• Maintenance Technician II (2nd Shift)

    Herbalife (Winston Salem, NC)
    …Electrical/Electronics + HVAC training /experience/ education + Food and Drug Administration ( FDA ) or other regulatory experience + Food manufacturing or ... packaging experience, and/or blending equipment, batching operation systems **PHYSICAL DEMANDS:** In general, the following physical demands are representative of those that must be met by an employee to successfully perform the essential functions of this… more
    Herbalife (11/05/25)
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  • Technician I, Manufacturing (2nd Shift)

    Herbalife (Winston Salem, NC)
    …diploma or GED equivalent. **PREFERRED QUALIFICATIONS:** + Food and Drug Administration ( FDA ) other regulatory . + Experience using high Speed Mixer, Dryers, ... Fitz mill, Sweco, scales and tablet presses. + Current Good Manufacturing Practices (CGMPS). At Herbalife, we value doing what's right. We are proud to be an equal opportunity employer, making decisions without regard to race, color, religion, sex, sexual… more
    Herbalife (11/05/25)
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  • Senior Manager, Quality

    ThermoFisher Scientific (Greenville, NC)
    …worldwide medical device and combination product portfolio. This role ensures adherence to global regulatory requirements ( FDA 21 CFR Parts 4, 210, 211, and 820; ... preferred. **Knowledge, Skills, Abilities** + Deep knowledge of global regulatory frameworks ( FDA , ISO, EU MDR, ICH). + Proven experience leading global… more
    ThermoFisher Scientific (12/10/25)
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  • Director, GxP Training

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …approaches. + Ensure training content is accurate, current, and aligned with global regulatory requirements ( FDA , EMA, ICH). **Compliance & Risk Management** + ... cross-functional teams. + Strong understanding of R&D functions and the regulatory landscape (GxP, ICH, FDA , EMA, etc.). + Proven ability to design and deliver… more
    Otsuka America Pharmaceutical Inc. (12/06/25)
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  • Advisor - Regulatory Compliance and Post…

    Lilly (Durham, NC)
    …and others as appropriate to determine the need and document the decision for FDA reporting or for notification to OUS regulatory agencies Generate, submit and ... This position is responsible for providing GMP/GxP support across the different regulatory reporting and inspection support that is provided by the RCPMR (… more
    Lilly (12/11/25)
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  • Sr. Analyst 1, QC Analytical Development Bioassay

    Fujifilm (Holly Springs, NC)
    …requirements * Ensures compendial method oversight and scientific guidelines (eg ICH, EMA, FDA , etc.) * Supports regulatory requests and inspections * Supports ... Manufacturing Practices (GMP) compliant laboratory operations in accordance with regulatory guidelines. This role executes analytical method transfers from clients… more
    Fujifilm (12/06/25)
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  • Product Support Specialist - MS

    Fujifilm (Raleigh, NC)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all job duties inherent… more
    Fujifilm (12/03/25)
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  • Clinical Consultant, MI - I

    Fujifilm (Raleigh, NC)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... Integration, Customer Service, etc.). + Adheres to the Company's quality and regulatory compliance requirements and ensures that all job duties inherent in the… more
    Fujifilm (12/02/25)
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  • Senior Upgrade Engineer, Medical Informatics:…

    Fujifilm (Raleigh, NC)
    …systems. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... factors, which may include customer impact, HCUS business priorities, and regulatory requirements. Normally receives little instruction on day-to-day work and… more
    Fujifilm (11/12/25)
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  • CPQ, Medical Informatics Marketing Manager…

    Fujifilm (Raleigh, NC)
    …others. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... into actionable user stories and system requirements. + Integrate input from regulatory , marketing, and implementation teams to maintain compliance and accuracy in… more
    Fujifilm (10/29/25)
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