• Laboratory Team Leader

    Catalent Pharma Solutions (Greenville, NC)
    …development, validation, and testing for oral solid dosage forms. It ensures high- quality data generation, regulatory compliance , and efficient project execution ... + Lead in the development of a climate of quality and safety within the teams, by identifying and...documented according to approved standard operating procedures, in general compliance with cGMPs and in a timely manner consistent… more
    Catalent Pharma Solutions (11/05/25)
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  • Senior Director, Global Clinical Development…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …develops, manufactures, and markets innovative products, with a focus on pharmaceutical products for the treatment of diseases and nutraceutical products for ... numerous compounds currently in the pipeline. In conjunction with Otsuka America Pharmaceutical , Inc., (OAPI), Otsuka has global strategies in place for the… more
    Otsuka America Pharmaceutical Inc. (11/18/25)
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  • Senior Development Scientist

    Catalent Pharma Solutions (Greenville, NC)
    …as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities. The Senior Development ... **The Role** + Work closely with analytical scientists, project management, quality , and commercial operations to ensure that formulation and process development… more
    Catalent Pharma Solutions (11/07/25)
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  • Senior Manager, IT Web Services

    Sumitomo Pharma (Raleigh, NC)
    …+ Exceptional attention to detail and a commitment to delivering high- quality , error-free solutions. + Experience within the pharmaceutical , biotech, ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in...propose solutions, and ensure align with corporate branding and compliance standards. + Oversee the full web development lifecycle… more
    Sumitomo Pharma (11/13/25)
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  • Analytical Chemist II

    Catalent Pharma Solutions (Greenville, NC)
    …independently performing routine and non-routine analytical testing in support of pharmaceutical products following all applicable safety, quality , and ... method validation for oral solid dosage forms, ensuring product quality and regulatory compliance . It contributes to...science degree with four years of professional experience in pharmaceutical analytical chemistry or; + BS or BA degree… more
    Catalent Pharma Solutions (11/05/25)
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  • Associate Director, Regulatory Affairs (Labeling)…

    ThermoFisher Scientific (Greenville, NC)
    …ensuring accurate record-keeping of decisions and minutes. + Manage global labeling compliance activities, including quality control, FDA-508 compliance , and ... Team is responsible for managing global labeling activities and ensuring compliance with international regulatory standards. This role coordinates all aspects of… more
    ThermoFisher Scientific (11/23/25)
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  • Assoc. Tech, Operations

    Merck (Durham, NC)
    …make our products. We work in the manufacturing plants with a "Safety First, Quality Always" mindset striving for continuous improvement. We work in the local plant ... connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. **Position Description:** Our… more
    Merck (11/24/25)
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  • Associate Director, Regulatory Affairs (Oncology)

    Sumitomo Pharma (Raleigh, NC)
    Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the US (Sumitomo Pharma America, Inc.), focused on addressing patient ... closely with Regulatory Operations in the electronic submission + Ensure compliance with global regulatory requirements and adherence to regulatory internal policies… more
    Sumitomo Pharma (10/11/25)
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  • Senior Specialist, Engineering

    Merck (Wilson, NC)
    …policies and Wilson site procedure for safety, quality , and regulatory compliance . + Review literature pertaining to pharmaceutical packaging in order to ... This involves leading root cause analysis investigations for equipment-related quality events. + Provides written scientific justification for proposed changes… more
    Merck (11/22/25)
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  • Manager, Cell Production - RMOMAL

    United Therapeutics (Research Triangle Park, NC)
    …maintaining compliance with regulatory standards, safety protocols, and internal quality systems. + Prepare and manage the cell expansion production schedule for ... We Are** We are the first publicly-traded biotech or pharmaceutical company to take the form of a public...brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of… more
    United Therapeutics (11/05/25)
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