• Sr R&D Software Engineer

    J&J Family of Companies (Halethorpe, MD)
    …**Primary Responsibilities:** + Design and implement embedded software for a class II medical device + Construction and maintenance of software requirements + ... a regulated industry + Version control and issue tracking systems + Medical device development, including ISO 62304 preferred + Linux use and development… more
    J&J Family of Companies (08/19/25)
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  • Senior Engineer, Materials R&D

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …+ Sound knowledge of material science and engineering principles + Working experience in medical device industry + Familiar with design control process and ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...medical device regulations + Knowledge of method...medical device regulations + Knowledge of method validation and six… more
    BD (Becton, Dickinson and Company) (08/17/25)
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  • Senior Microbiologist

    Stryker (Flower Mound, TX)
    …Provide guidance on cleaning, disinfection, sterilization, and biocompatibility for reusable medical device design. + Develop, review, and approve sterilization ... microbiological or biological testing, R&D, or sterility assurance within the medical device , pharmaceutical or regulated industry. Preferred Qualifications: +… more
    Stryker (08/16/25)
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  • Principal, QA- IDM (R1 - R4)

    Lilly (Indianapolis, IN)
    …project teams and participate in identifying specific software deliverables for SaMD (Software as a Medical Device ) and SiMD (Software in a Medical Device ... of product development, release, and life cycle management of MMA-mobile medical applications used in digital health. Ensure quality management system compliance… more
    Lilly (08/15/25)
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  • Future Opportunities - Join Our Talent Pipeline…

    AbbVie (North Chicago, IL)
    …industry experience (at least 4 years) with sufficient exposure to pharmaceutical, medical device , biologics and combination products, cosmetics, eye care or ... years in Quality Assurance with some project management experience in the pharmaceutical, medical device , biotechnology or related industry and 2+ years in… more
    AbbVie (08/15/25)
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  • Manager, Quality Engineering

    Hologic (Marlborough, MA)
    …management for medical devices. + Advanced knowledge of electromechanical and IVD medical device standards and best practices. **Skills** + Proven ability to ... accountability. **Experience** + 7+ years of quality engineering experience in the medical device industry, with a focus on electromechanical and IVD devices. +… more
    Hologic (08/14/25)
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  • Biomedical Equipment Technician

    Kelly Services (Cincinnati, OH)
    …for a Biomedical Equipment Technician for a long-term engagement at one of our Global medical device clients in Cincinnati, Ohio. The role is eligible for ... at Hiring Experts. This client is a company that's leading the way in medical device industry. + **Schedule** : On-site Monday through Friday 8am to 5pm +… more
    Kelly Services (08/13/25)
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  • Cleaning and Deburring Operator Days 7:00 AM…

    LSI Solutions (Victor, NY)
    …in 1986, located in beautiful Victor, New York, is a dynamic and growing medical device company with over 500 employees dedicated to advancing minimally invasive ... are searching for passionate people looking to make a difference in the medical device industry. By joining LSI SOLUTIONS(R) an ISO 13485 certified company, you… more
    LSI Solutions (08/13/25)
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  • Associate Director, Global Regulatory Affairs…

    Sanofi Group (Morristown, NJ)
    …year (3+ years preferred) of regulatory experience, preferably within the pharmaceutical/ medical device /biotech industry + Knowledge and understanding of complex ... and other R&D colleagues, as well as other stakeholders (eg, Legal, Medical , Marketing, Communications and Compliance). + Participates in the development, monitoring… more
    Sanofi Group (08/12/25)
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  • Staff Quality Engineer

    Stryker (Irvine, CA)
    …**Preferred:** + MS, CQE, or CRE. + Six Sigma Green or Black belt. + Medical device industry experience is strongly preferred. + Experience in interacting with ... agencies (FDA, MoH, TUV, etc.). + Understanding of US and International Medical Device Regulations. + Familiarity with ISO 13485, GDP, GMP. + Proven ability… more
    Stryker (08/09/25)
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