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
- Support problem solving, root cause analysis, identify potential solutions, and evaluate them against requirements
- Under supervision, conduct research and studies to support product design

Business Responsibilities

- 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
- With supervision, 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
- Contribute to the project as a team member

What you will need:

Minimum Qualifications (Required):

- Bachelor of Science in Engineering, Mechanical Engineering or BioMedical with 2+ years of work experience

Preferred Qualifications:

- Fundamental knowledge and understanding of mechanical engineering practices and tools, design principles within a regulated setting.
- 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

Travel Percentage: 10%

📌 Engineer Advanced Operations (Gurugram)
🏢 Stryker GmbH u0026 Co
📍 Gurugram