• Senior CQV Engineer

    Verista (The Woodlands, TX)
    …acquire new skills and learn from our experiences to enhance our collective expertise Senior CQV Engineer Responsibilities: + Designing validation plans. + ... validation documents, URS, IQ, OQ, PQ Requirements + 5-7 years of demonstrated CQV experience in GMP regulated (preferably Cell and Gene Therapy) environments +… more
    Verista (06/05/24)
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  • CQV Engineer / Validation…

    Verista (Columbus, OH)
    …new skills and learn from our experiences to enhance our collective expertise CQV Engineer Responsibilities: This role will require supporting the client in ... PQ protocols and summary reports, trace matrices with support and guidance from senior resources. The resource will be required to provide execution support as well.… more
    Verista (06/07/24)
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  • Sr Quality Engineer I - Automation and CSV

    Gilead Sciences, Inc. (Frederick, MD)
    …seeking a highly motivated individual to join us as a Sr Quality Engineer I, reporting to the Associate Director, Quality Engineering in our state-of-the-art ... + Provide Quality Engineering oversight for Commissioning, Qualification, and Validation ( CQV ) related activities. + Represent site in global matrix team towards… more
    Gilead Sciences, Inc. (05/07/24)
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  • Senior Validation Engineer 2

    Verista (Kalamazoo, MI)
    …acquire new skills and learn from our experiences to enhance our collective expertise Senior CQV Engineer Responsibilities: This role will require supporting ... the client site in Kalamazoo, MI. Resource will be required to draft validation and commissioning documentation including, change requests, system impact assessments, user requirement specifications, risk assessments, IQ, OQ, PQ protocols and summary reports,… more
    Verista (06/29/24)
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  • Senior Validation Engineer

    Takeda Pharmaceuticals (Social Circle, GA)
    …of my knowledge. **Job Description** **About the role:** Join Takeda as a Senior Validation Engineer where you will support site projects, technical transfers, ... environment. + At least 4 years of commissioning, qualification and validation ( CQV ). + Validation and system experience in the following applicable areas: +… more
    Takeda Pharmaceuticals (05/14/24)
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  • Kneat Implementation Engineer

    Verista (Fishers, IN)
    …our experiences to enhance our collective expertise Kneat Implementation Engineer Responsibilities: This position requires advanced learning; technical precision; ... independent judgment and discretion. Kneat Validation Engineers utilize Kneat Gx and CSV/ CQV experience to provide value added solutions to Verista clients. +… more
    Verista (06/08/24)
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  • Senior Validation Engineer I…

    Takeda Pharmaceuticals (Social Circle, GA)
    …environment. + At least 4 years of commissioning, qualification and validation ( CQV ). + Validation and system experience in the following applicable areas: ... Sterilization and aseptic processing validation. + Process and utility systems validation, temperature mapping, manufacturing equipment commissioning and qualification. + Protein purification from mammalian plasma and blood. + Technical experience of… more
    Takeda Pharmaceuticals (06/26/24)
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  • CSV Engineer /Analyst

    Verista (Indianapolis, IN)
    …new skills and learn from our experiences to enhance our collective expertise Senior CSV Engineer /Analyst Responsibilities: + Provide IT CSV support to implement ... trainings to maintain 100% compliance Requirements + Demonstrated experience in leading CQV activities specific to Process Equipment + Proficiency using PC and… more
    Verista (05/11/24)
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