• Legend Biotech USA, Inc. (Raritan, NJ)
    …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Senior CQV Specialist as part of the Commissioning and Qualification ... OverviewThis position will be responsible for providing Commissioning, Qualification and Validation support to the cGMP Clinical and Commercial Cell Therapy… more
    HireLifeScience (12/11/24)
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  • CQV Specialist / Senior

    Verista (Warren, NJ)
    …new skills and learn from our experiences to enhance our collective expertise Senior CQV Engineer Responsibilities: + Develop, author, and execute commissioning ... equivalent required + 5+ years of experience in commissioning, qualification, and validation ( CQV ) activities in a regulated environment, with a focus on gas… more
    Verista (01/08/25)
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  • CQV Specialist / Senior

    Verista (Warren, NJ)
    …new skills and learn from our experiences to enhance our collective expertise Senior CQV Engineer Responsibilities: + Prepare, author, and execute commissioning ... validation requirements + 5+ years of experience in CQV activities, with demonstrated expertise in gas system ...CQV activities, with demonstrated expertise in gas system validation and documentation + Strong skills in document authorship,… more
    Verista (01/08/25)
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  • Cleaning Validation Specialist

    Verista (Los Angeles, CA)
    …enhance our collective expertise CQV Engineer Responsibilities: The Cleaning Validation Specialist for Operations is responsible for ensuring the effective ... standards and company policies. This role involves the development, implementation, validation , and ongoing monitoring of cleaning procedures to ensure product… more
    Verista (12/22/24)
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  • Senior Specialist , Engineering…

    Takeda Pharmaceuticals (Boston, MA)
    …compliance standards + Own and/or author documentation associated with assigned CQV discipline(s); maintain and improve this documentation as necessary to maintain ... industry best-practices. + Develop and execute studies, commissioning, and validation protocols. Assist in deviation resolution, summarize results, and author… more
    Takeda Pharmaceuticals (11/22/24)
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