Intermediate Quality Engineer

Intermediate Quality Engineer

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year
• An excellent retirement savings plan with high employer contribution
• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity 

This position supports our Princeton, NJ location within the Point of Care business. As an Intermediate Quality Engineer, you’ll partner with Operations to help ensure manufacturing processes, materials, and products meet quality and regulatory requirements. You’ll support validation and qualification activities, investigate quality issues, review production documentation, and assess materials for commercial release while contributing to process improvement and operational excellence.

What You’ll Work On 

• Partner with Operations as a Quality representative to review production records, executed test methods, and material disposition decisions before commercial distribution.
• Review process and test method validation, equipment and facility qualification documentation, and calibration records; identify and resolve deficiencies before commercial use.
• Support nonconformance and deviation investigations, assess process risks, recommend mitigations, and help improve manufacturing and quality processes.
• Review and approve standard operating procedures and manufacturing work instructions, and conduct production-area audits to maintain compliance with cGMP, ISO, and internal quality standards.
• Collaborate with cross-functional teams to resolve day-to-day quality concerns, maintain accurate documentation, and support continuous improvement.

Required Qualifications 

• Bachelor’s degree in engineering, science or a related field; or an associate degree in a related field with an additional two years of experience
• 2+ years of experience in a manufacturing operations environment
• 1+ years of experience applying quality principles and practices
• Knowledge of and experience working within a 21 CFR Part 820, ISO 13485, and/or cGMP-regulated environment
• Strong communication and collaboration skills with the ability to work effectively across Operations and Quality teams
• Ability to meet applicable PPE requirements and perform role-related physical activities, including lifting up to 40 pounds, with or without reasonable accommodation
• Authorization to work in the United States without sponsorship

Preferred Qualifications

• 2+ years of experience in biotechnology manufacturing, preferably in a GMP and/or ISO 13485 environment

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