About this role
Quality Engineer, Level II at Elevaris Medical Devices. Location: Wilmington, Massachusetts, United States. Role: supporting investigations, facilitating nonconformance, supporting validation Requirements: 2+ years quality engineering in manufacturing preferred; knowledge of ISO 13485, 21 CFR 820, cGMP/QSR/MDR; experience with validations, CAPA, audits, supplier controls, SPC and statistical sampling. Category: Quality Assurance Seniority: Entry Level Tools: Microsoft Office Suite, Microsoft Visio, Microsoft Project Certifications: asq cqa, asq cqe Commitment: Full Time Workplace: Onsite Languages: English