Sr. Supplier Quality Engineer job opportunity at Abbott.

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DatePosted 30+ Days Ago bot
Abbott Sr. Supplier Quality Engineer
Experience: 6-years
Pattern: full-time
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loacation United States - Illinois - Lake Forest, United States Of America
loacation United States ..........United States Of America

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 114,000 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 Abbott is seeking a Senior Supplier Quality Engineer (SQE) to lead and support supplier quality activities across the product and service lifecycle. This role is responsible for ensuring that suppliers consistently meet Abbott’s quality, regulatory, and business requirements. The Senior SQE will act as a key technical and quality liaison between Abbott and its suppliers, driving continuous improvement, risk mitigation, and compliance with global regulations. This role also supports general QMS processes where applicable, including quality investigations What You'll Work On Lead supplier qualification, selection, and onboarding activities, including supplier risk assessments and quality agreements Develop and maintain supplier quality plans aligned with Abbott and regulatory requirements Serve as the primary quality contact for assigned suppliers Plan, conduct, and lead supplier audits (onsite and remote) to applicable standards (e.g., ISO 13485, FDA QSR, GMP) Evaluate audit findings, ensure timely and effective corrective actions, and verify closure Support internal, regulatory, and notified body inspections related to supplier quality Lead investigations of supplier nonconformances, deviations, and escapes Ensure robust root cause analysis and effective corrective and preventive actions (CAPA) Monitor supplier performance metrics and trends to proactively address risks Review and approve supplier‑initiated changes impacting product, process, or materials Assess regulatory and quality impact of changes and ensure proper implementation Collaborate with cross‑functional teams to ensure controlled and compliant changes Drive supplier quality improvement initiatives to enhance capability, reliability, and cost efficiency Mentor junior SQEs and contribute to the development of supplier quality best practices Support new product introductions (NPI) by ensuring supplier readiness and process validation Required Qualifications Bachelor’s degree in Engineering, Quality, or a related technical field 6+ years of experience in Supplier Quality, Quality Engineering, or Manufacturing Quality in a regulated industry Strong knowledge of FDA QSR, ISO 13485, GMP, and global regulatory requirements Proven experience conducting supplier audits and managing CAPAs Demonstrated ability to analyze data, assess risk, and make sound quality decisions Preferred Qualifications Experience in toxicology testing, medical devices, diagnostics, pharmaceuticals, or combination products ASQ certification (CQE, CQA) or equivalent preferred Experience with PPAP, APQP, FMEA, SPC, and process validation Strong project management and cross‑functional leadership skills Ability to travel domestically and internationally (up to ~25%) 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 $78,000.00 – $156,000.00 In specific locations, the pay range may vary from the range posted.       JOB FAMILY: Operations Quality       DIVISION: TOX ARDx Toxicology          LOCATION: United States > Lake Forest : J55       ADDITIONAL LOCATIONS:       WORK SHIFT: Standard       TRAVEL: Yes, 5 % 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)       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

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