• Sr. Embedded Software Engineer

    J&J Family of Companies (Danvers, MA)
    …into software specifications. + Design, development , and test software per medical device software development life cycle (IEC-62304) + Participate ... + Knowledge of QNX would be a big plus. + Experience in the medical device industry is strongly preferred. + Working knowledge of cardiovascular physiology… more
    J&J Family of Companies (07/24/25)
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  • Sr Prod Mgr Interv GI & Access

    Fujifilm (Boston, MA)
    …manager, senior product manager, product/technical director). + Minimum 8 years of medical device experience with strong clinical background. + Prior experience ... global R&D, operations, regulatory, global marketing, infection control, other companies/ device manufacturers, etc.) + Build and maintain strong relationships with… more
    Fujifilm (08/11/25)
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  • R&D Project Manager - Transducer Hardware…

    Philips (Cambridge, MA)
    …You've acquired 7+ years of professional experience with leading complex new product development projects in medical device regulated environment and proven ... skills include product quality and reliability metrics, risk management, and FMEA in medical device regulated environment. + You have a Bachelor's / Master's… more
    Philips (07/04/25)
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  • Technical Project Manager

    Actalent (North Reading, MA)
    …technically fluent and execution-driven Technical Program Manager (TPM) to lead development efforts across embedded systems, firmware, device drivers, ... hardware and software domains, with a strong emphasis on software development processes and release coordination. Responsibilities + Coordinate projects involving… more
    Actalent (08/12/25)
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  • Director, Regulatory Site CMC

    Takeda Pharmaceuticals (Boston, MA)
    By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... of scientific principles and regulatory CMC requirements relevant to global drug development and post-market support. Who has a proven ability to understand and… more
    Takeda Pharmaceuticals (06/04/25)
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  • Principal Regulatory Affairs Specialist

    Philips (Cambridge, MA)
    …a minimum of 8+ years' Regulatory Affairs experience within FDA regulated Medical Device /HealthTech product environments. Experience with Software as Medical ... will lead and provide regulatory oversight for critical new product development projects, ensuring our state-of-the-art Ultrasound Products meet FDA, and other… more
    Philips (06/28/25)
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  • Solutions Architect - Contact Center

    Insight Global (Quincy, MA)
    …a liaison between Business Units and Consumer Banking IT during design, development , testing, deployment, and ongoing maintenance phases, throughout the entire life ... starting on day one of employment, including options for medical , dental, and vision insurance. Eligibility to enroll in...due to a disability during the application or recruiting process , please send a request to Human Resources Request… more
    Insight Global (08/14/25)
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  • Supply Line Engineer - Silicon Photonics and New…

    Teradyne (North Reading, MA)
    …and develop alternative sources as needed. + Manage supplier's tooling and test process development to ensure the supplier has the capacity, flexibility and ... powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device more
    Teradyne (07/29/25)
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  • Sr. MES Opcenter OR Camstar Consultant - Remote

    Cognizant (Boston, MA)
    …cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Understand the ... paper Batch record and business process flow in collaboration with business SMEs Data-driven, user-centric,...of Electronic Lot History Records using Camstar Software for Medical Device / Pharma industries Implement and execute… more
    Cognizant (07/18/25)
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  • Senior Quality Engineer I - Design & Reliability…

    Integra LifeSciences (Braintree, MA)
    …participating on cross-functional project teams through all phases of the product development process , and assisting the technical team with planning, executing, ... related discipline with 5+ years of experience in Quality Assurance role for medical device or pharmaceutical manufacturing, or equivalent education and years of… more
    Integra LifeSciences (08/08/25)
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