• Medical Devices, Regulatory Specialist

    Meta (New York, NY)
    …team. You will get to work on wearables and Software as a Medical Device (SaMD) applications for the US and worldwide approvals.You will work on cutting-edge ... equivalent work experience 6. 3+ years of industry experience in medical device regulatory affairs or related industry 7. Experience working with minimal supervision… more
    Meta (07/10/25)
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  • Desktop Support Manager

    PSEG Long Island (Bethpage, NY)
    …all End User related products and services, including End User device support, software deployment, ticket processing, Identity Access Management, and collaboration ... of key processes, systems, tools, and best practices in end user device management, IT service management and collaboration tools * Knowledge of desktop,… more
    PSEG Long Island (07/02/25)
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  • Phadv I Screening /Optical

    City of New York (New York, NY)
    …to Regional Supervisor. - Import class lists/biographical information to Spot autorefractor device from ASHR. Provide vision screenings, using the Spot device . ... automated student health record). Export screening data from Spot device to ASHR. - Other duties as assigned by...accommodation to participate in the job application or interview process , contact Sye-Eun Ahn, Director of the Office of… more
    City of New York (06/29/25)
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  • Assistant General Counsel, Regulatory

    Cardinal Health (Albany, NY)
    …(EPR) regulations; and other product-specific environmental / sustainability drug and device lifecycle obligations and stewardship programs. This role will also ... color additive legislation and regulations, and EPR and other drug and device stewardship programs. This entails working with multiple business leaders across the… more
    Cardinal Health (06/18/25)
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  • Senior Staff GMP Internal Auditor

    Regeneron Pharmaceuticals (Troy, NY)
    …both drug substance manufacturing and aseptic filling, primary packaging and labeling, device assembly, and serialization operations. As a GMP Internal Auditor, a ... BS/BA and + Staff: 10+ years of related experience in Med Device /Biotech/Pharmaceutical industry + Senior Staff: 12+ years of related experience in… more
    Regeneron Pharmaceuticals (06/15/25)
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  • goodr Merchandiser - $20/hr

    ThirdChannel (Rochester, NY)
    …and after photos and written summaries, using ThirdChannel app on a smart device + Improve brand visibility and presentation for goodr products. + Ensure ... visit summary notes using our app on your smart device . (iOS version 15.0, Android version 10.0 or above)...DETAILS + Immediate start date upon completion of certification process + Brand Rep certification must be completed before… more
    ThirdChannel (05/21/25)
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  • Test Engineering Manager

    Data Device Corporation (Bohemia, NY)
    …Manager Department:Manufacturing Engineering Location:Bohemia, NY For more than 60 years,Data Device Corporation (DDC)has been recognized as a world leader in the ... individual will play a pivotal role in driving test engineering and process improvements, optimizing designs, and supporting production operations, directing a team… more
    Data Device Corporation (07/31/25)
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  • Manufacturing Software Validation Engineer

    Adecco US, Inc. (Buffalo, NY)
    …is to evaluate computerized systems based on applicability, functionality, and process and product safety. They will support management and maintenance of ... support to all Company Product Facilities in the Computerized System Validation Process . **Job Duties** + Implements and analyzes the applicability of the different… more
    Adecco US, Inc. (07/26/25)
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  • Software Validation Engineer

    Harmac Medical Products (Buffalo, NY)
    …is to evaluate computerized systems based on applicability, functionality, and process and product safety. They will support management and maintenance of ... support to all Harmac Medical Product Facilities in the Computerized System Validation Process . This is a full time, salaried (exempt) position. This is a HYBRID… more
    Harmac Medical Products (07/24/25)
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  • UL - Quality Systems Engineer

    Ultralife Corporation (Newark, NY)
    …investigation and response through the Return Material Authorization (RMA) process . Collaborate with manufacturing and product engineers on failure analysis. ... release processes for finished goods. + Monitor, support and promote process validation activities for new product introductions and current manufacturing… more
    Ultralife Corporation (07/31/25)
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