Remote Global RA Specialist — Medical Devices

A leading medical technology firm is seeking a Regulatory Affairs Specialist to join their RAQA team on a permanent, fully remote basis. In this role, you will lead regulatory submissions for EU MDR and FDA 510(k), and ensure compliance with various ISO standards. The ideal candidate will have a strong background in regulatory affairs and experience with Software as a Medical Device. This position offers the opportunity to shape global regulatory strategies in a collaborative environment.#J-18808-Ljbffr…