• Medical Device External Quality…

    AbbVie (North Chicago, IL)
    …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: The Manager, Medical Device External Quality is part of AbbVie's External and ... Product Quality Assurance group and reports to the Senior Manager, Medical Device External Quality. The role will be based out of Lake County, IL site. This role… more
    AbbVie (06/17/25)
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  • Project Engineer (Med Device )

    Element Materials Technology (Fairfield, OH)
    **Overview** Element has an opportunity for an *on-site* ** Medical Device Project Engineer** to join our rapidly expanding team in Fairfield, Ohio. This position ... scheduling, testing , data analysis and reporting. The Project Engineer will manage medical device testing projects, using standard and custom test frames across… more
    Element Materials Technology (06/19/25)
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  • Moment - Experience Partner - Life Sciences…

    Cognizant (Chicago, IL)
    …Global Pharmaceutical market and industry, including BioTech, Medical Device , Traditional Rx, enabling technologies and regulatory /compliance in the ... **Experience Partner - Life Sciences (Pharma / BioTech / Medical Device )** **Associate Director - Chicago/Midwest Remote**...to plan and run existing clients. You'll work with Consulting and other parts of Cognizant like Data, and… more
    Cognizant (07/11/25)
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  • Sr. Sales Executive/Managed Services- Life…

    NTT America, Inc. (San Francisco, CA)
    …now. We are currently seeking a Sr. Sales Executive/Managed Services- Life Sciences/Med Device (Remote) to join our team in San Francisco, California (US-CA), United ... in digital, cloud and automation across a comprehensive portfolio of consulting , applications, infrastructure and business process services. This is primarily a… more
    NTT America, Inc. (06/14/25)
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  • Associate Director, Quality Consulting

    IQVIA (Durham, NC)
    …in life science and quality consulting services. + MSc/MBA preferred. + GMP/ GxP consulting knowledge (Pharma & Medical Device ). + Proven track record in ... optimize their Quality Management Systems (QMS) in alignment with regulatory standards and industry best practices. + Partner with...Change Management (OCM) experience. **Required:** + 10+ years of consulting experience in Medical Device more
    IQVIA (06/19/25)
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  • Sr. Consulting /Principal Full Stack…

    RELX INC (Horsham, PA)
    …projects within LexisNexis Reed Tech Life Sciences. Our focus includes our cutting-edge medical device and drug product platforms, along with their ancillary ... a part of RELX, is a leading global provider of legal, regulatory , and business information. We help customers increase productivity and improve decision-making… more
    RELX INC (06/14/25)
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  • Director, Cybersecurity Regulatory Affairs

    IQVIA (Washington, DC)
    …guidelines, and apply these to services provided. * Stay current on US medical device regulatory requirements. Qualifications: * Bachelor's degree required; ... years of consulting or client facing experience preferred; direct healthcare and/or medical device experience preferred. * Should understand medical more
    IQVIA (07/10/25)
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  • Sr. Regulatory Affairs Specialist

    Cardinal Health (Boston, MA)
    …+ Bachelors in related field, preferred + 2+ years' experience in Medical Device Regulatory Affairs/Quality experience preferred + Certification ... Regulatory provides regulatory affairs and product development consulting services to enable pharmaceutical, medical and biotechnology companies to… more
    Cardinal Health (07/09/25)
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  • Senior Associate, Regulatory Operations

    Publicis Groupe (New York, NY)
    …Saatchi & Saatchi Wellness has provided consumer and professional marketing, strategic consulting , and medical education to pharmaceutical and wellness brands. ... submissions follow the protocols established by our pharmaceutical and medical /surgical device clients for promotional materials. This includes knowing… more
    Publicis Groupe (06/12/25)
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  • Post Market Surveillance Analyst III

    Abbott (Burlington, MA)
    …various types of product complaints. Independently assesses the complaint to determine if a medical device report needs to be filed with various global ... + 5 years related work experience **Preferred Qualifications** + 3+ years in MDR ( Medical Device Reporting) + Knowledge of the use, development, and … more
    Abbott (07/11/25)
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