• Sr. Manufacturing Design Engineer

    Actalent (Waltham, MA)
    …testing, process validation, and transfer to manufacturing within a regulated medical device development environment. Key Responsibilities: + Serve as a key team ... maintenance. + Perform fixture qualifications and verifications in collaboration with Quality and Manufacturing Engineering. + Support the development of assembly… more
    Actalent (04/23/25)
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  • Regulatory Affairs Program Manager

    Philips (Cambridge, MA)
    …Manager will play a critical role within Philips Patient Safety & Quality Organization, responsible for enhancing tracking and controlling systems to optimize ... systems and processes to ensure accurate and timely compliance of global Unique Device Identification (UDI) requirements. **Your role:** + Serves as a key liaison… more
    Philips (04/16/25)
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  • Distribution Protection Engineer

    Leidos (Framingham, MA)
    …challenging substation engineering problems. + Work with design engineers and perform quality reviews. + Collaborate directly with clients and other staff in remote ... + Determine appropriate conductor types, sizes, transformer sizes, and equipment applications . + Specify relay settings, fuse sizes, trip saver settings, and… more
    Leidos (02/14/25)
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  • Engineering Manager

    Dentsply Sirona (Waltham, MA)
    …frontend applications with Flutter a big plus. + Experience in the medical device software industry is a plus. Key Skills, Knowledge & Capabilities: + Strong ... portfolio of world class brands. Dentsply Sirona's products provide innovative, high- quality and effective solutions to advance patient care and deliver better… more
    Dentsply Sirona (04/01/25)
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  • Associate Director, Promotion Compliance

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …context required of promotional labeling materials for prescription drug and medical device products. Must be effective in managing work and resolving conflicts. ... context required of promotional labeling materials for prescription drug and medical device products. Must be effective in managing work and resolving conflicts.… more
    Otsuka America Pharmaceutical Inc. (04/17/25)
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  • Optical Calibration Engineer (SiPh Test Solutions,…

    Teradyne (North Reading, MA)
    …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... Teradyne (http://www.teradyne.com/) companies deliver manufacturing automation across industries and applications around the world! We attract, develop, and retain a… more
    Teradyne (05/01/25)
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  • Manager, Optical Instrumentation (SiPh Test…

    Teradyne (North Reading, MA)
    …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... Teradyne (http://www.teradyne.com/) companies deliver manufacturing automation across industries and applications around the world! We attract, develop, and retain a… more
    Teradyne (05/01/25)
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  • Front-End Developer (Data V)

    Harvard University (Cambridge, MA)
    68164BRAuto req ID:68164BRJob Code:I0757P Applications Professional III Department Office Location:USA - MA - Cambridge Business Title:Front-End Developer (Data ... + At least 2-3 years of professional experience developing web applications using React, Angular or similar frameworks + Demonstrated experience using… more
    Harvard University (04/12/25)
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  • Product Safety & Risk Engineering Expert

    Philips (Cambridge, MA)
    …strong knowledge in Risk Analysis Methodology (eg, FMEA, FTA, PHA). Knowledge/experience in Software as a Medical Device (SaMD), Model Based Systems Engineering ... Monitoring Systems/Products are safe, reliable, and compliant with all applicable regulatory/ quality standards. **Your role:** + Will guide and facilitate safety… more
    Philips (04/23/25)
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  • Sr Manufacturing Fixture Design Engineer

    Actalent (Newton, MA)
    …testing, process validation, and transfer to manufacturing within a regulated medical device development environment is essential. Responsibilities + Be a key team ... documentation + Perform fixture qualifications and verifications in conjunction with Quality and Manufacturing Engineering + Support the development of assembly and… more
    Actalent (04/26/25)
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