• Associate Director , Global

    BeOne Medicines (Emeryville, CA)
    **General Description:** The Associate Director , Global Regulatory Project Management (AD, Global RPM) is a strategic leader responsible for ... **Strategic Global Leadership** + Translate, implement, and advise on global regulatory strategies for development programs, ensuring alignment with business… more
    BeOne Medicines (12/31/25)
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  • Associate Director

    Sumitomo Pharma (Sacramento, CA)
    …of ** Associate Director , Regulatory Affairs (Oncology).** The Associate Director is part of the Global Regulatory Affairs (GRA) team based in ... the US. He/She will primarily function as a regional regulatory leader (RRL) and/or Global Regulatory Leader (GRL) for assigned products. This position is… more
    Sumitomo Pharma (10/11/25)
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  • Associate Director , IT…

    Bristol Myers Squibb (San Diego, CA)
    …of your application should be directed to Chat with Ripley. R1596697 : Associate Director , IT Regulatory , Clinical, and Enterprise Systems **Company:** ... to be the global leader in radiopharmaceuticals. **Job Description** The Assoc. Director , IT Regulatory , Clinical and Enterprise Systems is an integral part… more
    Bristol Myers Squibb (11/08/25)
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  • Associate Director

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to ... environment. **Job Description** + Oversee the capture, review, and dissemination of global regulatory news, public commenting opportunities, new and updated… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Associate Director Regulatory

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …grow and become your best self. Become a **maker of possible** with us. **The Associate Director of Regulatory Affairs** will provide regulatory support ... makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the...is not limited to the development and implementation of regulatory strategies for new product submissions, project management for… more
    BD (Becton, Dickinson and Company) (11/21/25)
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  • Associate Director , Global

    BeOne Medicines (Emeryville, CA)
    **General Description:** BeOne is seeking an Associate Director of GTS Governance, Risk, & Compliance (GRC) to build, enable and transform its risk management, ... in North America & LATAM regions. The GTS GRC Associate Director is a critical position within...security perspective across the organization. Working closely with the Director of Global GTS GRC, this position… more
    BeOne Medicines (11/14/25)
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  • Associate Director

    BeOne Medicines (Emeryville, 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 (12/23/25)
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  • Regulatory Affairs Associate

    GRAIL (Menlo Park, CA)
    … plans and activities to optimally position GRAIL products with the FDA and/or global health authorities. + Support the US Regulatory Affairs team in preparing ... North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. For more information,… more
    GRAIL (12/03/25)
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  • Associate Director , Global

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    **Job Summary** The Associate Director , Quality Operations will lead initiatives that drive operational excellence, enhance risk management practices, and ... practices. **Compliance & Governance** + Ensure quality operations comply with global regulatory requirements (eg, FDA, EMA, PMDA) and internal standards. +… more
    Otsuka America Pharmaceutical Inc. (12/17/25)
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  • Associate Director , Global

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products ... and transported in a controlled way that is in accordance with regulatory expectations and applicable cGMP/GDP quality standards. This role will direct Biologics… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Associate Director , Global

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    The Associate Director of Global Supplier Quality will be responsible for the execution of supplier quality audit and monitoring across the company's ... quality issues. + **Compliance & Documentation** + Ensure supplier compliance with global regulatory requirements (eg, FDA, EMA, ICH). + Prepare documentation… more
    Otsuka America Pharmaceutical Inc. (12/16/25)
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  • Associate Director , Global

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality oversight of ... are manufactured, packed, labelled, stored, and transported accordance with regulatory expectations and applicable cGMP/GDP quality standards. This role has… more
    Otsuka America Pharmaceutical Inc. (12/19/25)
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  • Associate Director , Global

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …assigned compounds to drive alignment of labeling content and strategy. + Partner with Global Regulatory Affairs to ensure that all labeling is aligned with the ... activities related to all global labeling components. + Represent Global Labeling on product-specific Regulatory and Cross-Functional teams, as appropriate.… more
    Otsuka America Pharmaceutical Inc. (12/18/25)
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  • Associate Director , Global

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    **Summary:** The Global Integrated Evidence Operations, Associate Director role oversees and coordinates the operational processes, digital system support, ... and governance for Global Integrated Evidence & Innovation (GIE&I), which includes responsibility...development lifecycle functions such as Discovery, Clinical Trials, and Regulatory . + Experience with digital technology to support management… more
    Otsuka America Pharmaceutical Inc. (12/17/25)
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  • Associate Director , Global

    AbbVie (Irvine, CA)
    …involving Tissue Management Science, Product Development, Clinical, Medical Affairs, Quality, Regulatory , Health Economics Outcomes Research, Global Access & ... all with a personal touch. For more information, visit https:// global .allerganaesthetics.com/. Follow Allergan Aesthetics on LinkedIn. Allergan Aesthetics | An… more
    AbbVie (12/23/25)
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  • Associate Director , Quality Risk…

    AbbVie (Irvine, CA)
    …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: The Associate Director / Director , Quality Risk Management is a ... fostering a culture of proactive risk identification, mitigation, and compliance with global regulatory and industry standards. Additionally, they will lead the… more
    AbbVie (12/16/25)
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  • Associate Director , Scientific…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    The Associate Director , Scientific Communications manages the execution of the core scientific and medical communications strategy for the relevant therapeutic ... Director , CNS Medical Communications Lead. **Key Responsibilities Include:** ** Global Scientific Communication Strategy** + Manage and deliver a comprehensive,… more
    Otsuka America Pharmaceutical Inc. (12/16/25)
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  • Associate Director , Clinical Trial…

    BeOne Medicines (Emeryville, CA)
    …Reporting to the Head/ Director of Clinical Trial Diversity, the Associate Director will operationalize BeOne's clinical trial diversity strategy through ... corporate functions to embed diversity into study design and site selection. The Associate Director will build trusted partnerships with sites, communities, and… more
    BeOne Medicines (11/06/25)
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  • Associate Director , ICSR Management…

    Ascendis Pharma (Palo Alto, CA)
    …We offer a dynamic workplace for employees to grow and develop their skills. The Associate Director , ICSR Management Team reports to the Director , Head, ICSR ... validated Drug Safety Databases (Argus preferred) + Experience with MedDRA coding and global safety reporting regulatory requirements. + Expert knowledge of FDA… more
    Ascendis Pharma (10/09/25)
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  • Associate / Medical Director

    Parexel (Sacramento, CA)
    …are expanding our esteemed Medical Sciences Team and seeking an Associate /Medical Director to support the growth of our Global Immunology and Inflammation ... Therapeutic Franchise. As an Associate / Medical Director , you will work closely with some of the...needed with the support of the designated Senior Medical Director / Global Head of TA (as appropriate)… more
    Parexel (10/11/25)
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