Job Description

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. KNOWLEDGE, SKILL, AND ABILITY In-depth experience in CAD tools such as Solid works is expected. Expertise in Robust Modeling and Detailing practices following the ASME guidelines. Strong Knowledge and application of GD&T including Tolerance stack-up analysis. Strong knowledge of metal manufacturing processes. Knowledge on 3D printing and additive manufacturing technologies is an add-on. Knowledge on Engineering Change management processes and PLM tools such as Agile, PTC Windchill is preferred. Strong understanding of medical device standards , guidelines and regulations per ISO 13485, ISO 14971 and Design controls ( 21 CFR Part 820). Ability to create, assess or review applicable product DHF deliverables such as Risk files, Sterilization reports, Bio-compatibility reports etc. along with support from relevant project stakeholders. Strong knowledge of Engineering fundamentals and application of same during concept generation or re-design of products. Able to effectively work with cross functional teams in a multinational matrix organization. Assist in the design of cutting-edge medical devices through prototyping, testing and modeling. Develop validation plans and conduct validation testing Assist in DFM (Design for Manufacturing) activities. Develop and test new manufacturing processes. Maintain working relationships with Suppliers. Support regulatory filings to various government bodies. Support pre-clinical and clinical research activities. Comply with the Health & Safety policies of the company and inform Management of unsafe working conditions. 7 to 10 years of experience. Skills & Experience 21 CFR Part 820, DFM, DFMA, Geometric Dimensioning And Tolerancing (GD&T), ISO 13485 Medical Devices, ISO 14971 Risk Management, Plastic Product Design, SolidWorks, Windchill 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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