• Director, Product Master Data IT Applications

    Teleflex (Morrisville, NC)
    …medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in ... meeting project objectives * Strong communication skills * Experience in an FDA regulated environment preferred * Project Management and/or Lean Six Sigma… more
    Teleflex (07/09/25)
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  • Director Research and Software Engineering

    RELX INC (Raleigh, NC)
    …strategy. This role ensures compliance with industry regulations (such as GxP and FDA 21 CFR Part 11), oversees daily operations, drives software development best ... delivery. + Design and implement scalable prototypes with a focus on velocity, quality , and flexibility. + Lead and mentor a small team of engineers; establish… more
    RELX INC (06/25/25)
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  • Sr Mfg Equipment Maintenance Technician - Nights

    ThermoFisher Scientific (High Point, NC)
    …to create significant contributions to the world. A day in the Life: + Follow quality standards in accordance with company policy, cGMP and FDA requirements. + ... Assist in the installation and maintenance of utilities systems and equipment components for electrical power distribution, instrumentation and controls, electrical machinery, responsible for knowledge of codes and standards. + Perform preventive and… more
    ThermoFisher Scientific (06/13/25)
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  • Clinical Research Coordinator

    Alaka'ina Foundation Family of Companies (Camp Lejeune, NC)
    …compliance with medical requirements and professional standards in terms of quality and appropriateness. Independent judgment is exercised to determine appropriate ... policies and procedures concerning the conduct of clinical trials, including FDA Good Clinical Practice (GCP), International Council on Harmonization (ICH)… more
    Alaka'ina Foundation Family of Companies (06/07/25)
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  • Manufacturing Production Operator

    Catalent Pharma Solutions (Greenville, NC)
    …development. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent ... and logbook entries are accurately documented and compliant with SOPs and FDA cGMP guidelines. + Assist with setup, manufacturing, and changeovers with adherence… more
    Catalent Pharma Solutions (05/31/25)
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  • Phlebotomist

    CSL Plasma (Wilmington, NC)
    …donor disconnect. + In compliance with SOPs and Food & Drug Administration ( FDA ) guidelines, performs venipuncture on donors to begin pheresis process. + Evaluates ... necessary corrections in order to expedite donation time and ensure product quality and donor safety. Ensures donation process is efficient and makes adjustments… more
    CSL Plasma (05/30/25)
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