Role: Project Validation Specialist Location: Anasco, PR Duration: 12 Months Job Description: The position is to support the European Union Medical Device Regulation (EU MDR) program at A asco, PR. The incumbent will be supporting the following activities to ensure conformance with EU MDR for technical filing of products manufactured at A asco, included in the EU MDR program. Data Gathering Participate in the discovery and compilation of required documentation to be updated as pa