• Senior Regulatory Affairs…

    Medtronic (Lafayette, CO)
    …in a more connected, compassionate world. **A Day in the Life** The Senior Regulatory Affairs Specialist (Sr. RAS) is responsible for working collaboratively ... EU Medical Device Regulation (MDR). The Sr. RAS translates regulatory requirements into actionable project or product...Minimum Requirements** + Bachelors degree with 4+ years of regulatory affairs experience in the medical device,… more
    Medtronic (11/18/25)
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  • Regulatory Affairs Specialist…

    BD (Becton, Dickinson and Company) (Louisville, CO)
    **Job Description Summary** The Regulatory Affairs Specialist II is responsible for implementation of strategies including domestic and international ... support through the product life cycle on product project teams (eg, developing regulatory strategies, timeline...with software and capital systems is a plus. + Regulatory Affairs Certification (RAC) desired ​ At… more
    BD (Becton, Dickinson and Company) (10/17/25)
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  • Senior Principal Regulatory Affairs…

    Bausch + Lomb (Denver, CO)
    …preferred + Minimum of 8 years in recent experience in strategic pharmacuetical Regulatory Affairs . This position does not work with medical device, cosmetics ... labeling, adpromo areas. Serve as a strategic advisor to project teams, ensuring regulatory compliance, influencing key...and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative… more
    Bausch + Lomb (09/06/25)
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  • Biomedical Equipment Support Specialist…

    Veterans Affairs, Veterans Health Administration (Grand Junction, CO)
    Summary Serves as a Biomedical Equipment Support Specialist (BESS) specialized in information systems within a Healthcare Technology Management (HTM) department at ... or deficiencies. Complies with applicable standards, policies, procedures, and regulatory requirements. Provides guidance and mentorship to expand professional… more
    Veterans Affairs, Veterans Health Administration (11/19/25)
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  • DOLA Contract Drafting Specialist /Contract…

    State of Colorado (Denver, CO)
    …of affordable housing. + Works with stakeholders such as: underwriter, development specialist , and/or program manager to incorporate the project description, ... statement of work; ensures that terms and conditions in the exhibits related to regulatory compliance are appropriate for the project type and the funding… more
    State of Colorado (11/22/25)
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  • Trial Master File (TMF) Specialist Oncology

    Sumitomo Pharma (Denver, CO)
    …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...quality concerns and oversee resolution of issues. + Develop project specific TMF plan and structure and update the… more
    Sumitomo Pharma (11/05/25)
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  • Sr Quality Assurance (QA) Specialist

    Danaher Corporation (Boulder, CO)
    …reports to the Sr Manager, Quality Systems and is part of the Quality and Regulatory Affairs group located in Boulder Colorado and will be an on-site role. ... which makes everything possible. The Sr Quality Assurance (QA) Specialist is responsible for providing administration, coordination, and maintaining the… more
    Danaher Corporation (10/21/25)
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