• 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 ... high-performance, scalable, data-centric, serverless microservices + Own and deliver software architecture, diagrams, design documents + Primary engineering lead,… more
    Otsuka America Pharmaceutical Inc. (08/08/25)
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  • Director Research and Software Engineering

    RELX INC (Raleigh, NC)
    Director of Research and Software Engineering for Life Sciences Are you ready for a leading role? Would you enjoy working on our cutting-edge products? About Us At ... concepts. About the Role The Director of Research & Software Engineering will lead the development of our regulated...ensures compliance with industry regulations (such as GxP and FDA 21 CFR Part 11), oversees daily operations, drives… more
    RELX INC (06/25/25)
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  • Software Engineer

    Eliassen Group (Raleigh, NC)
    ** Software Engineer** **Anywhere** **Type:** Contract-to-Hire **Category:** Development **Industry:** Life Sciences **Workplace Type:** Remote **Reference ID:** JN ... Jobs **Description:** Our client is hiring for an iOS Software Engineer to join their team in San Diego,...PLUS: Bluetooth experience & Any industry experience that has FDA requirements OR enterprise level company experience and documentation.… more
    Eliassen Group (08/08/25)
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  • Senior Manager, Regulatory Operations

    Sumitomo Pharma (Raleigh, NC)
    …including computer word processing, electronic document management systems, and regulatory publishing software . + Robust understanding of FDA and other health ... + Distributing, and archiving all incoming and outgoing communications with FDA and international counterpart agencies. + Understands evolving Health Authority (HA)… more
    Sumitomo Pharma (07/18/25)
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  • Site Sanitation Manager - 3rd Shift

    Perdue Farms, Inc. (Lewiston Woodville, NC)
    …interface with internal, external, customer and regulatory (USDA and/or FDA where applicable) inspectors regarding sanitation related non-conformance reports and ... ensuring strict enforcement of Perdue Farms Standards, USDA, FSIS, FDA , GFSI, OSHA and customer requirements. + Leads or...Equipment. + Training development using MS office or other software such as Alchemy. + FS risks mitigation (pathogens,… more
    Perdue Farms, Inc. (07/03/25)
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  • Fill Plant Team Lead

    Arc3 Gases (Dunn, NC)
    …direct medical plant operations in compliance with US Food and Drug Administration ( FDA ) regulations to provide quality medical gas products to our customers. The ... activities of medical plant operators. + Maintain all medical paperwork as per FDA requirements. + Run daily branch automated orders as per our established schedule.… more
    Arc3 Gases (06/20/25)
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  • Senior IT Infrastructure Engineer - Development…

    United Therapeutics (Research Triangle Park, NC)
    …their daughter's pulmonary arterial hypertension (PAH). Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial ... operation overhead on the team via scripting, orchestration platforms, and/or software defined platforms + Deploy standard service packages, workloads, and resources… more
    United Therapeutics (08/07/25)
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  • Sr Material Handler-Night Shift

    BioFire Diagnostics, LLC. (Durham, NC)
    …and manufacturing operations. This position ensures compliance with cGMP, ISO, FDA regulations, company policies, and safety guidelines while overseeing the physical ... supporting Manufacturing through timely replenishment activities. Utilizing Warehouse Management software , this role performs real-time electronic transactions to maintain… more
    BioFire Diagnostics, LLC. (07/22/25)
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  • Associate Director Quality Assurance, Data…

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …reviewed at appropriate intervals + Oversee the selection, validation, and implementation of software used for the generation of cGMP data + Conduct audits and gap ... time + Oversee the selection, validation, and implementation of software used for the generation of cGMP data +...to, 21 CFR Parts 11, 210, and 211, and FDA data integrity guidance KNOWLEDGE, SKILLS AND ABILITIES: Education:… more
    Glenmark Pharmaceuticals Inc., USA (08/08/25)
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  • Process Scientist II

    BD (Becton, Dickinson and Company) (Mebane, NC)
    …biotechnology, or related industries. * Experience working under GMP, regulated industries by FDA . or/and ISO 13485 is desirable. * Proficient with MS Office suite ... knowledge of data analysis and use of data analysis software like Minitab would be advantageous. **Job Description** We...industries. + Experience working under GMP, regulated industries by FDA . or/and ISO 13485 is desirable. + Proficient with… more
    BD (Becton, Dickinson and Company) (07/30/25)
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