• HPLC Scientist

    Eurofins (Lexington, MA)
    …including associated protocol/report documentation and presentations. + Conducts work in compliance with cGMP/GLP, safety, and regulatory requirements. + ... is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is… more
    Eurofins (05/24/25)
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  • Clinical Support Services Coordinator I

    Charles River Laboratories (Shrewsbury, MA)
    …Summary** Support all aspects of Clinical Support Services to ensure compliance with protocols, study documentation and applicable SOPS. Communicate with clients, ... ⦁ Prepare, review and ship clinical kits and supplies for clients in compliance with relevant Standard Operating Procedures (SOPs) under the guidance of senior… more
    Charles River Laboratories (05/14/25)
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  • Senior Manager, Clinical Management

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …Director.** **Establish communication flow with CRO and investigative sites to maximize compliance with study protocol.** **Provide oversight of ESP in its conduct ... corporate goals/vision and departmental** **policies and processes.** **- Assuring compliance with departmental, SOP, compliance , and corporate training**… more
    Otsuka America Pharmaceutical Inc. (05/13/25)
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  • Senior Sterilization Engineer

    Amgen (Cambridge, MA)
    …The successful candidate will lead collaborations with cross-functional teams to ensure compliance with regulatory standards and industry best practices. This ... extensively with internal and external stakeholders ie manufacturing, suppliers, quality, regulatory , senior management, etc. + Drive and influence key opinion… more
    Amgen (05/09/25)
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  • Research Scientist 1 - Immunochemistry

    Charles River Laboratories (Shrewsbury, MA)
    …management, interpretation, and reporting of study data and assuring the regulatory compliance of these projects, as appropriate. Additional responsibilities ... in accordance with company standard operating procedures and industry regulatory guidelines. This position will serve as the primary...in the direction and execution of assigned studies in compliance with regulations as they apply to the conduct… more
    Charles River Laboratories (03/04/25)
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  • Site Quality Head

    Curia (Hopkinton, MA)
    …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... is directly responsible for oversight of total quality and compliance operations at the assigned site. This role uses...to achieve a consistent approach to Quality Assurance and Regulatory Affairs + Acts as a key point of… more
    Curia (05/20/25)
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  • Laboratory Lead, Sanofi Intrepide US

    Sanofi Group (Cambridge, MA)
    …Execution & Excellence team on material and supply management, laboratory functions, and regulatory compliance + Support the coordination and management of legal ... (in vitro biology and in vivo pharmacology), Research lab operations, and pharmaceutical research experience in agile settings. They will maintain quality standards… more
    Sanofi Group (05/26/25)
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  • Field Reimbursement Manager, Hemophilia, NORTHEAST

    Sanofi Group (Boston, MA)
    …products. + Manage and adhere to all company policies and Legal and Regulatory guidelines. + Uphold and exemplify Sanofi's core values. **About You** **Basic ... a plus. + Minimum 10+ years' experience in the pharmaceutical or related healthcare industry + 4-7+ years ...in the patient home. + Must achieve and maintain compliance with all applicable Sanofi compliance policies,… more
    Sanofi Group (05/24/25)
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  • Associate Director, Digital Health Engagement…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …healthcare consulting, payer relations, or value-based care models. + Understanding regulatory and compliance requirements in healthcare engagement. + ... mental health. Candidates must be adaptable, results-oriented, and committed to compliance with all healthcare regulations. **EXPECTED TRAVEL** + 50-70% expected… more
    Otsuka America Pharmaceutical Inc. (05/23/25)
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  • Director, Global Scientific Communications Lead,…

    Takeda Pharmaceuticals (Cambridge, MA)
    …journals for the planning, integration, and execution of all publication activities in compliance with ICMJE, GPP and other standards as well as with Takeda's ... Ensure high scientific quality, alignment with medical strategy and adherence to compliance and legal requirements + Ensure and communicate regular updates to… more
    Takeda Pharmaceuticals (05/23/25)
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