• Senior Scientist, Drug/ Device Combo…

    Merck (Rahway, NJ)
    …+ Identify and implement process improvements by working collaboratively with device technical operations and manufacturing sites on existing and new ... **Job Description** As a Senior Engineer in Device Design and Process Development group,...ISO 14971 etc.) and industry standards related to medical device manufacturing is a plus. + Prior… more
    Merck (07/22/25)
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  • Associate Director, Device Technology

    Merck (Rahway, NJ)
    …Products, Device Development, Drug Delivery, Injection Moldings, Management Process , Manufacturing Compliance, Medical Devices, Product ... in injection molding, automation, complex assembly and packaging operations for medical device or combination product component manufacturing , with… more
    Merck (08/08/25)
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  • Distinguished Scientist, Device Tech & Eng…

    Merck (Rahway, NJ)
    **Job Description** Our company's Device Product & Process Development (DPPD) Team within our Device Development & Technology (DD&T) organization ... subject-matter expertise and knowledge of product and process development in the (bio)pharmaceutical and medical device...individual will be expected to apply their knowledge of product design and development, manufacturing process… more
    Merck (07/29/25)
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  • Device Development Associate Principal…

    Merck (Rahway, NJ)
    …**Job description** This position will be responsible for leading and implementing medical device and combination product design controls for both new products ... 5 years related experience + Experience with the development drug- device combination product or a medical ...inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here… more
    Merck (07/31/25)
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  • Senior Quality Engineer I - Medical Device…

    Integra LifeSciences (Plainsboro, NJ)
    …updated Quality System procedures for ISO/QSR, such as validation protocols, manufacturing procedures, product & material specifications, design & development ... updated Quality System procedures for ISO/QSR, such as validation protocols, manufacturing procedures, product & material specifications, design & development… more
    Integra LifeSciences (06/16/25)
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  • Senior Counsel (Medical Device )

    Fujifilm (Trenton, NJ)
    …integral part of the legal team providing support to the Medical Device businesses of FUJIFILM Healthcare Americas Corporation and FUJIFILM SonoSite, Inc., ... for working independently and collaboratively on legal issues affecting the Medical Device businesses to minimize risks of legal liability and ensure maximum legal… more
    Fujifilm (08/08/25)
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  • Sr Staff Scientist - Medical Device

    Astrix Technology (Essex County, NJ)
    …IVF Media solutions. + Provide biological risk assessments and technical support to manufacturing teams for process development and optimization. + Manage R&D ... **Sr Staff Scientist - Medical Device ** Science & Research Essex County, NJ, US...This high-impact, visible role is key to driving innovation, product improvements, and global expansion within the Life Sciences… more
    Astrix Technology (05/28/25)
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  • Medical Device , Endoscope Repair…

    Pentax Medical (Montvale, NJ)
    …CLINICALLY RELEVANT INNOVATION, and SIMPLICITY. Through leading edge R&D and manufacturing , PENTAX Medical provides endoscopic imaging devices and solutions to the ... global medical community. Position Opening: Medical Device , Endoscope Inspection Technician Why JOIN Us? We are...+ Proper use of microscope + Understand the repair process on endoscopes + Maintain knowledge and understanding of… more
    Pentax Medical (07/18/25)
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  • Associate Director, External Manufacturing…

    Merck (Rahway, NJ)
    …Partner Site Readiness, Assist with Technology Transfer, Develop and Execute Manufacturing Process Robustness Plans, Production Oversight. Minimum Education ... Operations will also assist in commercialization activities for New Product Introductions that require complex devices and other novel...manufacturing for MDCP (21 CFR Part 4, Medical Device Reporting, ISO 13485:2016, EU Medical Device … more
    Merck (05/19/25)
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  • Lead, Cleanroom Manufacturing Operator

    Integra LifeSciences (Plainsboro, NJ)
    …production schedule, available resources, and department priorities. Engage and support manufacturing process to assure timely completion and quality throughput. ... suite. + Actively engage in all areas of the manufacturing process . + Identify and resolve training...years of chemical processing experience or batch mixing in manufacturing environment in the Medical Device or… more
    Integra LifeSciences (07/28/25)
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