Quality Engineer

📋 Description

• Manage and execute assigned quality projects in an FDA Title 21 (820) environment
• Cross-functional support for rapid growth and continuous improvement
• Support in-house manufacturing operations
• Develop quality system procedures with cross-functional teams
• Assist in design development projects representing QA and customers
• Contribute to Continuous Improvement and Lean culture

🎯 Requirements

• Bachelor's degree in Engineering, Science, Technology or related field
• 3+ years of progressive medical device engineering experience
• Experience in FDA Title 21 CFR 820 environment
• Experience with manufacturing, development or quality engineering
• Knowledge of quality systems, change control, and inspection processes
• Ability to work cross-functionally and in cross-functional teams