• Market Development

    BlueVoyant (MD)
    Market Development Representative ( MDR ) Location: Remote in the United States Job Description: We are seeking a dynamic and detail-oriented Market ... Development Representative ( MDR ) to join our team. This individual contributor role will work collaboratively with our demand generation marketing team, operations team, and with our sales representatives to optimize the lead conversion processes… more
    BlueVoyant (01/04/25)
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  • Market Development

    Spindrift (Philadelphia, PA)
    …a critical role as we continue to grow our newest product across the US. The Market Development Representative ( MDR ) should be based in Philadelphia and ... will build the brand through direct account selling, distributor relationships, and in- market distribution, display and sampling execution. The MDR will maximize… more
    Spindrift (12/11/24)
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  • Market Development

    Catholic Health Initiatives (Bryan, TX)
    …primary care, Express Clinics, and imaging and diagnostic services. **Responsibilities** The Market Development Representative ( MDR ) will develop, ... Market services and service lines growth goals. The MDR will become acutely knowledgeable in specified service lines...and within guidelines set by the Executive Director of Market Development _(EDMD)_ . Coordinates internal sales… more
    Catholic Health Initiatives (12/14/24)
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  • Real Whirled Sales Development Program Full…

    Whirlpool Corporation (Benton Harbor, MI)
    …Second Rotation - Sell In:** After the SER role, participants are guided into a Market Development Representative ( MDR ) role. This position will be ... track your career trajectory in the Real Whirled Sales Development Program. Spend two years gaining a strong foundation...Whirlpool's brands, products, consumers, and how we go to market . **Your First Rotation - Sell Thru:** Participants apply… more
    Whirlpool Corporation (11/23/24)
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  • Senior MDR /Vigilance Manager

    Medtronic (Northridge, CA)
    …that monitors Medtronic's surveillance program including the intake, protocol development , evaluation, processing, and follow-up on adverse reports, participation in ... + Assess project issues and supports project team in development of resolutions to meet goals and objectives +...within the Responsibilities section of this job description are representative of those that must be met by an… more
    Medtronic (01/22/25)
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  • Senior Sales / Business Development

    RKON (Chicago, IL)
    …position: We are seeking an experienced and driven Senior Sales / Business Development Representative with deep expertise in the healthcare and pharmaceutical ... in providing IT migration and transformation services for the Mergers and Acquisitions market . RKON was recently recognized as one of the 100 best places to… more
    RKON (01/10/25)
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  • Principal Quality Mfg Engineer, Selution

    Cordis (Irvine, CA)
    development + Previous experience with product lifecycle (post market ) commercial support + Previous experience leading programs supporting business and ... **Overview** MedAlliance, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device… more
    Cordis (11/12/24)
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  • Regulatory Associate I / Regulatory Affairs - Days…

    LSI Solutions (Victor, NY)
    …employees dedicated to advancing minimally invasive surgical instruments through research, development , manufacturing, and marketing. We have doubled in size in just ... device regulations and standards to the company throughout the development cycle. Regulatory Associates monitor regulations, standards, policies, and guidance… more
    LSI Solutions (12/21/24)
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  • Sr Director Quality Management Systems

    BD (Becton, Dickinson and Company) (Warwick, RI)
    …internal audits, Notified Body assessments, FDA audits, adverse event reporting, post- market surveillance, and quality systems compliance. This position is key in ... internal audits, Notified Body assessments, FDA audits, adverse event reporting, post- market surveillance, and quality systems compliance. This position is key in… more
    BD (Becton, Dickinson and Company) (01/17/25)
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  • Senior Director, Product Development

    Globus Medical, Inc. (Methuen, MA)
    …technology division is searching for an enthusiastic Senior Director of Product Development to lead our navigation and computer vision team. This leadership position ... navigation program within Globus Medical and set the standard for product development , research and innovation within the industry. The position will be hands-on… more
    Globus Medical, Inc. (11/06/24)
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  • Principal Compliance Audit Specialist - Software…

