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Job Description:
Technical Responsibilities:
Assist with prototyping and bench testing
Support problem solving, identify potential solutions, and evaluate them against requirements
Under supervision, conduct research and studies to support product design
Code development time/resource estimation to support projects
Generate and review the necessary documents with project teams (requirements/design/architecture/bugs/test)
Business Responsibilities:
Interpret customer needs and understands design inputs
Understand the product’s intended use and clinical procedures
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:
Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success and contribute to the project as a team member
Learn procedures, policies, processes, systems, and technology required
Work on problems in limited scope; purposefully learn while gaining experience
Design, develop, modify, evaluate and verify software components for medical devices
In code reviews apply design principals, coding standards and best practices
Demonstrate ownership and integrity of work
Build stable relationships
Participate in code reviews applying design principals, coding standards and best practices
About Company:
