Description
Quality Assurance Specialist II role supporting Alphatec Spine’s quality system and QMS compliance for medical devices, including ISO 13485, 21 CFR 820, MDSAP, and other domestic and international regulatory requirements. The position involves auditing, document control support, CAPA facilitation, complaint handling, quality metrics, management review reporting, and cross-functional collaboration to maintain compliance and improve QMS processes. The job requires at least a bachelor’s degree and 2+ years of medical device experience, is full-time, based in the United States, and does not offer visa sponsorship.
