Senior Design Engineer

  • Company:
    Cyient Ltd
  • Location:
  • Salary:
    negotiable / month
  • Job type:
    Full-Time
  • Posted:
    2 weeks ago
  • Category:
    IT-Hardware/Networking | Telecom

Skill: iso 13485 , change control , validation , capa , quality control , product validation; Exp: 4-5 years; Celebrating its twenty-fifth anniversary in 2016, Cyient is an acknowledged leader in engineering design services, design-led manufacturing, networks and operations, data transformation, and analytics. We collaborate with our clients to help them achieve more and together shape a better future. We call it Designing Tomorrow Together. Our industry focus includes aerospace, defense, rail transportation, off-highway & industrial, power generation, mining, oil & gas, communications, utilities, geospatial, semiconductor and medical technology. We align closely with the business needs, goals, culture, and core values of our clients. This reflects in the deep, long-standing relationships we have developed and sustained with some of the leading names in these industries. LOCATION Hyderabad-LancoHIlls_SEZ JOB DESCRIPTION SUMMARY Product Design Engineer with experience in Medical Product Development, Design Verification and Validation, Design analysis, Test Method Validation, Change Control Management, Design Controls, Quality Control and Sustenance engineering. JOB DESCRIPTION Job Description Work in different phases in design process from Pre scope activates to Product launch for a multitude of products, parts, assemblies and subassemblies, including drafting, dimensioning, and tolerance. Product Validation and documenting results. Identifying early potential failure modes for a product by using DFMEA tool to assess the risk associated with those failure modes, to rank the issues in terms of importance and to identify carry out corrective actions to address the most serious concerns and Preventing design process mistakes Evaluating and optimizing the capability of the design to calculate the capability and if necessary optimize the design in an early stage with Tolerance Analysis by using Tolerance designer Carry out DHF remediation activities as per approved remediation plan. Perform risk management and risk analysis activities. Develop protocols and procedures. Carryout Root cause analysis and work on NC/CAPA resolution. Technical writing reports and technical justification. Develop understanding in functional / system testing of medical devices. Required Skills Closely work with Lead Engineer, developing the System requirements into proven functions with the right quality with in minimum time and with cost effective solutions. Familiarity with standards such as ISO 13485, 21 CFR 820 QMS. Should have good knowledge on Medical products Good knowledge on GD & T. Desired Skills Any experience on PLM software will be added advantage Qualification BTech( Mechanical) Exp 4-5 years

Quality Assurance

Degree: 

Experience: 4-5

Function: Quality / Process Control