• Parexel (Atlanta, GA)
    …motivated professional to join our Global Regulatory Affairs team as a CMC Regulatory Affairs Senior /Consultant. This role is critical to ensure ... contingency plans for CMC -related scenarios - Represent CMC Regulatory Affairs in cross-functional...for a Consultant level role, 7+ years for a Senior Consultant - Proven success in preparing regulatory more
    DirectEmployers Association (10/10/25)
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  • Parexel (Atlanta, GA)
    …strategic thinker with a passion for navigating the complex world of global regulatory affairs ? Do you thrive in cross-functional environments and love ... a dynamic and experienced Post-Approval Regulatory Strategy Lead to join our Regulatory Affairs team. In this pivotal role, you will be responsible for… more
    DirectEmployers Association (10/10/25)
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  • CMC Regulatory Affairs

    Parexel (Atlanta, GA)
    …motivated professional to join our Global Regulatory Affairs team as a CMC Regulatory Affairs Senior /Consultant. This role is critical to ensure ... contingency plans for CMC -related scenarios * Represent CMC Regulatory Affairs in cross-functional...for a Consultant level role, 7+ years for a Senior Consultant * Proven success in preparing regulatory more
    Parexel (10/11/25)
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  • Senior Principal Regulatory

    Bausch + Lomb (Atlanta, GA)
    …in assigned due diligence activities for business development and acquisitions. + Lead all CMC regulatory activities for IND, NDA, ANDA, and BLA submissions. + ... preferred + Minimum of 8 years in recent experience in strategic pharmacuetical Regulatory Affairs . This position does not work with medical device, cosmetics… more
    Bausch + Lomb (09/06/25)
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  • Senior Regulatory Affairs

    Parexel (Atlanta, GA)
    …strategic thinker with a passion for navigating the complex world of global regulatory affairs ? Do you thrive in cross-functional environments and love ... a dynamic and experienced Post-Approval Regulatory Strategy Lead to join our Regulatory Affairs team. In this pivotal role, you will be responsible for… more
    Parexel (10/11/25)
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  • Associate Director, Regulatory

    Sumitomo Pharma (Atlanta, GA)
    …highly motivated, and experienced individual for the position of **Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part of the ... Global Regulatory Affairs (GRA) team based in the US....the global regulatory lead (GRL) and the CMC regulatory lead in the formulation of … more
    Sumitomo Pharma (10/11/25)
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  • Director, Regulatory Affairs

    Sumitomo Pharma (Atlanta, GA)
    …seeking a dynamic, highly motivated, and experienced individual for the position of **Director Regulatory Affairs ** . The Director is part of the Global ... Regulatory Affairs (GRA) team based in the...collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports,… more
    Sumitomo Pharma (09/09/25)
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  • Senior Manager, Global Regulatory

    Otsuka America Pharmaceutical Inc. (Atlanta, GA)
    …with 5+ years' experience or Master's degree with 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, ... needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling,...the global regulatory team (GRL, regional leads, CMC -RA, labeling, medical writing, regulatory operations, etc.)… more
    Otsuka America Pharmaceutical Inc. (08/22/25)
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  • RA US Operations Excellence Manager

    Boehringer Ingelheim (Duluth, GA)
    …vision or to improve collaboration. The stakeholders will vary from USA GI Region, USA CMC , Corporate Affairs or regulatory agencies. + In partnership with ... Operations Excellence Partner is to partner with the USA Regulatory Affairs team in executing key strategic...initiatives to achieve USA priorities for RA and USA CMC objectives. This role is directly responsible for improving… more
    Boehringer Ingelheim (11/05/25)
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  • Associate Director, Small Molecule Analytical…

    Otsuka America Pharmaceutical Inc. (Atlanta, GA)
    …cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to ... drug substance and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement stability study protocols and timelines,… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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