About this role
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 BioMedical & • 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