Quality Engineer III

Quality Engineer III responsible for maintaining company compliance with FDA Quality System Regulations and ISO 13485 standards, providing customer-related quality and regulatory inquiries, and leading implementation of continuous improvement projects.

Requirements

• Bachelor's degree in engineering or equivalent
• 3 years working experience in manufacturing environment, preferably in medical devices with increasing responsibility
• Strong technical knowledge in required discipline
• Familiar with FDA QSR and ISO 13485
• Comprehensive technical knowledge including ERP system, statistics, SPC, geometric tolerance and mechanical drawing

Benefits

• Equal Opportunity Employer
• Encouragement of veterans and individuals with disabilities to apply