• Sr. Manager - Parenteral Operations (Nights)

    Lilly (Concord, NC)
    …group during asset delivery, process development, operations readiness, start-up, and validation of the parenteral (PAR) areas which include formulation, aseptic ... and Capabilities** + Bachelor's degree in a STEM or pharmaceutical related field of study. + At least 2...equipment, or system start up. + Qualification and process validation experience. + Manufacturing Execution Systems and electronic batch… more
    Lilly (07/09/25)
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  • Operations Manager - Night Shift

    Lilly (Concord, NC)
    …the project phase, the Operations Manager (OM) will support commissioning, qualification, and validation of the Device Assembly and Packaging (DAP) areas as well as ... or network collaboration. **Basic Qualifications:** + Bachelor's degree in a STEM or pharmaceutical related field of study. + At least 2 years working within… more
    Lilly (06/21/25)
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  • Tech 3, Utility Maintenance

    Fujifilm (Holly Springs, NC)
    …Practices (cGMP) documentation practices and quality standards in a Pharmaceutical Manufacturing plant. Utilities to include high-pressure steam boilers, process ... accurate maintenance records and documentation * Participates in overseeing validation and qualification activities to ensure compliance with regulatory requirements… more
    Fujifilm (06/10/25)
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  • Technician - Sterility Assurance TSMS (Night…

    Lilly (Durham, NC)
    …Parenteral Facility. As designated by management, additional support for qualification/ validation activities or other routine responsibilities within the TS/MS group ... including the execution of required studies. + Execute or assist in qualification/ validation activities to support the bioburden control of the facility or equipment… more
    Lilly (07/18/25)
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  • Scientist II, Manufacturing Sciences - Continuous…

    ThermoFisher Scientific (Greenville, NC)
    …**Key Responsibilities:** + Collaborate with cross-functional teams-including validation , operations, quality, analytical development, and process development-to ... and review batch records, protocols, and reports to support development, validation , and commercial production activities. + Support routine manufacturing operations… more
    ThermoFisher Scientific (06/18/25)
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  • Logistics Specialist

    Actalent (Clayton, NC)
    Job Title: Logistics Specialist Job Description A leading global pharmaceutical company is seeking a Logistics Specialist to join their brand new state-of-the-art ... material handling and storage equipment. The Logistics Specialist will ensure the validation of commercial products and oversee the physical handling of materials… more
    Actalent (09/06/25)
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  • Senior Director, Global Quality Strategy…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …candidate will have a strong background in quality management within the pharmaceutical industry and a proven track record of driving strategic initiatives. **Job ... Establish and maintain best practices for system qualification and validation . + **Document Management:** Oversee the document management system, ensuring… more
    Otsuka America Pharmaceutical Inc. (09/03/25)
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  • Associate Director, Small Molecule Analytical…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …drug substance and drug product at CDMOs + Design and lead method validation and implementation activities for drug substance and drug product ensuring compliance ... analysis techniques, fostering their professional growth and expertise in pharmaceutical stability studies. + Collaborate cross-functionally with analytical team… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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  • Manager, PVRM

    Sumitomo Pharma (Raleigh, NC)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... + Assist in signal detection activities including data assembly, signal validation , and signal evaluation. + Perform literature monitoring (with vendor support)… more
    Sumitomo Pharma (08/01/25)
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  • Director, Manufacturing Science and Technology

    ThermoFisher Scientific (Greenville, NC)
    …lab experiments + Post PPQ, full ownership of all continuous process validation activities + Lead and coordinate large-scale technical projects from initiation to ... a related field, or PhD. + 10 years of expertise in pharmaceutical processes, including DP characterization, stability profile understanding, and linking DP… more
    ThermoFisher Scientific (07/13/25)
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