Description
The Supplier Quality Manager will lead supplier quality projects, investigations, CAPA, audits, change management, risk control, and supplier performance improvement in a regulated medical device environment. The role requires a bachelor’s degree in engineering or a related field, five years of supplier quality or supplier development experience, knowledge of 21 CFR 820, ISO 13485, and ISO 14971, and direct experience with plant or supplier GMP auditing. The position is based in El Paso, Texas, and requires bilingual Spanish-English communication.
