• Phlebotomist II

    Kedplasma (El Paso, TX)
    …within the scope of EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Responsible for performing venipuncture on donors ... within the scope of EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR. **MAIN DUTIES AND RESPONSIBILITIES** **Core** + Self-introduction to donors… more
    Kedplasma (08/25/25)
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  • Operations Supervisor

    Biomat USA, Inc. (San Antonio, TX)
    …employees and supervise donor flow. * Learn and maintain thorough familiarity and compliance with all state and federal regulations, US Food and Drug Administration ... ( FDA )-approved Standard Operating Procedure Manual, Occupational Safety and Health...standards in accordance with Federal and State regulations, with FDA approved Standard Operating Procedure Manual, OSHA, CLIA and… more
    Biomat USA, Inc. (08/23/25)
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  • Senior Medical Science Liaison Genitourinary…

    Bayer (Dallas, TX)
    …Medical Inquires in collaboration with Medical Communications; + Adherence to SOP and FDA guidance for distribution of scientific information; + Adherence to SOP and ... compliance guidelines for all external contacts; + Prepares and...GI Oncology and Precision Medicine + Working knowledge of FDA , OIG requirements; + A minimum of 1 year… more
    Bayer (08/14/25)
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  • Plasma Center Manager

    Biomat USA, Inc. (Corpus Christi, TX)
    …campaigns to attract and retain donors. * Maintains thorough familiarity and ensures compliance with state and federal regulations, US Food and Drug Administration ( ... FDA )-approved Standard Operating Procedures, Occupational Safety and Health Administration...state and federal regulations, US Food and Drug Administration ( FDA )-approved Standard Operating Procedures, Occupational Safety and Health Administration… more
    Biomat USA, Inc. (08/08/25)
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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 ... performance metrics; to include labor, equipment uptime, preventive maintenance compliance , MTTR, MTBF, part usage, etc. **QUALIFICATIONS:** **Experience** Required… more
    Sysco (08/01/25)
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  • Global Support Engineer II - Surgical Robotics

    Medtronic (Dallas, TX)
    …as assigned/requested by management + All activities must be performed in compliance with the Quality System + Travel requirement (international possible): 20-40% ... in the operating room, so healthcare/surgical setting experience + Familiarity with FDA product requirements and regulatory guidelines + Experience with robotics or… more
    Medtronic (08/01/25)
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  • Assistant Professor, Clinical Faculty Appointment…

    MD Anderson Cancer Center (Houston, TX)
    …Center and/or other Houston area locations for clinical service. Administrative . Must assure compliance with standards of CAP, JCAHO, FDA , Medicare, and CLIA. . ... that the laboratory in which he/she is working complies with the CAP, JCAHO, FDA , Medicare, and CLIA regulations for accreditation. . Must be able to identify and… more
    MD Anderson Cancer Center (07/11/25)
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  • BioPharmaceutical Account Manager - Dallas East

    Lundbeck (Longview, TX)
    …including the full range of treatment options available. **Pharmaceutical Environment/ Compliance ** - Ability to apply knowledge of pharmaceutical and regulatory ... environment, including Lundbeck policies and procedures and FDA regulations regarding the promotion of pharmaceutical and medical products. Ability to apply… more
    Lundbeck (07/08/25)
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  • Field Customer Support Specialist I

    Charles River Laboratories (Houston, TX)
    …customer training, and product validations. * Responsible for completing all service and compliance documentation as required by company policy, cGMP and FDA . * ... proudly supported the development of ~85% of the drugs approved by the FDA in 2019. Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity… more
    Charles River Laboratories (06/28/25)
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  • Advanced Quality Assurance Specialist - Supplier…

    Bio-Techne (Austin, TX)
    …quality and regulatory standards. **Key Responsibilities:** Provides support ensuring compliance with all regulatory standards, systems, procedures, and practices. ... Includes ISO 13485, FDA QSR, MDSAP, IVDR, and other requirements relating to...+ Knowledge of cGMP, ISO 13485, MDSAP, IVDD/IVDR and FDA QSR preferred. **Why Join Bio-Techne:** **We offer competitive… more
    Bio-Techne (06/19/25)
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