• Engineer III, QA

    ThermoFisher Scientific (Greenville, NC)
    …We are seeking an experienced and meticulous QA Engineer III to join our Quality Assurance team as a Quality Validation Specialist. The ideal candidate will ... have a strong background in quality validation processes, excellent analytical skills, and a dedication to maintaining the highest standards of product quality .… more
    ThermoFisher Scientific (08/21/25)
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  • Sr Clinical Consultant, MI I

    Fujifilm (Raleigh, NC)
    compliance with all applicable requirements of the company's quality management system. + Maintains effective communications and working relationships with ... satisfaction and/or HCUS's future business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures that all job… more
    Fujifilm (08/11/25)
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  • Supervisor, Formulation Manufacturing (12 Hour…

    ThermoFisher Scientific (Greenville, NC)
    …to the operations activities in the assigned. Supervises operations employees of high- quality pharmaceutical products according to schedules, cost, and quality ... collaborating with employees to ensure that every product unit is of high quality and exceeds all current Good Manufacturing Practices (cGMPs). . Ensures that… more
    ThermoFisher Scientific (06/06/25)
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  • Lab Manager - Cell Processing Lab

    Novant Health (Charlotte, NC)
    …lymphocytes, and other cellular therapy products such as CAR-T. Monitors quality assurance activities and compliancewith regulatory entities including FACT, CLIA, ... NMDP, CIBMTR, and FDA . Responsible for qualification, validation, auditing of all critical...+ Provides leadership in achieving ongoing corporate objectives including quality , financial vitality, employee, and customer satisfaction. + Key… more
    Novant Health (08/19/25)
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  • Senior Technical Clinical Consultant (PACS,…

    Fujifilm (Raleigh, NC)
    …measurement/data mapping for project and or post go-live support cases in compliance with the company's quality procedures. **Company Overview** At FUJIFILM ... customization, and electronic delivery of technical clinical tools and supplements. + Compliance with respect to all applicable requirements of the company's … more
    Fujifilm (06/19/25)
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  • Packaging Tech 1-Night Shift

    BioFire Diagnostics, LLC. (Durham, NC)
    …interfaces + Execute production activities per approved Manufacturing Directions while maintaining compliance with all job-related SOPs + Quality + Ensure that ... processes and procedures in a timely manner, while maintaining compliance with all company and regulatory agency regulations +...deviation analysis, CAPA actions and other process equipment related quality concerns + Maintain all work areas in a… more
    BioFire Diagnostics, LLC. (08/23/25)
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  • Talent Pipeline - Analytical R&D - Future…

    Cambrex High Point (Durham, NC)
    …customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities ... Together with our customers, we aim to improve the quality of life for patients around the world. Start...of project tasks and deliverables + Responsible for ensuring compliance with cGMP and other regulatory guidelines. + Analyze… more
    Cambrex High Point (08/21/25)
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  • Manufacturing Cleaning Tech 1 - 2nd Shift

    BioFire Diagnostics, LLC. (Durham, NC)
    …interfaces + Execute production activities per approved Manufacturing Directions while maintaining compliance with all job-related SOPs Quality + Ensure that all ... processes and procedures in a timely manner, while maintaining compliance with all company and regulatory agency regulations +...deviation analysis, CAPA actions and other process equipment related quality concerns + Maintain all work areas in a… more
    BioFire Diagnostics, LLC. (07/31/25)
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  • RTP MES Systems Engineer

    Lilly (Durham, NC)
    …a culture of compliance aligned with internal and external computer system quality standards. + Advocate for quality improvement practices in EBR design and ... Computer Systems Validation in line with pharmaceutical computer system quality regulations (eg cGMP's, FDA 21 CFR Part 11) and other applicable regulations (eg… more
    Lilly (06/27/25)
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  • Associate Director, Engineering - Packaging…

    Merck (Wilson, NC)
    …packaging process and equipment issues, optimizing processes, and ensuring compliance . Effective collaboration with site-based and above-site based functional teams ... requires advanced skills in creating and improving business, technical, and compliance processes, and leading high-impact cross-functional teams. + Responsible to… more
    Merck (08/29/25)
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