• Medical Technologist

    UnityPoint Health (Sioux City, IA)
    …of conditions of any test or instrument, and equipment recalls from the FDA or the vendor. + Identifies and coordinates the requirements for the preventative ... with the Lawson requestors, UPH Supply Department, vendors, and the Technical Lab Manager to develop a process for an organized and cost effective supply ordering… more
    UnityPoint Health (01/06/26)
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  • Principal Engineer, Design Quality - Software

    Olympus Corporation of the Americas (Westborough, MA)
    …Affairs' efforts in creating submission materials for various regulatory domains including FDA , PMDA, and EU-MDR. **Job Duties** + Advise SW development teams on ... disability impairs your ability to email, you may call our HR Compliance Manager at 1-888-Olympus (###). **Let's realize your potential, together.** It is the policy… more
    Olympus Corporation of the Americas (01/06/26)
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  • Automation Engineer II

    Fresenius Medical Center (Ogden, UT)
    …effectively integrate automation/process re-designs, while ensuring compliance with generally accepted FDA and cGMP standards. + Lead change agent and the deployment ... with higher level problems that may arise. + Escalates issues to supervisor/ manager for resolution, as deemed necessary. + Assists with various projects as… more
    Fresenius Medical Center (01/06/26)
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  • Quality Coordinator

    ADM (Columbus, NE)
    …management. The Coordinator working with the Quality Superintendent and Quality Manager will delegate workload to other team members as needed and ... as needed, including shift coverage. + Maintains awareness of and adheres to all FDA , GMP, BATF, EPA, OSHA, and employer standards and guidelines; serving as an… more
    ADM (01/06/26)
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  • Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …grant proposals, and presentations. Works closely with the Principal Investigator, manager , and study team to address study needs, implement approved changes, ... in patient safety and protocol compliance. Adhere to all University of Pennsylvania, FDA and GCP guidelines. In addition to the responsibilities mentioned above, a… more
    University of Pennsylvania (01/06/26)
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  • Manufacturing Operator I/II (2nd shift)

    Novo Nordisk (Durham, NC)
    …shift will include a 10% shift differential** Relationships Reports to Shift Manager . Essential Functions + Setup, operate, monitor & control equipment, systems & ... one (1) year of experience in pharmaceutical solid dose manufacturing or other FDA regulated industry preferred + Ability to read, write & understand complicated… more
    Novo Nordisk (01/06/26)
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  • Engineer III, QA

    ThermoFisher Scientific (Rochester, NY)
    …internal, customer, and regulatory requirements. Under the direction of the Senior Manager , Quality Assurance this position is responsible for executing the customer ... Science or Engineering Degree preferred. + Working experience in a regulated ( FDA Quality System Regulations (21 CFR Part 820)) and certified International… more
    ThermoFisher Scientific (01/06/26)
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  • Senior Technical Support Engineer, MI - I

    Fujifilm (Little Rock, AR)
    …engineers. + Maintains a high level of success with yearly goals provided by your manager and metrics defined on a team level. + Working outside of normal business ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
    Fujifilm (01/05/26)
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  • Manufacturing Technician

    Mirion Technologies (Melbourne, FL)
    …environment. * Able to work overtime as required. * Experience in an ISO/ FDA /FAA work environment. * Flexible with work assignments. * Other duties as assigned ... by the team leader/ manager . Must demonstrate strong decision-making and leadership skills. * Experience in handling delicate components using ESD practices. * Must… more
    Mirion Technologies (01/04/26)
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  • Senior Analyst Internal Controls - SOX…

    Charles River Laboratories (Wilmington, MA)
    …or international travel is possible. ESSENTIAL RESPONSIBILITIES INCLUDE: * Work with Manager and team in facilitating the SOX 404 Program including scoping, setting ... worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that elevate your… more
    Charles River Laboratories (01/03/26)
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