Quality Manager - Medical Device - Litchfield, CT

This CMM Programmer/Quality Engineer will have insight into many different areas of Quality within an elite manufacturing organization. The aim is to balance activities to foster career growth within areas that are of most interest to the candidate. They will learn under a long tenured Quality Manager to strengthen both their technical and soft skills.

Client Details

As a pioneer in fineblanking technology, our client offers state-of-the-art solutions for precision-engineered components. Our comprehensive services, ranging from fineblanking to secondary finishing, cater to a wide range of industries, including automotive, electronics, and medical equipment.

Description

In this role, this CMM Programmer/Quality Engineer will:

• Quality System Oversight: Monitor and maintain the effectiveness of quality and reliability systems, ensuring adherence to industry standards and customer requirements.
• Documentation Management: Generate, maintain, and update accurate documentation related to quality, reliability, and manufacturing processes.
• Metrology and Inspection: Develop and execute CMM programs to verify part quality. Measure tool components and document findings for future reference.
• Problem Solving and Prevention: Implement detection systems to identify and eliminate potential quality and reliability issues.
• Data Analysis and Reporting: Prepare and present detailed reports on key performance indicators (KPIs) such as PPM, Cost of Quality, and NCRs.
• Quality Program Development: Develop, implement, and manage quality programs, including tracking, analysis, and problem-solving activities.
• Record Keeping: Maintain accurate and organized quality records, including customer complaints, control plans, quality alerts, and weekly logs.
• Calibration Management: Oversee and control the gauge calibration system to ensure measurement accuracy.
• Customer Support: Manage and submit timely customer PPAPs, ensuring compliance with customer-specific requirements.
• Process Improvement: Develop and implement control plans and in-process inspection records to optimize manufacturing processes.
• Non-Conformance Management: Issue NCRs, initiate containment actions, and write clear instructions and reports for corrective actions.
• Corrective Action Implementation: Lead 8-D corrective action investigations, document findings, and submit reports to customers.

Profile

A Successful Candidate will have:

• High school diploma or equivalent
• Experience regarding CMM Programming
• 5+ years of hands-on experience in quality assurance within a manufacturing environment or CQE certification
• Strong understanding of ISO9001 and IATF16949 standards and their application in quality management systems

Job Offer

On Offer for the Candidate is:

• Strong Compensation Package
• 4 day work weeks!
• Career Growth Focused
• Long Term Stability
• and more

APPLY TODAY! All relevant applicants will receive follow up within 72 hours.

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.