• cGMP Quality Control (QC)…

    University of Southern California (Los Angeles, CA)
    cGMP Quality Control (QC)...GLPs, GDPs). Experience with standard operating procedures in a cGMP laboratory setting. Demonstrated ability to work ... internal/external users in the university's current Good Manufacturing Practices ( cGMP ) facility. The Quality Control ...current Good Manufacturing Practices ( cGMP ) facility. The Quality Control (QC) Specialist is responsible for… more
    University of Southern California (06/09/25)
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  • cGMP Quality Control

    University of Southern California (Los Angeles, CA)
    cGMP Quality Control Lab TechnicianApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP ... laboratory tests as appropriate. + Complies with any quality control policies and procedures and maintains... laboratory experience, knowledgeable in use of specialized laboratory equipment. Working knowledge of lab procedures,… more
    University of Southern California (06/10/25)
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  • cGMP Quality Control (QC)…

    University of Southern California (Los Angeles, CA)
    cGMP Quality Control (QC) Specialized Laboratory...Practices ( cGMP ) facility. The cGMP Quality Control (QC) Specialized Lab ... TechnicianApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP - Quality - Control --QC--Specialized- Laboratory -Technician\_REQ20159957/apply) Keck School of Medicine Los Angeles, California… more
    University of Southern California (06/09/25)
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  • cGMP Process Development (PD) Specialized…

    University of Southern California (Los Angeles, CA)
    …Minimum Skills: Proficiency in operating and maintaining laboratory equipment used in cGMP manufacturing and quality control testing. Strong attention to ... cell therapy and cGMP manufacturing. + Prepares, calibrates, and maintains laboratory equipment for use. Participates in routine lab maintenance and ensures… more
    University of Southern California (06/11/25)
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  • cGMP Associate Director, Process…

    University of Southern California (Los Angeles, CA)
    …assay development and qualification for product testing. + Lead technology transfer to cGMP manufacturing and quality control , ensuring efficient scaling and ... and process development reports. Authoring CMC documentation. + Oversee lab setup and work with cGMP facility...2. Experience and knowledge of standard operating procedures in cGMP laboratory settings. 3. Ability to drive… more
    University of Southern California (06/09/25)
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  • cGMP Process Development (PD) Specialist

    University of Southern California (Los Angeles, CA)
    …tech transfer of processes) from cGMP manufacturing and assays to quality control . Develops and reviews standard operating procedures (SOP), protocols and ... execute projects. Provides training support to the manufacturing and quality control teams during tech transfer. +...GLPs, GDPs). Experience with standard operating procedures in a cGMP laboratory setting. Demonstrated ability to work… more
    University of Southern California (06/09/25)
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  • Bioseparations Associate I

    Charles River Laboratories (Northridge, CA)
    …of analysis (COA) for completed products. **Essential Responsibilities** * Performs product quality control (QC) and certificate of analysis (COA) creation. ... to making a positive impact on the world by providing the highest quality cellular material and services to biotech and pharmaceutical companies and research… more
    Charles River Laboratories (06/19/25)
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  • Plasma Center Manager

    Biomat USA, Inc. (Bellflower, CA)
    …management. Manages the daily operations of the center, supervising operations and quality control , and ensuring compliance with all applicable policies and ... production targets and quality goals at the agreed-upon cost structure. + Control center donor funds and ensure that all financial records are accurate and in… more
    Biomat USA, Inc. (05/14/25)
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  • Chemist I

    Element Materials Technology (Santa Fe Springs, CA)
    …test reports. The **Chemist I** is responsible for performing testing in a pharmaceutical Quality Control laboratory . All work will be conducted in ... experiments and observations + Assist in audit preparedness and for participating in quality audits with FDA, other Regulatory Agencies, and customers, as needed +… more
    Element Materials Technology (06/17/25)
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  • Operations Supervisor

    Biomat USA, Inc. (Van Nuys, CA)
    Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice ( cGMP ) and internal company procedures. * Supervise donor selection, plasma ... FDA approved Standard Operating Procedure Manual, OSHA, CLIA and cGMP . * Attend all required training sessions, staff meetings,...Manager and/or the Assistant Manager. * Assist in the control of center donor funds as determined by the… more
    Biomat USA, Inc. (06/11/25)
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  • Compliance Auditor

    Biomat USA, Inc. (Los Angeles, CA)
    …experience should demonstrate expertise in SOP development as well as an understanding of quality control principles and QA audit function + Expert knowledge in ... compliance and quality audits of donor center, warehouse, transportation and lab and other suppliers of services and goods auditing activities inspecting for… more
    Biomat USA, Inc. (06/17/25)
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  • Production Engineer

    Prose (Commerce, CA)
    …is processed through a proprietary algorithm and made-to-order in the Prose lab using natural active ingredients. Marrying emerging technologies with the best in ... the facility. The position requires working in a plant environment for a cGMP /ISO certified facility and travel between West and East coast facilities in California… more
    Prose (06/18/25)
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