• Shipping & Receiving Supervisor

    North Coast Seafoods (Boston, MA)
    …of Shipper/Receivers, ensuring adherence to company policies, safety regulations, and quality control standards. The Shipping & Receiving Supervisor will be ... inspection, and processing of incoming products, ensuring accuracy in quantity, quality , and documentation. + Manage the storage and organization of products… more
    North Coast Seafoods (06/12/25)
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  • Global Program Head, Neurology

    Sanofi Group (Cambridge, MA)
    …are conducted in compliance with current regulations, laws, and guidance from FDA , EMeA, and CHMP, as well as with Sanofi's policies and procedures. **About ... the task they are required to perform. Including accountability and maintaining compliance training for direct reports + Works cross functionally to select… more
    Sanofi Group (08/15/25)
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  • Sales Specialist, Diagnostic Oncology (Central…

    Fujifilm (Boston, MA)
    …policies, and procedures. + Effective communication within FUJIFILM IVD organization of sales, quality and compliance issues. + Utilization of the IVD reporting ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
    Fujifilm (08/14/25)
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  • Global Program Head, Neurology Development

    Sanofi Group (Cambridge, MA)
    …are conducted in compliance with current regulations, laws, and guidance from FDA , EMeA, and CHMP, as well as with Sanofi's policies and procedures. **About ... the task they are required to perform. Including accountability and maintaining compliance training for direct reports + Works cross functionally to select… more
    Sanofi Group (08/10/25)
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  • Scientist I

    AbbVie (Worcester, MA)
    …mostly through lab and/or pilot plant based activities. + Responsible for compliance with all applicable Corporate and Divisional policies and procedures. + ... handling of materials, controlled drug and radioactive compounds, GxP compliance , and animal care where applicable. Qualifications Qualifications + Bachelors… more
    AbbVie (08/08/25)
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  • R&D Regulatory Manager

    Grifols Shared Services North America, Inc (Worcester, MA)
    …staff + May have responsibility for maintaining a compliant medical device quality system for R&D and informing project teams of needed updates/changes **Additional ... responsibilities:** + Represent R&D Compliance in professional and industry organizations. **Knowledge, skills, & abilities:** Knowledge and understanding of FDA more
    Grifols Shared Services North America, Inc (08/01/25)
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  • Senior Embedded Software Engineer - Verification…

    Capgemini (Burlington, MA)
    …will drive verification strategies, manage a team of engineers, and ensure compliance with medical device regulations. **Your Role** . Lead Verification Strategy: ... and mentor a team of verification engineers, promoting a culture of quality , collaboration, and continuous improvement. . Test Development: Design and implement both… more
    Capgemini (07/31/25)
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  • Sr. Director, Global Scientific Engagement…

    Chiesi (Boston, MA)
    …ecosystems. + Direct global early access and compassionate use programs, ensuring compliance with varied regulatory frameworks (eg, FDA , EMA, and other ... than 6,000 employees (Chiesi Group). To achieve its mission of improving people's quality of life by acting responsibly towards society and the environment, the… more
    Chiesi (07/24/25)
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  • Manager, Research Programs

    Beth Israel Lahey Health (Burlington, MA)
    …and support to staff as needed.** **Oversees and ensures staff compliance with the research protocols of the department.** **Utilizes problem-solving skills ... of all aspects of clinical trials research complying with research SOPs, GCP, FDA and OHRP regulations; ensures adherence to regulations and educates study team… more
    Beth Israel Lahey Health (07/17/25)
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  • Pharmacovigilance (PV) Specialist

    Rhythm Pharmaceuticals (Boston, MA)
    …and aggregate reports. This may include the support of monitoring compliance , effective communication, and implementation of corrective and preventive actions, as ... needed. + Performs quality review of SAEs and SUSARs from clinical trials...with PV and safety activities to ensure and promote compliance with pharmacovigilance standards and operational consistency across programs.… more
    Rhythm Pharmaceuticals (07/12/25)
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