Technical Responsibilities:  

• Under supervision, design, develop, modify, and verify mechanical components for medical devices. 

• Assist with prototyping and bench testing. 

• Test prototypes to verify meet design requirements.  

• Support problem solving, root cause analysis, identify potential solutions, and evaluate them against requirements while maintaining traceability of components.  

• Under supervision, conduct research and studies to support product design and process development. 

• Under supervision, develop new test methods, fixtures, and inspection processes for evaluating prototypes. 

• Aid with specification development and testing of new materials and designs. 

• Ideate new design concepts and generate intellectual property. 

• Preform statistical analysis and present findings. 

• Contribute to Design Reviews. 

Business Responsibilities: 

• Basic understanding of customer needs and design inputs. 

• Understand the product’s intended use and clinical procedures. 

• Individual Design History File task ownership including testing and drawings. 

Med Device Compliance: 

• Understand fundamental industry standards, design requirements and test strategies which align with regulatory requirements.  

• With supervision, create or refine engineering documentation, such as the Design History file per company design control procedures. 

• Learn R&D procedures like design controls and risk management, per the Quality Management System.  

General Responsibilities:  

• With supervision, work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success. 

• Learn procedures, policies, processes, systems, and technology required. 

• Work on problems in limited scope; purposefully learn while gaining experience. 

• Demonstrate ownership and integrity of work.