Supplier Quality Engineer

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:

Supplier Quality Engineer  

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 Scarborough, ME location in the Infectious Disease, 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 Supplier Quality Engineer will help drive supplier quality performance, continuous improvement, and risk mitigation across the supply base. Acts as a key technical contributor partnering across functions to ensure supplier capabilities meet product, regulatory, and business requirements. Leads supplier quality activities and influences outcomes without direct authority.

What You’ll Work On

• Support onboarding of suppliers, including validation and readiness activities

• Contribute to supplier improvement plans to address performance gaps

• Collaborate with suppliers to improve process capability and product quality

• Track supplier quality metrics (PPM, defect rates, yield, escapes) and perform trend analysis

• Monitor supplier performance and identify risks and systemic issues

• Support supplier reviews and follow-up on improvement actions

• Investigate supplier-related defects, incoming issues, and field failures

• Own supplier nonconformance management, including containment, resolution, and closure of supplier-related issues

• Support root cause analysis and implementation of corrective and preventive actions (CAPA)

• Drive and own supplier corrective actions, ensuring timely and effective implementation and verification of effectiveness

• Communicate supplier quality issues and track resolution progress

• Support development and maintenance of inspection procedures and acceptance criteria

• Assist in optimizing incoming inspection strategies based on risk

• Provide guidance to inspection teams as needed

• Collaborate with Design Engineering, Manufacturing, Procurement, and Quality teams

• Provide input to supplier-related quality decisions

• Participate in cross-functional problem-solving efforts

• Analyze data to identify trends and opportunities for improvement

• Own suppliers change management processes, including review, risk assessment, approval, and implementation of supplier-initiated changes

Required Qualifications

• Bachelors in Engineering or related field, or equivalent combination of education and experience.

• 2-4 years Supplier Quality, Manufacturing Quality, or related experience.

Preferred Qualifications

• Experience working in regulated industry (e.g., medical device, pharmaceutical, automotive, aerospace) with knowledge of applicable standards (e.g., FDA, ISO 13485, ISO 9001, AS9100)

• Demonstrated experience leading supplier audits, including process, system, and compliance audits.

• Experience managing supplier corrective actions and verifying effectiveness of CAPAs.

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

$61,300.00 – $122,700.00

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

     

JOB FAMILY:

Operations Quality

     

DIVISION:

ID Infectious Disease

        

LOCATION:

United States > Scarborough : 10 Southgate Rd

     

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), Continuous standing 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