QA Technician I
Location: Plymouth, MN • Duration: 6 Months • 100% Onsite
About the role
Entry level individual contributor representing the most common entry point for this career stream. Works under direct supervision in the Good Manufacturing Practices (GMP) area. 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.
Responsibilities
- Maintain control of the product quality and the manufacturing process.
- DHR (Device History Record) review, both paper and electronic
- Assist with Quality Issues on the floor and product disposition
- Assist in ensuring all manufactured products align with applicable product specifications
Requirements
- HS Diploma or GED required
- 1-3 years of experience
Skills
- Knowledge of good documentation practices
- Production systems knowledge (MES/SAP/Windchill)
Benefits available after waiting period.
Benefits
- 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 coverage
- Hospital coverage
- Accident Insurance
- MetLife Legal
- MetLife ID Fraud
- MetLife Pet Insurance
- 401(k)
Schedule
Shift: 2pm to 1am