What you will do:

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, prototyping one or more options to provide proof of concept
Apply fundamental and some advanced concepts, practices and procedures for problem solving

Business Responsibilities:

Demonstrate advanced understanding of customer needs and design inputs. Demonstrate proficiency with product's intended use and clinical procedures. Learn how the financial models are constructed

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:

Under minimal supervision, work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success. 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. Works as key member of the team, collaborating with others and solidifying relationships

What You need:

Required Qualifications:

Preferred Qualifications:

Senior Design Engineer- Mechanical