulatory Affairs Specialist II in Lone Tree, CO. This hybrid role requires in‑office presence three days per week with two days remote, joining a global leader in implantable hearing devices. You will support FDA and Health Canada submissions, develop writing and regulatory strategies, and collaborate across regions to ensure compliant products. The ideal candidate has extensive regulatory affairs experience in medical devices, strong technical writing skills, #J-18808-Ljbffr
Vacancy posted 14 hours ago
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