• Medical Reviewer

    Cook Medical (West Lafayette, IN)
    …of medical writing tasks). Qualifications MD or DO with medical device experience preferred; however, nurse practitioners and physician assistants ... Understand and provide guidance on comprehensive, systematic searches of published medical literature; Participate in the planning, development , and delivery… more
    Cook Medical (07/15/25)
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  • Lead Secondary Packaging Development

    Lilly (Indianapolis, IN)
    …mechanical and thermal (for cold-chain products) hazards. **Responsibilities:** + Partner with Device development , Business Unit, and Human Factor teams to drive ... sales and continues to grow. DDCS supports the design, development , and commercialization of medical devices and...years of work experience in GMP regulated pharmaceutical and/or medical device industries is required. + Background… more
    Lilly (09/12/25)
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  • Clinical Evaluation - Senior Project Manager…

    Abbott (Plano, TX)
    …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...On** + Manage, provide guidance, and oversight of CER Medical Writers' development of Clinical Evaluation Reports… more
    Abbott (08/08/25)
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  • Senior Design Quality Eng

    Medtronic (Lafayette, CO)
    …for you. You will be tasked to provide quality engineering support in design and development of medical device products across the Acute Care and Monitoring ... Design Quality Engineer The Design Quality Engineer position is one of development , improvement, and innovation, through cross functional collaboration. If you pride… more
    Medtronic (08/15/25)
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  • Sr. Regulatory Affairs Specialist

    Caldera Medical (Westlake Village, CA)
    …your role as a Sr. Regulatory specialist, you will develop and implement medical device regulatory strategies to obtain timely approvals from worldwide ... provide regulatory input and guidance to cross-functional partners regulatory documentation for medical device approvals in compliance with EU MDR, MDSAP, NMPA,… more
    Caldera Medical (08/24/25)
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  • Senior Software Engineer, Linux Kernel & Driver…

    General Motors (Austin, TX)
    …bring-up of next-generation automotive computing platforms, focusing on Linux kernel development , device drivers, low-level system integration, diagnostics, and ... Or Work equivalent experience . 3+ years of experience in embedded Linux kernel development , device driver programming, and board bring-up. . Expertise in Linux… more
    General Motors (07/23/25)
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  • GPS Medical - Product Safety Assessments

    Lilly (Indianapolis, IN)
    …+ Previous experience supporting manufacturing or manufacturing quality issues. + Experience in device development and device risk management. + Background ... ** **Purpose:** The Clinical Research Physician (CRP) in GPS Medical has responsibilities associated with the development ,...Team Leaders and Business Unit Leadership + Regulatory (including Device and CMC regulatory) + Affiliate Medical more
    Lilly (07/31/25)
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  • Director of R&D - PAD

    Permobil (Lebanon, TN)
    …of design experience, 3+ years leading engineering teams, and expertise in hardware/software development , FDA Medical Device Design Controls, and project ... assistive devices to the market. You'll oversee both new product development and sustaining engineering, ensuring our portfolio remains at the forefront… more
    Permobil (08/08/25)
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  • Principal CoreValve Therapy Development

    Medtronic (Orlando, FL)
    …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… more
    Medtronic (09/11/25)
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  • Director, External Development

    Merck (West Point, PA)
    …on the mission of ExDM. Their reports will manage the execution of formulation, device development and cGMP drug product manufacturing at external providers as ... registration stability manufacturing by designing, developing and scaling-up the formulation, device , and manufacturing process. Driving drug product design from the… more
    Merck (09/06/25)
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