• PhD Research Associate - Emergency Medicine

    Integrative Emergency Services (Fort Worth, TX)
    …implementation programs; thorough knowledge of Good Clinical Practice Guidelines and FDA guidance Preferred: + Doctoral degree in epidemiology, biostatistics, health ... implementation programs; thorough knowledge of Good Clinical Practice Guidelines and FDA guidance PHYSICAL DEMANDS: The physical demands described here are… more
    Integrative Emergency Services (08/09/25)
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  • Sr. Operations Supervisor - Houston - Bellfort

    Biomat USA, Inc. (Houston, TX)
    …all state and federal regulations, US Food and Drug Administration ( FDA )-approved Standard Operating Procedure Manual, Occupational Safety and Health Administration ... highest production standards in accordance with Federal and State regulations, with FDA approved Standard Operating Procedure Manual, OSHA, CLIA and cGMP. + Attends… more
    Biomat USA, Inc. (08/08/25)
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  • Research Patient Care Assistant - Baytown

    Houston Methodist (Houston, TX)
    …meets appropriate Institutional Review Board (IRB), Federal Drug Administration ( FDA ), Institutional Council of Harmonization (ICH)/Good Clinical Practice (GCP), and ... conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than 1,387 clinical research… more
    Houston Methodist (08/08/25)
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  • Plasma Center Manager

    Biomat USA, Inc. (Corpus Christi, TX)
    …state and federal regulations, US Food and Drug Administration ( FDA )-approved Standard Operating Procedures, Occupational Safety and Health Administration (OSHA), ... state and federal regulations, US Food and Drug Administration ( FDA )-approved Standard Operating Procedures, Occupational Safety and Health Administration (OSHA),… more
    Biomat USA, Inc. (08/08/25)
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  • GMP Cleaning Manager

    ABM Industries (Houston, TX)
    …services, cleaning operations, and contract management, ensuring compliance with ISO, FDA , cGMP, and cleanroom standards. A strong, process-driven leader, the ... Experience with P&L analysis and financial reporting. + Familiarity with ISO, FDA , cGMP, and cleanroom operations. **Skills & Competencies:** + Self-starter with… more
    ABM Industries (08/07/25)
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  • Production Maintenance Technician III

    Sysco (Dallas, TX)
    …and industry standard safety policies and procedures - OSHA, NEC, NFPA, USDA, FDA , etc. Recognize, escalate, and action unsafe work conditions and engages with ... space, etc. Experience working in a food processing environment and familiar with USDA, FDA , and SQF policies and procedures Preferred + 1 year experience in a… more
    Sysco (08/01/25)
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  • Global Support Engineer II - Surgical Robotics

    Medtronic (Dallas, TX)
    …in the operating room, so healthcare/surgical setting experience + Familiarity with FDA product requirements and regulatory guidelines + Experience with robotics or ... Ability to read and understand schematics and engineering drawings + Familiar with the FDA 21 CFR, CGMP for Medical devices + Demonstrable skills in Microsoft Office… more
    Medtronic (08/01/25)
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  • QA Manager

    Kedplasma (Houston, TX)
    …Operates within the scope of EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has been made to make ... other Company standards and protocols to meet regulatory requirements of the FDA , EMEA, Customer Specifications, and other regulatory bodies, as required. . Ensures… more
    Kedplasma (07/26/25)
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  • Sr. Applications Support Specialist

    Fujifilm (Austin, TX)
    …when Fuji Dictation software is utilized. + Maintains a clear understanding of FDA requirements and ACR recommendation as well as local state regulations for ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
    Fujifilm (07/24/25)
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  • Research Coordinator II

    Houston Methodist (Houston, TX)
    …cellular therapies. The Expanded access program is a potential pathway from the FDA for a patient with a serious or immediately life-threatening disease or condition ... conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than 1,387 clinical research… more
    Houston Methodist (07/22/25)
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