Philips RespirTech in Plymouth, Minnesota seeks a Director of Regulatory Affairs to lead regulatory strategy and quality systems for RespirTech products. You will guide end-to-end regulatory activities from product inception to lifecycle management and liaise with FDA and Notified Bodies.
You will build teams, drive compliance with ISO 13485/14971 and 21 CFR 820, and shape the external regulatory landscape.
#J-18808-LjbffrRegulatory Affairs Director: MedTech Strategy & Quality in plymouth at Unknown Company
This position is listed as full time and onsite.