Quality Engineer II - Manufacturing - Southwick, MA

• Step into a visible, hands-on quality role!
• Own quality from raw material!

About Our Client

This organization is a well-established, multi-site manufacturing business supporting a diverse range of technically demanding industries. They combine advanced in-house capabilities with a strong culture of safety, accountability and continuous improvement.

Job Description

• Design, document and implement process control, testing and inspection methods, including SPC.
• Lead root cause analysis using structured problem-solving tools and implement effective corrective and preventive actions.
• Manage and support large quality and process improvement projects, ensuring timelines, resources and communication are aligned.
• Conduct internal quality system audits and support ongoing compliance with quality standards.
• Facilitate CAPA meetings, track actions and ensure timely and sustainable resolution.
• Lead APQP activities to ensure effective product and process validation.
• Develop, maintain and report quality system metrics to support data-driven decision making.
• Partner with engineering teams to use historical performance data to prevent recurrence of issues.
• Apply quality and engineering tools such as DOE, DFM, FMEA, GD&T, process capability and Six Sigma methodologies.
• Support MRB activities, including failure analysis and disposition decisions.
• Develop and lead blueprint reading and quality training for new hires in collaboration with HR.

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

• 3-5 years of recent, relevant experience in a manufacturing environment.
• Strong understanding of manufacturing processes, tooling and production controls.
• Solid working knowledge of ISO 9001 quality systems; auditing experience preferred.
• Experience with medical systems and ISO 13485 audits is highly desirable.
• Bachelor's degree in Engineering or Certified Quality Engineer (CQE) certification preferred.

What's on Offer

• Be part of a safety-first, values-driven culture that genuinely invests in its people.
• Work in a technically diverse manufacturing environment supporting multiple industries.
• Gain exposure to advanced manufacturing processes and quality systems across multiple sites.
• Enjoy a competitive total rewards package, including bonus, 401(k) match and education support.
• Join a business that values collaboration, accountability and continuous improvement.

Contact

Jenny Ly

Quote job

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