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QC Analyst I​/II-Microbiology; 2nd Shift

Job in Memphis, Shelby County, Tennessee, 37544, USA
Listing for: Planet Pharma
Full Time position
Listed on 2026-01-04
Job specializations:
  • Quality Assurance - QA/QC
  • 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
Position: QC Analyst I/II-Microbiology (2nd Shift)

QC Analyst I/II-Microbiology (2nd Shift)

Leveling:

  • QC I set Pay: $21/hr
  • QC II set Pay: $24/hr (Must have at least 2 years of relevant experience)
Position Summary (QC I)

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 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 SOP and GCP to ensure data integrity and traceability
  • Participates in maintaining proper overall operation of department (physical inventories, logs, documentation, filing, etc.)
  • Assists 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
  • Performs all other related duties as assigned
Qualifications (QC I)
  • Bachelor's degree in biology or a 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 the company's 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, microscope, Endosafe® Instrumentation, PCR, BacT/ALERT systems
Position Summary (QC II)

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 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 SOP and GCP 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 Practices (cGMP) guidance (CFR, USP, EP, ICH, etc.)
  • Responsible for assisting with routine laboratory upkeep and organization
  • 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
  • Performs other related duties as assigned
Qualifications (QC II)
  • Bachel…
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