About this opportunity
Michael Page lists this Senior Quality Engineer opportunity in danvers, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Overview
A leading aerospace manufacturer is seeking an experienced Senior Quality Engineer to drive continuous improvement across a fast‑paced production environment. This role blends strategic quality leadership with hands‑on problem‑solving and cross‑functional influence. The organization is a leading provider of aerospace components known for its technical expertise and commitment to high‑reliability products. With a strong global presence and a collaborative engineering culture, it supports customers across commercial, military, and industrial sectors.
Description
Solve real‑time production quality issues, partnering with manufacturing, engineering, and operations to quickly diagnose defects and prevent repeat issues.
Run structured root‑cause investigations using 5‑Why, Ishikawa, fishbone, and data analysis to drive long‑term corrective actions.
Review and disposition nonconforming material daily through MRB activities, including documentation, parts evaluation, and cross‑functional decisions.
Analyze quality data and trends (scrap, defects, escapes, RMA patterns) and translate insights into improvement projects.
Work directly on the production floor, observing processes, verifying compliance to drawings/specs, and supporting operators and technicians.
Own customer and supplier quality communication, ensuring timely responses, documentation, and follow‑through.
Lead continuous improvement projects that reduce defects, improve throughput, and strengthen process capability.
Support audits (internal, customer, regulatory) and maintain readiness through documentation and process adherence.
Qualifications
Solve real‑time production quality issues, partnering with manufacturing, engineering, and operations to quickly diagnose defects and prevent repeat issues.
Run structured root‑cause investigations using 5‑Why, Ishikawa, fishbone, and data analysis to drive long‑term corrective actions.
Review and disposition nonconforming material daily through MRB activities, including documentation, parts evaluation, and cross‑functional decisions.
Analyze quality data and trends (scrap, defects, escapes, RMA patterns) and translate insights into improvement projects.
Work directly on the production floor, observing processes, verifying compliance to drawings/specs, and supporting operators and technicians.
Own customer and supplier quality communication, ensuring timely responses, documentation, and follow‑through.
Lead continuous improvement projects that reduce defects, improve throughput, and strengthen process capability.
Support audits (internal, customer, regulatory) and maintain readiness through documentation and process adherence.
Job Offer
Competitive salary ranging from $ to $ USD.
Comprehensive benefits package to support your well‑being.
Opportunities for professional development and career growth.
Collaborative and supportive work environment.
Be a part of a respected organization in the Business Services industry.
If this sounds like the right opportunity for you, apply now to join a company that values quality and innovation!
Desired Skills and Experience
Skilled in structured root‑cause analysis and corrective action methodologies (RCCA, 5‑Why, fishbone).
Proficient in interpreting engineering drawings, specifications, and technical data to support quality decisions.
Effective cross‑functional communicator with the ability to influence teams and drive resolution in fast‑paced manufacturing environments.
MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.