• Quality Assurance Programmer/Analyst - Medical

    Techtronic Industries North America, Inc. (Anderson, SC)
    …Outlook, Teams, OneNote) required. + Experience interacting with Senior Management. + FDA 21 CFR 820 and ISO 13485 knowledge preferred. **OTHER REQUIREMENTS** + ... a plus + Experience with SAP a plus + Experience with CMM Manager a plus Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled We endeavor to make… more
    Techtronic Industries North America, Inc. (12/05/25)
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  • Kitting Specialist

    Caris Life Sciences (Phoenix, AZ)
    …hazardous materials. + Carry out tasks as assigned by the supervisor and /or manager . **Required Qualifications** + High school diploma or equivalent. + 1-2 years of ... various inventory transactions. + Experience working in a regulated GMP/ FDA regulated or diagnostic testing/ pharmaceutical (CAP/CLIA) organization and environment.… more
    Caris Life Sciences (12/05/25)
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  • Biostatistician

    Olympus Corporation of the Americas (Center Valley, PA)
    …+ Ensure compliance with regulatory standards relevant to medical devices (eg, FDA , EMA, PMDA), quality systems/SOPs, data integrity and audit readiness. + Lead ... 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 (12/05/25)
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  • Clinical Sciences Program Director

    University of Colorado (Aurora, CO)
    …administrative lead for clinical research. + Work with DFA, clinical research manager and clinical trials finance coordinator to monitor and execute finance duties ... tasks include local and central IRB submissions, maintaining clinical trial records, FDA submissions, and acting as a liaison between industry, grants and contracts,… more
    University of Colorado (12/04/25)
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  • Maintenance Technician

    BD (Becton, Dickinson and Company) (Grayson, GA)
    …to the maintenance department. + Knowledgeable and complies with requirements for GMPs, FDA , USDA, OSHA, EPA and ISO as related to maintenance functions. + Familiar ... technical information as needed. + Act as a backup for the Facilities Manager , as required **Physical Requirements:** + Heavy lifting and maneuvering of over 100… more
    BD (Becton, Dickinson and Company) (12/04/25)
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  • Clinical Research Budget Analyst

    University of Washington (Seattle, WA)
    …for a Clinical Research Budget Analyst (Budget Analyst). Reporting to the CTO Manager of Trial Start-up and Special Projects, the Budget Analyst position is ... and reputational risks by ensuring strict compliance with the CMS and the FDA regulations and guidelines. CTO Budget Analyst is a key position in maintaining… more
    University of Washington (12/03/25)
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  • Quality Supervisor

    Conagra Brands (Menomonie, WI)
    Reporting to the Quality manager at our Menomonie, WI facility, local producers of Swiss Miss and more, you will provide guidance, technical assistance, and ... (GMPs) and procedures, and HACCP plans + Understanding of government regulations ( FDA , USDA) Relocation assistance is available for this position. Preference will be… more
    Conagra Brands (12/03/25)
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  • Production Supervisor

    Danaher Corporation (Chaska, MN)
    …on strategic plans to achieve long-term objectives. This position reports to the Manager of Production Operations and is part of the Hardware Operations Leadership ... experience applying lean manufacturing principles (eg, Kaizen, 5S, Gemba). + Knowledge of FDA , QSR, ISO, or GMP compliance requirements. + Proven track record of… more
    Danaher Corporation (12/02/25)
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  • Union Utility Mechanic/Helper

    CBRE (Ridgefield, CT)
    …work on varied shifts. + Work under general supervision of the CBRE Sr. Account Manager at a GMP regulated facility maintaining FDA quality standards. + Document ... all work within a Computerized Maintenance Management System. + Assist licensed mechanics to maintain, adjust, and repair a variety of machines and equipment used to support building, manufacturing, and R&D operations. + Perform all work assigned within the… more
    CBRE (12/02/25)
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  • Senior Clinical Research Director, Rare

    Sanofi Group (Cambridge, MA)
    …Briefing regulatory documents, Common Technical Document for submission to regulatory bodies ( FDA , EMA, PMDA etc ) and answers to questions from health authorities. ... Collaborate on key medical and clinical questions with the Global feasibility manager to prepare and interpret feasibility and competitive intelligence results +… more
    Sanofi Group (12/02/25)
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