• Multi-Specialty Account Manager

    Lundbeck (Waco, TX)
    …(IDNs, Medicare, Medicaid, Commercial) using Lundbeck resources. **Pharmaceutical Environment/ Compliance ** - Apply knowledge of pharmaceutical and regulatory ... Multi-Specialty Account Manager - Waco, TX Requisition ID: 6706 Location: Waco,...accountability and adherence to Lundbeck policies and procedures and FDA regulations regarding the promotion of pharmaceutical and medical… more
    Lundbeck (07/29/25)
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  • Engineering Manager II

    Abbott (Austin, TX)
    …and vendors. + Develops and implements engineering systems and procedures to ensure compliance with FDA , GMP, and other applicable regulations. + Ensures a ... overseeing engineering processes to ensure strict adherence to quality and regulatory standards, while guiding a diverse team toward achieving operational… more
    Abbott (06/13/25)
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  • Senior cGMP Specialist - Cyclotron

    Houston Methodist (Houston, TX)
    …service focus and application of positive language principles + Familiar with quality, compliance and FDA regulatory requirements for Good Laboratory ... and meet quality requirements. + Conducts internal inspections and audits to ensure compliance with Federal Drug Administration ( FDA ) regulations and cGMP Core… more
    Houston Methodist (08/13/25)
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  • Quality Specialist

    CSL Plasma (Port Arthur, TX)
    …role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and ... facility compliance with CSL procedures and policies, cGMP, OHSA, FDA , and other regulations, as applicable, and develop center responses for deficiencies.… more
    CSL Plasma (08/09/25)
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  • Production Lead

    Kedplasma (Pharr, TX)
    …center activities with SOPs and other company standards and protocols to meet the regulatory requirements of the FDA , EMEA, customer specifications and other ... compliant plasma collections under the direction of the Center Manager . Operates within the scope of EU Guidance on...scope of EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has… more
    Kedplasma (07/04/25)
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  • Senior Operations Supervisor

    Biomat USA, Inc. (Odessa, TX)
    …the daily activities of donor floor operations, supervising staff, and supporting compliance with regulatory and quality standards. The Senior Operations ... of operational priorities, and provides direct support to the Center Manager in driving performance, donor satisfaction, and continuous improvement. **Primary… more
    Biomat USA, Inc. (08/16/25)
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  • Sr. Operations Supervisor - Houston - Bellfort

    Biomat USA, Inc. (Houston, TX)
    …the daily activities of donor floor operations, supervising staff, and supporting compliance with regulatory and quality standards. The Senior Operations ... of operational priorities, and provides direct support to the Center Manager in driving performance, donor satisfaction, and continuous improvement. **Primary… more
    Biomat USA, Inc. (08/08/25)
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  • Medical Screener

    Kedplasma (San Antonio, TX)
    …procedure and plasma collection, including donor set-up, monitoring and disconnect in compliance with Standard Procedures and FDA guidelines, as needed. + ... and screening donors under the direction of the Center Manager . Operates within the scope of EU Guidance on...scope of EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has… more
    Kedplasma (08/15/25)
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  • Phlebotomist II

    Kedplasma (El Paso, TX)
    …of the donor during the plasmapheresis process under the direction of the Center Manager . Operates within the scope of EU Guidance on Good Manufacturing Practice and ... FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Responsible for performing...the plasmapheresis process under the direction of the Center Manager . Operates within the scope of EU Guidance on… more
    Kedplasma (08/21/25)
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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 ... by management + All activities must be performed in compliance with the Quality System + Travel requirement (international...understand schematics and engineering drawings + Familiar with the FDA 21 CFR, CGMP for Medical devices + Demonstrable… more
    Medtronic (08/01/25)
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