• Daiichi Sankyo, Inc. (Bernards, NJ)
    …partners to ensure robust development of assay, participate in HA interaction for drug -related CDx topics/questions, and attend device company HA meetings as ... and tactical role and deliverables of Global Regulatory Strategy in the Drug and Device Development and Commercialization process.Experience with developing and… more
    HireLifeScience (05/29/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …research areas centered around rare diseases and immune disorders. Summary: The Associate Director , Laboratory Data Management is accountable for the end-to-end ... vendors to ensure high quality of laboratory data deliverables to support drug development processes and global submissions. This position provides leadership within… more
    HireLifeScience (05/13/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders. JOB SUMMARYThe Senior Director , Head Medical affairs Quality Assurance in Global RD/PV QA is accountable ... QA RDPVQA, and oversees multiple levels of direct reports (Directors, Associate Directors, Managers, contractors as applicable) across the Global Quality teams… more
    HireLifeScience (04/25/25)
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  • Associate Director , Drug

    Merck (West Point, PA)
    **Job Description** The Associate Director - Device Tech Transfer is a leadership role within the Device Development and Technology Organization. This ... and combination products, with a focus on autoinjectors, prefilled syringes, and other drug delivery systems. The Associate Director will collaborate with… more
    Merck (06/12/25)
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  • Associate Director , External…

    Merck (West Point, PA)
    …Operations, Drug Delivery Systems and Devices within our Manufacturing Division ( Associate Director ). This role serves as a Virtual Plant Manager - ... contact for all dealings between our Company and the External Partner, the Associate Director External Manufacturing Operations is accountable for establishing a… more
    Merck (05/19/25)
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  • CDx Associate Director , Global…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …partners to ensure robust development of assay, participate in HA interaction for drug -related CDx topics/questions, and attend device company HA meetings as ... strategic and tactical role and deliverables of Global Regulatory Strategy in the Drug and Device Development and Commercialization process. + Experience with… more
    Daiichi Sankyo Inc. (05/29/25)
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  • Associate Director , Laboratory Data…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders. **Summary:** The Associate Director , Laboratory Data Management is accountable for the ... vendors to ensure high quality of laboratory data deliverables to support drug development processes and global submissions. This position provides leadership within… more
    Daiichi Sankyo Inc. (05/14/25)
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  • Associate Director , Promotion…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …and approves content and context required of promotional labeling materials for prescription drug and medical device products. Must be effective in managing work ... and context required of promotional labeling materials for prescription drug and medical device products. Must be effective in managing work and resolving… more
    Otsuka America Pharmaceutical Inc. (04/17/25)
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  • Associate Director , R&D…

    Bristol Myers Squibb (Princeton, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Bioanalytical Biomarker Category Manager will directly report ... into the Specialty Clinical Laboratories global category Director . This position is responsible for supporting and delivering procurement related activities in… more
    Bristol Myers Squibb (06/13/25)
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  • Director , Global Clinical…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …management experience, will support position at entry ( Associate Director / Director ). + An advanced understanding of drug development principles and ... the clinical safety, efficacy, medical usefulness and value of drug or medical device product candidates. +...research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for … more
    Otsuka America Pharmaceutical Inc. (04/17/25)
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