• cGMP Quality Control (QC) Specialist

    University of Southern California (Los Angeles, CA)
    …cell therapy. Demonstrated passion for solving complex scientific issues. Experience with Food and Drug Administration regulations and clinical trials. Extensive ... leadership experience. Salary Range: The annual base salary range for this position is $87,576.76 - $92,000. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and… more
    University of Southern California (09/08/25)
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  • EHS Specialist II

    Abbott (Sylmar, CA)
    …Management Systems (EMS), and other regulatory requirements + Aligns with US Food and Drug Administration (FDA) regulations, Company policies, operating ... procedures, processes, and task assignments **Required Qualifications** + Environmental work experience, Bachelor's Degree in environmental studies, health sciences, or an equivalent academic field + Experience working in a broader enterprise/cross division… more
    Abbott (09/07/25)
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  • Medical Device Regulatory Affairs Development…

    Abbott (Santa Clara, CA)
    …Management Systems (EMS), and other regulatory requirements. + Complies with US Food and Drug Administration (FDA) regulations, international regulations and ... other regulatory requirements, company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. + Performs other… more
    Abbott (09/06/25)
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  • Technician, Mechanical Installation

    Fujifilm (Sacramento, CA)
    …by the Manager, High Field Operations. + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ... ISO 13485 standard requirements and all other applicable laws, regulations, and standards. **Qualifications** Experience: + Minimum five (5) years previous service-related experience. + Demonstrated ability at operating installation tools and test equipment. +… more
    Fujifilm (08/30/25)
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  • Sr. Clinical Research Monitor

    Children's Hospital Los Angeles (Los Angeles, CA)
    …in clinical research compliance and/or regulatory research Preferred: * Knowledge of Food and Drug Administration (FDA) regulations and International Conference ... on Harmonization (ICH) and Good Clinical Practice (GCP) guidelines governing the protection of human research subjects. * Experience using Clinical Trial Management Systems (CTMS) and Electronic Medical Records (EMR). **Education/Licensure/Certification:** *… more
    Children's Hospital Los Angeles (08/28/25)
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  • Senior Operations Supervisor

    Biomat USA, Inc. (Bakersfield, CA)
    …thorough familiarity and compliance with all state and federal regulations, US Food and Drug Administration (FDA)-approved Standard Operating Procedure Manual, ... Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP) and internal company procedures. + Supervises donor selection, plasma collection and all manufacturing records… more
    Biomat USA, Inc. (08/28/25)
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  • Clinical Research Associate I - Miriad IBD Biobank…

    Cedars-Sinai (Los Angeles, CA)
    …and kits. + Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. + ... Maintains research practices using Good Clinical Practice (GCP) guidelines. + Maintains strict patient confidentiality according to HIPAA regulations and applicable law. + Participates in required training and education programs. **Department-Specific Duties… more
    Cedars-Sinai (08/27/25)
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  • Engineer II, Product Analysis

    Abbott (Sylmar, CA)
    …Management Systems (EMS), and other regulatory requirements. + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, ... Company policies, operating procedures, processes, and task assignments. + Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors **Required Qualifications** + Bachelors Degree (… more
    Abbott (08/27/25)
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  • Software Quality Engineer II

    Abbott (Sylmar, CA)
    …Management Systems (EMS), and other regulatory requirements. + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, ... Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. **Required Qualifications** + Bachelor's Degree in… more
    Abbott (08/20/25)
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  • Senior Operations Supervisor

    Biomat USA, Inc. (Van Nuys, CA)
    …thorough familiarity and compliance with all state and federal regulations, US Food and Drug Administration (FDA)-approved Standard Operating Procedure Manual, ... Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP) and internal company procedures. + Supervises donor selection, plasma collection and all manufacturing records… more
    Biomat USA, Inc. (08/16/25)
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