Quality Systems Engineer: Medical Device Compliance & Audits

Cretex Medical is seeking a Quality Systems Engineer to support and administer the QMS across ISO 9001, ISO 13485, and FDA QSR requirements. You will lead internal and supplier audits, develop corrective actions, and drive continuous improvement through data analysis and BI-driven insights. Responsibilities include documenting changes, training, and ensuring regulatory compliance. A Bachelor’s degree in a STEM field and 5+ years’ experience in regulated environments are required.