• PV and GCP QA Quality Advisor

    Lundbeck (Deerfield, IL)
    PV and GCP QA Quality Advisor Requisition ID: 6548 Location: Deerfield, IL, US Do you want to join a team where the mission is meaningful, the challenges are ... GCP and PV audits, in line with R&D Quality steering documents. + Provide unsupervised GCP /GcLP/PV...R&D Quality steering documents. + Provide unsupervised GCP /GcLP/PV expertise as applicable and compliance advice in areas… more
    Lundbeck (06/24/25)
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  • GCP QA CAPA Manager

    IQVIA (Durham, NC)
    …in Life Science or related field. + At least 5 years' experience in ** GCP Quality Assurance** within pharmaceutical, technical, or related areas. + Considerable ... knowledge of GCP , clinical trial, regulations, and quality assurance auditing techniques. + Fluent English language capabilities. **Skills** + Ability to work… more
    IQVIA (06/14/25)
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  • GCP Process Lead, FSP Clinical Compliance

    ThermoFisher Scientific (Greenville, NC)
    …Your expertise will be crucial in determining and successfully implementing advanced quality assurance processes. **Role:** GCP Process Lead, FSP Dedicated ... (Mon-Fri) **Environmental Conditions** Office **Job Description** **Job Summary** As the GCP Compliance and Process Lead at Thermo Fisher Scientific, you will… more
    ThermoFisher Scientific (04/11/25)
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  • Practice Architect 2- GCP

    TEKsystems (Dallas, TX)
    …communication and change control standards. * Maintain client satisfaction while ensuring quality and governance of GCP solutions. Practice & Product Line ... experience you've been searching for? We're looking for a GCP Practice Architect 2 to join our team. A...is a leadership-level role focused on Google Cloud Platform ( GCP ) delivery and practice development. The role oversees consulting… more
    TEKsystems (06/18/25)
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  • Director, Clinical Quality and Compliance

    Danaher Corporation (Austin, TX)
    …the job include: + Bachelor's degree in science with 14+ years of clinical quality / GCP experience within the device industry OR Master's degree in science with ... 12+ years of clinical quality / GCP experience within the device industry + Knowledge of US requirements and regulations related to Good Clinical Practice with… more
    Danaher Corporation (03/29/25)
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  • Clinical Project Quality Manager

    Sanofi Group (Morristown, NJ)
    …assess areas of study risk and leads the preparation and delivery of Project/Study specific quality reviews. Advises on GCP quality issues and risks, while ... in the pharmaceutical industry, with at least 5 years' experience in GCP clinical and/or GCP quality operations-related roles (eg, GCP auditing, clinical… more
    Sanofi Group (06/25/25)
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  • GCP Solution Executive Lead

    TEKsystems (Chicago, IL)
    …significant value. * Provide authoritative technical guidance, architectural oversight, and quality assurance across the portfolio of GCP projects delivered ... requires: Position Overview We are seeking a visionary and strategic Google Cloud Platform ( GCP ) Solution Executive (SE) Lead to lead our dynamic team of GCP more
    TEKsystems (06/26/25)
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  • Head of Feasibility

    Sanofi Group (Swiftwater, PA)
    …training in GCP methods + Proven track record in delivering high quality GCP -compliant Clinical Trials + Clinical Trial experience preferred + Knowledge of ... up to date, consistent and accurate reports on operational components of ICH- GCP compliance, quality standards and regulatory considerations for his /her… more
    Sanofi Group (05/01/25)
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  • Associate Director, Clinical and Safety…

    Takeda Pharmaceuticals (Boston, MA)
    …Management and Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical development, medical affairs ... **About the role:** The Associate Director, Clinical and Safety Quality Compliance is responsible for ensuring the quality...and GCP /GVP regulations including FDA, EU, MHRA, PMDA and ICH.… more
    Takeda Pharmaceuticals (04/25/25)
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  • Associate Director, Clinical Program…

    Takeda Pharmaceuticals (Boston, MA)
    …Management and Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical development, medical affairs ... **Job Description** **About the role:** Associate Director, Clinical Program Quality Investigations is responsible for ensuring the compliance of...and GCP /GVP regulations including FDA, EU, MHRA, PMDA and ICH.… more
    Takeda Pharmaceuticals (04/16/25)
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