Description
Responsibilities may include:* Participation in the generation and evaluation of new concepts and prototypes, including analysis and bench testing
* Development of test methods and/or test fixtures to evaluate product performance
* Develop and conduct measurement systems analyses (gage R&R studies) on test methods and equipment
* Development of various design control records
* Planning and Execution of design verification protocols, testing and reports
* Work with Suppliers to provide test fixtures, components, assemblies and prototypes
Experience and skills:
* Experience with FDA class II or III medical devices preferred
* Thorough understanding of design principles, GD&T, DFM, mechanical testing, and measurement systems
* Relevant experience includes design considerations such as tight tolerances and design implications for quality control for high-volume manufacturing processes
* Ability to understand challenges quickly and organize multiple projects concurrently, and must adapt rapidly to changing work assignments
Must be results driven and action oriented, maintain careful attention to detail to ensure accurate, precise execution of work tasks and procedures and work well in a team environment.
KEYWORDS: ISO 13485, 13485, MEDICAL DEVICE, DESIGN, ENGINEER, SOUTH EAST, ENGLAND, CONTRACT, PROTOTYPE, DRAWINGS, INJECTION, PLASTICS, MOULDING
To find out more about Real please visit www.realstaffing.com