Medline Industries seeks a Manager Regulatory Affairs at our Eagan, MN hybrid site to oversee regulatory activities for medical device divisions. You will lead cross-functional teams, coordinate regulatory submissions, and ensure compliance across pre- and post-market activities.
The role requires a Bachelor’s in Regulatory Affairs, Life Sciences, or Engineering with 4+ years of medical device regulatory experience, plus strong communication with regulators and stakeholders.
#J-18808-LjbffrRegulatory Affairs Manager - Medical Devices in eagan at Unknown Company
This position is listed as full time and hybrid.