23 developer positions at Center for Devices and Radiological Health (CDRH)

FDA Development of a Queryable Technological Parameter Library for Energy-Based Surgical Devices Indexed by Indications for Use (IFU)

Center for Devices and Radiological Health (CDRH) | United States | about 19 hours ago

benchmarks, compare device specifications against cleared predicates, and identify gaps in submitted data. Furthermore, the outcomes of this project may further the development of FDA guidance documents

FDA Postdoctoral Fellowship - Identification Criteria Development for Extractables and Leachables Non-Targeted Analysis

Center for Devices and Radiological Health (CDRH) | Silver Spring, Maryland | United States | about 19 hours ago

development and validation for extraction, sample analysis using GC-MS and LC-MS, development of criteria for compound identification and quantification of substances contained in polymeric and other materials

FDA Development of a General Surgery Devices Database and Analysis to Identify Key Technological Attributes and Trends

Center for Devices and Radiological Health (CDRH) | Silver Spring, Maryland | United States | about 19 hours ago

: You will collaborate with review staff to develop a database of robotic surgical device technologies across the Office of Product Evaluation and Quality (OPEQ). This project will help categorizing key

FDA Fellowship - Development of Medical Device Extractable Database and Toxicological Risk Assessment Approaches

Center for Devices and Radiological Health (CDRH) | Silver Spring, Maryland | United States | about 19 hours ago

(CDRH), Office of Science and Engineering Laboratories (OSEL). Medical Device Extractable and Leachable Database Project : This project will offer the opportunity to develop databases of containing

FDA Interventional Radiological Imaging and Visualization (IRIS) Fellowship

Center for Devices and Radiological Health (CDRH) | Southern Md Facility, Maryland | United States | about 19 hours ago

emerging medical technology domains: interventional and autonomous systems, extended reality technologies, and novel imaging validation and evaluation methodologies. This integrated project aims to develop

FDA Digital Pathology Image Analysis Fellowship

Center for Devices and Radiological Health (CDRH) | Silver Spring, Maryland | United States | about 19 hours ago

focused on the development of methods and tools in support of our regulatory science efforts in evaluating computational pathology (CPATH) devices. As a fellow, you will have the opportunity to learn about

FDA Research Opportunity - Pediatric and Perinatal Devices

Center for Devices and Radiological Health (CDRH) | Silver Spring, Maryland | United States | about 19 hours ago

: The Pediatric and Perinatal Devices Program within the FDA’s Center for Devices and Radiological Health (CDRH) conducts regulatory science research aimed at advancing the development and evaluation of medical

FDA Fellowship - Strategic Modernization of Regulatory Taxonomy: Energy Based Surgical Devices

Center for Devices and Radiological Health (CDRH) | Silver Spring, Maryland | United States | about 19 hours ago

consumer confidence in devices marketed in the U.S. Research Project: To optimize Total Product Life Cycle (TPLC) oversight, strategic structure in categorization needs to be developed and implemented

FDA Artificial Intelligence and Machine Learning Fellowship

Center for Devices and Radiological Health (CDRH) | Southern Md Facility, Maryland | United States | about 19 hours ago

to minimize algorithmic bias. Develop expertise in evaluating AI devices that can adapt and learn post-deployment, including understanding evolving algorithms and creating methodologies to assess algorithm

FDA Methodological Evaluation of Validation Approaches for AI/ML-Based Predictive Medical Devices for Regulatory Settings

Center for Devices and Radiological Health (CDRH) | United States | about 19 hours ago

methodological frameworks used to evaluate their safety and effectiveness. Specifically, you will: Develop proficiency in conducting structured landscape analyses of FDA device submissions (510(k), De Novo, PMA