• Principal Software Development Engineer

    Lumen (Raleigh, NC)
    …digitally connect the world and shape the future. **The Role** The Principal Software Development Engineer plans, designs, architects, and builds multiple highly ... may include checks for criminal records and/or motor vehicle reports and/or drug screening, depending on the position requirements. For more information on these… more
    Lumen (09/03/25)
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  • ​Cybersecurity Principal Engineer (Breach…

    Truist (Charlotte, NC)
    …of America) **Please review the following job description:** The Cybersecurity Principal Engineer (Breach and Attack Simulation) is responsible for designing, ... or other classification protected by law. Truist is a Drug Free Workplace._** EEO is the Law (https://www.eeoc.gov/sites/default/files/2022-10/EEOC\_KnowYourRights\_screen\_reader\_10\_20.pdf) Pay… more
    Truist (08/27/25)
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  • Principal Process Engineer

    Lilly (Durham, NC)
    …better for people around the world. + **Responsibilities** The Senior Principal Process Engineer provides technical leadership and expertise for production ... pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (eg, healthcare and/or dependent day care… more
    Lilly (08/26/25)
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  • Principal Software Engineer - Cloud

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    **Job Description** We're looking for a Principal Software Engineer to join our growing team and lead the development and strategy for our Digital Medicine ... business days. **Company benefits:** Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death &… more
    Otsuka America Pharmaceutical Inc. (08/08/25)
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  • Principal Software Engineer--Payments

    Truist (Charlotte, NC)
    …(United States of America) **Please review the following job description:** The Principal Payments Software Engineer is a top-level engineering team lead responsible ... or other classification protected by law. Truist is a Drug Free Workplace._** EEO is the Law (https://www.eeoc.gov/sites/default/files/2022-10/EEOC\_KnowYourRights\_screen\_reader\_10\_20.pdf) Pay… more
    Truist (08/08/25)
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  • Talent Pipeline- Principal Scientist…

    Cambrex High Point (Durham, NC)
    …a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug ... North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances,… more
    Cambrex High Point (08/13/25)
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  • Sr. Principal Scientist - Molecule Steward

    Lilly (Concord, NC)
    …The Molecule Steward is the subject matter expert for the Concord Site Drug Product manufacturing and will provide local technical leadership and expertise for ... + Serve as technical subject matter expert for all topics related to drug product manufacturing. + Expected to provide technical direction on deviations, production… more
    Lilly (07/29/25)
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  • Principal Engineer - Electrical Power…

    GE Vernova (Wilmington, NC)
    …is conditioned upon the successful completion of a background investigation. The drug screen requirement in the background check process is not required if ... in certain areas. Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach, a 24/7 nurse-based resource; and… more
    GE Vernova (07/29/25)
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  • Principal Medical Writer

    IQVIA (Durham, NC)
    …Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing. **Essential Functions:** + Take a leading ... new/unusual document types/customer requirements. + In depth knowledge of drug development, medical writing, and associated regulations. Good understanding of… more
    IQVIA (08/31/25)
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  • Senior Principal Regulatory Affairs…

    Bausch + Lomb (Raleigh, NC)
    …to ensure the stringent accuracy of information for creation of cosmetics, OTC Drug Facts and nutritional/natural health products in the US and/or Canada + ... Formulate, lead, and drive integrated regulatory strategies across CMC and clinical/non-clinical, labeling, adpromo domains + Lead all CMC regulatory activities for IND, NDA and ANDA submissions and OTC products and dietary supplements + Plan, author, review,… more
    Bausch + Lomb (09/06/25)
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