• FM (Johnston, RI)
    …combining property loss prevention with insurance protection. **Summary** The Corporate Affairs Contracts Specialist II role is responsible for providing ... guidance documents as needed; and (v) supports contract review workflow. The Corporate Affairs Contracts Specialist II supports the Corporate Affairs more
    DirectEmployers Association (09/24/25)
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  • Regulatory Affairs Specialist

    J&J Family of Companies (Raynham, MA)
    …to any necessary consultation processes. We are searching for the best talent for a ** Regulatory Affairs Specialist II** to support our Spine business. _This ... and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** Regulatory more
    J&J Family of Companies (10/25/25)
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  • Regulatory Affairs Specialist

    Cardinal Health (Mansfield, MA)
    **_What Regulatory Affairs contributes to Cardinal Health_** Regulatory provides regulatory affairs and product development consulting services to ... submissions as well as clinical research and manufacturing process consulting. Regulatory Affairs plans, coordinates and implement regulatory strategies… more
    Cardinal Health (10/29/25)
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  • Principal Regulatory Affairs

    Bausch + Lomb (Providence, RI)
    …with ongoing regulatory training related to products. + Works closely with the Regulatory Affairs labeling group in order to assess and determine the impact ... + Bachelor degree preferred or equivalent + Minimum of 6 years in Regulatory Affairs or relevant experience in a regulated environment + 2+ years of ad/promo… more
    Bausch + Lomb (10/15/25)
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  • Senior Principal Regulatory Affairs

    Bausch + Lomb (Providence, RI)
    …preferred + Minimum of 8 years in recent experience in strategic pharmacuetical Regulatory Affairs . This position does not work with medical device, cosmetics ... Strong business acumen and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative ideas to promote a successful … more
    Bausch + Lomb (09/06/25)
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  • Trial Master File (TMF) Specialist Oncology

    Sumitomo Pharma (Providence, RI)
    …ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements. + ... follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that SMPA studies...transfer of TMF is sufficient to support any potential regulatory filings. + Champion best practices for building and… more
    Sumitomo Pharma (11/05/25)
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