• Eisai, Inc (NJ)
    …provider business relationships in alignment with global strategies.Review and approve Clinical Quality Assurance audit plans and reports.Review and respond to ... procurement experience, minimum 7 years pharmaceutical/clinical outsourcing.In-depth understanding of GCP / GLP guidelines, audit processes and agency regulatory… more
    HireLifeScience (04/26/24)
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  • Good Clinical Practice ( GCP ) Senior…

    GE HealthCare (Boston, MA)
    **Job Description Summary** The Good Clinical Practice ( GCP ) Senior Quality Assurance ( QA ) Auditor is crucial in ensuring that clinical trials are ... of quality assurance processes. + Quality Metrics and Reporting: QA Auditors may...system (QMS) improvements. + Overall, the role of a GCP Quality Assurance Auditor is… more
    GE HealthCare (05/06/24)
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  • Global Compliance Quality Assurance

    GE HealthCare (IN)
    …adaptation of quality assurance processes + Overall, the role of a GCP Quality Assurance Oversight Team Leader is critical for maintaining the ... **Job Description Summary** The Global Compliance Quality Assurance R&D / GCP...role: This role is responsible for providing Leadership and QA oversight to the PDx R&D & GCP more
    GE HealthCare (05/06/24)
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  • Sr. Manager / Associate Director Quality

    Kelly Services (Burlington, MA)
    Quality team. They will play a key role in expanding and shaping US-based Quality culture, including GCP and GLP compliant business units. This is a ... **Sr. Manager/ Associate Director - Quality Assurance ** **Burlington, MA** **Direct Hire**...individual will report to the Sr. Director of Global GCP / GLP compliance and while working closely with… more
    Kelly Services (04/04/24)
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  • Sr. Manager/Associate Director, Quality

    Frontier Medicines (Boston, MA)
    … at Frontier, where precision meets purpose. In this pivotal role, you'll oversee GCP / GLP Quality Assurance activities, ensuring meticulous adherence to ... RA/ QA as we navigate the complexities of quality assurance with precision and purpose. Requirements...not limited to: US CFR, EU CTD, and ICH GCP + Familiarity with electronic document management systems and… more
    Frontier Medicines (04/03/24)
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  • Senior Manager/Director of Quality

    HistoWiz (Long Island City, NY)
    …by accelerating histopathology and enabling global collaboration. We are looking for a Quality Assurance Specialist interested in joining our mission and serving ... position is accountable for the execution of assigned company GLP QA audit activities ensuring that the...field + At least 5 years of experience in Quality Assurance working at a CRO, pharma,… more
    HistoWiz (05/07/24)
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  • Director R&D Quality Excellence & Data…

    BeiGene (San Mateo, CA)
    …maintaining a balanced, proactive, and phase appropriate approach to GCP , GVP and GLP Quality Assurance . This position will be primarily responsible for ... and operations and develop improvement strategies. + Assisting R&D Quality GCP , GVP and GLP ...Quality and cross-functional functions in the identification of training needs + Promoting continuous improvement by partnering with… more
    BeiGene (05/01/24)
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  • Senior BioServices Project Manager

    IQVIA (Durham, NC)
    …visits to foster business development. + Working closely with Medical Writing and Quality Assurance to ensure timely completion of project deliverables. + ... years' related experience. + Or equivalent combination of education, training and experience in GLP laboratory environment....needed for this role:** + Understanding of regulatory guidelines ( GLP , GCP ) and the ability to work… more
    IQVIA (04/24/24)
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  • Manager, Clinical Laboratory Accessioning - RTP

    GRAIL (Durham, NC)
    …and work with the Laboratory Supervisor, the Technical Supervisor on the laboratory's quality control and quality assurance procedures, technical and ... of CAP/CLIA certified Laboratory Supervisory experience + Thorough understanding of CAP, CLIA, GLP , and GCP regulations + Strong communicator with ability to… more
    GRAIL (03/08/24)
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  • Clinical Scientist

    Actalent (Kansas City, MO)
    …skills/SOP writing including method development. + Microbiology, microscopy, aseptic technique. + Quality assurance and analysis of data prepared by other ... use of micro pipettors, biosafety cabinets, incubators, and centrifuges. + Operating in a GLP , GMP, or GCP environment. Skills & Qualifications : + Masters… more
    Actalent (05/01/24)
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  • Validation Engineer III

    Teva Pharmaceuticals (West Chester, PA)
    …must be skilled in data integrity, manufacturing and laboratory equipment qualification, and GCP , GLP and cGMP regulatory procedures. The Validation Engineer III ... site aligns with corporate standards and cGMP guidelines + Work with QA /Manufacturing group members to initiate and implement corrective and preventive actions +… more
    Teva Pharmaceuticals (04/17/24)
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