• Medical Devices , Regulatory

    Meta (New York, NY)
    …a scientific discipline or equivalent work experience 6. 3+ years of industry experience in medical device regulatory affairs or related industry 7. ... regulatory affairs specialist to join our medical devices compliance team. You will get...get to work on wearables and Software as a Medical Device (SaMD) applications for the US… more
    Meta (10/08/25)
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  • Post-Doctoral Regulatory Affairs

    Boehringer Ingelheim (Ridgefield, CT)
    **Description** The Clinical Development and Medical Affairs Fellow is a post-doctoral pharmacist position that will obtain broad exposure to BI US Medical ... functions including, but not limited to -- Medical Affairs and Scientific Communications, clinical operations, translational medicine and clinical pharmacology,… more
    Boehringer Ingelheim (08/30/25)
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  • Director of Scientific Affairs , COP

    Colgate-Palmolive (New York, NY)
    …+ DDS, DMD, or PhD. + Minimum of 10 years of experience in scientific affairs , medical affairs , or a related scientific role within the pharmaceutical, ... range of oral health needs. The Director of Scientific Affairs for Colgate Oral Pharmaceuticals is a pivotal role... medical device , or consumer healthcare industry. +… more
    Colgate-Palmolive (10/15/25)
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  • Supervisory Biomedical Engineer

    Veterans Affairs, Veterans Health Administration (West Haven, CT)
    …available for patient care activities. Responsible for compliance and reporting of medical device cybersecurity incidents and isolation for facilities under ... to manage a recall and safety alert program including medical device hazard investigations and assures compliance...assures compliance with the patient safety goals, the Safe Medical Devices Act (SMDA), and TJC requirements.… more
    Veterans Affairs, Veterans Health Administration (10/08/25)
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  • Sr. Innovation Product Manager, Neurodegenerative

    Danaher Corporation (New York, NY)
    …core labs, Define product vision, roadmap, and key requirements in collaboration with R&D, regulatory , medical affairs , and commercial teams + Build and ... 9+ years relevant experience + Product Management experience in diagnostics, biotechnology, medical devices or related fields with hands-on leadership in… more
    Danaher Corporation (10/14/25)
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  • Senior Manager, Global Regulatory

    Pfizer (Groton, CT)
    …You Will Achieve** You will represent Pfizer as an approval liaison in the regulatory affairs team assisting with diagnostics regulatory tasks. You will ... to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. Regulatory Affairs more
    Pfizer (10/19/25)
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  • Director, Data Science (RWE & GenAI), Diagnostics…

    Danaher Corporation (New York, NY)
    regulatory , market access, and post-market). You'll collaborate with clinical, regulatory /quality, R&D, medical affairs , IT/security, and our Operating ... and visualization tools. + Proven experience analyzing RWE/RWD (EHR, claims, registries, device logs) for clinical, regulatory , or market access impact. Travel,… more
    Danaher Corporation (10/03/25)
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  • Field Clinical Engineer

    Philips (Stamford, CT)
    …. This role also acts as a critical link between Clinical Research, Medical Affairs , Research and Development, Training and Education, marketing and the ... to supporting the implementation, training, and troubleshooting of Philips medical devices and systems during clinical studies....that can be brought back to internal teams (Clinical Affairs , R&D, Medical Affairs ). +… more
    Philips (10/17/25)
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  • Sr Medical Science Liaison, Selution…

    Cordis (New York, NY)
    …key clinical and scientific insights to internal stakeholders-such as Clinical Development, Medical Affairs , and Commercial teams, helping shape strategy and ... and medical information between KOLs, other investigators and the company's Medical Affairs , Marketing and R&D groups. + Propose strategic solutions to… more
    Cordis (10/21/25)
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  • Senior Clinical Project Manager (Remote)

    Stryker (New York, NY)
    …directly supporting clinical device research or similar experience in a medical device scientific area. + Understanding of industry clinical research ... safety, quality and integrity of data, compliance with relevant SOPs and regulatory requirements and completes studies on-time and on-budget. **What you will do**… more
    Stryker (10/22/25)
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  • Clinical Research Coordinator

    WMCHealth (Valhalla, NY)
    …reimbursement requests at the conclusion of patient's participation in protocol + Regulatory Affairs : Responsible for preparing and submitting new research ... and as the operational liaison for other research organizations, funding agencies and regulatory bodies. + Assists in training PIs and other research staff on the… more
    WMCHealth (10/11/25)
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  • Director, CCIA Product Portfolio Strategy…

    Danaher Corporation (New York, NY)
    …Managers towards it; build and maintain strong relationships with R&D, Clinical & Regulatory Affairs , Marketing, Operations, and Quality + Own & improve Beckman ... lifecycle management within the Diagnostics industry or a related field (eg, Medical Device , Pharmaceuticals, Biotechnology, Life Sciences) and a deep knowledge… more
    Danaher Corporation (08/13/25)
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