Job description

• Join a global leader supporting aerospace and medical innovation • Drive quality improvements with advanced engineering tools and systems About Our Client Our client is a globally recognized manufacturer serving highly regulated, technology-driven industries where quality and precision are critical to success. Their products contribute to applications that improve lives and support mission-critical performance across demanding markets. Job Description • Lead non-conformance investigations and drive root cause corrective actions (CAPA) initiatives. • Manage MRB, RMA, and quality documentation processes to ensure compliance and operational excellence. • Support supplier quality activities, including audits and performance evaluations. • Assist with customer, internal, and third-party audits across multiple quality certifications. • Analyze manufacturing and quality data using tools such as Minitab and Excel to identify improvement opportunities. • Develop and execute validation protocols including IQ, OQ, and PQ activities. • Implement and maintain SPC/SQC programs to improve process capability and product quality. • Create and maintain quality plans, PFMEAs, control plans, and inspection documentation. • Conduct capability studies and variation reduction initiatives to enhance manufacturing performance. • Develop training materials and provide quality-related training across the organization. • Support metrology and inspection activities, including CMM and advanced measurement systems. • Collaborate cross-functionally with engineering, operations, and production teams to resolve quality concerns and improve processes. 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. The Successful Applicant • Bachelor's degree in Engineering, preferably Mechanical, Electrical, or Chemical Engineering. • Minimum 2 years of experience in a manufacturing environment. • Experience within aerospace, medical device, or other regulated manufacturing industries is highly preferred. • Working knowledge of quality systems including CAPA, MRB, RMA, FMEA, SPC, and validation activities. • Experience supporting ISO 9001, AS9100, ISO 13485, or similar quality standards. • Strong problem-solving, analytical, and root cause investigation skills. • Proficiency with Microsoft Excel and quality data analysis tools. • Strong communication and collaboration skills across cross-functional teams. • ASQ Certified Quality Engineer (CQE) certification is a plus. • Knowledge of GD&T, CMM programming, SolidWorks, or AutoCAD is advantageous. What's on Offer • Opportunity to support products that impact aerospace safety and medical innovation. • Join a stable, globally recognized organization with a strong quality-focused culture. • Gain exposure to advanced manufacturing processes and engineering technologies. • Work on high-visibility projects with cross-functional collaboration and career growth opportunities. • Be part of a team committed to continuous improvement, technical excellence, and operational success.

Requirements

Must-haves

Join a global leader supporting aerospace and medical innovation
Drive quality improvements with advanced engineering tools and systems
Lead non-conformance investigations and drive root cause corrective actions (CAPA) initiatives.
Manage MRB, RMA, and quality documentation processes to ensure compliance and operational excellence.
Support supplier quality activities, including audits and performance evaluations.
Assist with customer, internal, and third-party audits across multiple quality certifications.
Analyze manufacturing and quality data using tools such as Minitab and Excel to identify improvement opportunities.
Develop and execute validation protocols including IQ, OQ, and PQ activities.
Implement and maintain SPC/SQC programs to improve process capability and product quality.
Create and maintain quality plans, PFMEAs, control plans, and inspection documentation.
Conduct capability studies and variation reduction initiatives to enhance manufacturing performance.
Develop training materials and provide quality-related training across the organization.
Support metrology and inspection activities, including CMM and advanced measurement systems.
Collaborate cross-functionally with engineering, operations, and production teams to resolve quality concerns and improve processes.
The Successful Applicant
Bachelor's degree in Engineering, preferably Mechanical, Electrical, or Chemical Engineering.
Minimum 2 years of experience in a manufacturing environment.
Working knowledge of quality systems including CAPA, MRB, RMA, FMEA, SPC, and validation activities.
Experience supporting ISO 9001, AS9100, ISO 13485, or similar quality standards.
Strong problem-solving, analytical, and root cause investigation skills.
Proficiency with Microsoft Excel and quality data analysis tools.
Strong communication and collaboration skills across cross-functional teams.

Nice-to-haves

Experience within aerospace, medical device, or other regulated manufacturing industries is highly preferred.
ASQ Certified Quality Engineer (CQE) certification is a plus.

Application prep

Use the role’s language and application details while tailoring your materials.

Platform: careers-page
Effort: medium