Work Flexibility: Hybrid

What you will do:

• Under supervision, design, develop, modify, and verify mechanical components for medical devices; sssist with prototyping and bench testing and support problem solving, root cause analysis, identify potential solutions, and evaluate them against requirements; conduct research and studies to support product design

• 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; learn R&D procedures like design controls and risk management, per the Quality Management System; work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success.
• Learn procedures, policies, processes, systems, and technology required; 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 Need:

Required-

Bachelor of Science in Engineering, Mechanical Engineering or Bio Medical &

Experience- 4 years- 6 years

Preferred Qualifications:

• Fundamental knowledge and understanding of mechanical engineering practices and tools, design principles within a regulated environment.
• Basic knowledge of design and concept generation CAD( Creo Preferred) or CAE modeling tools; analysis tools and statistical methods and materials and manufacturing methods
• Ability to read and Interpret complex drawings

Travel Percentage: 20%