• Senior Specialist , Medical

    Merck (Wilson, NC)
    **Job Description** **Job Description** This Senior Specialist , MDCP Operations Lead position will serve as the primary medical device and combination ... advocating for processes that are both compliant and pragmatic. **Responsibilities** The Senior Specialist , MDCP Operations Lead position is responsible for… more
    Merck (09/21/24)
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  • Senior Cardiac Device Technician

    Swedish Health Services (Seattle, WA)
    **Description** The Senior Device Tech works with physicians, mid-levels, clinical staff and office staff to effectively, efficiently and accurately fulfill the ... and implantable loop recorders, as well as management of remote transmissions. The senior device technician will work closely with device clinic… more
    Swedish Health Services (08/19/24)
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  • Senior Regulatory Affairs Specialist

    Abbott (Plymouth, MN)
    …help of international regulatory affiliates. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Interfaces directly with ... ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more
    Abbott (08/30/24)
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  • Senior Principal Regulatory Affairs…

    Medtronic (Minneapolis, MN)
    …minimum of 5 years of relevant experience + Or minimum 5 years of medical device regulatory affairs experience with Master's degree **Preferred experience:** + ... affairs support for Class I, II and Class III medical devices. The Sr Principal Regulatory Affairs Specialist...4+ years of medical device industry experience with US FDA… more
    Medtronic (09/17/24)
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  • Senior Regulatory Affairs Specialist

    Abbott (Sylmar, CA)
    …ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements world-wide are ... Sylmar, CA currently has an on-site opportunity for a ** Senior Regulatory Affairs Specialist ** with our Cardiac...device regulations or with EU and other international medical device regulations and submissions. + Ability… more
    Abbott (09/25/24)
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  • Senior Regulatory Specialist

    BD (Becton, Dickinson and Company) (Covington, GA)
    …Minimum of 4 years' experience in Regulatory (to include some experience within medical device ); experience in areas of product registration, compliance or ... **Job Description Summary** Senior Regulatory Affairs Specialist - hybrid...+ Must have knowledge of the US and European medical device regulations. + Must have technical… more
    BD (Becton, Dickinson and Company) (09/15/24)
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  • Senior Regulatory Affairs Specialist

    Medtronic (Minneapolis, MN)
    …profile_ + Bachelor's degree in a technical discipline + Minimum 4 years of medical device regulatory experience with Bachelor's degree + Or minimum 2 years ... efficiently, with more predictable procedure times and outcomes. The ** Senior Regulatory Affairs Specialist ** develops strategies for...of medical device regulatory experience with an advanced… more
    Medtronic (09/06/24)
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  • Regulatory Affairs Senior Specialist

    Kelly Services (Redondo Beach, CA)
    **Title** : Regulatory Affairs Specialist ( Senior Level) **Pay** : $38-$50/hr depending on experience **Shift** : M-F, standard working hours. **Hybrid** role ... **Temp to hire** **Overview:** We are seeking a Regulatory Affairs Specialist ( Senior Level) to ensure company compliance with US FDA 510(k), Health Canada… more
    Kelly Services (08/22/24)
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  • Senior Regulatory Specialist

    Medtronic (Irvine, CA)
    …forward and remain a global medical technology and solutions leader. The ** Senior Regulatory Affairs Specialist ** will be vital in launching new products and ... sustaining the current product portfolio. The senior specialist complies with US and EU...Requires a Baccalaureate degree Minimum of 4 years of medical device regulatory affairs experience or advanced… more
    Medtronic (09/18/24)
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  • Senior Specialist , Clinical…

    Edwards Lifesciences (Atlanta, GA)
    …(RT), Operating Room Technician (ORT), or Cardiovascular Technician (RCIS) or related medical device , clinical, or Certification in RDCS (Registered Diagnostic ... + Knowledge and understanding of cardiovascular science + Moderate understanding of medical device regulatory requirements and documents, device more
    Edwards Lifesciences (09/04/24)
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  • Senior Oncology Specialist

