• Senior Manager , Global…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …pharmaceutical and/or healthcare industry. - Knowledge and experience with preparation of global regulatory submissions (IND, CTA , NDA or BLA, MAA). - RAC ... **Position Summary** Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription… more
    Otsuka America Pharmaceutical Inc. (11/20/25)
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  • Associate Director, Regulatory CMC (Small…

    BeOne Medicines (San Mateo, CA)
    **_General Description:_** BeOne is seeking an experienced and energetic regulatory professional to manage, evaluate, and complete regulatory projects consistent ... responsible for development of strategies, planning, drafting, and managing CMC-related regulatory submissions and HA interactions to meet the aggressive timelines… more
    BeOne Medicines (09/23/25)
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  • Director, Program Management

    Bristol Myers Squibb (San Diego, CA)
    …in nearly all phases of research and drug development, including global regulatory submissions (IND/ CTA through NDA/BLA/MAA/JNDA/ NDA China) and lifecycle ... planning including annual and long-term portfolio processes. + May serve as a matrix manager for Program Management resources assigned to the asset. + Supports DD PM… more
    Bristol Myers Squibb (11/20/25)
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