QC Technologist
Abbott
2 - 5 years
Louisiana
Posted: 23/05/2026
Job Description
JOB DESCRIPTION:
QC Technologist
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and 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 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 around the world 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 a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
Abbott Rapid Diagnostics is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.
The QC Technologist position is located within Abbott’s SAMHSA‑certified Toxicology Laboratory in Gretna, LA. The individual in this role will be responsible for preparing calibrators and controls, performing annual verifications, assisting in method development and QC review, and other duties for which the individual is qualified on an as-needed basis.
What You’ll Work On
Preparation and verification of calibrators, controls, internal standards, and annual verification samples.
Complete preparation and verification activities promptly based on inventory and expiration dates.
Ensure full compliance with current SOPs and regulatory guidelines.
First review and data entry of chromatographic data from annual verifications and QC (LC / GC / Screening) verifications.
Complete all associated paperwork to properly document verification assessments.
Must meet SAMHSA and CAP‑FDT criteria.
Update and review QC in the BioRad Unity Program.
Maintain documentation for validation assessments and written communication with the Responsible Person.
Ensure compliance with current SOPs and regulatory requirements.
Adhere to all security procedures to protect the confidentiality of donor and proprietary method information.
Follow all current SOPs and applicable regulatory guidelines.
Required Qualifications
BS in a science field or 5+ years of relevant laboratory experience
Previous experience in extraction and first review
Previous experience processing data associated with GC/MS and LC‑MS/MS (using MultiQuant)
Preferred Qualifications
Advanced understanding of:
Analytical techniques and procedures
Laboratory instrumentation
GC/MS and LC‑MS/MS data review
R&D requirements for SAMHSA, CAP‑FDT, and relevant regulatory bodies
Laboratory Information Systems (LIS) and related systems
Strong communication skills with Supervisory staff; ability to maintain written communication records
Ability to present data neatly and in an organized fashion
Ability to detect chromatographic issues and suggest or implement corrective actions
Work Environment
Climate-controlled office and testing laboratory environment
May be potential exposure to toxic or hazardous materials
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
$17.15 – $34.25/hourIn specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Operations Quality
DIVISION:
TOX ARDx Toxicology
LOCATION:
United States > Gretna : 1111 Newton Street
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
No
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Awkward/forceful/repetitive (arms above shoulder, bent wrists), 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), Exposure to temperatures below 60 degrees Fahrenheit/16 degrees Celsius or above 85 degrees Fahrenheit/28 degrees Celsius on a regular basis, Keyboard use (greater or equal to 50% of the workday), Lift, carry, push or pull weights of more than 20 pounds/9 kilos on a regular/daily basis, Routine work with chemicals, Work requiring repeated bending, stooping, squatting or kneeling, Work with human blood or other potentially infectious materialsAbbott 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
About Company
Abbott is a global healthcare company developing medical devices, diagnostic tools, nutritional products, and medicines. It focuses on improving health outcomes across areas like heart disease, diabetes, and infectious diseases, with a strong emphasis on research and innovation.
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