Quality Engineer

Cyient Limited; Sacramento (CA); On-site; USD 90,000 - 120,000; Full time

Job summary

Cyient Limited is seeking a Quality/MRB specialist to review and evaluate nonconforming materials through the MRB process, coordinate with Design/Manufacturing Engineering, Quality, Inspection, and other functions, and perform root-cause analysis to drive corrective actions.

You will inspect parts when required, review drawings and GD&T, maintain MRB documentation, and support dispositions such as Use-As-Is, Rework, Repair, or Scrap while ensuring traceability and compliance.

Qualifications

• Review and evaluate nonconforming materials, parts, components, and assemblies through the MRB process.
• Review and process NCR/ QN and other nonconformance documentation.
• Coordinate and discuss quality issues with stakeholders including Design Engineering, Manufacturing Engineering, Quality, Inspection, Supplier Quality, Procurement, Planning, Operations, and other functions.
• Physically inspect nonconforming parts when required to understand the actual defect/condition and support technical evaluation.
• Review engineering drawings, specifications, inspection reports, dimensional results, and other technical documentation.
• Strongly understand and interpret engineering drawings, tolerances, and GD&T requirements.
• Evaluate nonconformances for potential impact on form, fit, function, performance, manufacturability, assembly, and downstream operations.
• Coordinate with Engineering and other stakeholders to support MRB dispositions such as Use-As-Is, Rework, Repair, Return to Vendor, and Scrap, in accordance with applicable authorization requirements.
• Organize and conduct regular Quality Clinic meetings with relevant stakeholders.
• Present and discuss open nonconformances, recurring defects, aging issues, and critical quality concerns during Quality Clinic meetings.
• Track Quality Clinic action items, responsible stakeholders, target dates, and follow up until closure.
• Drive timely closure of MRB/NCR/QN and aging quality issues.
• Perform or support Root Cause Analysis (RCA) and Corrective/Preventive Actions using 5-Why, Fishbone, 8D, or similar methodologies.
• Analyze recurring defects and quality trends and support actions to reduce rejection, rework, and scrap.
• Support First Article Inspection (FAI/FAIR) activities when required.
• Maintain appropriate MRB documentation, approvals, supporting evidence, and traceability.
• Understand, adopt, implement, and consistently follow all applicable Quality, MRB, Engineering, Manufacturing, and customer-defined processes and procedures.
• Support implementation of new/revised processes and identify opportunities for process improvement.
• Participate in internal, customer, and regulatory quality audits as required.
• Escalate critical or aging quality issues to appropriate stakeholders when necessary.

Responsibilities

• Review and evaluate nonconforming materials, parts, components, and assemblies through the MRB process.
• Review and process NCR/ QN and other nonconformance documentation.
• Coordinate and discuss quality issues with stakeholders including Design Engineering, Manufacturing Engineering, Quality, Inspection, Supplier Quality, Procurement, Planning, Operations, and other functions.
• Physically inspect nonconforming parts when required to understand the actual defect/condition and support technical evaluation.
• Review engineering drawings, specifications, inspection reports, dimensional results, and other technical documentation.
• Strongly understand and interpret engineering drawings, tolerances, and GD&T requirements.
• Evaluate nonconformances for potential impact on form, fit, function, performance, manufacturability, assembly, and downstream operations.
• Coordinate with Engineering and other stakeholders to support MRB dispositions such as Use-As-Is, Rework, Repair, Return to Vendor, and Scrap, in accordance with applicable authorization requirements.
• Organize and conduct regular Quality Clinic meetings with relevant stakeholders.
• Present and discuss open nonconformances, recurring defects, aging issues, and critical quality concerns during Quality Clinic meetings.
• Track Quality Clinic action items, responsible stakeholders, target dates, and follow up until closure.
• Drive timely closure of MRB/NCR/QN and aging quality issues.
• Perform or support Root Cause Analysis (RCA) and Corrective/Preventive Actions using 5-Why, Fishbone, 8D, or similar methodologies.
• Analyze recurring defects and quality trends and support actions to reduce rejection, rework, and scrap.
• Support First Article Inspection (FAI/FAIR) activities when required.
• Maintain appropriate MRB documentation, approvals, supporting evidence, and traceability.
• Understand, adopt, implement, and consistently follow all applicable Quality, MRB, Engineering, Manufacturing, and customer-defined processes and procedures.
• Support implementation of new/revised processes and identify opportunities for process improvement.
• Participate in internal, customer, and regulatory quality audits as required.
• Escalate critical or aging quality issues to appropriate stakeholders when necessary.

Job description

• Review and evaluate nonconforming materials, parts, components, and assemblies through the MRB process.
• Review and process NCR/ QN and other nonconformance documentation.
• Coordinate and discuss quality issues with all relevant stakeholders, including Design Engineering, Manufacturing Engineering, Quality, Inspection, Supplier Quality, Procurement, Planning, Operations, and other functions.
• Physically inspect nonconforming parts when required to understand the actual defect/condition and support technical evaluation.
• Review engineering drawings, specifications, inspection reports, dimensional results, and other technical documentation.
• Strongly understand and interpret engineering drawings, tolerances, and GD&T requirements.
• Evaluate nonconformances for potential impact on form, fit, function, performance, manufacturability, assembly, and downstream operations.
• Coordinate with Engineering and other stakeholders to support appropriate MRB dispositions such as Use-As-Is, Rework, Repair, Return to Vendor, and Scrap, in accordance with applicable authorization requirements.
• Organize and conduct regular Quality Clinic meetings with relevant stakeholders.
• Present and discuss open nonconformances, recurring defects, aging issues, and critical quality concerns during Quality Clinic meetings.
• Track Quality Clinic action items, responsible stakeholders, target dates, and follow up until closure.
• Drive timely closure of MRB/NCR/QN and aging quality issues.
• Perform or support Root Cause Analysis (RCA) and Corrective/Preventive Actions using 5-Why, Fishbone, 8D, or similar methodologies.
• Analyze recurring defects and quality trends and support actions to reduce rejection, rework, and scrap.
• Support First Article Inspection (FAI/FAIR) activities when required.
• Maintain appropriate MRB documentation, approvals, supporting evidence, and traceability.
• Understand, adopt, implement, and consistently follow all applicable Quality, MRB, Engineering, Manufacturing, and customer-defined processes and procedures.
• Support implementation of new/revised processes and identify opportunities for process improvement.
• Participate in internal, customer, and regulatory quality audits as required.
• Escalate critical or aging quality issues to appropriate stakeholders when necessary.