• Lead CQV Engineer /Analyst

    Verista (New Brunswick, NJ)
    …and learn from our experiences to enhance our collective expertise Lead CQV Engineer /Analyst Responsibilities: + Authoring, editing, and executing technical ... process knowledge + Understanding validation documents, URS, IQ, OQ, PQ + Lead CQV efforts for facilities and utilities, including HVAC, water systems, and building… more
    Verista (09/22/24)
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  • CQV Engineer

    Actalent (Somerset, NJ)
    Job Title: CQV Engineer Job Description Assisting in development, review, and approval of cGMP documents including, but not limited to: Master Validation Plans, ... design documentation. Providing expertise and solutions to issues regarding CQV Lifecycle documentation in regards for applicable FDA/EMEA Regulations. Supporting… more
    Actalent (09/28/24)
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  • Qualification Engineer (4 Openings)

    PDS Tech Inc (Morris Plains, NJ)
    …for an experienced **Qualification Engineers in Morris Plains, NJ.** **Qualification Engineer (4 Openings)** Start: **ASAP** Location: **Morris Plains, NJ - Onsite** ... of relevant experience in the pharmaceutical industry, with a focus on CQV activities. This experience should include hands-on experience in executing validation… more
    PDS Tech Inc (09/23/24)
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  • Documentation Control Lead / Project…

    Verista (New Brunswick, NJ)
    …our experiences to enhance our collective expertise Associate Project Engineer Responsibilities: + Manage validation documentation in automated systems, including ... test scripts, and validation reports. + Collaborate with the CQV and engineering teams to ensure documentation aligns with...test scripts, and validation reports. + Collaborate with the CQV and engineering teams to ensure documentation aligns with… more
    Verista (09/22/24)
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  • Validation Engineer III

    Sanofi Group (Ridgefield, NJ)
    **Job Title:** Validation Engineer III **Location:** Ridgefield, NJ **About the Job** We deliver 4.3 billion healthcare solutions to people every year, thanks to the ... to patients and their families. Your job, as Validation Engineer III within our Quality Assurance (QA) Validation group,...deviations. + Demonstrate ability to manage medium to complex CQV projects. + Responsible for peer review of validation… more
    Sanofi Group (09/28/24)
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  • Lead CSV Engineer /Analyst

    Verista (New Brunswick, NJ)
    …our experiences to enhance our collective expertise Lead CSV Engineer /Analyst Responsibilities: + Authoring, editing, and executing technical commissioning, ... for production equipment and analytical instruments. + Collaborate with engineering and CQV teams to align automation validation activities with project timelines. +… more
    Verista (09/22/24)
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