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Cognate: QC Analyst -BioAssay
Job in
Memphis, Shelby County, Tennessee, 37544, USA
Listed on 2026-10-05
Listing for:
The Fountain Group
Full Time
position Listed on 2026-10-05
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst -
Healthcare
Data Scientist
Job Description & How to Apply Below
Job Title: QC Bioassay Analyst I/II
Location: Memphis, TN
Pay Rate: $21.13–$24.50/hr.
Duration: 4 months
Schedule: Monday–Friday, 8:00 AM–4:30 PM; overtime as needed
Training: 1 month, Monday–Friday, 8:00 AM–5:00 PM
Job Description
- Perform QC testing using cell-based immunological in vitro assays, including MLR, cytotoxicity, HLA-restriction, CTLp, and cell proliferation assays.
- Perform mammalian cell culture using aseptic techniques and established cell culture procedures.
- Execute molecular biology-based assays and laboratory testing according to approved methods and SOPs.
- Review QC test results for accuracy, precision, and compliance with established requirements.
- Perform study design, data analysis, statistical analysis, and preparation of written and oral test reports.
- Enter test observations and results into trending databases and support periodic data trending.
- Maintain QC laboratory inventories, testing logs, documentation, and records.
- Support laboratory investigations, including OOS and CAPA activities.
- Follow cGMP/GLP requirements, SOPs, and Good Documentation Practices to maintain data integrity and traceability.
- Bachelor’s degree in Biological Sciences or a related field preferred.
- 1–2 years of applicable laboratory, biotechnology, cell therapy, or related industry experience, or an equivalent combination of education and related work experience.
- Cell-based immunological in vitro assays
- Mammalian cell culture
- Aseptic technique
- Cell proliferation assays
- Cytotoxicity assays
- MLR (Mixed Lymphocyte Reaction)
- HLA-restriction assays
- CTLp assays
- Molecular biology-based assays
- cGMP / 21 CFR 210 and 211
- GLP
- Good Documentation Practices (GDP)
- SOP compliance
- QC testing and results review
- OOS investigations
- CAPA
- Data integrity and traceability
- Statistical/data analysis
- QC data trending
- Biotech or cell therapy laboratory experience
- QC laboratory operations
- Experience with trending databases
- Laboratory documentation and product release testing
- Experience supporting quality improvement initiatives
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