

New · posted Oct 21
Abbott · Medical Devices
Quality Assurance Engineer
- Madison, WI
- On-site
- Full-time
- Associate & Specialist
Open until filled
The role
This position supports Operations within the Cancer Diagnostics business.
As a Quality Assurance Engineer, you will partner with Facilities, Service & Metrology, Process and Controls Engineering, Instrument Production, Reagent Manufacturing, Quality Control, and other areas of Operations. Depending on the assigned area, you will provide Quality oversight of products, materials, manufacturing and QC laboratory equipment and processes, instrumentation, facilities, utilities, and associated systems through qualification and validation, risk management, investigations, change control, and continuous improvement.
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.
What you need
Required Qualifications
- Bachelor's degree in a science or technical field; or an associate degree in a science or technical field plus two (2) years of relevant experience in lieu of a bachelor's degree.
- Three (3) or more years of experience in a manufacturing operations environment.
- One (1) or more years of experience applying quality principles and practices in an assigned area such as Design Transfer, Risk Management, or Manufacturing Quality.
- One (1) or more years of experience with process or test method validation, equipment qualification, or related quality engineering activities
- Demonstrated ability to work in an FDA 21 CFR 820, ISO 13485, ISO 9001, and/or cGMP-structured environment.
- Ability to travel up to 15%, including possible overnight or weekend travel, and comply with applicable personal protective equipment requirements.
- Authorization to work in the United States without sponsorship and ability to perform the essential duties with or without accommodation.
Preferred Qualificationsnice to have
- Three (3) or more years of experience in medical device, biotechnology, pharmaceutical, or other regulated manufacturing environments.
- Experience supporting manufacturing processes, equipment, instrumentation, facilities, utilities, or Quality Control operations.
- Knowledge of equipment qualification, process validation, test method validation, and associated risk management principles.
- Experience supporting calibration, preventive maintenance, environmental monitoring, or equipment lifecycle management programs.
- Familiarity with manufacturing automation, process controls, and computerized systems in regulated environments.
- Experience supporting design and technology transfer activities, manufacturing process improvements, or implementation of new equipment and processes.
- Experience with electronic Quality Management Systems (eQMS), Product Lifecycle Management (PLM), or equipment asset management systems.
- Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or other relevant professional certification.
What you'll do
What You'll Work On
- Provide Quality Engineering oversight of manufacturing processes, instruments, equipment, facilities, utilities, and automated systems throughout their lifecycle, including qualification, validation, maintenance, calibration, and continuous improvement activities.
- Review and assess engineering and manufacturing changes for potential impacts to product quality, process performance, equipment qualification, validated state, and regulatory compliance.
- Lead or support investigations involving manufacturing deviations, nonconformances, out-of-specification results, equipment failures, calibration issues, and process or environmental monitoring excursions.
- Support risk assessments, support root-cause investigations, and develop or evaluate corrective and preventive actions (CAPA) to address quality issues and drive sustainable improvements.
- Provide Quality Engineering oversight of design and technology transfer activities, including manufacturing readiness, equipment and process qualification, verification and validation, risk management, and implementation of new or modified products and processes into Operations.
- Partner with engineering and operational teams to evaluate process improvements, equipment modifications, automation and control system changes, and manufacturing or QC testing requirements.
- Review and approve applicable Quality Management System records, engineering documentation, qualification and validation records, investigations, and change controls to ensure compliance with established procedures and regulatory requirements.
- Exercise independent Quality Engineering judgment when evaluating technical issues, identifying compliance risks, and recommending appropriate actions to maintain product quality and process control.
Pay and benefits
$61,300 – $122,700 a year
Employer providedThe base pay for this position is
$61,300.00 – $122,700.00
In specific locations, the pay range may vary from the range posted.
Free medical coverage option (HIP PPO plan)
Retirement savings plan with high employer contribution
Tuition reimbursement
Freedom 2 Save student debt program
FreeU education benefit
Career development
Where you'll work
Madison, WIOn-siteOpen in Maps (opens in a new tab)
More jobs in Madison, WIWorking conditions
Standard
TRAVEL
No
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/
Connect with us at abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, and on Facebook at https://www.facebook.com/AbbottCareers.
JOB FAMILY
Quality Assurance
DIVISION
ONCO Cancer Diagnostics
LOCATION
United States > Madison : 1 Exact Lane

From the posting
About Abbott
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 recognized as one of the best big companies to work for, as well as one of the best places to work for diversity, working mothers, female executives, and scientists.
Equal opportunity, accessibility and legal noticesAbbott's statements, word for word
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.
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.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
Job intelligence
The context around this role
Live data · October 21, 2026
Salary intelligence
How the pay compares
This role's midpoint is 13% above the US median for Quality Assurance roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US175 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $61,300 | — | $122,700 |
| All US (middle half) | $59,000 | $81,500 | $93,750 |
This role: Abbott's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 21, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 904 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Abbott's own promotion track.
Career resources on Quality Assurance
Skills DNA
What this role leans on
How many of the posting's 26 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Quality systems and risk11
- Validation and qualification7
- Lab testing and methods6
- GMP and compliance5
- Investigations and CAPA4
- Collaboration and leadership3
- Documentation and SOPs1
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices
- FDAFDA OOS guidance(official source, opens in a new tab)Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
Company hiring pulse
Abbott on Regulatory Jobs
- 83
- Open roles
- 78
- Distinct roles
- 30
- Locations
By discipline
- Quality55 66%
- Regulatory26 31%
- Compliance & Safety2 2%
By level
- Senior & Principal40 48%
- Associate & Specialist25 30%
- Manager15 18%
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Quality Assurance Engineer at Abbott
Open until filled. $61K–$123K a year, employer provided.

