Quality Engineer

Boyd•Grand Rapids, MI

23d•Onsite

About The Position

The Quality Engineer supports APQP activities, develops and maintains PFMEAs, Control Plans, and Work Instructions, and manages the PPAP submission process. The role investigates non-conformances, leads corrective actions, and identifies process improvement opportunities to ensure compliance with ISO 9001, IATF 16949, and customer-specific requirements. The Quality Engineer also monitors supplier performance, supports internal and supplier audits, and partners with production, engineering, suppliers, and customers to maintain product reliability, reduce defects, and support continuous improvement. The position is on-site in Grand Rapids, Michigan. The physical demands include sitting and standing, moving around an office and production floor, working at a computer workstation, bending, twisting, lifting and reaching, and periodically lifting up to 40 pounds.

Requirements

Bachelor’s degree in Engineering, Quality, Manufacturing, or a related field, or equivalent experience.
3–5 years of experience in Quality Engineering, Quality Assurance, or a similar role.
Strong understanding of APQP, PPAP, FMEA, SPC, and MSA.
Knowledge of blueprint reading, drawing interpretation, and GD&T.
Familiarity with ISO 9001 and IATF 16949 quality management systems.
Hands-on experience with measurement tools, hand gauges, and testing equipment.
Strong communication skills with customers, suppliers, and all levels of the organization.
Problem-solving skills using 8D and 5-Why methodologies.
Organizational and project management skills, with the ability to work independently.
Proficiency in Microsoft Office, including Excel, Word, Outlook, and PowerPoint.
Ability to prepare and present data clearly in reports and meetings.
Ability to sit and stand, move around an office environment and production floor, work at a computer workstation, bend, twist, lift, and reach, and periodically lift up to 40 pounds.

Nice To Haves

Experience in high-volume manufacturing; automotive or industrial experience is preferred, and OEM experience is a plus.
Knowledge of Lean Manufacturing and Six Sigma principles.
Preferred experience in automotive or medical manufacturing.

Responsibilities

Support APQP activities.
Develop and maintain PFMEAs, Control Plans, and Work Instructions.
Manage the PPAP submission process.
Investigate non-conformances and lead corrective actions.
Identify opportunities for process improvements.
Help ensure compliance with ISO 9001, IATF 16949, and customer-specific requirements.
Monitor supplier performance.
Support internal and supplier audits.
Partner with production, engineering, suppliers, and customers to maintain product reliability, reduce defects, and support continuous improvement.
Perform other job-related duties requested by the supervisor.