• Parexel (Springfield, IL)
    …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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  • CMC Regulatory Affairs…

    Parexel (Springfield, IL)
    …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 (Springfield, IL)
    …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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  • Associate Director, Regulatory…

    Sumitomo Pharma (Springfield, IL)
    …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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  • Senior Manager, Global Regulatory…

    Otsuka America Pharmaceutical Inc. (Springfield, IL)
    …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. (11/20/25)
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  • Senior , Program Management- (North…

    AbbVie (North Chicago, IL)
    …to use their broad understanding of Product Development, Manufacturing, Quality and Regulatory Affairs to translate the business objectives into actionable ... landscape for device and combination product industrialization, global quality and regulatory requirements and pathways for approval/market access in programs to… more
    AbbVie (11/18/25)
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  • Senior Scientist, Engineering II

    AbbVie (North Chicago, IL)
    …innovative medicines. In the course of our work, we collaborate with early-stage CMC , Quality Assurance, Regulatory Affairs , Internal and External ... . Job Description Purpose: We are looking for an experienced and versatile Senior Scientist II/Mechanical Engineer to join our Injection Device Development team to… more
    AbbVie (11/08/25)
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  • Associate Director, Small Molecule Analytical…

    Otsuka America Pharmaceutical Inc. (Springfield, IL)
    …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. (11/25/25)
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