• 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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  • Senior Regulatory Affairs Specialist

    Hologic (Marlborough, MA)
    …with R&D, Quality, Clinical, and Marketing, you will prepare and manage regulatory submissions , technical files, and documentation to meet US, EU, ... Senior Regulatory Affairs Specialist Newark, DE, United...capital equipment products + Proven expertise preparing and maintaining regulatory submissions and technical files for mature… more
    Hologic (07/19/25)
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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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  • Principal Reg Affairs Specialist

    Medtronic (Boston, MA)
    …and related regulatory standards. Proven experience in global regulatory submissions and product approvals. Excellent communication and leadership ... world. **A Day in the Life** Job Summary: Principal Regulatory Affairs Specialist As a Principal ...or performs coordination and preparation of document packages for regulatory submissions from all areas of company,… more
    Medtronic (07/30/25)
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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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  • Research Data Specialist - GYN 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. + Bachelor's ... The **Research Data Specialist (RDS** ) will support the Gynecologic (GYN)...and the monitoring of patient status. The Research Data Specialist will be responsible for the collection, management, and… more
    Dana-Farber Cancer Institute (06/24/25)
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  • Environmental Health and Safety Specialist

    WIN Waste Innovations (Brockton, 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 (06/12/25)
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  • Senior Specialist , Data Science

    Merck (Cambridge, MA)
    …(GenAI) to enhance document authoring processes, thereby improving efficiency and compliance in regulatory submissions . The candidate will play a key role in ... influence scientists to adapt to positive change. * Experience with regulatory submissions and understanding of the review process. * Familiarity with… more
    Merck (07/08/25)
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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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  • 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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