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Quality Control Analyst-Microbiology
Job in
Memphis, Shelby County, Tennessee, 37544, USA
Listed on 2026-01-05
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
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.
PositionTitle:
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 – MicrobiologyJob 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.
- 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.
- 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
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.
- 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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