Intern FY 2026-27

Work Flexibility: Hybrid or Onsite 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 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. What you need: 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. Travel Percentage: None Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World's Best Workplaces! For more information, visit: www.stryker.com Work Flexibility Remote – Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location. Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based. Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category. Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.