Our client is a leading provider of sheet metal fabrication and injection molding services, complemented by capabilities in welding, powder coating, blanking, and a variety of other manufacturing processes. Serving both the industrial and medical device sectors, the company is certified to ISO 9001 and ISO 14001 standards. Operations are based in a state-of-the-art, 160,000 sq. ft. facility staffed by approximately 200 employees. This role presents an exciting opportunity to join a dynamic organization with a broad product portfolio and diverse customer base, offering a fast-paced, stimulating work environment where each day brings new challenges and opportunities.
The Quality Engineer is responsible for analyzing reports and returned products, recommending appropriate corrective actions. Prepares documentation for inspection and testing procedures. Executes PPAP, APQP, Control Plans, and FMEA documentation, with a solid background in Continuous Improvement Processes. Gathers information from customers and communicates it internally and to vendors to ensure customer specifications and expectations are met or exceeded. Collaborates with various departments and divisions regarding current and future product configurations. Facilitates corrective actions and verifies the effectiveness of their implementation. Coordinates technical aspects related to product documentation and addresses manufacturing challenges. Contributes to the development and maintenance of policies and procedures for configuration management activities. Establishes standards and procedures for inspection and quality assurance, as assigned. Engages with vendors to resolve quality-related issues, as needed. Operates in an open office environment.
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.
APQP, FMEA, Corrective Action, Control Plan, & Root Cause Analysis Experience. Understanding of ISO 9001 standard. Familiarity with ISO 13485 and ISO 14001 is a nice to have. Ability to communicate with suppliers and customers. Background in automotive or medical device industries. Sponsorship not provided.
Salary ranging from $75,000 - $90,000. Cigna Health Insurance. Excellent 401(k) matching. 2 weeks PTO.
Thomas Graf
Job Reference: JN-102025-6851768