The Associate Design Assurance Quality Engineer role supports product development teams in delivering high-quality medical devices while optimizing core design control processes. Key responsibilities include ensuring compliance with FDA, GMP, and ISO regulations, leading root cause analysis for quality issues, and driving continuous improvement initiatives through risk management and process validation. The position requires cross-functional collaboration with manufacturing, regulatory, and clinical departments to align product requirements with production controls. This opportunity appeals to engineers seeking to work in a fast-paced, regulated environment with a strong focus on innovation and operational excellence. The role offers a collaborative culture, opportunities for professional growth in quality system development, and requires approximately 10% travel.
