Lead Quality & Regulatory Engineer Medical Devices

STERIMED US is seeking a Quality & Regulatory Engineer to lead the site Quality and Regulatory activities at our Ridgeville, SC facility. You will ensure effective execution of the QMS, regulatory compliance with FDA QMSR/21 CFR 820, ISO 13485, and cGMP, and provide technical guidance across multiple functions. The role covers quality system activities, regulatory documentation, investigations, and continuous improvement within a medical device packaging environment, reporting to Site Leadership