Abbott Posted October 14, 2026

Sr. Supplier Quality Engineer

New Brighton, Minnesota, United States FULL_TIME
Quality Senior
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About this opportunity

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 122,000 colleagues serve people in more than 160 countries.

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 New Brighton, MN location on our Structural Heart team.

Supplier Development Quality Engineer responsible for activities related to supplier selection and evaluation, material qualification, supplier performance and receiving inspection.  Contributes to the development, establishment and maintenance of supplier quality engineering methodologies, systems and practices which meet company and regulatory requirements.

What You'll Work On

Support supplier selection, evaluation, qualification, and ongoing performance management activities.

Contribute to the development, implementation, and continuous improvement of Supplier Development Quality policies, procedures, methodologies, and systems.

Provide quality engineering support to Purchasing, Manufacturing, R&D, Receiving Inspection, and Operations teams.

Review and approve supplied product drawings, specifications, and component quality plans.

Develop and maintain supplied product inspection plans, receiving inspection requirements, and first article inspection processes.

Provide engineering guidance related to statistical analysis, measurement techniques, Gage R&R studies, sampling plans, and inspection methods.

Assess supplier capabilities through supplier audits, technical reviews, on-site visits, and quality system evaluations.

Lead and support supplier quality audits, including both internal and external supplier assessments.

Drive supplier corrective actions and follow-up activities to ensure root cause identification and sustainable corrective action implementation.

Manage supplier-related nonconforming material investigations and participate in Material Review Board (MRB) activities.

Support CAPA activities, supplier exceptions, and implementation of quality system improvements.

Monitor supplier performance through scorecards, KPI tracking, and supplier performance reviews.

Develop and maintain supplier quality agreements and supplied data agreements.

Apply systematic problem-solving methodologies to identify, prioritize, communicate, and resolve supplier quality issues.

Partner with manufacturing and quality teams to address supplier-related production issues and drive process improvements.

Design and conduct experiments to support process optimization and continuous improvement initiatives.

Participate on cross-functional project teams as the Supplier Quality representative.

Prepare technical documentation including audit reports, supplier agreements, quality procedures, nonconformance reports, and corrective action documentation.

Develop reports and dashboards to support supplier performance monitoring and executive reporting.

Ensure compliance with FDA regulations, ISO standards, and internal quality system requirements.

Build strong partnerships with suppliers and cross-functional stakeholders to drive continuous improvement and operational excellence.

Travel domestically and internationally as needed to support supplier management activities.

Required Qualifications

Bachelor's degree in Engineering, Manufacturing Engineering, Biomedical Engineering, or a related technical discipline.

5+ years of experience in Supplier Quality Engineering, Supplier Development, Manufacturing Quality, or a related quality function.

Strong knowledge of FDA Quality System Regulations, GMP, and ISO 13485 requirements.

Experience conducting supplier audits, supplier qualification activities, and supplier performance evaluations.

Experience managing CAPA activities, supplier corrective actions, nonconforming materials, and root cause investigations.

Strong technical writing skills, including audit reports, supplier quality agreements, procedures, and corrective action documentation.

Experience with quality engineering tools and methodologies such as FMEA, CAPA, Statistical Analysis, Root Cause Analysis, and Gage R&R.

Proficiency with SAP or similar ERP systems and experience using data analysis/reporting tools such as Power BI.

Strong communication, collaboration, and project management skills.

Ability to travel up to 25%, including occasional international travel.

Preferred Qualifications

Medical device industry experience.

ISO 13485 auditor certification or significant auditing experience, including both internal and supplier audits.

Experience with Windchill, CatsWeb, or similar quality management systems.

ASQ Certified Quality Engineer (CQE), Six Sigma, Lean Manufacturing, or related certification.

Experience supporting New Product Development (NPD), supplier qualification, and component/material validation activities.

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:  www.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 www.abbott.com , on Facebook at www.facebook.com/Abbott , and on Twitter @AbbottNews.

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 details

Seniority
Senior
Function
Quality
Therapeutic area
Not listed
Location
New Brighton, Minnesota, United States
Employment type
FULL_TIME

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 249 comparable Senior Quality roles across 63 biopharma companies.

249Comparable roles tracked
235Currently active
63Companies hiring similar roles
33Countries represented

Salary context

63 of 249 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Quality Control Chemist, Senior (Data Review) · Merck KGaA $25/hr – $39/hr (≈ $52,000–$81,120/yr)
Highest disclosed · Assoc Director, Quality Assurance · Gilead Sciences, Inc. $182,070/yr – $235,620/yr
Peer group range $66,560 – $208,845 (median $118,800)

Where these roles are based

Top locations among the 249 comparable roles

United States129
Ireland20
United Kingdom10
Spain9
China7
Switzerland7

+ 27 more countries

Seniority mix

249 of 249 peers have a known seniority level

Senior165
Associate Director46
Principal38

Therapeutic area mix

0 of 249 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
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Function Therapeutic area Seniority Country
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Function Therapeutic area Seniority Country
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ModernaTX, Inc. · Cambridge, United States · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.