Quality Engineer I, Medical Devices (Entry Level)

Regulatory Jobs; Plymouth (MN); On-site; USD 51,000 - 101,000; Full time

Benefits offered by this job

Health coverage

401(k) plan

Tuition reimbursement

Education benefits

Job summary

Abbott is a global healthcare leader with a Plymouth, MN location for the Quality Engineer I role in the Electrophysiology division. This position supports quality assurance programs to ensure products meet standards and regulatory requirements.

You will engage cross-functional teams and apply structured problem-solving to drive improvements in quality and compliance. The role emphasizes collaboration, documentation, and data analysis, with opportunities to grow within a multinational company

Qualifications

• Bachelor’s degree in engineering or technical field.
• 0-2 years engineering experience.
• Ability to work in a matrixed and geographically diverse environment.
• Team player and individual contributor in a fast-paced setting.
• Strong verbal and written communications.
• Multitasks, prioritizes, and meets deadlines.
• Strong organizational and follow-up skills with attention to detail.

Responsibilities

• Ensure compliance with corporate and divisional policies and procedures.
• Initiate and complete technical activities for current and future programs.
• Prepare reports, publish findings, and present to stakeholders.
• Analyze problems using engineering principles and devise innovative solutions.
• Apply engineering concepts and develop leadership in a specialty area.
• Support QMS, EMS, and regulatory requirements across the division.
• Identify opportunities for risk reduction and cost improvements.

Skills

Communication skills

Time management

Attention to detail

Teamwork

Multitasking

Organizational skills

Education

Bachelor’s degree in engineering

Job description

Abbott is a global healthcare leader with a Plymouth, MN location for the Quality Engineer I role in the Electrophysiology division. This position supports quality assurance programs to ensure products meet standards and regulatory requirements.

You will engage cross-functional teams and apply structured problem-solving to drive improvements in quality and compliance. The role emphasizes collaboration, documentation, and data analysis, with opportunities to grow within a multinational company