Quality Engineer I

Abbott seeks a Quality Engineer I for its Plymouth, Minnesota Electrophysiology division to support quality assurance programs, policies, and processes for cardiac medical devices. The role involves technical problem-solving, regulatory compliance, and cross-functional collaboration to ensure product quality and adherence to established standards.

Responsibilities

• Support and maintain quality assurance programs, policies, procedures, and controls for medical devices
• Initiate and complete technical activities for new or improved products and processes
• Prepare reports and presentations to communicate quality findings and analysis
• Analyze data and provide recommendations to senior staff regarding quality-related issues
• Identify opportunities to ensure compliance with FDA, ISO 13485, and other applicable regulations

Requirements

• Bachelor's degree in engineering or technical field, or equivalent education and work experience
• 0-2 years of engineering experience
• Strong verbal and written communication skills across organizational levels
• Ability to multitask, prioritize, and meet deadlines in fast-paced environments
• Experience working in matrixed, geographically diverse business environments
• Strong organizational skills and attention to detail