• Senior Representative, Regulatory

    Catalent Pharma Solutions (Bloomington, IN)
    …and combination products throughout the product lifecycle. **The main responsibility of a Senior Regulatory Affairs specialist is to serve as a regulatory ... direct management and guidance regarding the organization's cGMP compliance and regulatory affairs for biologics , sterile injectables, cell and gene therapy,… more
    Catalent Pharma Solutions (09/10/24)
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  • Sr. Specialist , Regulatory Project…

    West Pharmaceutical Services (Exton, PA)
    …Requisition ID: 66496 Date: Sep 12, 2024 Location: Exton, Pennsylvania, US Department: Regulatory Affairs Description: **Who We Are:** At West, we're a dedicated ... Regulatory Project Management (RPM) role is responsible for management of regulatory affairs projects associated with West's global portfolio of medical… more
    West Pharmaceutical Services (09/11/24)
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  • R&D Regulatory Specialist

    Belcan (Los Angeles, CA)
    …years of experience in positions of increasing responsibility within Regulatory Affairs or related field within the Biologics , Biotech or Pharmaceutical ... R&D Regulatory Specialist Job Number: 351627 Category: Research Scientist Description: Job Title: R&D Regulatory Specialist Pay Rate: $40 / hr Location:… more
    Belcan (08/29/24)
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  • Quality Assurance Specialist

    University of Pennsylvania (Philadelphia, PA)
    …programs and resources, and much more. Posted Job Title Quality Assurance Specialist ( Regulatory ) CVPF(Center for Cellular Immunotherapy) Job Profile Title ... Research Coordinator Senior Job Description Summary The Quality Assurance Specialist will work within the Clinical Cell and Vaccine Production Facility (CVPF) for… more
    University of Pennsylvania (08/11/24)
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  • Analytical Methods Specialist

    Merck (De Soto, KS)
    …in Research & Development, Bioprocess Technology Solutions, Production, Quality Control, and Regulatory Affairs to qualify new reference standards + Conducts in ... and management of the reference standard program for two US veterinary biologics sites + Participates, collaborates in, and/or leads cross-functional project teams… more
    Merck (09/11/24)
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  • Site Quality Head

    Curia (Albuquerque, NM)
    …processes, and services to achieve a consistent approach to Quality Assurance and Regulatory Affairs . + Direct quality and compliance process improvements and ... Quality Systems function. + Direct and manage the Quality Assurance Product Specialist function. + Includes coordination of lot release / coordination of… more
    Curia (09/11/24)
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  • Biologist

    Insight Global (De Soto, KS)
    …colleagues from R&D, Bio Technology Solutions-Analytics, Production, Quality Control, and Regulatory Affairs to support qualification of new reference standards ... Job Description Insight Global is seeking a Reference Specialist for fortune 100 company in the pharmaceutical...the maintenance of the reference management program for US biologics sites - Maintains compliance according to USDA guidelines… more
    Insight Global (09/12/24)
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