Validation Engineer – Medical Device Packaging

The role supports packaging validation and testing activities for sterile and non‑sterile medical device packaging systems, assisting senior engineers with studies, protocols, data analysis, and documentation. The engineer collaborates with cross‑functional teams to ensure compliance with FDA QSR, ISO 13485, ISO 9001, MDR, and CMDR standards while contributing to risk assessments, continuous improvement, and on‑site support as needed.