• Sr. Regulatory Affairs Specialist

    Medtronic (Mansfield, MA)
    …requirements + Directs or performs coordination and preparation of document packages for regulatory submissions from all areas of company, internal audits and ... compassionate world. **A Day in the Life** The Senior Regulatory Affairs Specialist (Sr. RAS) is responsible...considering both domestic and international regulations + Prepare 510(k) submissions and technical documents to support CE mark and… more
    Medtronic (07/01/25)
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  • Sr. Regulatory Affairs Specialist

    ConvaTec (Lexington, MA)
    …departments including but not limited to QC and legal in order to support regulatory submissions . **Travel Requirements** Position may involve travel up to 25% ... regulations and guidance documents to ensure complete and scientifically sound product submissions , as required. + Generate and execute regulatory strategies for… more
    ConvaTec (08/02/25)
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  • Regulatory Affairs Specialist - Post…

    Canon USA & Affiliates (Boston, MA)
    ** Regulatory Affairs Specialist - Post Market - req1434** **OVERVIEW** Reporting to the Director Regulatory Affairs, the Regulatory Affairs Specialist ... handling, coordination of product recalls, FMI processes, processing electronic submissions and state registrations. **RESPONSIBILITIES** + Remote position, **west… more
    Canon USA & Affiliates (06/07/25)
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  • Submission Ready Standards Specialist

    Takeda Pharmaceuticals (Boston, MA)
    …providing Submission Ready Standard Application during the preparation of high quality regulatory submissions and a wide range of supporting documentation across ... . **How you will contribute:** + Also the SRS Specialist will also be expected to drive, support and...the submission build activities for both paper and electronic regulatory submissions , ensuring submissions are… more
    Takeda Pharmaceuticals (08/09/25)
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  • Research Data Specialist - GI Oncology

    Dana-Farber Cancer Institute (Boston, MA)
    …tracking systems (STIP) and laboratory binders. + May be responsible for IRB and regulatory submissions and maintenance of regulatory files. **For Bone ... Research Program at Dana-Farber Cancer Institute is seeking a **Research Data Specialist ** to join our program. The GI Oncology Clinical Research Program supports… more
    Dana-Farber Cancer Institute (06/24/25)
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  • Environmental Health and Safety Specialist

    WIN Waste Innovations (Worcester, MA)
    WIN Waste Innovations is currently seeking an EHS Specialist that will be responsible for routine operations support, assistance, and coordination. The Specialist ... each assigned site with administrative environmental and safety systems, reports, and submissions . What You'll Do Training and Meetings + Implement safety and… more
    WIN Waste Innovations (08/09/25)
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  • Mortgage Loan Oversight Specialist

    City National Bank (Boston, MA)
    *COMMAND CENTER SPECIALIST * WHAT IS THE OPPORTUNITY? The Command Center Specialist will monitor production, quality, and timeliness of workflow of Residential ... implement policies for uniformity and quality standards, and ensure compliance to regulatory requirements. As the Subject Matter Expert, they will conduct root cause… more
    City National Bank (08/07/25)
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  • Research Data Specialist - Thoracic…

    Dana-Farber Cancer Institute (Brookline, MA)
    …tracking systems (STIP) and laboratory binders. + May be responsible for IRB and regulatory submissions and maintenance of regulatory files. + Bachelor's ... information; and the monitoring of patient status. The Clinical Research Data Specialist will be responsible for the collection, management, and quality assurance… more
    Dana-Farber Cancer Institute (08/08/25)
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  • Sustainability Reporting Specialist

    DuPont (Marlborough, MA)
    …Careers (https://careers.dupont.com/us/en/whyjoinus) **Future Electronics Sustainability Reporting Program Specialist ** DuPont is seeking a professional with a ... content and contribute to the execution of key non-financial disclosures including submissions to CDP, Ecovadis, and other scorecards as needed + Monitor external… more
    DuPont (05/17/25)
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  • Associate Director/Principal Medical Writer

    Sanofi Group (Cambridge, MA)
    …in a timely manner for study start, conduct and completion, as well as regulatory submissions according to company standards and procedures with the ultimate aim ... who has an extensive experience with the preparation of clinical documents and regulatory dossiers and has demonstrated leadership skills as submission lead. As an… more
    Sanofi Group (07/31/25)
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