QC Technician
Job description
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.
Job Summary
We are seeking a Quality Control Analyst I-Microbiology to support our Cell Therapy Manufacturing Facility located in Memphis, TN.
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.
The following are responsibilities related to the Quality Control Analyst I-Microbiology position:
- Primary responsibility entails processing samples from the cleanrooms, including non-viable particulate, viable air and surface sampling, and personnel monitoring.
- Performs growth promotion of raw materials.
- Performs Gram stain and classic microbiology techniques.
- Performs bioburden and endotoxin testing of raw materials, in-process samples and finished products and responsible for shipping samples to sub-contractors for additional testing.
- Prepares environmental excursion reports and conducts laboratory investigations.
- Receives raw materials and supplies for the QC laboratory. Maintains laboratory supplies, media and reagents inventory.
- Adheres to standard operating procedures and good documentation practices to ensure data integrity and traceability.
- Responsible for routine laboratory upkeep and organization.
- Will be expected to be responsible for performing sterility testing using the BacT Alert system.
- Will be expected to be responsible for performing mycoplasma testing.
- Will be expected to be responsible for processing preliminary and advanced IDs of microorganism recoveries.
Job Qualifications
The following are minimum qualifications related to the Quality Control Analyst I-Microbiology position:
- Bachelor's degree in Biology or relevant scientific discipline required.
- 0-2 years of relevant laboratory experience or experience in a cGMP/FDA regulated industry preferred.
- Ability to work independently or as a team member.
- Demonstrated knowledge in Microbiology and aseptic techniques required.
- Detail-oriented with strong written and verbal communication skills.
- Ability to problem-solve and troubleshoot as necessary.
- Familiarity with laser particle counters, viable air samplers, microscope, Endosafe® Instrumentation, PCR, BacT/ALERT systems.
The pay range for this position is $22.12 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.
IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.
About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.
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