Job Description

Work Flexibility: Hybrid

What you will do-

• Evaluating the design's overall effectiveness, cost, reliability and safety and create and review material part specifications and bills of material.
• Generation and checking of drawings for manufacturing - Drafting to Stryker and GD&T standards (Good experience required in DFMEA, DFM, GD&T, Tolerance Stack-up.)
• Manage multifunctional projects both short term and long term and Knowledge of manufacturing process, engineering change process, Design Verification and Validation, Design and Risk Management documents.
• Should Understand cross-functional roles & responsibilities as outlined by the Quality System and achieves communal goals of R&D projects
• Collaborate with internal manufacturing partners, contract manufacturers, designers and product specialists to optimize designs for manufacturability.
• Ability to set up new test methods, verification and validation activities knowledge
• Should have expertise of defining verification and validation methods.
• Proven Expertise in Material Selection Knowledge (materials specific to medical devices).
• Awareness about ISO13485 and International standards, and norms

What you will need-

Required skills-

• Educational Qualification of BE/B.Tech/ME/M. Tech in Mechanical Engineering with strong work experience of 9-12 years out of which Minimum 7 years in similar role of product development
• Good Product Design & Development Experience particularly for medical devices and concept designing and development and proofing by hand calculation, FEA reports / Problem Solving Skills.
• Experience of designing electromechanical devices from scratch and good 3D CAD modeling skills (Creo).
• Prototype Development and Testing - Should have clarity of prototype development methods

Preferred skills-

• Excellent verbal and written communication skills
• Good at Project Management and Documentation
• Should have good problem solving skills

Travel Percentage: 10%