Job Summary

• Primary responsibilities include working in Quality Engineering and with other functional groups in support of new product/process development, quality operations or quality assurance.
• Utilizing Quality Engineering tools/processes in development and implementation of practices for the effective and efficient development, transfer, and maintenance of products/processes throughout the product lifecycle.
• Ensure that development activities follow design control requirements, product is tested per applicable standards, European Essential Requirements are met per the MDR, and product is properly transferred to manufacturing.

Matching Summary

Skills & Requirements

Key Requirements

• Bachelor's degree in a related field
• 4 – 6 years of experience
• Medical device or regulated industry experience
• Master's degree preferred
• Knowledge of GD&T desirable
• Thorough knowledge of GMP and QSR requirements
• Thorough knowledge of design control and V&V
• Project management skills
• Auditing and problem-solving skills
• Six Sigma and Business Excellence tools

Work Rights