Overview
Technical Responsibilities:
• Under minimal supervision, research, design, develop, modify, and verify components/modules for medical devices.
• Translate design inputs to engineering specifications and produce sub-system level designs.
• Develop and analyze solutions.
• Apply fundamental and some advanced concepts, practices and procedures for problem solving.
• Troubleshoot engineering design issues, develop and propose solutions to design. Implement design changes effectively and efficiently.
Med Device Compliance:
• Follow fundamental industry standards, design requirements and test strategies which apply to regulatory requirements.
• Independently create or refine engineering documentation, such as the Design History file.
• Follow R&D procedure like design controls and risk management, per the Quality Management System.
General Responsibilities:
• Quickly process and assimilate procedures, policies, processes, systems, and technology required.
• Work on complex problems, applying advanced experience and learnings.
• Demonstrate ownership and prioritize work with minimal supervision.
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