QC Technologist

Jobfu; Gretna (LA); On-site; USD 24,000 - 47,000; Full time

Job summary

Abbott in Gretna, LA is seeking a QC Technologist to support our SAMHSA‑certified toxicology laboratory. You will prepare calibrators and controls, verify data, and assist with method development, documentation, and QC review to ensure accuracy and regulatory compliance.

The role requires a BS in a science field or 5+ years of lab experience, plus experience with GC/MS and LC‑MS/MS (MultiQuant). Strong communication and meticulous record‑keeping are essential for success in this position.

Qualifications

• BS in a science field or 5+ years of relevant laboratory experience.
• Experience with GC/MS and LC-MS/MS data review is required.
• Ability to follow SOPs and regulatory guidelines.
• Strong documentation and data entry skills.
• Good communication with supervisory staff.

Responsibilities

• Prepare calibrators, controls, and verification samples as required.
• Review chromatographic data and document verification assessments.
• Maintain QC records in the Unity/BioRad system.
• Assist in method development and QA activities.
• Ensure compliance with safety and regulatory requirements.

Skills

Extraction

Data analysis

Quality control

Documentation

Communication

SOP compliance

Education

BS in science field

5+ years lab experience

Tools

GC/MS

LC-MS/MS

MultiQuant

LIS

Job description

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 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 What You’ll Work On Preparation & Verification • 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. Data Review & Documentation • 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. QC Program Management • 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. Security & Compliance • 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) required. 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. Competencies: Physical Requirements • 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 Work Environment • Climate‑controlled office and laboratory environment • Potential exposure to toxic or hazardous materials • Domestic travel may be required for subpoenas/testimony or travel to other domestic Alere offices. 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. The base pay for this position is $17.15 – $34.25 per hour. In specific locations, the pay range may vary from the range posted.