×
Register Here to Apply for Jobs or Post Jobs. X

Senior Specialist Quality Assurance - Supplier Quality

Job in Des Plaines, Cook County, Illinois, 60019, USA
Listing for: Regulatory Jobs
Full Time position
Listed on 2026-11-04
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 86700 - 173300 USD Yearly USD 86700.00 173300.00 YEAR
Job Description & How to Apply Below
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 Des Plaines, IL location in the Abbott Molecular
, 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 Specialist Quality Assurance
- Supplier Quality
will support in the selection, approval, and maintenance of the division's approved suppliers by performing supplier quality system assessments, monitoring supplier performance, and driving supplier corrective action and/or improvement activities.

What You’ll Work On
  • Independently conducts and leads audits across supplier and TPM network.
  • Maintain and strengthen Quality System effectiveness by ensuring adherence to regulatory requirements, site procedures, and corporate quality policies.
  • Provides guidance and trains colleagues, provides mentoring to one or more junior level auditors.
  • Participates as SME in audits, provides compliance, and strategic solutions to complex quality issues.
  • May lead projects that are cross-functional in scope, directly influence project direction and scope, champions new initiatives and acts as the catalyst for change.
  • Maintains and demonstrates understanding of global standards, regulations, and regulatory bodies.
  • May assume managerial responsibilities as needed.
  • May mentor less senior level members of the group
  • Develop innovative, compliant, and practical solutions to complex quality challenges that support organizational goals and operational excellence.
  • Communicate effectively with management, suppliers, and cross-functional partners to drive project direction, quality strategy, and business results.
Required Qualifications
  • Bachelors Degree
  • Minimum 7 years in Quality or related field experience;
    Less experience may be appropriate with advanced degree.
Preferred Qualifications
  • Knowledge of applicable US and non-US Quality System Requirements and other relevant regulations for medical devices. Previous experience with regulatory body. Knowledge of Good Manufacturing Practices (GMPs), Quality System standards and regulatory requirements such as 21 CFR 820; ISO 13485; IVDD; etc.
  • Certified ISO Lead Auditor qualification or equivalent is required. Excellent written and verbal communication skills.
The base pay for this position is

$86,700.00 – $

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

JOB FAMILY:

Operations Quality

DIVISION:

AMD Molecular

LOCATION:

United States >
Des Plaines : DP01

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:

EEO is the Law link
- Espanol:

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 , on Linked In at , and on Facebook at

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

Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary