What you will do:
Technical Responsibilities:
• Conduct or design advanced prototyping and testing
• Conduct advanced problem solving, identify potential solutions, and evaluate them against component and sub-system requirements
• Conduct and design research and studies to support advanced product design
• Translate user needs to design inputs/specifications and produce advanced component and sub-system level designs
• Analyze and correct complex product design issues, using independent judgment
• Independently balance design tradeoffs while designing a component of the system
• Develop and design software systems per requirements and architecture defined
• Code development time/resource estimation to support projects
• Generate and review the necessary documents to support the project. (requirements/design/architecture/bugs/test)
Business Responsibilities:
• Advance solutions by applying in-depth knowledge of customer needs, market and competitive offerings
• Apply detailed knowledge of clinical procedures to author design inputs
• Support Voice of Customer sessions internally and with clinicians
• Demonstrate developing financial acumen
Med Device Compliance:
• Be proficient with and mentor others in usage of industry standards, including design requirements and test strategies per applicable regulations
• Lead creation and refinement of engineering documentation, such as the Design History file
• Follow and mentor others on 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 as a leader on the team
• Identify and support the creation of or improvements to procedures, policies, processes, systems, and technology
• Support and execute segments of complex product development to advance projects through the design /development/launch process
• Contribute to product development from concept through release
• Deliver high quality results with passion, energy and drive to meet business priorities
• Build relationships and influence across the engineering groups within the business
• Design, develop, modify, evaluate and verify software components for medical devices
• In code reviews apply design principals, coding standards and best practices

Minimum Qualifications (Required):
• Bachelor's degree in Software Engineering/ Computer Science or related discipline & 4+ years of work experience

Preferred Qualifications (Strongly desired):
Technical Skills:
• Knowledgeable programming skills. Design new components applying various concepts design concepts and patterns
Design and Development Skills:
• Knowledgeable with integrated development environments (IDE) for projects
• Knowledgeable with tools for static/dynamic analysis, memory management, code coverage and techniques for analyzing software
• Knowledge in integration and deployment processes
Software Process Skills:
• Software Development Life Cycle processes
• Knowledge in creating estimates for code implementation time/resource for assigned tasks and projects
• Knowledge from using Application Lifecycle Management /Traceability tools.
• Knowledge of regulatory and compliance standards applied to the SDLC (Software Development Life Cycle)