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QC Analyst -Microbiology

Job in Memphis, Shelby County, Tennessee, 38118, USA
Listing for: Integrated Resources, Inc
Apprenticeship/Internship position
Listed on 2026-06-04
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
    Data Scientist, Medical Science
Salary/Wage Range or Industry Benchmark: 21.13 USD Hourly USD 21.13 HOUR
Job Description & How to Apply Below
Position: QC Analyst I-Microbiology
Quality Control Analyst I (QC I) QC Microbiology Department

Location: Memphis, TN
Duration: 6 months
Schedule: Sunday Thursday, 2:00 PM 11:00 PM

Interview Process: Virtual interview (45 minutes)

Pay Rate: $21.13/hour (QCI)

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, micro

    Product, Endosafe Instrumentation, PCR, and BacT/ALERT systems.

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