• Quality Chemical Laboratories (Wilmington, NC)
    Quality Chemical Laboratories (QCL), a pharmaceutical testing, manufacturing, and development lab in Wilmington, is seeking a highly motivated scientist for our ... technology transfer into cGMP manufacturing, familiarity with analytical techniques, regulatory requirements, and early phase cGMP manufacturing is preferred. QCL… more
    Appcast IO CPC (01/20/26)
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  • AI Solutions Manager, Life Sciences R&D…

    Deloitte (Charlotte, NC)
    …serve + Limited immigration sponsorship may be available Preferred: + Understanding of pharmaceutical regulatory data and regulatory filing requirements and ... analytics solutions + 4+ years of experience with Life Sciences Pharmaceutical R&D regulatory data lifecycle . Experience to include introducing new technologies… more
    Deloitte (01/15/26)
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  • Sr. Regulatory Affairs Specialist…

    Grifols Shared Services North America, Inc (Clayton, NC)
    regulatory experience. + Minimum 5 years of related technical and/or regulatory experience in pharmaceutical industry or an equivalent combination of ... experience. + 6 to 7 years related technical and/or regulatory experience in pharmaceutical industry, or an equivalent combination of education and experience.… more
    Grifols Shared Services North America, Inc (12/05/25)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    … intelligence and collaborates with SMEs to interpret the impact of regulatory changes to the pharmaceutical environment. **Job Description** + Oversee ... The Associate Director of Regulatory Intelligence leads the collection and dissemination of...new and updated regulations and guidance that may impact pharmaceutical practices, procedures and controlled documents. + Lead weekly… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Regulatory Affairs Associate Director, IVD

    GRAIL (Durham, NC)
    …clinical affairs, quality, or program management within the IVD, medical device, or pharmaceutical industries is required. + Regulatory affairs and IVD device ... Regulatory Affairs Certification (RAC) preferred. + Experience in pharmaceutical clinical, statistical, or regulatory settings-especially in oncology,… more
    GRAIL (11/24/25)
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  • Director, Operational Technology

    United Therapeutics (Research Triangle Park, NC)
    …external and internal resources at all levels + Broad knowledge of the regulatory requirements for pharmaceutical applications + Working skills and experience ... are as follows:** **Who We Are** We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public… more
    United Therapeutics (12/23/25)
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  • Import/Export Specialist II

    ThermoFisher Scientific (Greenville, NC)
    …in logistics, supply chain management, or Customs Broker license. + Knowledge of pharmaceutical regulatory standards (FDA, DEA) is a plus. + Strong analytical, ... providing solutions to take essential products from pre-clinical to the market. Pharmaceutical products come in many different dose forms including inhalations, oral… more
    ThermoFisher Scientific (01/18/26)
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  • Lead QA Technician

    ThermoFisher Scientific (Greenville, NC)
    …Technician, you will play a critical role in ensuring product quality and regulatory compliance within pharmaceutical manufacturing operations. As part of the ... phase of drug development. With global operations, we support active pharmaceutical ingredients (APIs), biologics, cell and gene therapy, viral vectors, formulation,… more
    ThermoFisher Scientific (12/25/25)
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  • Associate Director, Global Labeling

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …or other scientific field. + 6-8 years of relevant experience in pharmaceutical regulatory /labeling environment and/or drug development + Knowledge of scientific ... to drive alignment of labeling content and strategy. + Partner with Global Regulatory Affairs to ensure that all labeling is aligned with the product global… more
    Otsuka America Pharmaceutical Inc. (12/18/25)
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  • Laboratory Equipment Specialist

    Reckitt (Wilson, NC)
    …management of laboratory equipment. Ensure compliance with cGMP guidelines, global pharmaceutical regulatory requirements (FDA, MHRA, EMA), relevant industry ... of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With… more
    Reckitt (01/15/26)
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