<div><b>Job Title: Project Validation Specialist III_US<br /> Location (On-site, Remote, or Hybrid?): Anasco, PR (Onsite)<br /> Contract Duration: Contract until 01/05/2027<br /> Work Hours: M-F Business Hours</b><br /> </div> <div><b>Summary Description:</b><br /> The position is to support the European Union Medical Device Regulation (EU MDR) program. The incumbent will be supporting the following activities to ensure conformance with EU MDR for technical filing of products manufactured , included in the EU MDR program.</div> <ul> <li>Data Gathering Participate in the discovery and compilation of required documentation to be evaluated.</li> <li>Gap Assessments Assess of all manufacturing documentation such as product device master record (drawings, specifications, bill of materials, production router/instructions, procedures, labeling), process flow charts, incoming inspe...