Laboratory Technician

4 weeks ago


Memphis, United States Integrated Resources, Inc ( IRI ) Full time

Job Title: Quality Control


Location: Memphis, TN


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


Schedule: Tuesday-Friday 11:30am – 10pm



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.
  • Performing routine environmental monitoring sampling in clean rooms; Performing Good Documentation Practices on paperwork; Required to be gown qualified
  • The position requires the utmost attention to detail, good organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation.
  • 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 in 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 and efficient workflow of all required testing documentation ensuring timely submission relative to product release dates.
  • Perform all other related duties as assigned.
  • Performing routine environmental monitoring sampling in clean rooms; Performing Good Documentation Practices on paperwork; Required to be gown qualified


Qualification:

  • Bachelor's degree in biology or relevant scientific discipline preferred.
  • Highschool diploma or equivalent 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 Clean Room environment with full gowning requirements.


Preferred Qualification:

  • 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.

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