• CQV / Validation Engineer

    Verista (Indianapolis, IN)
    …of an electrical engineer + Bachelor's Degree or equivalent required. + 2 -4 years of applicable industry experience + Proficiency using PC and Microsoft Office ... cGMP's, and regulatory standards to support team in compliance of validation effort + Independent verification of testing against specifications + Managing… more
    Verista (05/29/24)
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  • Senior CQV / Senior Validation

    Verista (Germantown, WI)
    …and learn from our experiences to enhance our collective expertise Senior CQV Engineer Responsibilities: + Managing the responsibilities on multiple simultaneous ... point of escalation and issue management on client projects + Designing validation plans + Designing and executing engineering studies for critical process parameter… more
    Verista (07/06/24)
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  • CQV Engineer / Validation

    Verista (Germantown, WI)
    …new skills and learn from our experiences to enhance our collective expertise CQV Engineer Responsibilities: + Managing and working collaboratively with clients' ... + Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as… more
    Verista (07/11/24)
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  • Senior CQV Engineer / Senior…

    Verista (Kalamazoo, MI)
    …skills and learn from our experiences to enhance our collective expertise Senior CQV Engineer Responsibilities: + Designing validation plans. + Conducting ... the team maintains) clear, detailed records of qualification and validation , and change control activities for future compliance audits...onsite in Kalamazoo, MI + 5-7 years of demonstrated CQV experience in GMP regulated (preferably Cell and Gene… more
    Verista (07/06/24)
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  • Senior Engineer I, Validation

    Bristol Myers Squibb (Bothell, WA)
    …+ Experience with equipment/utility/facility qualifications and general commissioning, qualification and validation CQV practices are required. + Experience with ... Read more: careers.bms.com/working-with-us . **Position Summary** + The Sr. Engineer I, Validation is a skilled ...or equivalent + 5+ years of commissioning, qualification, and validation ( CQV ) experience within technical and regulated… more
    Bristol Myers Squibb (08/19/24)
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  • Associate Director, Site Technical Services

    BeiGene (Hopewell, NJ)
    …regulatory compliance and achieving commercial success. Reviews, authors and works with CQV validation of start-up Green-Field Project. Works with Drug ... required to work closely with both manufacturing, quality, and engineer associates. + Maintaining the validation sample...of cGMP and Data Integrity principles. + Minimum of 2 years' experience in metrology and CMMS management. +… more
    BeiGene (07/13/24)
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