• Sr. Validation Engineer, Process…

    Danaher Corporation (Fargo, ND)
    …substance, and drug product + Mentor junior validation associates in Process Validation , cGMP regulations, and principles of Quality by Design + Develop and ... world. We bring together deep scientific expertise, an unwavering commitment to quality , and a collaborative spirit to drive progress. Whether you're launching your… more
    Danaher Corporation (12/07/25)
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  • Validation Analyst II

    Curia (Albuquerque, NM)
    …to ensure validation work is efficiently integrated into production and quality timelines. This role may also support investigations related to validation ... compliant with regulatory expectations. + Coordinate with cross-functional teams (eg, Quality , Manufacturing, Engineering) to ensure validation efforts align… more
    Curia (11/06/25)
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  • Senior Manager, SSD Product Validation

    Micron Technology, Inc. (Longmont, CO)
    …and validation , strong leadership capabilities, and a passion for quality and innovation. **Responsibilities:** Validation Strategy & Execution + Define ... We are seeking a highly qualified and strategic Senior Manager, SSD Product Validation Engineering to lead validation efforts across multiple SSD programs. This… more
    Micron Technology, Inc. (11/07/25)
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  • Manager, Validation Command, Edge Lab

    Auburn University (Auburn, AL)
    …to lead multidisciplinary teams, translate sponsor priorities into actionable validation plans, and produce defensible, high- quality outputs. Demonstrated ... AU **Division Name** Samuel Ginn Col of Engineering **Position Title** Manager, Validation Command, Edge Lab **Job Class Code** JA34 **Appointment Status** Full-time… more
    Auburn University (11/12/25)
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  • Senior Software Engineer

    Microsoft Corporation (Redmond, WA)
    …everyone can thrive at work and beyond. **Responsibilities** + Develop and modify quality validation plans, procedures, and software tools and programs used to ... a hand in evolving our engineering solutions and strategies for the validation of quality on personal computing devices. As part of the Surface Post Launch… more
    Microsoft Corporation (12/12/25)
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  • Sr. Cleaning Validation Engineer II

    Gilead Sciences, Inc. (La Verne, CA)
    …including implementation of new projects. + Coordinates the activities of assigned validation and contract personnel, ensuring the quality of completed work. ... to the completion of projects through the development of validation schedules, project plans, master plans, validation ...and harmonization of Standard Operating Procedures, leveraging existing Gilead Quality Systems. + Work with Quality to… more
    Gilead Sciences, Inc. (11/22/25)
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  • Validation Engineer III

    AbbVie (Branchburg, NJ)
    …years of significant engineering and/or operational experience. + Process and Cleaning Validation Experience + Equipment Qualification (IOQ/PQ) + Quality System ... up to regulatory scrutiny. + 6+ years of overall experience in Manufacturing, Quality or Engineering including 4 major validation subjects (eg Computer,… more
    AbbVie (12/29/25)
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  • Process Engineer

    Insight Global (Raynham, MA)
    …Background in pharma or med device industries with emphasis on quality and validation Scrap validation Quality NRs General Process Engineer Knowledge of ... investigations by implementing effective corrective actions. It also involves supporting quality systems such as CAPA and deviation management, assisting with… more
    Insight Global (12/16/25)
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  • Software Validation Specialist

    VTI Life Sciences (San Diego, CA)
    …to maintain and inspire professional excellence by providing Commissioning, Qualification, Quality Engineering, Automation and Validation Services to the ... companies in the Life Sciences industry. We are looking for a Software Validation Specialist to be responsible for ensuring that computerized systems and software… more
    VTI Life Sciences (11/07/25)
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  • CMM Programmer

    Actalent (Watertown, CT)
    …degree in Engineering, Life Sciences, or related field. + 3+ years' experience in validation or quality in a regulated industry. + PC-Dmis programming + ... impact on patient safety. + Identify and document non-conformances in product quality or processes. + Conduct root cause analysis for non-conformances and implement… more
    Actalent (12/25/25)
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