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Quality Control Analyst-Microbiology

Job in Memphis, Shelby County, Tennessee, 37544, USA
Listing for: Integrated Resources, Inc ( IRI )
Apprenticeship/Internship position
Listed on 2026-01-05
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 21 - 24 USD Hourly USD 21.00 24.00 HOUR
Job Description & How to Apply Below

Overview

Base pay range: $21.00/hr - $24.00/hr this range is provided by Integrated Resources, Inc (IRI). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Position

Title:
QC Analyst I & II - Microbiology

Location: Memphis, TN

Duration: 6-months to a year with a possibility of converting to FTE

Schedule: Tue-Sat 2pm-11pm

QC Analyst I – Microbiology

Job Description:

  • 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 – QC Analyst I
  • 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 – QC Analyst I
  • 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 an internship program.
  • Ability to work in 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, BacT/ALERT systems
QC Analyst II

Job Description:

  • The Quality Control Analyst II for the QC Microbiology Department will be responsible for performing routine environmental monitoring, product testing, and raw material testing.
  • The position requires the utmost attention to detail, very strong 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 – QC Analyst II
  • Performs sterility testing and endotoxin testing of raw materials, in-process samples and finished products.
  • Performs growth promotion of microbial media.
  • Performs environmental monitoring, including air viable particulate, non-viable particulate and surface sampling and personnel monitoring
  • Prepares environmental monitoring excursion reports and conducts minor laboratory investigations.
  • 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
  • Assists the QC Supervisor/Leads with managing proper overall operation of department (physical inventories, logs, documentation, filing, etc.)
  • Maintains familiarity with QC-relevant current Good Manufacturing…
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