• Production Maintenance Mechanic - Third Shift

    Merck (Wilson, NC)
    …direction of Maintenance Coach, sets up, adjusts, repairs, and maintains all pharmaceutical process equipment + Performs calibrations and maintains industrial ... Participates in the establishment and improvement of new and existing process equipment. Provides technical specifications and information to Research and… more
    Merck (05/28/25)
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  • API Manufacturing Associate I - (12-hour Night…

    Novo Nordisk (Clayton, NC)
    …for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our ... injectable and oral treatment supply chains. Our newer Active Pharmaceutical Ingredients (API) facility in Clayton, NC sits on 825,000 square-feet of… more
    Novo Nordisk (05/29/25)
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  • Data Governance and Quality Analyst

    Chiesi (Cary, NC)
    …care and consumer-facing self-care). We are proud to be the largest global pharmaceutical group to be awarded B Corp Certification, a recognition of high social ... many other enriching diversities. Chiesi USA Chiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent… more
    Chiesi (05/13/25)
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  • Associate Manager, I&C

    Fujifilm (Holly Springs, NC)
    …and operational reliability of the site instruments through an effective calibration process . This role sets the direction and manages the development of the ... Health Administration (OSHA) regulations, and cGMP) + Identifies opportunities for process or system improvements and implements the respective strategies + Ensures… more
    Fujifilm (05/03/25)
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  • QA Floor Support Supervisor (Day Shift) - Device…

    Lilly (Durham, NC)
    …attributes are met (ie, deviations / observations, procedures, production records, validation protocols, change controls, and engineering documents). + Ability to ... School Diploma or equivalent + 5 years of experience supporting pharmaceutical manufacturing operations. **Additional Preferences:** + Bachelor's degree in a… more
    Lilly (04/19/25)
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  • Analytical Quality Assurance Specialist

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …well-positioned to successfully emerge as a leading integrated research-based pharmaceutical company. POSITION SUMMARY: The Analytical Quality Assurance (AQA) ... side by side on the floor acting as an in- process quality assurance expert for microbiology and chemistry laboratory...+ Support in the development of methods transfer and validation , troubleshooting, cross validation , IQ/OQ protocols +… more
    Glenmark Pharmaceuticals Inc., USA (03/18/25)
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  • Associate Director, Clinical Laboratory

    GRAIL (Durham, NC)
    …to other groups and escalate priorities as needed. + Ensure stability studies, validation protocols, and other process improvement and new assay projects are ... United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com… more
    GRAIL (05/20/25)
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  • Quality Representative - Floor Support Parenteral

    Lilly (Concord, NC)
    …the facility. As the project progresses, this role will transition to site-based process team supporting one of the following manufacturing areas: + Formulation + ... for a diverse cross-functional staff in Quality, the project team, and area process teams, including mentoring and training of new Quality and other project staff… more
    Lilly (04/26/25)
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  • Associate - QA Compliance - CSV and DI

    Lilly (Durham, NC)
    …functional areas, projects, and systems comply with corporate Computer System Validation (CSV) standards. This position is responsible for maintaining the life ... operational processes. Additionally, the candidate will utilize Computer System Validation methodologies to ensure regulatory compliance, consistency, and sustainment.… more
    Lilly (05/09/25)
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  • Associate Director, Commercial Quality Assurance

    Catalent Pharma Solutions (Greenville, NC)
    …continuous improvement philosophy focused on improved compliance, right-first-time and process efficiency while creating an environment of open communication, ... Candidate** + PhD with at least 7 years of professional experience in QA/QC pharmaceutical manufacturing or; + Master's degree with at least 9 years of professional… more
    Catalent Pharma Solutions (05/06/25)
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