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%
