Medline Industries, LP is seeking a Senior Regulatory Affairs Specialist to lead global regulatory projects for devices. This remote US-based role emphasizes strategy, submissions, and cross-functional teamwork.
You will prepare regulatory strategies for new devices, launches, and post-market changes, manage filings (510(k), CE), monitor regulatory updates, and drive adherence to FDA guidelines with up to 10% travel when needed.
#J-18808-LjbffrSenior Regulatory Affairs Lead — Global Submissions Remote in northern at Unknown Company
This position is listed as full time and able to be worked remotely.