    Amgen (Abilene, TX)
    …years of sales and/or marketing experience within pharmaceutical, biotech, healthcare, or medical device industries. + Product or hospital sales experience in ... you are meant to be in this meaningful role. ** Senior Oncology Specialist -Abilene, TX** **Live** **What...the clinical and economic benefits of the products to medical professionals. Our Senior Oncology Specialists achieve… more
    Amgen (09/08/24)
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  • Senior Provider Solutions Specialist

    HCA Healthcare (Overland Park, KS)
    …diversity and inclusion thrive? Submit your application for our Sr Provider Solutions Specialist opening with Overland Park Regional Medical Center today and ... of the HCA Healthcare team. **Benefits** Overland Park Regional Medical Center, offers a total rewards package that supports...apply! **Job Summary and Qualifications:** Summary of Duties: The Senior Provider Solutions Specialist serves as a… more
    HCA Healthcare (09/26/24)
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  • Senior Therapy Development…

    Medtronic (Milwaukee, WI)
    …with experience coordinating programs + Thorough working knowledge of medical terminology, medical procedures and the medical device industry + Excellent ... **A Day in the Life** **Bring your talents to a leader in medical technology and healthcare solutions.** **Rooted in our long history of mission-driven innovation,… more
    Medtronic (09/25/24)
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  • Senior Staff Clinical Evaluation…

    Stryker (MI)
    …industry analyses to develop best practices. Stryker **Instruments** is seeking a ** Senior ** **Clinical Evaluation Specialist ** to be based remotely anywhere in ... the United States. **What you will do** As the ** Senior ** **Clinical Evaluation Specialist ** , you will...conclusion on the overall benefit-risk profile of the subject device , in collaboration with a Medical Expert… more
    Stryker (09/26/24)
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  • Senior Training Specialist

    Integra LifeSciences (Plainsboro, NJ)
    …employees in a medical device regulated environment. The Senior Training Specialist will assess training needs, develop curriculum, and deliver ... what's possible and making headway to help improve outcomes. The ** Senior Training Specialist - Operations** will create and conduct training programs to enhance… more
    Integra LifeSciences (09/12/24)
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  • Senior Specialist Quality Assurance

    Abbott (Alameda, CA)
    …for diversity, working mothers, female executives, and scientists. **The Opportunity** The Senior Specialist Quality Assurance will participate as a lead member ... they apply to the development, verification, validation, use, and maintenance of medical device software. In addition (but not limited to these activities), you… more
    Abbott (09/07/24)
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  • In-house Senior Clinical Research…

    Edwards Lifesciences (Mann, PA)
    …**What else we look for (Preferred):** + Experience managing clinical trials within medical device industry + Prior clinical research experience with Class III ... to optimize patient outcomes. We are searching for a Senior Clinical Research Specialist to join Edwards....through execution and close out + Experience in Surgical therapies/ medical device product + Knowledge of cardiovascular… more
    Edwards Lifesciences (08/03/24)
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  • Senior Regulatory Affairs Specialist

    Abbott (Pomona, CA)
    …of experience in Regulatory Affairs + Three plus years in an IVD or medical device manufacturing environment + 510k submission experience + Technical file ... mothers, female executives, and scientists. **The Opportunity** The position of ** Senior Regulatory Affairs Specialist ** is within our Toxicology Business… more
    Abbott (08/28/24)
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  • Senior CAPA Specialist

    Stryker (Mahwah, NJ)
    …or applicable technical field. + Minimum 3+ years' experience working in a medical device or pharmaceutical regulated environment with 2+ years' experience ... etc.). + Ability to gain knowledge and understanding of US and International Medical Device Regulations. + Experience in supporting Quality Systems (eg Audits,… more
    Stryker (09/21/24)
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  • Senior Staff Regulatory Affairs…

    Stryker (San Jose, CA)
    …regulated environment required + Minimum 4 years of full-time work experience in medical device regulatory affairs required + Demonstrated applied knowledge of ... FDA and international medical device regulations/standards (eg EU MDR) $127,400 - $210,100 salary plus bonus eligible + benefits. Actual minimum and maximum may… more
    Stryker (08/30/24)
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