Global Regulatory Affairs Specialist, Medical Devices
Listed on 2026-10-07
-
Healthcare
Healthcare Compliance, Medical Device Industry, Medical Science Liaison
Coloplast is seeking a Regulatory Affairs Specialist to manage day-to-day regulatory tasks for medical devices across assigned geographies. You will prepare submissions, monitor status, and support post-market surveillance, change analysis, and vigilance reporting while ensuring design history file documentation stays current.
The role requires 3+ years in regulatory affairs within the medical device industry, familiarity with FDA and EU regulations, and CE marking/Health Canada experience is a
The Global Regulatory Affairs Specialist, Medical Devices position in the Legal, Management & Operations field is open for applications.
We invite applications for the Global Regulatory Affairs Specialist, Medical Devices position located in Minneapolis, MN, United States.
The following position is for a Global Regulatory Affairs Specialist, Medical Devices with Coloplast.
Our group is growing, and we are hiring a Global Regulatory Affairs Specialist, Medical Devices in Minneapolis, MN, United States.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).