• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …as well as other research areas centered around rare diseases and immune disorders. Summary CMC Lead is responsible for supporting the overall CMC strategies ... based on the project needs and the respective development stage of the project. The CMC Lead will support the Sr. CMC Lead on complex and/or late-stage… more
    HireLifeScience (04/21/24)
    - Save Job - Related Jobs - Block Source
  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …centered around rare diseases and immune disorders.Summary The Associate Director , RACMC, is responsible for the regulatory CMC (Chemistry, Manufacturing ... serve as G-RACMC lead or regional submission lead . Provide regulatory guidance and strategy to CMC sub-team and G-RA teams along with other functional teams… more
    HireLifeScience (06/07/24)
    - Save Job - Related Jobs - Block Source
  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …The Technology Management (mAb, Drug Substance, Drug Product, or New Modality) Lead is responsible for the management of technology transfer of the manufacturing ... (mAb, Drug Substance, Drug Product, or New Modality) manufacturing, evaluates CMC risks for appropriate escalation, recommends transition milestones and ensures a… more
    HireLifeScience (04/21/24)
    - Save Job - Related Jobs - Block Source
  • Associate Director , Global…

    Bristol Myers Squibb (New Brunswick, NJ)
    …(including participating/leading HA meetings); and/or post-approval submissions. In this role, the GRS- CMC Associate Director , Biologics will serve as the ... Sciences (GRS) and Global Product and Supply (GPS). The GRS- CMC Associate Director , Biologics will...of global change management. **Position Responsibilities** + Represent regulatory CMC on and/or lead matrix teams for… more
    Bristol Myers Squibb (06/13/24)
    - Save Job - Related Jobs - Block Source
  • Associate Director , Principal…

    Bristol Myers Squibb (Summit, NJ)
    …careers.bms.com/working-with-us . **Position Summary** Bristol Myers Squibb is seeking an Associate Director , Principal Product Leader within the Cell Therapy ... The Principal PQL will support the Global Product Quality Lead (PQL) by providing supportive quality oversight of the...+ May act as author or Quality reviewer of CMC sections of regulatory submissions and response to global… more
    Bristol Myers Squibb (05/30/24)
    - Save Job - Related Jobs - Block Source
  • Associate Director , Business…

    Mitsubishi Chemical Group (Jersey City, NJ)
    …on real-world evidence, and creating hope for all facing illness. The Associate Director , Business Development will seek out potential business opportunities ... efficiently communicating with excellent facilitation. The incumbent will also lead initial partnership, licensing and/or acquisition negotiations with sufficient… more
    Mitsubishi Chemical Group (06/07/24)
    - Save Job - Related Jobs - Block Source
  • Associate Director , System Support,…

    Bristol Myers Squibb (Summit, NJ)
    …or more areas (ie, research, analytical, quality, engineering, manufacturing, regulatory CMC , or IT). + Proven ability to understand complex processes/problems and ... through various formats (eg presentations, written proposals, reports, correspondence, lead meetings, face-to-face dialogue, etc.) + Proficiency in data analytics… more
    Bristol Myers Squibb (06/11/24)
    - Save Job - Related Jobs - Block Source
  • Regulatory Operations Specialists - II…

    ManpowerGroup (Rahway, NJ)
    …and providing CVM/FDA support for labeling and chemistry, manufacturing, and controls ( CMC ) submissions. + The specialist position also works as part of a ... compendium; obtains US Free Sales Certificates. + The specialist may lead /support teams on various regulatory topics; optimize procedures, processes, and… more
    ManpowerGroup (06/12/24)
    - Save Job - Related Jobs - Block Source