Quality Engineer MRB
Accord Technologies Inc.
Position: Quality Engineer MRB
Location: North Hollywood, CA (Onsite)
Industry: Aerospace / Manufacturing
Position type: FTE
Overall Experience: 5 10 Years
MRB Experience: Minimum 2 Years Mandatory
| Required Skills | No of years of Exp |
| Quality control /Manufacturing | |
| Part Inspection | |
| Disposition /MRB | |
| NCR/NCMR/nonconformance | |
| Material handling | |
| Mechanical Engineering OR Aerospace domain |
Job Summary
We are looking for an experienced Quality Engineer with 5 10 years of overall experience and a minimum of 2 years of hands-on Material Review Board (MRB) experience , preferably in the aerospace/manufacturing industry.
The role requires hands-on involvement in nonconformance evaluation, physical inspection of parts when required, coordination with cross-functional stakeholders, conducting Quality Clinic meetings, and driving quality issues through timely disposition and closure.
Key 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 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.
Required Experience & Skills
- 5 10 years of overall Quality/Manufacturing Engineering experience.
- Minimum 2 years of hands-on MRB experience Mandatory.
- Strong experience in nonconformance management and MRB disposition processes.
- Experience with NCR/NCMR/QN or equivalent quality notification systems.
- Strong engineering drawing and GD&T interpretation skills.
- Hands-on ability to inspect and evaluate parts when required.
- Good understanding of manufacturing and inspection processes.
- Experience in Root Cause Analysis, Corrective Action, 8D, 5-Why, Fishbone, and CAPA.
- Experience conducting or coordinating Quality Clinic / cross-functional quality meetings.
- Strong stakeholder management, communication, coordination, and follow-up skills.
- Knowledge of AS9100 and AS9102 is preferred.
Preferred Manufacturing Experience
Experience in aerospace or precision manufacturing involving:
- Machining
- Sheet-metal fabrication
- Castings and forgings
- Mechanical assemblies
- Heat treatment
- Special processes
Qualification
- Bachelor's degree or Diploma in Mechanical, Manufacturing, Aerospace, Industrial Engineering, or equivalent discipline .
- 5 10 years of relevant industry experience.
- Minimum 2 years of direct MRB experience is mandatory.
- Aerospace manufacturing experience is preferred.
Key Competencies
- MRB & Nonconformance Management
- Engineering Drawing & GD&T Interpretation
$90k - $125k
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