• Director , Global Regulatory Affairs CMC

    Takeda Pharmaceuticals (Boston, MA)
    …as GRA CMC Product Lead. + Represents and contributes to Regulatory, Pharmaceutical Development , and Commercial project teams throughout clinical development ... - including preparation of NDA/NLA/MAA. + Equivalent industry experience in Pharmaceutical Development , Analytical Development , Production, Quality Assurance… more
    Takeda Pharmaceuticals (12/24/25)
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  • Director , Ophthalmology Discovery

    J&J Family of Companies (Cambridge, MA)
    …Skills:** **Preferred Skills:** Collaborating, Developing Others, Drug Discovery Development , Leadership, Pharmaceutical Microbiology, Product Knowledge, ... Learn more at https://www.jnj.com **Job Function:** Discovery & Pre-Clinical/Clinical Development **Job Sub** **Function:** Biological Research **Job Category:** People… more
    J&J Family of Companies (01/10/26)
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  • Associate Director , Global Labeling

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …Center at: https://www.ic3.gov , or your local authorities. Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, ... scientific field. + 6-8 years of relevant experience in pharmaceutical regulatory/labeling environment and/or drug development +...or for payment of money during the job application process . We do not require any financial, credit card… more
    Otsuka America Pharmaceutical Inc. (12/18/25)
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  • Director , Specialty Sales - Remote

    Option Care Health (Boston, MA)
    …and brightest talent in healthcare. **Job Description Summary:** The Specialty Sales Director will develop and implement the Specialty business sales plan that ... They will be responsible for the execution of sales, marketing, and business development activities in their geographic area of responsibility. It will be imperative… more
    Option Care Health (12/11/25)
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  • Associate Director , Global Regulatory…

    Takeda Pharmaceuticals (Cambridge, MA)
    …Legal, and Regulatory review functions within the Commercial Material Review Process (CMRP). Provide regulatory guidance during development , review, approval, ... and promotion for prescription medicines. + Experience in prescription medicine promotion development and review process . + Strong interpersonal skills with… more
    Takeda Pharmaceuticals (10/29/25)
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  • Medical Director Pharmacovigilance, Rare…

    Takeda Pharmaceuticals (Boston, MA)
    …: Takeda Development Center Americas, Inc. is seeking a Medical Director Pharmacovigilance, Rare Disease & PDT with the following duties: serve as Global ... By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application… more
    Takeda Pharmaceuticals (12/27/25)
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  • Director , Global Regulatory Lead…

    Takeda Pharmaceuticals (Boston, MA)
    …inclusive of regulatory and/or related experience. + Solid working knowledge of drug development process and regulatory requirements. Knowledge of FDA is a must. ... the "Apply" button, I understand that my employment application process with Takeda will commence and that the information...lasting impact on patients worldwide. Join Takeda as a Director , Global Regulatory Lead Oncology where you will be… more
    Takeda Pharmaceuticals (10/30/25)
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  • Associate Director , Quality Risk…

    Bristol Myers Squibb (Devens, MA)
    …effective risk and issue management. + As part of the upstream protocol authoring process , partner with Drug Development , to embed Quality by Design principles ... their personal lives. Read more: careers.bms.com/working-with-us . Job Description The Associate Director , RBQM - HOCT, ICN will mainly be responsible for developing… more
    Bristol Myers Squibb (01/10/26)
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  • Associate Director , CMC Project Management

    WuXi AppTec (Natick, MA)
    …years of relevant pharmaceutical or biotech industry experience in CMC process development and/or GMP manufacturing. + Working knowledge and understanding of ... years of pharmaceutical or CRO/CMO industry experience, preferably in API process R&D and manufacturing and/or Drug Product R&D and manufacturing. + Prior… more
    WuXi AppTec (01/10/26)
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  • Associate Director , External Manufacturing…

    AbbVie (Worcester, MA)
    development and planning skills coupled with necessary knowledge of pharmaceutical development , manufacturing and supply activities. *Issue identification and ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , External Manufacturing will be the main supplier relationship contact… more
    AbbVie (11/21/25)
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