• Specialist Manufacturing: NPI, Upstream…

    Amgen (Holly Springs, NC)
    …us and transform the lives of patients while transforming your career. ** Specialist Manufacturing** **:** **NPI, Upstream Process Owner** **What you will do** Let's ... world. In this vital role you will communicate and interface between the GMP manufacturing teams in the Amgen North Carolina (ANC) Biologics Drug Substance… more
    Amgen (08/17/25)
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  • QA Specialist - Stat Sort

    Lilly (Concord, NC)
    …related to final classification of defects and routine defect investigations. The QA Specialist - Stat Sort also supports training and qualification of ... facility and Quality System from the ground up. **Role Description:** The QA Specialist - Stat Sort is responsible for providing manual visual inspection of the… more
    Lilly (08/13/25)
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  • IBM Maximo EAM Specialist

    NTT DATA North America (Greenville, NC)
    **IBM Maximo EAM Specialist - 25-05059** **100% Remote** **6+ Mths Duration** **W2 or C2C** NTT DATA's Client is seeking an IBM Maximo EAM Specialist with15 ... Maximo systems under 21 CFR part 11 compliance under GMP practices and 2 years successful deployment of MAS...version change upgrades for existing enterprise systems + MAS Specialist creating and executing UAT testing, IQ/OQ/PQ/PV development, and… more
    NTT DATA North America (06/03/25)
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  • Manufacturing Specialist II - Cell Therapy

    Kelly Services (Winston Salem, NC)
    **Manufacturing Specialist III - Cell Processing** **Location: Winston Salem NC** **Contract Role, 12 month long with potential to convert** **Hourly Pay Rates: ... product freezing and storage, and driving continuous improvement. The Manufacturing Specialist III is also responsible for mentoring team members, leading… more
    Kelly Services (07/30/25)
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  • Deviation Specialist (On Site)

    ThermoFisher Scientific (Greenville, NC)
    …Schedule** **Environmental Conditions** **Job Description** **Job Title: Deviation Specialist (On Site)** **Location:** Greenville, North Carolina **Department:** ... Manufacturing Technology **Reports To:** **Job Summary:** The Deviation Specialist is responsible for identifying, documenting, investigating, and resolving… more
    ThermoFisher Scientific (07/30/25)
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  • QA Specialist III, Quality on the Floor…

    ThermoFisher Scientific (Greenville, NC)
    …hr shift/nights **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Office, Some degree of PPE (Personal Protective ... area and quality management + Performs quality review and approval of procedures, training documents, and forms of moderate to high complexity + Performs quality… more
    ThermoFisher Scientific (07/23/25)
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  • Deviation Specialist

    Kelly Services (Greenville, NC)
    **Job Title:** Deviation Specialist **Location:** Greenville, NC **Schedule:** 8:00-5:00 Will be responsible for identifying, documenting, investigating, and ... and provide insights for continuous improvement initiatives. o Participate in training programs to enhance knowledge and skills related to deviation management… more
    Kelly Services (08/13/25)
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  • Senior Commissioning/Validation Specialist

    Stantec (Raleigh, NC)
    …group for an enthusiastic, diligent and experienced Commissioning / Validation Specialist . In this role you will prepare and implements project ... FDA or similar facilities where drug products are manufactured, stored in GMP conditions and distributed, including computerized and automated systems which require… more
    Stantec (08/07/25)
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  • QA Specialist III - Batch Release

    ThermoFisher Scientific (Greenville, NC)
    …(Days) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Office **Job Description** **POSITION SUMMARY** In this ... area and quality management + Performs quality review and approval of procedures, training documents, and forms of moderate to high complexity + Performs quality… more
    ThermoFisher Scientific (07/20/25)
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  • Senior Specialist , Utilities Engineering

    Merck (Wilson, NC)
    …approvers. + Perform a thorough review of engineering records and related GMP documentation, identifying and resolving discrepancies in a timely manner, and ... implementing corrective actions to improve the execution/review process. + Develop training material. Working as a subject matter expert (SME), provide necessary … more
    Merck (08/19/25)
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