• Principal Process Controls…

    Regeneron Pharmaceuticals (East Greenbush, NY)
    Regeneron is currently looking for a Principal/ Staff Process Controls & Validation Engineer for the Labeled Drug Product fill/finish manufacturing ... transfer to post-commercial lifecycle management activities. As a Principal/Staff Process Controls & Validation Engineer **,** a typical day might include… more
    Regeneron Pharmaceuticals (07/29/25)
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  • Engineer II, Process

    Danaher Corporation (Fargo, ND)
    …discovery, development and delivery of solutions that safeguard and improve human health. The Process Validation Engineer II is part of the Technical ... groundwork for vital new discoveries worldwide. You will be a part of the Process Validation team and report to the Process Validation Manager… more
    Danaher Corporation (07/03/25)
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  • Sr. Validation Engineer

    Danaher Corporation (Fargo, ND)
    …System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Senior Validation Engineer , Process Validation ... starting materials, drug substance, and drug product + Mentor junior validation associates in Process Validation , cGMP regulations, and principles of Quality… more
    Danaher Corporation (06/08/25)
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  • Sr. Engineer I - Validation

    Terumo Medical Corporation (Elkton, MD)
    …product, and new product development process and production equipment/ process validation requirements. The Senior Validation Engineer I uses their ... Validation Engineer I position is specifically accountable for leading process validation activities to ensure the transferred process is… more
    Terumo Medical Corporation (08/02/25)
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  • Validation Engineer

    System One (Cranbury, NJ)
    …closely with senior validation engineers to develop cleaning and process validation master plans. The Validation Engineer will author and execute ... Job Title: Validation Engineer Location: Cranbury, NJ Type:...(IOQ/PQ), and final reports. + Experience in qualification and process validation . + Strong understanding of regulatory… more
    System One (08/15/25)
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  • Senior Engineer

    Amgen (Thousand Oaks, CA)
    … Engineering team in the Drug Product Technologies organization. Working with the Principal Engineer Process Validation Manager of Amgen Thousand Oaks (ATO) ... products to patients through demonstrated excellence in aseptic processing, technology transfer, process characterization, process validation and continuous … more
    Amgen (07/24/25)
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  • Quality Validation Engineer

    Actalent (Los Angeles, CA)
    Quality Validation Engineer Job Description The Quality Validation Engineer is responsible for the validation documentation of equipment, processes, ... including Master plans, IQ/OQ/PQ, and Final Reports. This role involves executing validation protocols and writing final reports while ensuring adherence to Quality… more
    Actalent (08/18/25)
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  • Silicon Validation Engineer

    Meta (Burlingame, CA)
    …of silicon, hardware, software, and content. The Reality Labs team seeks a Silicon Validation Engineer .As a Silicon Validation Engineer , you will ... leading the effort to ensure high-quality silicon delivery. **Required Skills:** Silicon Validation Engineer , Reality Labs Responsibilities: 1. Assist in the… more
    Meta (08/01/25)
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  • Engineer - Validation I/II…

    Grifols Shared Services North America, Inc (Clayton, NC)
    …and services in more than 110 countries and regions. **Location:** Clayton NC **Overview:** The Engineer I - Validation / Engineer II - Validation ... manages and completes all phases of assigned equipment, facilities, utilities and process qualification and validation activities. * Facilitates cross functional… more
    Grifols Shared Services North America, Inc (08/13/25)
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  • Senior Principal Validation Engineer

    Curia (Albuquerque, NM)
    Senior Principal Validation Engineer in Albuquerque, NM Build your future at Curia, where our work has the power to save lives. The Senior Principal ... Validation Engineer oversees Validation Contractors...Review and approve qualification, validation , re-qualification, and re- validation documents for equipment and manufacturing process more
    Curia (07/04/25)
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