• Project Engineer - Medical

    Intertek (Boxborough, MA)
    Project Engineer - Medical Device Testing, Boxborough, MA Intertek is a Nationally Recognized Testing Lab (NRTL) and leading provider of quality and ... quality, safety, and sustainability to life. What are we looking for? The Project Engineer is responsible for independently performing testing and evaluation on… more
    Intertek (04/12/25)
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  • Engineer I, Medical Device

    Amgen (Cambridge, MA)
    …team. Join us and transform the lives of patients while transforming your career. Engineer I - Medical Device Design Control Documentation Specialist **What ... and New Product Introduction program milestones + Participate in project execution according to the Robust Design paradigm and...- ISO 13485; Risk Management - ISO 14971; EU Medical Device requirements - Council Directive 93/42/EECStrong… more
    Amgen (05/09/25)
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  • Staff Device Engineer

    Takeda Pharmaceuticals (Lexington, MA)
    …support lifecycle management of commercial combination product. The Staff Device Engineer has extensive experience in medical devices for drug delivery ... of my knowledge. **Job Description** **Primary** **Role:** The Staff Device Engineer will lead technical efforts for...with medical device and combination device regulations. + Lead project execution activities… more
    Takeda Pharmaceuticals (05/02/25)
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  • Lead Project Team Support Engineer

    Fujifilm (Boston, MA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... **Position Overview** The LEAD PROJECT TEAM SUPPORT ENGINEER -MI provides remote...manages. + Maintains an expert working knowledge of current medical imaging products and related technologies. + May be… more
    Fujifilm (05/08/25)
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  • Sr. Project Engineer , SDS

    Fujifilm (Boston, MA)
    …of Synapse product implementation, fromsolution validation phases through product go-live. The Project Engineer (PE) must have wellrounded knowledge in all areas ... + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
    Fujifilm (04/25/25)
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  • Engineer I, Components

    Teleflex (Mansfield, MA)
    …is expected to have a basic understanding of development, manufacturing, design control, medical device regulation, and project management. They will be ... Engineer I, Components **Date:** Apr 29, 2025 **Location:**...global provider of product development and production services for medical device manufacturers. We set ourselves apart… more
    Teleflex (04/30/25)
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  • Principal Systems Engineer

    Olympus Corporation of the Americas (Westborough, MA)
    …product security, cybersecurity, and equipment development oversight. Extensive knowledge of medical device design control requirements, system design and ... project and engineering leadership in all phases of device development, as well as ensure compliance to applicable...for manufacturability and testability is required. Deep understanding of medical device standards, and experience in their… more
    Olympus Corporation of the Americas (03/29/25)
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  • Sr. Cybersecurity Engineer

    Olympus Corporation of the Americas (Westborough, MA)
    …and/or supporting the development and implementation of security measures specific to medical device technologies. This role focuses on protecting computer ... systems, networks, and sensitive data integral to medical device functionality and patient safety. The primary responsibilities include overseeing all phases of… more
    Olympus Corporation of the Americas (03/29/25)
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  • Senior Engineer , Combination Products…

    Amgen (Cambridge, MA)
    …experience with 5+ years of experience in operations/manufacturing environment. + Medical device industry experience and regulated work environment experience. ... the lives of patients while transforming your career. Senior Engineer **What you will do** Let's do this. Let's...Regulation - 21CFR820, Risk Management - ISO 14971, EU Medical Device requirements - Council Directive 93/42/EEC.… more
    Amgen (05/09/25)
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  • Sr. Manufacturing Engineer I

    Integra LifeSciences (Mansfield, MA)
    …provide technical expertise and project management in the areas of medical device manufacturing process development and validation, DFM, COGs management, ... and Manufacturing to develop and sustain surgical products for the neurosurgical medical device industry. + Manufacturing process technical expert who can… more
    Integra LifeSciences (04/05/25)
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  • Staff Manufacturing Engineer

    Integra LifeSciences (Mansfield, MA)
    …provide technical expertise and project management in the areas of medical device manufacturing process development and validation, DFM, COGs management, ... and Manufacturing to develop and improve surgical products for the neurosurgical medical device industry. * Recognized manufacturing process technical expert who… more
    Integra LifeSciences (03/20/25)
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  • Senior Engineer , Design Transfer…

    Amgen (Cambridge, MA)
    …of progressive experience as an engineer or scientist in relevant fields ( medical device development, manufacturing, etc.) + Proven track record of executing ... various global manufacturing sites. This role requires a deep understanding of medical device design, manufacturing processes, and regulatory requirements. Key… more
    Amgen (05/09/25)
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  • Engineer III - Combination Product…

    Takeda Pharmaceuticals (Lexington, MA)
    …relevant experience, Master's degree preferably within the biopharmaceutical industry or medical device development and commercialization is desired. + Hands ... releases. The ideal candidate will be a hands-on technical individual, providing project and engineering support in device and/or system identification,… more
    Takeda Pharmaceuticals (03/11/25)
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  • Sr. Engineer , Developer Productivity…

    Medtronic (Newton, MA)
    …well-versed in designing, implementing, and managing DevOps practices within the healthcare, medical device , or robotics software industry. This includes deep ... potential to work a hybrid schedule.** As a Sr. Engineer , you will play a pivotal role in accelerating...DevOps and cloud space, particularly those relevant to the medical device and healthcare sectors **Required Qualifications**… more
    Medtronic (04/12/25)
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  • Principal Systems Engineer

    ZOLL Medical Corporation (Chelmsford, MA)
    …devices. + Knowledge and experience developing products under FDA and European Community medical device regulations and standards. + Excellent verbal and written ... devices. + 7+ years' experience as a systems engineer , leading the architectural design and systems engineering of...and systems engineering of complex, real time embedded system medical devices. + Project management experience and… more
    ZOLL Medical Corporation (04/24/25)
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  • Electrical System Engineer (Teradyne, North…

    Teradyne (North Reading, MA)
    …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device more
    Teradyne (04/23/25)
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  • Imaging Service Engineer ( Medical

    Fujifilm (Boston, MA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... **Position Overview** An Imaging Service Engineer II is responsible for performing scheduled and...of this job: This position typically works in usual medical , clinical working environments, including sites under construction. **The… more
    Fujifilm (04/29/25)
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  • HTM Clinical Engineer 2

    Beth Israel Lahey Health (Charlestown, MA)
    …inclusion of terms for vendor compliance. + Assists with monitoring of medical device hazards/recalls and reports and ensures appropriate follow-up. Coordinates ... making a difference in people's lives.** The HTM Clinical Engineer II supports and advances patient care by applying...the internal and external medical device product recalls and alerts to… more
    Beth Israel Lahey Health (03/13/25)
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  • Staff Engineer , Software Design Quality

    Abbott (Burlington, MA)
    …of FDA regulations and guidance, ISO 13485, ISO 14971, Software Standards (eg, 62304), EU Medical Device Regulations and MDSAP + Experience with medical ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (03/08/25)
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  • Principal Software Engineer - Global IT…

    Medtronic (Boston, MA)
    …TO HAVE** (Preferred Qualifications) + Strongly Preferred: + Previous Healthcare or Medical Device experience + Strong experience building multi-platform mobile ... with FHIR and HL7v2 standards + Building software classified as Software as a Medical Device (SaMD) + Understanding of EHR technologies such as EPIC, Cerner,… more
    Medtronic (04/23/25)
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