• Software Quality Engineer - Automation Engineer…

    Teradyne (North Reading, MA)
    …all testing outcomes align with project requirements. + Interact closely with product managers, development teams, and QE colleagues to understand project ... powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your ...and product testing objectives. + Collect, analyze, and interpret test… more
    Teradyne (08/23/25)
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  • EMC Test Engineer (Semi Test Engineering; North…

    Teradyne (North Reading, MA)
    …support to drive EMC/EMI compliance projects across engineering teams throughout the product development lifecycle. + Ability to support and maintain Teradyne ... powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your ... Product EMC Certification to current requirements by performing EMC… more
    Teradyne (08/13/25)
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  • Quality Engineering Manager (On-Site)

    embecta (Holdrege, NE)
    …Assurance, Mathematics/Statistical or Science related field required + 3+ years in Medical Device /Pharma Manufacturing, Validation, PFMEA + 1+ years management ... plant are established and documented to provide a safe and effective product . Build sound technical and organizational competence within area of responsibility.… more
    embecta (08/08/25)
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  • Sr. Supplier Quality Engineer (ASIC), Project…

    Amazon (Redmond, WA)
    …US as a refugee or granted asylum. A day in the life - Collaborates with product development teams as owner of ASIC quality system requirements - Acts with ... Kuiper's quality system to ensure early detection of process excursions improving product reliability and wafer yields in volume manufacturing - Test and inspection… more
    Amazon (07/25/25)
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  • Remote Account Manager - Endoscopy

    Medtronic (Duluth, GA)
    …+ Bachelor's Degree with emphasis in Life Sciences, Medicine, or Business preferred + Medical device experience + Experience working in SFDC + Experience selling ... in a defined geographic area. The RAM will serve as a customer facing product expert responsible for educating physicians and nurses on the clinical advantages of… more
    Medtronic (09/22/25)
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  • Engineer I - Shift 1

    US Tech Solutions (Southington, CT)
    …in the manufacture of medical devices industry or combination of medical device or pharmaceutical industry. **Responsibilities:** * This includes writing and ... Development Plans and project plan schedules for each product family to be changed. * Overseeing Artwork Change...Development Pan) and any associated Validations for this Medical Packaging name change. * Coordinating with additional site… more
    US Tech Solutions (07/08/25)
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  • Director, Scientific Publications

    Organon & Co. (Plymouth Meeting, PA)
    …Director will support all aspects of global biomedical publications development , with minimal supervision. **Responsibilities** + Lead the end-to-end publications ... development align to therapeutic area strategy across the portfolio...strategic, value driven publications for small molecule, biologic and device assets from pipeline to market. + Establishes credibility… more
    Organon & Co. (09/04/25)
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  • Associate or Area Manager (Chicago, IL) - Johnson…

    J&J Family of Companies (Chicago, IL)
    …in assigned territory. Requirements + A minimum of 5+ years' experience in cardiovascular medical device sales. + Proven track record of selling into a Cath ... in accordance with all state and federal laws and regulations governing the medical device industry. Preferred + Bachelors degree preferred or 10 years… more
    J&J Family of Companies (09/20/25)
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  • Project Manager-HealthCast

    Medtronic (Lafayette, CO)
    …leverages cross functional teams to evaluate, develop and manage projects for new product development and ongoing lifecycle management of products, processes and ... planning, project team, and line management. + Manages the development and implementation process of a company's products and...management experience. Nice to Have: + 10+ years of medical device software project management experience with… more
    Medtronic (09/18/25)
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  • Quality Systems Manager

    PCI Pharma Services (Philadelphia, PA)
    …requiring systemic solutions + Ensure compliance with FDA regulations, ISO 13485, Medical Device Directive, and other applicable standards and regulations ... Demonstrated expertise in quality management systems and regulatory requirements (FDA, ISO 13485, Medical Device Directive) + Strong knowledge of cGMP and other… more
    PCI Pharma Services (09/16/25)
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