Job description
Work Flexibility: Hybrid What you will do:
- Under minimal supervision, research, design, develop, modify, and verify components/modules for medical devices and work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success
- 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
- Demonstrate proficiency with product’s intended use and clinical procedures. 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
- 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- Bachelor of Science in Engineering, Mechanical Engineering or Bio. Medical & Experience- 5 years -7 years Technical ability to create engineering drawings and models, applying GD&T and CAE tools Preferred skills-
- Working knowledge and understanding of mechanical engineering practices and design principles
- Demonstrated ability to apply knowledge of materials and manufacturing processes to product design
- Ability to Communicate basic plans and technical information to team members Travel Percentage: None