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Quality Control Technician

Integrated Resources, Inc ( IRI )
Memphis, TN Contractor
POSTED ON 6/4/2026
AVAILABLE BEFORE 7/3/2026

Title: Quality Control Analyst I (QC I) – QC Microbiology Department


Location: Memphis, TN


Duration: 6 months (Temp to Hire)


Schedule: Sunday–Thursday, 2:00 PM – 11:00 PM


Interview Process: Virtual interview (45 minutes)



Position Summary

  • The Quality Control Analyst I for the QC Microbiology Department will be responsible for performing processing of routine environmental monitoring samples, product-release testing, and raw material testing.
  • The position requires the utmost attention to detail, good organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment with minimal supervision are essential for success.


Essential Duties and Responsibilities

  • Performs environmental monitoring, including air viable particulate, non-viable particulate and surface sampling and personnel monitoring.
  • Receives raw materials and supplies for the QC laboratory and maintains laboratory supplies, media and reagents inventory.
  • Adheres to standard operating procedures and good documentation practices to ensure data integrity and traceability.
  • Participates with maintaining proper overall operation of department (physical inventories, logs, documentation, filing, etc.).
  • Responsible for assisting with routine laboratory upkeep and organization.
  • Utilizes GMP systems such as MODA and other laboratory computer systems.
  • Reviews test results of other QC analysts for accuracy and precision and maintains an efficient workflow of all required testing documentation, ensuring timely submission relative to product release dates.
  • Perform all other related duties as assigned.


Qualifications

  • Bachelor's degree in biology or relevant scientific discipline required.
  • Minimum 0–2 years relevant laboratory experience or experience in a cGMP and/or FDA regulated industry, or a combination of education and related work experience required.
  • May consider less education and professional experience upon successful completion of Client’s internship program.
  • Ability to work in a Clean Room environment with full gowning requirements.
  • Ability to work independently or as a team member.
  • Detail-oriented with strong written and verbal communication skills.
  • Demonstrated knowledge in Microbiology and aseptic techniques.
  • Ability to problem-solve and troubleshoot as necessary.
  • Familiarity with laser particle counters, viable air samplers, microProduct, Endosafe® Instrumentation, PCR, and BacT/ALERT systems.

Salary : $20 - $21

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