Intern

What you will do:

The individual will work as an individual contributor who will be part of a team working on following :

• With supervision, works with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success.
• With supervision, designs, develops, modifies, evaluates and verifies mechanical components for medical devices.
• Learn procedures, policies, processes, systems, and technology required.
• Assists with prototyping and bench testing.
• Support problem solving, root cause analysis, identify potential solutions, and evaluate them against requirements.
• Under supervision, conduct research and studies to support product design.
• Works on problems in limited scope; purposefully learns while gaining experience.
• Demonstrates ownership and integrity of work.
• Builds stable relationships and contributes to the project as a team member.
• Interpret customer needs and understands design inputs.
• Understand the products 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.

• Full time M. Tech -Engineering, Mechanical Engineering or relevant streams
• Fundamental knowledge and understanding of mechanical engineering practices and tools, design principles within a regulated environment.
• Basic knowledge of design and concept generation CAD or CAE modeling tools.
• Basic knowledge of analysis tools and statistical methods.
• Basic knowledge of materials and manufacturing methods.
• Ability to read and Interpret complex drawings.
• Must be flexible, independent and self-motivated
• Ability to conceptualize, eager to learn and detail orientation.
• Strong written and oral communication skills.

Work Flexibility