Job Summary

• This role plays a critical part in protecting patients and advancing product quality by ensuring robust, effective corrective and preventive action processes.
• You will influence how quality decisions are made across the site and beyond, shaping behaviors, strengthening compliance, and enabling continuous improvement.
• Develop and deliver training to ensure consistent and compliant use of corrective action processes and systems across all user groups.

Matching Summary

Salary

Base: $72,500.00 - $157,200.00; Bonus/Equity: bonus eligible; Benefits: benefits

Skills & Requirements

Key Requirements

• Bachelor's degree in science, engineering, or related discipline
• 2+ years of experience in a manufacturing environment
• 2+ years of experience in quality systems, quality engineering, or related regulated function
• Experience interacting with regulatory or notified bodies
• Experience applying U.S. and international medical device regulations
• Prior experience supporting quality system audits
• Experience working across multiple sites or within a matrixed or corporate quality structure

Work Rights