• Merck & Co. (North Wales, PA)
    …information.- Maintains up-to-date awareness in the areas of literature-related copyright compliance , adverse event reporting, and information storage ... to:Monitors the quality, accuracy, and timeliness of biomedical literature screening, adverse event reporting, abstracting, and indexingAssists with the… more
    HireLifeScience (08/13/24)
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  • Evergreen Requisition - Global MDR…

    Olympus Corporation of the Americas (Center Valley, PA)
    Global MDR Analyst II is responsible for supporting medical device adverse event reporting within the complaint handling process. This position is ... follow-up/ good faith effort to obtain additional information for Adverse Events or reported event by collaborating...MDR Analyst II will maintain quality documents to ensure compliance with global medical device guidance documents.… more
    Olympus Corporation of the Americas (08/01/24)
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  • Evergreen Requisition - Global MDR…

    Olympus Corporation of the Americas (Center Valley, PA)
    …ISO13485, 21CFR820, 21CFR806 and 21CRF803 and will also have a an understanding of global adverse event reporting criteria (For example: Europe, China, ... locations you would consider. * Olympus is looking for Global MDR Submissions Analyst III. Hiring Location: US **Job...5 or more years of medical device experience including adverse event reporting. + Complaint Handling/ Customer… more
    Olympus Corporation of the Americas (08/01/24)
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  • Associate Manager, Compliance , Training…

    Sumitomo Pharma (Trenton, NJ)
    …Pharmacovigilance (PVRM) and non-PVRM vendor(s) (eg Commercial) and will be responsible for adverse event handling and reporting and for general PVRM operations, ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...+ Manages the annual review and release of companywide Adverse Event (AE) policy training, ensuring that… more
    Sumitomo Pharma (08/27/24)
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  • Specialist, Clinical Literature Information…

    Merck (North Wales, PA)
    …information. Maintains up-to-date awareness in the areas of literature-related copyright compliance , adverse event reporting, and information storage ... to:** + Monitors the quality, accuracy, and timeliness of biomedical literature screening, adverse event reporting, abstracting, and indexing + Assists with the… more
    Merck (08/12/24)
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  • Director, Post Market Surveillance

    Integra LifeSciences (Princeton, NJ)
    Global Post Market Surveillance Program. This includes Complaint Handling, Adverse Event Reporting, Health Hazard Evaluations (HHEs), Field Actions, and ... a team of direct reports responsible for Complaint Handling, Adverse Event Reporting, Health Hazard Evaluations, Field...of the organization globally to identify and alert of compliance in time to resolve potential adverse more
    Integra LifeSciences (08/07/24)
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  • Associate Clinical Research Manager (aCRM)…

    Merck (Trenton, NJ)
    …and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. The aCRM ... and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. + o Reviews… more
    Merck (08/27/24)
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  • Clinical Research Manager (CRM) - Immunology…

    Merck (Trenton, NJ)
    …and country regulations, Our Company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. The CRM ... and country regulations, our Company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. + Reviews… more
    Merck (08/27/24)
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  • CRA - Monitor

    System One (Yardley, PA)
    …+ Supply Management: Ensure clinical trial supplies are managed and tracked efficiently. + Adverse Event Reporting: Ensure all adverse events are reported ... provides input, necessary support, and oversight for the high-quality execution of global clinical trials. This position also provides support for documentation of… more
    System One (08/29/24)
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  • Senior Technical Services Manager- Cattle (Upper…

    Merck (Trenton, NJ)
    …vaccination programs and protocol for use of pharmaceuticals, product use directions, adverse event reporting, dealing with Ruminant health issues in customer's ... for Ruminant products and programs, including response to product inquiries and adverse reports in accordance with internal, FDA, CFIA and USDA regulatory policies.… more
    Merck (08/01/24)
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  • Engineer, Principal Quality

    Olympus Corporation of the Americas (Center Valley, PA)
    …Olympus operations across the areas of HHAs and Field Actions, complaint handling, adverse event reporting, CAPA and Post Market Surveillance activities in ... and/or support continuous improvement and sustaining efforts for the global processes and systems to assure compliance ,...the global processes and systems to assure compliance , harmonization, and efficiency. **Job Duties** + Leads a… more
    Olympus Corporation of the Americas (08/30/24)
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  • Complaints Director

    Olympus Corporation of the Americas (Center Valley, PA)
    …both domestic and international with specific expertise in; Complaint Handling, Adverse Event Reporting, Field Actions/Recalls, Regulator Inspections, product ... ) compliance and quality assurance. + Demonstrated experience leading global change initiatives and integrations for multi-site and multi-product businesses. +… more
    Olympus Corporation of the Americas (08/29/24)
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  • Senior Engineer, Health Hazard Assessment - Remote

    Olympus Corporation of the Americas (Center Valley, PA)
    …across the areas of Risk Management, HHAs and Field Actions, complaint handling, adverse event reporting, CAPA and Post Market Surveillance activities in support ... occurs in a timely manner to address safety and compliance areas of our business and to ensure proper...expert guidance for the HHA teams. + Collaborates with global /regional leaders on relevant HHAs and interacts with Legal… more
    Olympus Corporation of the Americas (07/02/24)
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