Work Flexibility: Hybrid

What you will do:

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

• Experience 5 years -7 years , medical device experience

• Good CAD working knowledge - CREO and One PLM ( Windchill); drawing creation and interpretation understanding.

Preferred Skills:

• Translate design inputs to engineering specifications and produce sub-system level designs

• Demonstrate proficiency with product’s intended use and clinical procedures

• Develop and analyze solutions, prototyping one or more options to provide proof of concept

Travel Percentage: 10%