• Clinical Research Director, Immunology…

    Sanofi Group (Cambridge, MA)
    …progress study execution + Oversee the execution of clinical studies in compliance with internal SOPs, GCP, ICH guidelines and other regulations + Review ... the pharmaceutical industry, academia, or government agencies such as the NIH, FDA , or other equivalent national or international public health and regulatory… more
    Sanofi Group (09/04/25)
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  • Maintenance Technician - Night Shift

    Colgate-Palmolive (Morristown, TN)
    …maintenance standards, document activities in systems like SAP, and ensure compliance with regulatory requirements.** + **Participation in Projects and Improvements: ... departments.** + **Adhere to Standards: Follow environmental, health, safety, and quality standards while maintaining workplace housekeeping and engaging in regular… more
    Colgate-Palmolive (09/04/25)
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  • Value Evidence and Outcomes Liaison - (AK, OR, WA)

    Boehringer Ingelheim (Portland, OR)
    …(C-suite). + Collaborates with other Value Evidence Liaisons (regional, national, quality , policy, government) as necessary to address customer needs related to ... systems and tools (ie, Veeva CRM) in accordance with compliance guidelines. + Communicates account and project activities as...understanding of FDMA 114, 21st Century Cures, new draft FDA Guidance on Payor Communication and Unapproved Uses, as… more
    Boehringer Ingelheim (09/03/25)
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  • Lab Assistant, General Lab

    Charles River Laboratories (Cleveland, OH)
    …Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, ... we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science...development of 86% of the drugs approved by the FDA in 2021. **Equal Employment Opportunity** Charles River Laboratories… more
    Charles River Laboratories (09/03/25)
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  • Site Services Manager

    ZOLL Medical Corporation (Atlanta, GA)
    …sleep disorders. Our core product is the WatchPAT(R)️ family, a revolutionary FDA -cleared portable home sleep apnea test device, that is based on proprietary ... patients and provide testing to promote wellness and enhance overall quality of life. WatchPAT(R)️ is commercially available within major markets including… more
    ZOLL Medical Corporation (09/02/25)
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  • Clinical Research Associate (CRA) - A

    ManpowerGroup (Lake Forest, IL)
    …Conduct site qualification, initiation, monitoring, and close-out visits + Ensure compliance with protocols, GCP, and regulatory requirements + Perform source ... years of clinical research experience, including site monitoring + Strong understanding of FDA regulations and GCP + Experience with medical devices or in vitro… more
    ManpowerGroup (08/31/25)
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  • Supervisor Pharmacy

    Arkansas Children's (Little Rock, AR)
    …and generic substitution. 7. Assures that all medications meet the highest standards in quality and preparation of the final dosage form and that all drug products ... patients. 9. Performs drug information activities. Reviews patients and assesses compliance with AC criteria for food-drug interactions, breast milk drug assessment,… more
    Arkansas Children's (08/31/25)
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  • Manager, Mechanical Design Engineering-…

    Curtiss-Wright Corporation (Santa Clarita, CA)
    …debug of electronic systems + Extensive experience with SolidWorks, including FEA and FDA add-ons (thermal, vibration, shock, fluid flow) + VPX & VME Electronics ... for fee payment, and therefore become the property of Curtiss-Wright._ ** Compliance Statement** This position may require exposure to export-controlled information… more
    Curtiss-Wright Corporation (08/29/25)
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  • Automation Systems Technician II (1st Shift)

    Grifols Shared Services North America, Inc (Clayton, NC)
    …Fall Protection Training. (Internal Training Provided) + Responsible for maintaining CGMP compliance by insuring a high level of cleanliness and organization. + ... and resource planning. + Work with internal and external customers including Quality , Plasma Operations, and Logistics to analyze and solve issues that may… more
    Grifols Shared Services North America, Inc (08/28/25)
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  • Clinical Research Specialist - Neuromodulation

    Dignity Health (Phoenix, AZ)
    …in compliance with applicable regulations, guidelines, and policies (ie FDA , OHRP, IRB) + Collaborates with Investigator to identify adverse events/ serious ... We are extremely proud to be a nationally recognized center for quality quaternary care, medical education and research. St. Joseph's includes the internationally… more
    Dignity Health (08/28/25)
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