What are the responsibilities and job description for the Manufacturing Quality Engineer position at Isometric Micro Molding, an NMT Company?
Job Description
The Quality Engineering Technician plays a critical role in ensuring the quality and integrity of our products and processes. As a member of the Quality department, you will work closely with cross-functional teams to implement quality initiatives and ensure compliance to regulatory requirements.
Key Responsibilities
- Coordinate CAPA activities within QMS procedures
- Perform calibration system administration
- Train others to established procedures
- Perform First Article inspections
- Perform Gage R&R studies
- Assist in the development and writing of procedures
- Recommend adjustments to the assembly or production process
- Inspect, test, or measure materials or products being produced
- Measure products with CT scanner, calipers, gauges, micrometers, vision systems, or other measurement equipment
- Discuss inspection results with those responsible for products
Requirements
- Associate's degree in related technical field, or 2 years of relevant experience required
- Understand print and specification reading processes with GD&T concepts
- Ability to inspect a variety of equipment & methods experience
- Medical molding and validation experience preferred
- Independent initiative required
- Ability to work in a procedure-based system and follow guidelines
- Detail and Quality oriented
- Knowledge of clean room practices preferred
- Solid understanding of ISO13485 or ISO9001 continuous improvement
Benefits
- Comprehensive benefits package including medical, dental, and vision options
- 401(k) program with Company match available after 90 days
- Paid time off, personal days, and holidays
- Opportunities for professional growth and development
- Collaborative and dynamic work environment
The Quality Engineering Technician plays a critical role in ensuring the quality and integrity of our products and processes. As a member of the Quality department, you will work closely with cross-functional teams to implement quality initiatives and ensure compliance to regulatory requirements.
Key Responsibilities
- Coordinate CAPA activities within QMS procedures
- Perform calibration system administration
- Train others to established procedures
- Perform First Article inspections
- Perform Gage R&R studies
- Assist in the development and writing of procedures
- Recommend adjustments to the assembly or production process
- Inspect, test, or measure materials or products being produced
- Measure products with CT scanner, calipers, gauges, micrometers, vision systems, or other measurement equipment
- Discuss inspection results with those responsible for products
Requirements
- Associate's degree in related technical field, or 2 years of relevant experience required
- Understand print and specification reading processes with GD&T concepts
- Ability to inspect a variety of equipment & methods experience
- Medical molding and validation experience preferred
- Independent initiative required
- Ability to work in a procedure-based system and follow guidelines
- Detail and Quality oriented
- Knowledge of clean room practices preferred
- Solid understanding of ISO13485 or ISO9001 continuous improvement
Benefits
- Comprehensive benefits package including medical, dental, and vision options
- 401(k) program with Company match available after 90 days
- Paid time off, personal days, and holidays
- Opportunities for professional growth and development
- Collaborative and dynamic work environment
