• Senior Manager, Fleet & Sample Operations-2

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …inventory of pharmaceutical samples to field representatives. + Ensure compliance with regulatory tracking and reconciliation requirements. + Coordinate with ... working with field support or commercial operations teams. + Knowledge of compliance requirements related to pharmaceutical samples. **Preferred:** + … more
    Otsuka America Pharmaceutical Inc. (05/16/25)
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  • Global Quality Auditor - Technology Audit…

    Sanofi Group (Framingham, MA)
    …role represents the intersection of quality assurance, technological innovation, and regulatory compliance in a forward-thinking pharmaceutical environment. ... technology and diverse talents to secure product launches and support compliance through audits, inspections, regulatory surveillance, and advocacy. Grounded… more
    Sanofi Group (05/23/25)
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  • Validation Lead, Quality Assurance

    Astellas Pharma (Westborough, MA)
    …in compliance with user requirements, process parameters and global regulatory guidelines. The successful candidate will foster compliance across a ... of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We… more
    Astellas Pharma (03/25/25)
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  • Global Head of Pharma Sales

    Applied Materials (Gloucester, MA)
    …IoT, and automation to optimize production efficiency, ensure regulatory compliance , and drive real-time decision-making. We empower pharmaceutical companies ... platforms, or manufacturing automation software. + Strong understanding of **GMP, regulatory compliance (FDA, EMA), and pharma manufacturing processes** .… more
    Applied Materials (05/10/25)
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  • Project Manager II

    Adecco US, Inc. (Cambridge, MA)
    …Healthcare & Life Sciences is hiring a contract Project Manager II for our Pharmaceutical partner in Cambridge, MA. The anticipated hourly wage for this position is ... The overall scope of this position is to manage CMC development and Pharmaceutical Technical activities in support of new R&D compounds, Life Cycle Management… more
    Adecco US, Inc. (05/09/25)
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  • Director, Quantitative Pharmacology, Clinical…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    Otsuka Pharmaceutical Company is a global healthcare company with the corporate philosophy: "Otsuka-people creating new products for better health worldwide." Otsuka ... develops, manufactures and markets innovative products, with a focus on pharmaceutical products to meet unmet medical needs and nutraceutical products for… more
    Otsuka America Pharmaceutical Inc. (04/17/25)
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  • Associate Director, Clinical Research, Value…

    Takeda Pharmaceuticals (Lexington, MA)
    …IIR within assigned TA in accordance with all applicable internal legal and compliance policies as well as external US-specific regulatory guidelines. + Partners ... development (eg, thru Patent Exclusivity expiration). + Thorough understanding of legal, compliance , and regulatory guidelines related to the conduct of a… more
    Takeda Pharmaceuticals (05/03/25)
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  • Lead Quality Systems Auditor

    Fresenius Medical Center (Waltham, MA)
    …required + Minimum 10+ years' experience in quality management, regulatory compliance , quality engineering and auditing in the pharmaceutical or medical ... broad expertise related to the principles and application of quality conformity and regulatory compliance + Strong analytical and conceptual skills + Ability to… more
    Fresenius Medical Center (05/13/25)
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  • VP Clinical Development, Oncology

    Sumitomo Pharma (Boston, MA)
    …during IND submissions, clinical study reports, and NDA/MAA filings. + Collaborate with regulatory affairs team to ensure compliance with regulatory ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations...considered confidential. ** Compliance ** : Achieve and maintain Compliance with all applicable regulatory , legal and… more
    Sumitomo Pharma (05/15/25)
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  • Director, Clinical Trial Reporting

    Takeda Pharmaceuticals (Boston, MA)
    …regulations and standards for associated technologies and development programs to ensure regulatory submission compliance . + Ensure that technologies used in ... to standards for all development programs and marketed products to ensure regulatory submission compliance . + Manage team of employees and contractors to… more
    Takeda Pharmaceuticals (05/19/25)
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