QC Technologist

Abbott LaboratoriesGretna, LA
18h$17 - $34Onsite

About The Position

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 114,000 colleagues serve people in more than 160 countries. About Abbott Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. Our diagnostic solutions are utilized in hospitals, laboratories, and clinics worldwide. The crucial information derived from our tests, instruments, and informatics systems is often the first step in patient care decision-making for hundreds of health conditions, ranging from heart attacks to blood disorders, infectious diseases, and cancers. 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. Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies 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 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 the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity 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. Shift: Monday- Friday 8:00 AM- 5:00 PM

Requirements

  • 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) required.
  • Ability to lift and/or move 25 pounds
  • Full range of body movement
  • Vision and hearing corrected to acceptable norms
  • Math and reasoning skills to develop and communicate laboratory procedures and reports
  • Ability to cope with stress from:
  • Production obligations
  • Legal proceedings
  • Ability to read and comprehend SOPs, 49 CFR Part 40, and CAP‑FDT guidelines
  • Ability to transcribe data legibly
  • Strong communication skills with employees and supervisors
  • Ability to provide operational input and recommendations

Nice To Haves

  • 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.

Responsibilities

  • 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.
  • Expect 100% accuracy with no administrative errors.
  • 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.

Benefits

  • Career development with an international company where you can grow the career you dream of.
  • Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies 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 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 the best place to work for diversity, working mothers, female executives, and scientists.
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