• Associate Director, Global Product Quality - GMP…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …+ Cross-functional Leadership:Collaborate with Regulatory Affairs, Technical Operations, Manufacturing , and Supply Chain to ensure alignment and integration ... field (Master's or PhD preferred). + 8+ years of experience in pharmaceutical quality, regulatory affairs, or technical operations. + Proven expertise in managing… more
    Otsuka America Pharmaceutical Inc. (12/10/25)
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  • Director, GxP Training

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …oversee GxP training programs for all regulated functions (eg, R&D, Manufacturing , Clinical, Quality). + Implement innovative learning solutions leveraging adult ... Organizational Development, or related field preferred. + 10+ years in pharmaceutical or life sciences industry with significant experience in GxP compliance… more
    Otsuka America Pharmaceutical Inc. (12/06/25)
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  • CMC Regulatory Affairs Senior/Consultant - Small…

    Parexel (Raleigh, NC)
    …applications and post-approval changes Cross-Functional Collaboration * Partner with manufacturing , quality, and external organizations to address CMC-related issues ... Experience & Expertise * 4-6 years of CMC regulatory experience in the pharmaceutical industry for a Consultant level role, 7+ years for a Senior Consultant… more
    Parexel (10/11/25)
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  • Team Lead, Automated Visual Inspection (12-hour…

    ThermoFisher Scientific (Greenville, NC)
    …to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Fluctuating Temps hot/cold, Loud Noises ... at Thermo Fisher Scientific, you'll play a key role in ensuring our pharmaceutical products meet quality standards. This position allows you to bring your skills… more
    ThermoFisher Scientific (10/11/25)
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  • Senior Specialist, Engineering

    Merck (Wilson, NC)
    …support to the Wilson Site. The site includes an Energy Center, Vaccine Manufacturing Facility, Quality Labs, and a Packaging facility. This support position will ... system process improvement and optimization **Preferred** + cGMP in a pharmaceutical environment + Formal problem-solving techniques, such as root cause analysis… more
    Merck (12/13/25)
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  • Principal Scientist 2 - ARD

    Cambrex High Point (High Point, NC)
    …to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing ... and more! Your Future Matters. Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety,… more
    Cambrex High Point (12/04/25)
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  • Associate Director, Engineering - MDCP Technical…

    Merck (Wilson, NC)
    …+ Demonstrated technical leadership in medical device and combination product manufacturing , assembly and packaging sites and functional areas + Experience with ... and written communications **Preferred** + Eight plus years in medical device, pharmaceutical or in biotech organizations + Eight plus years in design control,… more
    Merck (12/04/25)
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  • Sr IT Architect

    ThermoFisher Scientific (Greenville, NC)
    …unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo ... The **Pharma Services Group (PSG)** provides end-to-end drug development and manufacturing services. The **Automation and Digital Solutions** team drives smart… more
    ThermoFisher Scientific (11/26/25)
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  • Operator II- 3rd Shift

    ThermoFisher Scientific (Asheville, NC)
    …Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Some degree of PPE ... creating top-tier scientific tools. **Location/Division Specific Information:** The Asheville Manufacturing site is in the Laboratory Products Division within Thermo… more
    ThermoFisher Scientific (11/23/25)
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  • Senior Manager, Quality Assurance Technical

    Fujifilm (Research Triangle Park, NC)
    pharmaceutical environment. This role reviews and approving Good Manufacturing Practice (GMP) documentation (eg, batch records), leads investigations and root ... place for you. From our Bioprocess Innovation Center to our cGMP-compliant manufacturing site, we thrive on collaboration, creativity, and purpose. Whether your… more
    Fujifilm (11/12/25)
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