• Sr Embedded Software Test Engineer

    J&J Family of Companies (Danvers, MA)
    …+ Knowledge of QNX would be a big plus. + Experience in the medical device industry is strongly preferred. + Working knowledge of cardiovascular physiology ... impact health for humanity. Learn more at https://www.jnj.com **Job Function:** R&D Product Development **Job Sub** **Function:** R&D Software/Systems… more
    J&J Family of Companies (11/26/25)
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  • Senior Post Market Quality Engineer

    Hologic (Marlborough, MA)
    …knowledge of FDA Quality System Regulations (especially Design Control), ISO 13485, EU Medical Device Regulation, ISO 14971, Risk Management, GMP, and GDP. + ... Engineer** , you will lead quality engineering efforts for on-market medical devices. This role is responsible for evaluating post-market feedback, investigating… more
    Hologic (10/10/25)
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  • Sr. Software Tool Engineer

    Medtronic (Newton, MA)
    …PhD with 0 years of relevant experience **Preferred Qualifications** + Knowledge of Medical device software development, IEC-62304 and FDA guidance in a ... to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference...to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference… more
    Medtronic (11/24/25)
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  • Robotic Instructional Design Manager

    Medtronic (Boston, MA)
    …+ Or advanced degree with a minimum of 3 years prior relevant experience. + Medical Device or Regulated Industry Experience + The ability to travel 25-50% **Nice ... to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference...to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference… more
    Medtronic (11/12/25)
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  • Director, Quantitative Clinical Pharmacology Lead

    Takeda Pharmaceuticals (Cambridge, MA)
    …within each At Takeda, we are transforming the pharmaceutical industry through our R&D -driven market leadership and being a values-led company. To do this, we ... Pharmacology (QCP) and Data and Quantitative Sciences (DQS) to the R&D organization and the external scientific community through high-value participation at… more
    Takeda Pharmaceuticals (09/25/25)
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  • Product Development Engineer

    J&J Family of Companies (Danvers, MA)
    …of role responsibilities **Preferred Qualifications:** + Master of Science degree + Medical Device product development experience + Knowledge in medical ... health for humanity. Learn more at https://www.jnj.com **Job Function:** R&D Product Development **Job Sub** **Function:** Biomedical Engineering **Job Category:**… more
    J&J Family of Companies (11/07/25)
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  • Clinical Development Portfolio Director-Patient…

    Philips (Cambridge, MA)
    …the right fit if:** + You have a minimum of 15+ years' combined experience in Medical Device Clinical Research and Medical Device development within FDA ... and Medical functions, as well as cross-functionally with Regulatory, R&D , Quality, HEMAR, Biostatistics and Data Management, Clinical Development, and other… more
    Philips (11/05/25)
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  • Software Engineer - C /Matlab

    Capgemini (Boston, MA)
    …impact patient care and clinical outcomes. **Your role** + Design and develop standalone medical device applications using modern C on Linux OS. + Lead the ... + 5 years of experience in application software development, with 2 years in the medical device or other regulated industries. + Bachelor's or Master's degree in… more
    Capgemini (11/20/25)
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  • Executive Account Director/ Sr Account Director…

    ThermoFisher Scientific (Boston, MA)
    …organizational expertise, and **_deep industry knowledge across the pharmaceutical, biotech, or medical device sectors_** , along with a proven track record ... business development and key account management in a related Pharmaceutical, Biotech or Medical Device sales industry + Experience in global sales with diverse… more
    ThermoFisher Scientific (09/21/25)
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  • Principal Quality Assurance Engineer

    Hologic (Marlborough, MA)
    …+ In-depth understanding of FDA Quality System Regulations, ISO 13485, and Medical Device Directive. + Expertise in compliance issues and regulatory ... a focus on integrity and compliance. **Experience:** + Minimum 12+ years in the medical device industry. + Proven track record in quality system strategy, risk… more
    Hologic (11/24/25)
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