Global Supplier Quality Engineer II

Role: Global Supplier Quality Engineer II supporting supplier quality assurance for Integra's manufacturing in Columbia, MD. Responsibilities: conduct supplier audits per GMP, ISO, and regulatory standards; maintain supplier quality documentation; support QC, purchasing, and production with technical quality assessments; lead supplier change requests, validation, CAPA, and non-conformance investigations; participate in continuous improvement, internal and third-party audits, and supplier management meetings. Qualifications: bachelor's or master's in engineering or sciences; minimum 3 years in quality or manufacturing, with experience in medical device or pharma; working knowledge of ISO 9001, ISO 13485, 21 CFR 820, with regulatory environment familiarity; strong analytical, collaborative skills, and ability to interpret technical data. High-Value: Medical device/pharma manufacturing, supplier quality management, audits, validation, cGMP compliance, ISO standards; hybrid onsite in Columbia, MD with travel up to 25%, potentially international. Work setup: hybrid (minimum 3 days onsite).