• Microbiology Analyst

    Actalent (Hercules, CA)
    …Engage in method development, modification, verification, and assist with method validation testing. + Participate in method transfer activities and suitability ... Skills + Proficiency in aseptic technique. + Experience with cleaning and disinfection validation . + Strong knowledge of GMP and GLP standards. Additional Skills &… more
    Actalent (01/13/26)
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  • Senior Laboratory Technician

    BioLife Plasma Services (Social Circle, GA)
    By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... is expected. BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. **OBJECTIVES/PURPOSE** Responsible for sample results release, maintenance… more
    BioLife Plasma Services (01/10/26)
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  • Export Trade Compliance Specialist

    Integra LifeSciences (Princeton, NJ)
    …exports. This position's focus will be classification and Country of Origin validation , and is responsible for validating, maintaining, and updating tariff codes ... CDOP/ECO approval for Trade Compliance department + Dedicated assistance in country-of-origin validation + Assist Manager and Team with trade sanctioned country due… more
    Integra LifeSciences (01/10/26)
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  • Method Development Scientist (HPLC)

    Actalent (St. Louis, MO)
    …and SOP generation. + Experienced in HPLC method development and validation + Demonstrate proper laboratory safety and housekeeping practices through weekly ... and troubleshoot analytical instrumentation and workspace as needed. + Perform method validation and/or qualification testing as needed. + Author and/or review SOPs… more
    Actalent (01/10/26)
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  • Quality Calibration Technician II

    Integra LifeSciences (Braintree, MA)
    …calibration systems and compliance requirements. + Support installation, qualification, and validation of new instruments and equipment, ensuring adherence to ISO ... 13485, ISO 14971 is preferred **Preferred Skills** + Experience in Biotech/ Pharmaceutical or Medical Device manufacturing facilities. + Familiarity with equipment… more
    Integra LifeSciences (01/07/26)
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  • Senior Analyst, QC Chemistry, US Site (Hopewell,…

    BeOne Medicines (Pennington, NJ)
    …laboratory to ensure timely and compliant generation and reporting of in- process , release, and stability test results in support of manufacturing operations. ... preventive actions (CAPAs). + Participate in transfer and method validation activities, including protocol preparation, protocol execution, and report preparation.… more
    BeOne Medicines (01/06/26)
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  • Lab Robotics and Automation Engineer

    Eurofins US Network (West Point, PA)
    …to and exceeding customer expectations. + Participate in the computer system validation process for diverse laboratory equipment such as automated liquid ... believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO...+ Experience in System Development Life Cycle and instrument validation . + Experience in a GLP or GMP laboratory,… more
    Eurofins US Network (12/30/25)
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  • SAP Cutover lead

    NTT DATA North America (Plano, TX)
    …Office 365 app suite SAP Cutover experience with S4 Private cloud Pharmaceutical industry experience with GxP Validation requirements Collaborative with internal ... business, IT, infrastructure, and third-party systems in a GxP Environment ( validation ), Act as the single point of contact for all cutover-related activities.… more
    NTT DATA North America (12/23/25)
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  • Principal Project Management Consultant (On-site…

    CBRE (Lebanon, IN)
    …site. The Project Management Team supports project delivery at a major pharmaceutical company. The primary responsibility of the Program Management Principal is to ... activities may include a combination of Commissioning, Qualification, and/or Validation for facilities, equipment, and computerized systems. Implement projects while… more
    CBRE (12/13/25)
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  • QC Specialist (LIMS Implementation)

    Astrix Technology (Redwood City, CA)
    …within the LIMS system, supporting product release, and driving continuous process improvements. The QC Specialist will collaborate cross-functionally with Quality ... define and document user requirements and functional specifications. + Author and execute validation protocols (IQ/OQ/PQ) in accordance with 21 CFR Part 11 and GxP… more
    Astrix Technology (12/12/25)
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