Quality Engineer III

Title: Quality Engineer III

Location: Saint Paul, MN

Duration: 12 Months

100% Onsite Qualifications

• 3–5 years experience
• Medical Device Quality experience (Ops or Manufacturing)
• Strong working knowledge of FDA/ISO regulations (13485, 14971, etc.)
• Ability to ramp up quickly

Responsibilities

• Support Quality integration activities including:
• Acceptance Activities and Inspection Plans
• Data Integrity Risk Assessments (DIRA)
• Validation Master Plans (VMPs)
• Hazard Analysis activities
• Assist with SOPs, Work Instructions, and occasional training
• Occasionally write/execute test protocols and report.

Consultants Eligible Benefits Upon Waiting Period

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account (for High-Deductible Health Plans)
• Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
• Supplemental Life Insurance
• Short Term Disability (coverage varies by state)
• Long Term Disability
• Critical Illness, Hospital coverage, Accident Insurance
• MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
• 401(k)

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.

Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.