    Medtronic (Minneapolis, MN)
    …partners on compliance gaps, data, and/or resulting corrective actions. * Own development of training and awareness programs for SaMD, SiMD, and product security ... security enhancement. * Possess understanding of Software Bill of Material (SBOM) development and maintenance for the purposes of vulnerability monitoring. * Possess… more
    Medtronic (01/16/25)
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  • Sr. Design Quality Engineer

    Medtronic (Carlsbad, CA)
    …in Medtronic we focus on providing Engineering support for Design and Development , Quality Compliance, and Risk Management activities across the Ventilation Service ... are conducted in compliance with the FDA Quality System Regulations and EU MDR requirements. This position will focus on software design changes. * Responsible for… more
    Medtronic (01/17/25)
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  • Specialist, Regulatory Compliance

    Danaher Corporation (Richmond, IL)
    …registration maintenance, device listing, regulatory requirements, Importer and Authorized Representative actions. + Experience with ISO 13485:2016, IVD/ MDR ... to bring IVD (In-Vitro Diagnostic), Research (RUO) and Laboratorial products to market and support activities related to Quality Management System (QMS) to ensure… more
    Danaher Corporation (12/20/24)
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  • Quality Manager

    Actalent (Emerson, NJ)
    …and international markets. Responsibilities + Serve as the appointed Management Representative . + Lead, coordinate, author, and review regulatory filing documents. + ... files, including 510(k) submissions, Device Master files, technical files, and post- market surveillance for product changes and new products. + Collect documentation… more
    Actalent (01/22/25)
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  • Senior Program Manager - Neuro Science

    Medtronic (Juncos, PR)
    …and programs in the released product space, including regulatory (ie MDR ) compliance remediation, manufacturing capacity expansion, product design enhancement, and ... management skills, business acumen, and domain knowledge in medical device operations and development . This is a hybrid position with the expectation of being onsite… more
    Medtronic (01/22/25)
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  • Senior Manager, Medical Device Quality Systems

    AbbVie (North Chicago, IL)
    …serves as Deputy Person Responsible for Regulatory Compliance under EU MDR 2017/745, providing compliance subject matter expertise to internal business partners, ... Serves as the Deputy Person Responsible for Regulatory Compliance under EU MDR 2017/745, supporting quality management supervision under the direction of the… more
    AbbVie (01/16/25)
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  • Manager, SW Design Quality -Digital Products

    Medtronic (Los Angeles, CA)
    …you will be asked to manage and guide the design quality engineers in the pre- market design and sustaining space. You will be responsible to drive development of ... implements all quality aspects of the company's design and development of new and sustaining medical device products** or...to ensure project planning is complete end-to-end, for both pre- market and post- market activities. + Manages activities… more
    Medtronic (01/15/25)
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  • Prin Design Assurance Engineer, Systems Risk…

    Medtronic (Los Angeles, CA)
    …members from Systems Engineering, R&D/ Design, Manufacturing Operations, Pre & Post Market Quality, and Regulatory Affairs to ensure the successful execution of ... function as the subject matter expert that leads risk management development activities & generating tailored risk documentation outputs across different components… more
    Medtronic (01/22/25)
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  • Regulatory Coordinator - Days - 8:00am to 5:00pm

    LSI Solutions (Victor, NY)
    …to obtain market approvals in the USA (510(k), Canada, Europe (MDD/ MDR ), Australia, and ROW ensuring all US/EU/CA requirements and corporate policies and ... and Regulatory compliance with all standards that govern the design, development , manufacturing, and distribution of our medical devices. REPORTS TO: REGULATORY… more
    LSI Solutions (01/23/25)
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  • Principal Systems Risk Management Engineer

    Medtronic (Mounds View, MN)
    …risk assessments for product released to the field. + Experience in product development . + Experience owning and authoring risk analyses and assessments. + Knowledge ... regulations: FDA 21 CFR Part 820, EU 217/745 (EU MDR ) + Familiarity with these standards: ISO 13485, ISO...within the Responsibilities section of this job description are representative of those that must be met by an… more
    Medtronic (01/22/25)
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