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, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

Working at Abbott:

At Abbott, you can do work that matters, grow, and learn, care for yourself and your 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 a 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 worldwide 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 the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Lake Forest, IL location in the Core Lab, Diagnostics Division. We’re empowering smarter medical and economic decision-making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott’s diagnostics instruments, providing lab results for millions of people.

The Senior Professional Quality (Commodities) will conduct quality-related activities to deliver consistent, high-quality documents, services, products, and processes.

What You’ll Work On

• Develops and executes local quality strategies aligned with divisional and business objectives.

• Translates strategic priorities into executable long‑range programs, projects, and tactical activities.

• Provides compliant, innovative, and practical solutions to complex quality and operational challenges.

• Represents the function on cross‑functional initiatives, influencing project scope, direction, and outcomes.

• Communicates effectively and contributes quality expertise across one or more QA functions, providing guidance to professionals and technicians as appropriate.

• Demonstrates strong knowledge of applicable regulatory standards and ensures compliance with division and corporate Quality System policies and procedures.

• Maintains and improves the effectiveness of ADD’s Quality System subsystems and key processes by identifying and mitigating compliance risks.

• Supports and drives risk management strategies, making independent, risk‑based decisions aligned with site policies, Quality System requirements, and business objectives.

• Reviews and approves supplier risk management documentation and supports quality‑related improvements and investments.

• Investigates complex complaints and provides direction and approval for defect resolution related to supplied materials.

• Reviews and approves supplier investigations, root cause analyses, and corrective and preventive actions (CAPAs).

• Provides quality oversight and approval for mold, assembly automation, and manufacturing equipment qualification activities, and supports supplier monitoring and performance management.

• Acts as Process Owner and/or Subject Matter Expert for design control, documentation, and change management activities; participates in internal and external audits and supports major site, divisional, and supplier projects.

Required Qualifications

• Apprenticeship or bachelor’s degree in Life Science, Engineering, or closely related discipline is required OR relevant combination of education or experience.

• At least 8 years work experience in Quality or related filed experience; Less experience may be appropriate with advanced degree.

• Has experience in the health care industry.

• Has a history of completing successful cross-functional projects and driving positive compliance outcomes required.

Preferred Qualifications

• Experience with plastic injection molded components, validation, qualification, change control CAPA and quality engineering.

• Experience in using Power BI or other applications to display and monitor key metrics related to supplier performance.

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:

https://abbottbenefits.com/

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, and on Facebook at https://www.facebook.com/AbbottCareers.

The base pay for this position is

$86,700.00 – $173,300.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Operations Quality

DIVISION:

CRLB Core Lab:

LOCATION:

United States > Lake Forest : CP01

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

Yes, 25 % of the Time

MEDICAL SURVEILLANCE:

Not Applicable

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday), Work requiring repeated bending, stooping, squatting or kneeling

Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

• EEO is the Law link

• English: http://webstorage.abbott.com/common/External/EEO_English.pdf

• EEO is the Law link

• Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf