• Veterans Benefits Administration (Hartford, CT)
    Summary Vocational Rehabilitation Specialist (VRS) position is within the Veteran Readiness and Employment (VR&E) Program. The Vocational Rehabilitation ... Specialist (VRS) carries out all duties related to assisting...the full performance level without further competition when all regulatory , qualification, and performance requirements are met. Selection at… more
    Upward (08/09/25)
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  • Regulatory Affairs Specialist

    Medtronic (North Haven, CT)
    …alleviate pain, restore health, and extend life for patients around the world. As a Regulatory Affairs Specialist , you will play a vital role in supporting ... with strong organizational skills. + Knowledge of document control systems and regulatory submission tools + Regulatory Affairs Certification (RAC-Devices)… more
    Medtronic (10/04/25)
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  • Principal Regulatory Affairs

    Medtronic (North Haven, CT)
    …in a more connected, compassionate world. **A Day in the Life** As a **Principal Regulatory Affairs Specialist ** at Medtronic, you will play a critical role ... **Nice to Have: Preferred Qualifications** + 7+ years of medical device regulatory affairs with roles showing increasing responsibility. + Strong leadership… more
    Medtronic (10/04/25)
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  • Senior Principal Regulatory Affairs

    Bausch + Lomb (Hartford, CT)
    …degree or equivalent; Master's degree preferred + Minimum of 8 years in Regulatory Affairs with experience in the consumer product (Rx/OTC, OTC Monograph, ... 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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  • Senior Principal Regulatory Affairs

    Bausch + Lomb (Hartford, CT)
    …Bachelor degree or equivalent, Master degree preferred + Minimum of 8 years in Regulatory Affairs or relevant experience in a regulated environment + Ability to ... 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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  • Supervisory Biomedical Equipment Support…

    Veterans Affairs, Veterans Health Administration (West Haven, CT)
    Summary Supervisory Biomedical Equipment Support Specialist is responsible for the hospital-wide Healthcare Technology Management (Clinical Engineering) Program ... Supervisory Biomedical Engineer CBTD-12805833-25-EF or Supervisory Biomedical Equipment Support Specialist JOA CBTD-12805834-25-EF Requirements Conditions of Employment You must… more
    Veterans Affairs, Veterans Health Administration (10/08/25)
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  • Supervisory Biomedical Engineer

    Veterans Affairs, Veterans Health Administration (West Haven, CT)
    …a medical equipment management program compliant with applicable healthcare standards and regulatory agencies. Ability to manage a recall and safety alert program ... Biomedical Engineer JOA: CBTD-12805833-25-EF or Supervisory Biomedical Equipment Support Specialist JOA CBTD-12805834-25-EF Requirements Conditions of Employment You must… more
    Veterans Affairs, Veterans Health Administration (10/08/25)
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  • Senior PD PMO Specialist

    Medtronic (North Haven, CT)
    …for released surgical products, collaborating across departments such as R&D, Quality, Regulatory Affairs , and Marketing. You'll help drive effective execution ... the Life** Join Medtronic's Surgical Operating Unit as a Sr PD PMO Specialist in our Robotic Surgical Technologies (RST) Released Product Management (RPM) Project… more
    Medtronic (10/03/25)
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  • Controls Assessment & Testing Senior…

    M&T Bank (Bridgeport, CT)
    …Risk, and internal partners such as the Risk Division, Internal Audit, and Regulatory Affairs . + Work is accomplished with periodic direction. The position ... programs that informs how to align practices with business objectives and regulatory requirements, including (but not limited to) developing complex process maps,… more
    M&T Bank (07/24/25)
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  • Regional Director of Medical Staff Services, East…

    Hartford HealthCare (Norwich, CT)
    …works collaboratively with the East Region Vice President of Medical Affairs , the Medical Executive Committee and additional medical staff leaders (appointed, ... goals and plans are realized, and there is adherence to the requirements of regulatory and accreditation bodies that are relevant to the organized medical staff. Key… more
    Hartford HealthCare (10/09/25)
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  • Post-Doctoral Fellow - Clinical Development…

    Boehringer Ingelheim (Ridgefield, CT)
    …of required trial documents, contracts and necessary approvals + All Regulatory Requirements are satisfied prior to trial/site initiation + Where necessary, ... for CRAs, investigators and site staff + In collaboration with Trial Resource Specialist and with support from CRAs as appropriate, ensures collection of required… more
    Boehringer Ingelheim (08/30/25)
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  • Executive Director, ExpMED Oncology Targeted…

    Boehringer Ingelheim (Ridgefield, CT)
    …and facilitation skills. + Strong track record of interactions with regulatory affairs authority, international societies and other relevant stakeholders. ... of Concept studies), ideally clinical specialization hematology, oncology or organ specialist . Solid relationships with key stakeholders. + Sound medical and… more
    Boehringer Ingelheim (09/18/25)
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