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
Job Summary:
As a Supplier Quality Engineer, to review the process parameters, review Supplier process capabilities, Sourcing and assessing the vendors, Participating in Quality Audits & review of all quality documentation
Yrs of Experience: 2 to 6 yrs
Roles & Responsibilities:
Review engineering and manufacturing specifications to identify materials needed for product / Assembly.
Conduct drawing and certification reviews.
Review Supplier APQP, PPAP packages & validate customer requirements are met.
Maintaining detailed reports on supplier quality, including defect rates and areas that result in flaws.
Providing technical advice and guidance to suppliers to reduce defect rates.
Assess supplier process controls to ensure product is manufactured to meet requirements.
Collate and evaluate supplier quality data to identify process improvement opportunities within the supply chain.
Review and Ensure Quality Clinic Procedures are being fulfilled.
Execute Corrective Action & Preventive actions Request and Reports.
Document corrective action requests and verify effectiveness of actions implemented.
Maintain relevant ISO/ AS/FDA compliant procedures as they pertain to the Supplier Quality function.
Review and validate QN Supplier Inputs.
Evaluate Supplier(s) root cause and assess corrective action for each defect submitted.
Supports and co-ordinates with Customers and Suppliers in all technical issues
Mandatory Skills:
Manufacturing Process Planning knowledge.
Knowledge on different manufacturing processes & special processes.
Knowledge of using GD&T & blueprint reading.
Knowledge in QC tools/documentation like FAIR, APQP/PPAP, FMEA, MSA, SPC, etc.,
Working experience in Aerospace/ Automobile/ Medical/ Rail/ Composites domain.
Working knowledge on CAD tools CATIA/ Siemens NX/ CREO/ Solid works.
Desired skills:
Knowledge on using AS9100 and AS9102/ ISO9001/ FDA Quality System Regulation, ISO 13485, and the Medical Device Directive.
Hands on experience on Minitab/ MS office Suite (Advance Excel, Word, Power point) is an added advantage.
Knowledge of Risk Management standard – ISO 14971
Six sigma/Supplier Quality/Quality certification from recognized body is an added advantage.
Skills & Experience
ISO 13485:2003- Quality in Medical Devices, Quality Assurance, Quality assurance in Software and manufacturing, Quality Control, Quality Engineering Certification, Supplier Quality
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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