Job Description

QC Technologist I

Schedule: Wednesday thru Saturday ( 3:45pm-2:15am, 4x10s)

About the Role

The QC Technologist I plays a key role in supporting the quality and reliability of diagnostic products by performing laboratory testing in a cGMP environment. This position conducts quality control testing on reagents, IVD materials, and personnel swabs to ensure product safety, efficacy, and compliance with established acceptance criteria before release.

This role offers hands‑on laboratory experience using scientific techniques such as spectrophotometry, PCR, pipetting, and more. The QC Technologist I collaborates closely with Manufacturing, Technology Transfer, and other cross‑functional teams to support data collection, validations, and new product qualifications.

What You’ll Do

Quality Control Testing

• Perform QC testing on incoming reagents used in FilmArray and other diagnostic product lines.
• Execute routine testing on raw materials, consumables, and finished products following established inspection and laboratory protocols.
• Set up and report results for the personnel swab testing program.
• Coordinate and execute repeat testing as needed.

Documentation & Compliance

• Ensure accurate and efficient QC data entry and documentation.
• Maintain QC records in accordance with the Quality System.
• Communicate deviations and atypical results to supervisors; assist in applying corrective measures.
• Update inspection documentation as needed.

Operational Support

• Maintain QC areas to ensure a clean, organized, and contamination‑free environment, including participation in routine cleaning and swabbing.
• Maintain supply levels and coordinate repairs/calibrations for instruments and equipment.
• Support cross‑departmental projects and validations as assigned.
• Learn and adopt new techniques or workflows required for new product lines.
• Assist new staff with standard QC protocols as needed.

Qualifications

Required

• High School Diploma, GED, or equivalent.
• Associate’s degree in a life science or related field;
  OR one (1) year of bioMérieux QC experience plus completion of in‑house molecular biology training (in lieu of degree).
• Minimum 6 months of academic or professional laboratory experience.
• Proficiency with standard laboratory pipettes.
• Intermediate proficiency with MS Office (Outlook, Teams, Word, Excel).
• Strong organizational skills with high attention to detail.
• Ability to make timely decisions under pressure.
• Strong teamwork and communication skills.

Preferred

• Previous experience in a cGMP environment.

Working Conditions & Physical Requirements

• Ability to sit or stand for prolonged periods.
• Ability to wear PPE correctly for most of the day.
• Ability to lift, move, or adjust objects up to 50 lbs.
• No domestic or international travel required.
• Laboratory environment with required PPE and standard biosafety practices.

About the QC Reagents Team

The QC Reagents group is part of the Global Quality organization and plays a vital role in ensuring the quality and consistency of diagnostic products used worldwide. Team members work collaboratively in a fast‑paced laboratory environment with strong support for training, development, and cross‑functional partnership.