• Analytical Laboratory Clerk, Research…

    Catalent Pharma Solutions (St. Petersburg, FL)
    …but also support CMC development activities in support of client regulatory filings. Activities are performed in accordance with specifications, standard operating ... procedures, approved test methods and/or protocols, regulatory requirements, and St. Petersburg's Quality departmental policies. The **Analytical Laboratory Clerk,… more
    Catalent Pharma Solutions (09/17/25)
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  • Senior Director, Head of Clinical Data Management

    CSL Behring (King Of Prussia, PA)
    …clinical data, ensuring they are leveraged effectively to drive decision-making, regulatory compliance , and patient-centric outcomes. Responsibilities + Lead the ... SOPs, and quality standards aligned with GCP, GCLP, and regulatory expectations. + Collaborate with Clinical Operations, Biostatistics, Clinical Programming… more
    CSL Behring (09/16/25)
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  • RD&A Process Scientist

    Kerry (IN)
    …world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier ... process. He/she will focus on process optimizations, scale-ups, solving regulatory and other hurdles to new products and technologies introductions.… more
    Kerry (09/16/25)
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  • Sr. Research Scientist, Process and Mfg Excellence

    Herbalife (Torrance, CA)
    …contract manufacturing sites to ensure timely product launches, smooth commercial production, and compliance with quality and regulatory standards as well as on ... routinely with Herbalife global cross functional teams including Quality, Procurement, Regulatory Affairs, Project Management and Supply Chain as well as raw… more
    Herbalife (09/13/25)
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  • Associate Marketing Manager, Cardiology

    GE HealthCare (Arlington Heights, IL)
    Compliance : Ensure all marketing activities are compliant with regulatory and corporate guidelines. **Key Capabilities:** + Project management and organizational ... Cross-Functional Coordination: Collaborate with internal teams (Sales, Training, ComOps, Regulatory , Medical) to ensure alignment and support for product… more
    GE HealthCare (09/13/25)
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  • Associate Director, Immunoassay

    Charles River Laboratories (Shrewsbury, MA)
    …and assignments meet client needs. o Maintain the scientific, safety, and regulatory compliance integrity of the entire bioanalytical process. o Provide ... skills. Demonstrated independent analytical and problem-solving abilities. Full understanding of regulatory requirements of study types assigned, as well as Testing… more
    Charles River Laboratories (09/11/25)
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  • Senior Director, Quantitative Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …Lead in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. ... functional experts across the R&D organization, such QS, Research, Biostatistics, Regulatory Affairs, DMPK, Pharm Sci, and Clinical Science providing leadership and… more
    Takeda Pharmaceuticals (09/11/25)
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  • Associate Research Scientist: LC/MS, HPLC

    ThermoFisher Scientific (Lawrenceville, NJ)
    …the employee, to gain direct experience working onsite at a pharmaceutical / biopharmaceutical company, all while maintaining full-time benefits. **Summary:** The ... related compounds in biological samples to support drug development and regulatory filings. **Essential Functions:** * Perform method development, method validation,… more
    ThermoFisher Scientific (09/10/25)
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  • Research Analyst I - Bioanalytical Chemistry

    Charles River Laboratories (Mattawan, MI)
    …+ Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, ... with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling… more
    Charles River Laboratories (09/06/25)
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  • CRA ll

    Abbott (Alameda, CA)
    …+ Manage clinical monitoring activities and overall site management ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, ... Federal Regulations, department procedures and applicable regulatory requirements. + Responsible for assisting senior staff in planning study conduct, designing case… more
    Abbott (09/05/25)
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