The Staffing Resource Group, Inc
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http://www.srg-us.com
http://www.srg-us.com
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Environment: A global leader and trusted supplier in the pharma, biotech and specialty ingredients markets. Headquartered in Basel, Switzerland, the company is focused on advanced manufacturing, high-quality control systems, regulatory expertise, and research and development (R&D) capabilities. The company s products and services include active pharmaceutical ingredients (API), stem cell therapies, drinking water sanitizers, vitamin B compounds, organic personal care ingredients, industrial preservatives and microbial control solution to combat viruses, bacteria and other dangerous pathogens.
Key responsibilities:
QC Analyst
Posted: 10/28/2024
2024-10-28
2025-01-06
Employment Type:
Contract
Division: Life Sciences
Job Number: JN -102024-19831
State: Texas
Job Description
QC Analyst
SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
- Title: QC Analyst
- Location: Houston, TX
- Industry: Pharmaceutical
- Hours: 7:00PM-7:30AM (2-2-3 schedule)
- Salary: up to $31.41/ hr Paid Weekly (Benefits are Available)
- Employment Type: Contract
Environment: A global leader and trusted supplier in the pharma, biotech and specialty ingredients markets. Headquartered in Basel, Switzerland, the company is focused on advanced manufacturing, high-quality control systems, regulatory expertise, and research and development (R&D) capabilities. The company s products and services include active pharmaceutical ingredients (API), stem cell therapies, drinking water sanitizers, vitamin B compounds, organic personal care ingredients, industrial preservatives and microbial control solution to combat viruses, bacteria and other dangerous pathogens.
Key responsibilities:
- Performs Quality Control assays for product release of cell therapy products and Stability Studies.
- Maintain data and follow cGMP regulations including writing deviations and other Quality documentation.
- Performs Quality Control (QC) biological/cell based testing of Cell Therapy release and stability samples during 3rd shift. Typical test methods performed include flow cytometry based assays, but analyst may also perform proliferation, ELISA, cell counts (manual and automated), and immunofluorescence microscopy/spectroscopy assays.
Actively participates in support of Cell Therapy technology transfer activities and validation of analytical methods including training on new methodology, setup of new equipment, generation of method standard operating procedures (SOPs), and execution of validation protocols. - Performs general lab and equipment maintenance duties.
Key requirements:
- Bachelor's Degree required
- GMP experience
- Working knowledge of Immunofluorescence, Sample Handling and Flow Cytometry.
EOE/ADA
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