• Engineering Manager (Silicon Photonics 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 ... oversee the design, development, and implementation of advanced test systems, ensuring high- quality and innovative solutions that meet the needs of our customers.… more
    Teradyne (07/24/25)
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  • Senior Software Engineer

    Candela Corporation (Marlborough, MA)
    …and/or commercialization of. These programs are supported by Candela's global clinical, regulatory , and quality teams and are managed through our Product ... MA** State/Territory **Massachusetts** Candela Corporation is a leading global aesthetic device company with a comprehensive product portfolio and a global… more
    Candela Corporation (07/01/25)
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  • CGMP Manufacturing Operator

    Aerotek (Fall River, MA)
    …assigned. **Essential Skills** + Experience with cGMP is required. + Experience in medical device or pharmaceutical industry. + Experience in machine operation ... activities in each area. + Adhere to all cGMPs, compliance/ regulatory mandates, and quality requirements. + Wear...a Cleanroom Assembler or Operator. + Experience as a Medical Device Assembler or Operator. + Ability… more
    Aerotek (08/09/25)
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  • Optical Calibration Engineer (SiPh Test Solutions,…

    Teradyne (North Reading, MA)
    …and enforce quality assurance protocols to meet industry standards and regulatory requirements. + Training: Provide training and guidance to technical staff on ... powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device more
    Teradyne (07/31/25)
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  • Facilities Manager (R&D Site)

    Mentor Technical Group (Boston, MA)
    …the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, ... programs. + Conduct routine safety observations to ensure compliance with regulatory agencies, company environmental, health, and safety policies, procedures and… more
    Mentor Technical Group (06/10/25)
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  • Principal Software Project Manager

    Medtronic (Boston, MA)
    …execute concurrent, interdependent projects. + Knowledge of medical device R&D, product development, and clinical/ regulatory procedures; including ... charge in ensuring customer satisfaction design integrity, and impeccable quality across each milestone. Join our esteemed team as...as a Subject Matter Expert + Comprehensive knowledge of medical device standards and regulations (eg, IEC… more
    Medtronic (07/29/25)
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  • Digital Biomarker Innovation Clinical Lead

    Sanofi Group (Cambridge, MA)
    …will design and lead exploratory studies, early data generation and device evaluation programs to foster high-confidence, high-value digital biomarker (DBM) ... develop research hypotheses grounded in clinical relevance, then design high- quality experiments to inform patient-centric decisions + Deliver scientific leadership… more
    Sanofi Group (07/22/25)
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  • Lead Product Security Engineer (R&D Cytology)

    Hologic (Marlborough, MA)
    …department in our Diagnostics division is looking for a Security Engineer experienced in medical device and/or instruments security and systems to join our team, ... architecture diagrams. + Collaborate with cross-functional teams (Product Engineering, DevSecOps, Regulatory , Quality ) to integrate security into the product… more
    Hologic (07/12/25)
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  • Sr Product Development Engineer

    J&J Family of Companies (Danvers, MA)
    …degree, or demonstrated ability with a Master's degree. + Thorough understanding of Medical Device Design Controls and Product Life cycle + Knowledge of ... test protocols, reports, and engineering rationales to support both quality and regulatory documentation. + Develop Test...Suite. **Preferred:** + Product development experience in Class 3 Medical Device engineering + MSc/MEng Preferred +… more
    J&J Family of Companies (07/31/25)
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  • Business Development Mgr, ESD (East Coast)

    Fujifilm (Boston, MA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... with a Master's degree. + Minimum 8 years of medical device industry experience in a clinical...evolving situations and needs + Strong commitment to delivering high- quality work and upholding HCUS values. + Proficiency in… more
    Fujifilm (07/24/25)
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