• Principal Engineer, R&D

    Terumo Neuro (Aliso Viejo, CA)
    …**Job Description:** Support and lead teams in the development of medical device products, including writing or verifying specifications; maintaining ... prototypes meet their requirements. Job duties: + Develop new product concepts and products. + Provide engineering design and...Engineering. 2. Ten (10) to twelve (12) years of medical device industry experience. 3. Strong written… more
    Terumo Neuro (09/16/25)
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  • Senior Director, Quality Assurance - Site Quality…

    Lilly (Pleasant Prairie, WI)
    …compliance with cGMPs, policies, procedures and standards that are required to support parenteral manufacturing, device assembly, and packaging. They effectively ... the world. Lilly is designing and building a Next-Generation Parenteral and Device Assembly/Packaging Facility in Kenosha County, Wisconsin. This is an exciting… more
    Lilly (08/08/25)
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  • Director Senior Global Regulatory Lead

    CSL Behring (King Of Prussia, PA)
    …select roles, manager of Regional Regulatory Leads at CSL's global facilities that support assigned product /s or TA related products. Coaches and ensures ... innovative, scientificallyc sound regulatory vision / strategies for assigned product /s with a patient centric-focus, leveraging appropriate business insights and… more
    CSL Behring (09/19/25)
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  • Manager, Quality Assurance & Quality Control

    Danaher Corporation (Richmond, IL)
    medical , or technical field and 5+ years' experience with increasing responsibility in medical device /IVD + Experience working within a medical device ... Control for Leica Biosystems Richmond is responsible for providing leadership and support of daily quality operations including QC finished goods and raw material… more
    Danaher Corporation (08/08/25)
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  • Director, Software Engineering

    Abbott (Sylmar, CA)
    …diverse and growing portfolio of digital health products, including software as a medical device (SaMD), connected devices, and digital health platforms. This ... field + Minimum 12 years of proven experience in Connectivity development within the medical device / life sciences / digital health space, 5+ years being… more
    Abbott (08/13/25)
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  • Territory Manager, Acute

    Abbott (Boston, MA)
    …Bachelor's degree required; Graduate Degree preferred . Minimum of five years of medical device sales experience within the Cardiovascular field . Experience ... and Technical knowledge of Abbott CentriMag Circulatory and Respiratory support system and other complimentary products in the Acute...customer relationships . Track record of success in prior Medical Device sales roles . In depth… more
    Abbott (08/26/25)
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  • R&D Electrical Engineer

    Actalent (Santa Clara, CA)
    …R&D Electrical Engineer Job Description We are seeking a hands-on engineer to support product validation and final-stage development. This role focuses on ... + Redline and update technical documentation as needed. + Support product validation efforts to ensure functionality...and readiness for release. Essential Skills + Proficiency in medical device validation processes. + Experience with… more
    Actalent (09/17/25)
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  • Staff Software Verification Engineer, R&D

    Stryker (Redmond, WA)
    …* Experience with software test equipment and test methodologies * Experience in a medical device or regulated product development environment (21 CFR 820 ... Quality System requirements and best practices. Check out the product you'll support here: Stryker Emergency Care...regulations and ISO 13485 medical device standards) * Master's or Bachelor's… more
    Stryker (08/30/25)
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  • Associate Area Manager/Area Manager (Kansas City,…

    J&J Family of Companies (Kansas City, MO)
    …+ A minimum of 3+ years of sales experience with 2+ years experience in cardiovascular medical device sales. + A minimum 10+ years of sales experience with 5+ ... the best talent for Associate Area Manager/Area Manager to support clients in the Kansas City, MO area. **About...years experience in cardiovascular medical device sales. (Area Manager requirement) +… more
    J&J Family of Companies (09/24/25)
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  • Quality Control Inspector I, 2nd Shift

    Integra LifeSciences (Plainsboro, NJ)
    …of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations ... specific to incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in the medical more
    Integra LifeSciences (09/15/25)
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