Work Flexibility : Hybrid
Who we want : What you will do :
Technical Responsibilities :
- Under supervision, design, develop, modify, and verify mechanical components for medical devices
- Assist with prototyping and bench testing
- Support problem solving, root cause analysis, identify potential solutions, and evaluate them against requirements
- Under supervision, conduct research and studies to support product design
Business Responsibilities :
Interpret customer needs and understands design inputsUnderstand the product’s intended use and clinical proceduresMed Device Compliance :
Understand fundamental industry standards, design requirements and test strategies which align with regulatory requirementsWith supervision, create or refine engineering documentation, such as the Design History file per company design control proceduresLearn R&D procedures like design controls and risk management, per the Quality Management SystemGeneral Responsibilities :
With supervision, work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project successLearn procedures, policies, processes, systems, and technology requiredWork on problems in limited scope; purposefully learn while gaining experienceDemonstrate ownership and integrity of workBuild stable relationshipsContribute to the project as a team memberMinimum Qualifications (Required) :
Bachelor of Science in Engineering, Mechanical Engineering or BioMedical & 0+ years of work experiencePreferred Qualifications (Strongly desired) :
Technical Skills :
Fundamental knowledge and understanding of mechanical engineering practices and tools, design principles within a regulated environment.Basic knowledge of design and concept generation CAD or CAE modeling toolsBasic knowledge of analysis tools and statistical methodsBasic knowledge of materials and manufacturing methodsAbility to read and Interpret complex drawingsTravel Percentage : 10%