• Mission Support and Test Services (North Las Vegas, NV)
    …MSTS offers our full-time employees highly competitive salaries and benefits packages including medical , dental, and vision; both a pension and a 401k; paid time off ... We are seeking a self-motivated Senior Engineer to serve as the Instrument & Control (I&C) Engineer who will participate in planning, specifying, scheduling,… more
    DirectEmployers Association (10/08/25)
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  • Merck & Co. (Rahway, NJ)
    …guidance & standards: 21 CFR Part 421 CFR 82021 CFR 210/ 211EU Medical Device RegulationUSP USP FDA Guidance for Industry, Container Closure Systems ... Human Factor Engineering, Manufacturing Processes, Mechanical Engineering, Mechanical Testing, Medical Device Quality Systems, Microscopies, Negotiation, Optical… more
    HireLifeScience (10/29/25)
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  • Terumo Medical Corporation (Elkton, MD)
    …(TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high-quality medical devices used in a broad range of applications for ... of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in...with FDA regulations, ISO standards, GMP requirements specific to medical devices and all national regulations. 2.… more
    DirectEmployers Association (08/13/25)
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  • Teradyne (Agoura Hills, CA)
    …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... and embedded algorithms for Digital, DC, AC & RF instrument calibration in the ATE equipment using C/C++/C# and...development of HW error budget and offline & online validation of these error terms using statistical analysis techniques… more
    DirectEmployers Association (09/11/25)
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  • Battelle Memorial Institute (Columbus, OH)
    instrument design. + Experience in reverse engineering, verification and validation , and/or device processing for fabrication of integrated circuits + ... security solutions ranging from design, verification, and testing of electronic devices , integrated circuits, and embedded systems. + Support semiconductor device more
    DirectEmployers Association (10/07/25)
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  • Teradyne (North Reading, MA)
    …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... products. This role will be instrumental in ensuring the validation of new designs and modification of existing designs...and have a strong background in system, sub-assembly, and instrument assembly. + Support the assembly and verification of… more
    DirectEmployers Association (10/25/25)
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  • Teradyne (Agoura Hills, CA)
    …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... the accuracy, reliability, and compliance of test equipment used in product validation and manufacturing environments. Leadership & Strategy + Lead a team of… more
    DirectEmployers Association (09/04/25)
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  • Instrument & Medical Device

    Cognizant (Highland Heights, KY)
    **About the role** As an ** Instrument & Medical Device Validation Specialist** , you will make an impact by ensuring software installed on laboratory ... validation test cases and protocols for instruments and medical devices . . Create infrastructure and data...considered:** . Extensive experience in instrument or medical device validation within a… more
    Cognizant (10/27/25)
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  • Instrument and Medical

    Cognizant (Highland Heights, KY)
    **About the role** As an ** Instrument / Medical Device Validation Specialist** , you will make an impact by ensuring software installed on laboratory ... you need to have to be considered** + 6-10+ years of experience in Instrument / Medical Device validation within a regulated (GxP) environment. + Strong… more
    Cognizant (10/16/25)
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  • Senior Validation Test Engineer…

    Cognizant (Highland Heights, KY)
    …accordance with EMA guidelines. The ideal candidate will have strong Instrument / Medical device validation experience and will be crucial to ensure ... years of extensive experience in instrument or medical device validation within a... validation test cases and protocols related to Instruments/ Medical devices validation . + Conduct… more
    Cognizant (10/17/25)
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  • Validation Specialist - Medical

    Cognizant (Highland Heights, KY)
    …**What you need to have to be considered** + 6-10+ years of experience in Instrument / Medical Device validation within a regulated (GxP) environment. + ... **About the role** As an ** Validation Specialist - Medical Devices...with EMA guidelines and IT SOPs in pharmaceutical or medical device settings. + Experience with risk… more
    Cognizant (10/16/25)
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  • Process Instrument Technician

    CBRE (Indianapolis, IN)
    …and DO2 Transmitters, Pressure and Temperature controllers, Delta V Foundation Field bus, Device Net, PLC controlled devices and all related data and ... Process Instrument Technician Job ID 237928 Posted 22-Oct-2025 Service...have a good understanding with the Installation/ Qualification and Validation processes and demonstrate good documentation skills and practices.… more
    CBRE (09/16/25)
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  • Verification and Validation Test Engineer

    DEKA Research & Development (Manchester, NH)
    …for a Verification and Validation Test Engineer to work in a dynamic medical device R&D environment. Test Engineering is a high-visibility role with a ... excellent verbal and written communication skills + Experience in medical devices , knowledge of FDA Quality System...Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience preferred About DEKA:… more
    DEKA Research & Development (10/30/25)
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  • Validation Analyst 2

    PCI Pharma Services (Rockford, IL)
    …**Process/Cleaning Validation Focus:** Background in Packaging, Pharmaceutical, Bio-Pharmaceutical, and/or Medical Devices . Must be able to properly gown and ... across our global network to pioneer and shape the future of PCI. The ** Validation Analyst II** is responsible for overall validation project ownership of… more
    PCI Pharma Services (08/09/25)
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  • AI Evaluation Engineer, Device Intelligence

    Danaher Corporation (Washington, DC)
    …especially for medical devices and AI/ML-based software as a medical device (SaMD). + Familiarity with quality management systems and standards relevant ... about the Danaher Business System which makes everything possible. The AI Evaluation Engineer, Device Intelligence will be a key member of the AI Product and Imaging… more
    Danaher Corporation (10/28/25)
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  • Associate Principal Scientist, Combination Product…

    Merck (Rahway, NJ)
    …& standards:** + 21 CFR Part 4 + 21 CFR 820 + 21 CFR 210/ 211 + EU Medical Device Regulation + USP <1> + USP <697> + FDA Guidance for Industry, Container Closure ... Human Factor Engineering, Manufacturing Processes, Mechanical Engineering, Mechanical Testing, Medical Device Quality Systems, Microscopies, Negotiation, Optical… more
    Merck (10/29/25)
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  • Medical Supply Technician (Sterile…

    Veterans Affairs, Veterans Health Administration (Albuquerque, NM)
    …the reprocessing of RME are responsible for knowing what reusable instruments, equipment, medical devices or supplies are used (inventory) in their clinical ... or sterilized according to the SOP and manufacturer's guidelines. Single-use (disposable) medical devices will not be reused or re-sterilized.All personnel must… more
    Veterans Affairs, Veterans Health Administration (10/16/25)
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  • Senior MDI System Administrator

    Novant Health (NC)
    …seeking a Senior MDI System Administrator to lead the operational management of our Medical Device Integration (MDI) systems. This role is critical to ensuring ... seamless data flow from biomedical devices and lab instruments into our electronic ...Epic, Cerner, or other EMR platforms. + Knowledge of medical device standards and regulatory compliance. +… more
    Novant Health (10/23/25)
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  • Laboratory Application Scientist

    Unither Pharmaceuticals (Rochester, NY)
    …needed Laboratory or analytical development experience in pharmaceutical manufacturing or medical device background required SPECIFIC SKILLS: Must have previous ... in cGMP environment Knowledge of LIMS use and development Strong knowledge in instrument and software validation Ability to evaluate data, perform trend… more
    Unither Pharmaceuticals (09/27/25)
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  • Director, Hardware and Systems Engineering (R&D)

    Hologic (San Diego, CA)
    …a leadership role requiring a proven level of technical expertise, ideally within Medical Device and Diagnostics space, and a successful cross-functional leader ... evaluation methods, labeling per 21 CFR 809). + Oversee instrument /cartridge verification and validation (including wet bench), environmental/EMC/safety… more
    Hologic (10/30/25)
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