• Specialist, Clinical Apps - MRI

    Fujifilm (Boston, MA)
    …system enhancement suggestions. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ... ISO 13485 standard requirements and all other applicable laws, regulations, and standards. **Qualifications** + Experience + Minimum three (3) years clinical MR experience. + Educational requirements: + Degree from accredited Radiology Technologist Program. +… more
    Fujifilm (07/02/25)
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  • Senior Technical Clinical Consultant (PACS,…

    Fujifilm (Boston, MA)
    …by upper-level management. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO ... 13485 standard requirements and all other applicable laws, regulations and standards. + Comply with and pass all requirements for vendor credentialing as part of gaining access to hospitals and facilities to perform assigned job duties. **Qualifications:** +… more
    Fujifilm (06/19/25)
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  • Director Environment, Health & Safety…

    Staples (Framingham, MA)
    …(Transportation & Disposal), Emergency Planning, Hazardous Chemical - Right to Know laws, Food Safety & Defense, State, County, local specific codes, and norms . ... to safety training as required by OSHA, EPA, DOT, FMCSA and the US FDA . Works closely with Risk Management and field operations leaders to analyze incident &… more
    Staples (08/08/25)
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  • Microbiology Technician II

    Integra LifeSciences (Braintree, MA)
    …components, manufactured sub-assemblies and final product. Must have working knowledge of US Food and Drug Administration regulations, ISO 13485, and other ... studies. + Assist in preparing for and participating in FDA audits, customer audits, etc. + All other duties...regulated product preferred environment. + Familiarity with application of FDA and/or ISO quality standards in a government regulated… more
    Integra LifeSciences (08/08/25)
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  • Quality Control Technician II, Analytical

    Integra LifeSciences (Boston, MA)
    …components, manufactured sub-assemblies and final product. Must have working knowledge of US Food and Drug Administration regulations, ISO 13485, and other ... (CAPAs). + Assist in preparing for and participating in FDA audits, customer audits, etc. + All other duties...regulated product preferred environment. + Familiarity with application of FDA and/or ISO quality standards in a government regulated… more
    Integra LifeSciences (07/31/25)
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