An IVI RMA (In-Vitro Fertilization Returned Materials Authorization) job typically involves managing the return and replacement process for medical or laboratory products used in fertility treatments. Professionals in this role ensure that returned materials comply with quality standards, investigate defects or issues, and coordinate with suppliers or manufacturers. They may also document return processes, analyze trends in product failures, and support continuous improvement efforts. This position is commonly found in fertility clinics, medical laboratories, or biotech companies specializing in reproductive health.