Reality Labs is seeking experienced medical devices quality management professionals to drive the establishment and ongoing operations of a quality management system (QMS) compliant with 21 CFR, EU MDR, and ISO 13485 for the organization. You will work cross functionally in an organization that is primarily consumer electronics focused but has a growing medical device portfolio of hardware and software products. You will be both an internal consultant to other functions adopting new SOPs and act as an owner of key QMS and Design Control initiatives.