CREO/Solid Works Engineer with GD&T and PLM 21 views

Cyient is a global engineering and technology solutions company.As a Design, Build, and Maintain partner for leading organizations worldwide, we take solution ownership across the value chain to help clients focus on their core, innovate, and stay ah

Cyient is a global engineering and technology solutions company.As a Design, Build, and Maintain partner for leading organizations worldwide, we take solution ownership across the value chain to help clients focus on their core, innovate, and stay ahead of the curve. We leverage digital technologies, advanced analytics capabilities, and our domain knowledge and technical expertise, to solve complex business problems. With over 15,000 employees globally, we partner with clients to operate as part of their extended team in ways that best suit their organization’s culture and requirements. Our industry focus includes aerospace and defence, healthcare, telecommunications, rail transportation, semiconductor, geospatial, industrial, and energy. Job Description Bachelor of Engineering /Technology in Mechanical, Production or Automobile Engineering. Minimum freshersand 3+ years of Product design experience. In-depth experience in CAD tools such as Pro-E Creo and Solid works is expected. Experience in Robust Modeling and Detailing practices. Knowledge and application of GD&T including Tolerance stack-up analysis. Knowledge of Design of Plastic parts, Metal Parts and Tool Design. Knowledge on Engineering Change management processes and PLM tools such as Agile, PTC Windchill is preferred. Able to effectively work with cross functional teams in a multinational matrix organization. Superior written and verbal communication skills required. Good attitude and team player. Nice to Haves Master’s in Mechanical engineering, Production or Automobile Engineering. Medical device domain experience Experience in concept development, prototyping and bench testing Experience in lab procedures and testing using Instron Has good understanding of the FDA and other applicable standards relevant to medical devices Has good understanding of DHF deliverables and DHF remediation activities. Knowledge of medical device standards, guidelines and regulations per ISO 13485, ISO 14971 and Design controls ( 21 CFR Part 820). Experience in working with large, multi-site, global organizations. Electro-mechanical medical devices experience is a plus. Skills & Experience Creo, GD&T, SolidWorks Cyient is an Equal Opportunity Employer. Cyient recruits, employs, trains, compensates, and promotes regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, veteran status, and other protected status as required by applicable law. We are proud to be a diverse and inclusive company where our people can focus their whole self on solving problems that matter.

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