• Sr. Scientist, Drug/ Device Combination…

    Merck (Rahway, NJ)
    … design control activities in the following aspects: + Lead and contribute device development design controls for the assigned projects. + Prepare materials ... and thoroughness. + Lead the implementation and/or ensure effective execution of the device development strategy and design controls for the assigned projects… more
    Merck (09/06/25)
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  • Associate Director - QA - Medical

    Lilly (Indianapolis, IN)
    …oversight for quality system activities performed by Quality Assurance in the medical device complaint handling area. To support implementation and maintenance ... Support complaint related activities associated with new product launches + Support device development processes by providing complaint analyses of predicate… more
    Lilly (08/20/25)
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  • Associate Director, Device Technology

    Merck (West Point, PA)
    …Director of Device Technology is a key leadership role within the Device Development and Technology Organization. This position is responsible for building ... or PhD) preferred. + Minimum of 8 years of experience in pharmaceutical, biologic, medical device or combination product engineering, with at least 4 years in… more
    Merck (09/06/25)
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  • Lead Systems Engineer, Medical

    Hologic (Newark, DE)
    Lead Systems Engineer, Medical Device Newark, DE, United States **Are you a strategic thinker, problem solver, and visionary leader ready to shape the future of ... medical device innovation? Join Hologic as our...cross-functional teams on large, complex, and technically challenging product development projects, driving the full design life cycle from… more
    Hologic (09/13/25)
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  • Medical Device Assembler

    Kelly Services (Irvine, CA)
    …to support production demand and new product development . **Position Summary:** As a Medical Device Assembler, you will play a key role in developing and ... Medical Device Assemblers...Follow process instructions to build catheters to meet product development and launch commitments. + Meet catheter manufacturing yield… more
    Kelly Services (09/04/25)
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  • Sr. Software Tool Engineer

    Medtronic (Mounds View, MN)
    …+ OR PhD with 0 years of relevant experience **Preferred Qualifications** + Knowledge of Medical device software development , IEC-62304 and FDA guidance in a ... you will play a critical part in enhancing and streamlining our software development , testing, and quality assurance processes. You will develop a variety of tools,… more
    Medtronic (09/06/25)
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  • Cardiac Device Specialist Cardiac…

    HonorHealth (AZ)
    …to make a difference. From our Ambassador Movement to our robust training and development programs, you can select where and how you want to make an impact. ... area. The comprehensive network encompasses six acute-care hospitals, an extensive medical group with primary, specialty and urgent care services, a cancer… more
    HonorHealth (07/24/25)
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  • Senior Manager, Regulatory Affairs - Device

    AbbVie (North Chicago, IL)
    …CFR Parts 3, 4, GCP, GLP, 210/211, 820 QSR (Design Control), European Medical Device Directives and Regulation (MDR/IVDR), ISO 13485, MDSAP, technical standards, ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...the Regulatory Affairs functional areas, Operations, and Research & Development (R&D) organizations. Represents RA Device on… more
    AbbVie (09/11/25)
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  • R&d Engineer

    Actalent (Irvine, CA)
    Job Title: Clinical Development Engineer Job Description A medical device company developing a novel transcatheter therapy for valvular heart disease is ... to work independently in a fast-paced, collaborative environment. + Proficiency in medical device and clinical development , particularly in cardiovascular… more
    Actalent (09/03/25)
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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 ... Staff Software Verification Engineer you will collaborate with product development teams to coordinate software testing throughout the ...regulations and ISO 13485 medical device standards) * Master's or Bachelor's… more
    Stryker (08/30/25)
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