• Parexel (Springfield, IL)
    …innovative treatment options to patients. We are currently seeking a dedicated and detail-oriented ** Regulatory CMC Project Manager ** to join a growing, ... requirements. Project Management: Serve as the project manager for meetings, adhering to best...Project Management). + 3+ years proven experience in regulatory affairs, particularly in CMC (Chemistry, Manufacturing,… more
    DirectEmployers Association (12/12/25)
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  • Senior Manager , CMC Global…

    Otsuka America Pharmaceutical Inc. (Springfield, IL)
    …of regulatory guidelines and perspective to the cross-functional team. Serve as CMC regulatory lead on global project teams (Pharmaceutical Development, ... domestic/international travel. **Job Description** + Develop and implement global CMC regulatory strategies for late-stage development, marketing applications… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Senior Manager , Global Regulatory

    Otsuka America Pharmaceutical Inc. (Springfield, IL)
    …of the associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external functional business units ... associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external...needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling,… more
    Otsuka America Pharmaceutical Inc. (11/20/25)
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  • Manager , Quality Control

    Xeris Pharmaceuticals, Inc. (Chicago, IL)
    …Participating in the preparation of analytical, testing, and specification sections of regulatory submissions and communications * Adhering to CMC /QC budgets 2. ... **Overview** The Manager of Quality Control position is a hands-on...events * Ability to effectively work with R&D scientists, CMC engineers, Supply Chain, Regulatory Affairs, and… more
    Xeris Pharmaceuticals, Inc. (01/14/26)
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  • Senior Manager , Global Product Quality…

    Otsuka America Pharmaceutical Inc. (Springfield, IL)
    regulatory submissions for OPDC R&D products. Performs quality reviews of CMC sections of regulatory submissions. + Authors and maintains Standard Operating ... The Senior Manager , Global Product Quality - Biologics is responsible...Subsidiaries ensure Compliance with local and global requirements and regulatory requirements. + Interfaces with project teams… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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