Work Flexibility: Hybrid

What you will do:

• Under supervision, design, develop, modify, and verify mechanical components for medical devices; assist with prototyping and bench testing; conduct research and studies to support product design.
• Support problem solving, root cause analysis, identify potential solutions, and evaluate them against requirements
• Interpret customer needs and understands design inputs and understand the product’s intended use and clinical procedures
• Understand fundamental industry standards, design requirements and test strategies which align with regulatory requirements
• With supervision, create or refine engineering documentation, such as the Design History file per company design control procedures and work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success.
• Learn R&D procedures like design controls and risk management, per the Quality Management System
• Work on problems in limited scope; purposefully learn while gaining experience
• Demonstrate ownership and integrity of work; build stable relationships and contribute to the project as a team member.

What you will need-

Required:

• Bachelor of Science in Engineering, Mechanical Engineering

• Work experience- 3 years - 5 years

• Basic knowledge of design and concept generation CAD or CAE modeling tools; GD&T and Design Documentation; analysis tools and statistical methods

Preferred Qualifications :

• Fundamental knowledge and understanding of mechanical engineering practices and tools, design principles within a regulated environment.
• Basic knowledge of materials and manufacturing methods
• Ability to read and Interpret complex drawings

Travel Percentage: None