• Senior Quality Assurance Area Specialist I - Msat…

    Novo Nordisk (Durham, NC)
    …department. Position will also be responsible for the production activities & validation . Ensuring relevant compliance issues are addressed & handled in close ... product release + Quality oversight, review & approval of validation activities associated with projects, new systems, changes to...system, such as 21 CFR Part 11, GAMP5, ISO, Data Integrity preferred + Experience with Risk Assessment &… more
    Novo Nordisk (04/26/25)
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  • DeltaV Engineer

    ManpowerGroup (Raleigh, NC)
    …protocols, and draft validation plans. + Monitor and analyze test equipment, data , and identify root causes of production problems. + Create databases and ... validation schedules, document test results, and prepare compliance reports....2 years of DeltaV experience preferred. + Experience in validation within a regulated environment. + Greenfield project experience.… more
    ManpowerGroup (04/19/25)
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  • Engineer, Quality Assurance

    Revlon (Oxford, NC)
    …solving. + **Culture** + Drive culture change, to one that is data -driven, fact-based, and quality-oriented, without sacrificing plant capacities and output. + **Q** ... Assesses the impact of deviations, CAPAs, and associated change request on the validation status of equipment and/or systems. + Assess changes via NPD, change… more
    Revlon (04/09/25)
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  • QA Director - Site Investigations & Quality…

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …at the site. Stakeholder: + Responsible for coordination with Production/R&D/QA/QC/ Validation for various activities + Lead and coordinate with stakeholders ... for APR activities + Periodic review of SOP-s of QA/Production/Warehouse/QC/ Validation /IT etc. Innovation: + Operate in compliance of cGMP, 21CFR, USP, EP and ICH… more
    Glenmark Pharmaceuticals Inc., USA (04/07/25)
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  • QA Engineer, DSM Operations - Nights

    Fujifilm (Holly Springs, NC)
    …and equipment specifications, functional specifications, traceability matrices, qualification protocols, validation plans, and validation summary reports * ... GMP Quality Assurance and/or similar role * Experience in Validation , cGMP manufacturing operations and/or Quality oversight, in an...& IT Systems, and methodologies * Understanding of GAMP5, Data Integrity, and application of 21 CFR Part 820… more
    Fujifilm (03/26/25)
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  • Regional Manager of Southeast CQV Services

    VTI Life Sciences (Raleigh, NC)
    …(preferred but not required). They must have previous Engineering and/or Validation experience. The candidate will have some business development responsibilities ... Relevant, professional experience, ideally within Life Sciences industry, specifically Validation , Commissioning and Qualification within the Pharmaceutical, Biologic, Biotechnology… more
    VTI Life Sciences (03/12/25)
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  • Sr Quality Assurance Representative - Digital…

    ThermoFisher Scientific (Greenville, NC)
    …(PSG) of Thermo Fisher Scientific, ensuring compliance to regulations for computer system validation (CSV) and assurance with respect to data integrity, computer ... sites, work to support computerized system compliance from system design, validation and verification, release, maintenance, change management, and retirement for… more
    ThermoFisher Scientific (04/26/25)
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  • Senior Technical MES Lead

    NTT DATA North America (Greenville, NC)
    **Req ID:** 315139 NTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, ... into MES solutions across various ISA-95 layers, ensuring proper data modeling and defining sources of truth. + Proven...necessary updates to meet client specifications. + Familiarity with validation tools such as Kneat and HP ALM. +… more
    NTT DATA North America (04/02/25)
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  • Principal Scientist II

    Cambrex High Point (Durham, NC)
    … data analysis and draft reports for analytical method development and validation * Demonstrate ability to correctly analyze data /results and interpret ... routine work independently and to evaluate, troubleshoot and interpret generated data . Demonstrated understanding of method development and qualification / … more
    Cambrex High Point (03/20/25)
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  • QC Technician III

    Kelly Services (Charlotte, NC)
    …This role involves independently executing complex analytical methods, interpreting chromatographic data , and contributing to method development and validation . ... documentation in compliance with cGMP/GLP standards. + **Method Development & Validation :** Participate in the development, optimization, and validation of… more
    Kelly Services (05/07/25)
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