Abbott

QA Specialist III

Abbott Westfield, Massachusetts, United States · $33K–$66K/yr

Hospitals and Health Care · 10,001+ employees

Yesterday
qa Mid (2-5 yrs) Full-time United States
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About the role

The QA Specialist ensures that all commercial and clinical products are manufactured and sterilized in accordance with internal procedures before release. They are responsible for reviewing manufacturing documentation, managing non-conforming materials, and maintaining compliance within the quality system.

What they look for

Quality assurance Documentation review Lot history records Non-conforming material reports SAP Design history files Compliance Troubleshooting Quality improvement Sterilization processes Clinical product coordination Auditing Manufacturing documentation

Requirements

Candidates must have a High School Diploma or GED and a minimum of 4 years of related work experience. The role requires solid knowledge of business concepts, quality system environments, and the ability to perform complex assignments with considerable judgment.

Benefits

Medical coverage Retirement savings plan Tuition reimbursement Student debt program Education benefit

Full description

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.

JOB DESCRIPTION:

QA Specialist III

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 Westfield Indiana location in the Structural Heart Division. Hours are 3:00pm to 11:30pm Mon - Fri, with occasional Saturday overtime.

 

MAIN PURPOSE OF THE ROLE The Quality Assurance Specialist position exists to ensure that all units, either commercial or clinical product, have been manufactured and sterilized in accordance with internal procedures prior to release.

 MAIN RESPONSIBILITIES

  • Reviews Manufacturing documentation by obtaining all lot history records and non-conforming material reports and ensuring that they are compiled in accordance with internal procedures.
  • Tracks Documentation discrepancies by maintaining a mechanism by which discrepancies with manufacturing documentation can be tracked to determine trends, etc.
  • Notifies Manufacturing personnel of documentation issues by providing feedback immediately upon discovery of issues, and, on a periodic basis, informing manufacturing personnel in a more formal manner of discrepancies with manufacturing documentation.
  • Confines discrepant materials by maintaining a Quarantine area whereby discrepant materials are physically located until they are resolved and can be released.
  • Releases product by performing the necessary transactions in SAP in the sterile cycle to release product upon receipt of the Product Release Authorization and completion of LHR review.
  • Reviews and approves Design History Files by obtaining and verifying the contents of DHFs and approving the Engineering Order authorizing release into the Archive department.
  • Advises Manufacturing personnel and project leaders by functioning as the "expert" in the area of documentation compliance.
  • Coordinates Clinical product by completing appropriate paperwork to release clinical product to approved sites.
  • Audits materials or the work of others through the examination, inspection, measurement, or test of raw materials, components, sub assemblies and documentation.

Required Qualifications 

-High School Diploma / GED  

-Minimum 4 years Related work experience. -Applies solid knowledge of business concepts, procedures and practices, and a complete understanding fundamentals in a functional area, and working knowledge of other related disciplines. -Will perform this job in a quality system environment. -Performs complex assignments usually without established procedures. -Assignments require considerable judgment, initiative, creativity and leadership in troubleshooting, suggesting alternatives, and making recommendations for continuous quality improvement.

Preferred Qualifications: 

Associates Degree or some college credits performed

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 X @AbbottNews. 

The base pay for this position is

$15.80 – $31.60/hourIn specific locations, the pay range may vary from the range posted.

     

JOB FAMILY:

Operations Quality

DIVISION:

SH Structural Heart

LOCATION:

United States > Westfield: 1820 Bastian Court

ADDITIONAL LOCATIONS:

WORK SHIFT:

Standard

TRAVEL:

No

MEDICAL SURVEILLANCE:

No

SIGNIFICANT WORK ACTIVITIES:

Not Applicable

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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