• Research Technician I

    Charles River Laboratories (Horsham, PA)
    …and overall well being. * Collect and record research data in compliance with Good Laboratory Practice Regulations (GLPs), study protocols and Standard Operating ... pertinent information. * Review documentation of functions performed as part of quality control requirements. * Retrieve and view Standard Operating Procedures using… more
    Charles River Laboratories (08/23/25)
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  • Engineer, Manufacturing, Sciences, and Technology

    Catalent Pharma Solutions (Greendale, IN)
    …Greendale, Indiana. Catalent is committed to a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer ... CMOs, or similar client-based environments is preferred. + Knowledge of GMPs, FDA regulations, and documentation procedures required. + Experience in quality more
    Catalent Pharma Solutions (08/23/25)
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  • Sr. R&D Software Engineer - Shockwave Medical

    J&J Family of Companies (Santa Clara, CA)
    …Functions** + Design and develop software for medical device product(s) in full compliance with the company's Design Control requirements and consistent with FDA ... for knowing and planning activities consistent with the company's quality policy and quality objectives. + Responsible for ensuring lab notebooks are documented… more
    J&J Family of Companies (08/23/25)
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  • Bioinformatician - Urology, Chan lab (onsite)

    Houston Methodist (Houston, TX)
    …bioinformatics pipelines, application or hardware related issues as they arise. ** QUALITY /SAFETY ESSENTIAL FUNCTIONS** + Maintains compliance with guidelines set ... for the medical directors. + Validates and performs audits of scheduled bioinformatics quality assurance tasks, including but not limited to new versions of publicly… more
    Houston Methodist (08/22/25)
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  • Plant Engineering Projects Leader

    Leprino Foods (Fort Morgan, CO)
    …improvements. + Supervise contractors and consulting services, inspecting completed work for quality and compliance . + Develop CAD designs and update mechanical, ... and technical drawings while ensuring they align with regulatory standards (OSHA, FDA , building codes). + Coordinate project work with production schedules to reduce… more
    Leprino Foods (08/22/25)
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  • Scientist I, Production

    Cole-Parmer (Raleigh, NC)
    …and troubleshooting abilities + Adherence to quality systems with special regard to FDA , ISO 13485 and GMP / OSHA compliance + QC testing of components ... as well as document generation and completion. Key Responsibilities: + Execution of quality system procedures + Proper execution of SOPs and work instructions for… more
    Cole-Parmer (08/20/25)
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  • Sr. Software Engineer

    Envista Holdings Corporation (Quakertown, PA)
    …and diverse mix of professionals spanning engineering, operations, regulatory and quality backgrounds that work collaboratively in the fast-paced medical device ... an Agile framework. + Assures that deliverables meet all relevant quality , safety, regulatory, serviceability, and reliability requirements. + Reviews code proposals… more
    Envista Holdings Corporation (08/20/25)
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  • Capital Project Engineering Management Expert

    Nestle (Solon, OH)
    …and feedback process for projects + Monitors processes for compliance with quality and GMP requirements in accordance with FDA and OSHA regulations + ... own initiative, without first questioning its impact in relation to product safety/ quality , people safety and the environment. No compromises will be tolerated… more
    Nestle (08/20/25)
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  • Transfusion Safety Officer

    Children's Hospital Boston (Boston, MA)
    …and clinical staff to enhance transfusion safety through education, audits, quality improvement, transfusion event review, and active surveillance of the blood ... and appropriate regulatory agencies. + Collaborates with physicians, nursing, and quality programs to ensure clinical policies and procedures are compliant with… more
    Children's Hospital Boston (08/20/25)
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  • Scientist, Cell Culture Process Development…

    Gilead Sciences, Inc. (Foster City, CA)
    …technology development and platform process evolution projects for increased productivity, high quality product, and speed to clinic. + Contribute to design of and ... + Author and review experimental protocols and reports. + Ensure high- quality , timely documentation in electronic laboratory notebooks and reports. + Contribute… more
    Gilead Sciences, Inc. (08/20/25)
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