Job Description

Work Flexibility: Hybrid
What you will do:

• Under minimal supervision, research, design, develop, modify, and verify components/modules for medical devices.
• Translate design inputs to engineering specifications and produce sub-system level designs; Develop and analyze solutions, prototyping one or more options to provide proof of concept.
• Demonstrate understanding of customer needs and design inputs; Demonstrate proficiency with product's intended use and clinical procedures.
• Responsible risk-taking and risk management.
• Follow fundamental industry standards, design requirements and test strategies which apply to regulatory requirements.
• Independently create or refine engineering documentation, such as the Design History file.
• Working knowledge of (V&V) of medical device , Design verification testing, Design confidence testing, and product validation experience
• Follow R&D procedure like design controls and risk management, per the Quality Management System- ISO 13486, ISO 14971, EUMDR/ MDD requirements

Minimum Qualifications (Required):

• Preferable Bachelor's/ Master's in Mechanical Engineering can consider Biomedical engineering as well; 2- 6 years of relevant work experience in product development of mechanical engineering.
• Experience and hands on with design tools like Creo, Windchill, release of design through change management. Good to have hands on with UG NX.
• Skilled in interpreting design, analyzing and driving design changes, and collaborating across different functions for DFM, design for inspection, material selection.
• Basic working level of GD&T and tolerance analysis
• Good to have understand medical domain and clinical setting.

Travel Percentage: 10%