• Quality Control Analyst IV

    Catalent Pharma Solutions (Chelsea, MA)
    ** Quality Control Analyst IV - Tech...Niro SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North America. ... Catalent Pharma Solutions is hiring a Quality Control (QC) Analyst IV...IV who is a key analytical leader in a cGMP (Good Manufacturing Practices) laboratory capable of both clinical… more
    Catalent Pharma Solutions (07/19/25)
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  • Quality Control Analyst III

    Catalent Pharma Solutions (Chelsea, MA)
    ** Quality Control Analyst III**...knowledge of cGMP 's and their application to Quality Control required; + Ability to effectively ... SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North...in North America. Catalent Pharma Solutions is hiring a Quality Control Analyst III who… more
    Catalent Pharma Solutions (08/02/25)
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  • Quality Control Analyst II

    Catalent Pharma Solutions (Chelsea, MA)
    ** Quality Control Analyst II** **Position...SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North America. ... and drug products according to standard operating procedures. The Quality Control Analyst compiles data...determine root causes of OOTs and/or OOSs according to cGMP standards required + Ability to troubleshoot and repair… more
    Catalent Pharma Solutions (08/08/25)
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  • Senior Quality Control

    Nitto Denko Corp. (Milford, MA)
    …and QC reports, documents analytical procedures, and authors QA documents. The Sr. QC Analyst may review the work of other analysts, schedule work within the lab, ... manner in support of project plans in accordance to cGMP guidelines + Review analytical data for compliance with...related discipline + 8+ years' experience as a QC chemist/ analyst . + Interpersonal skills to lead and train less… more
    Nitto Denko Corp. (07/19/25)
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  • Quality Control Analyst II

    Nitto Denko Corp. (Milford, MA)
    About this opportunity : The QC Analyst II is responsible for conducting routine and non-routine analyses of raw materials, in-process materials and finished ... products in accordance with cGMP guidelines. The appropriately trained individual may provide training...related discipline + 2-5 years' experience as a QC analyst /chemist in a GMP environment + Experience and familiarity… more
    Nitto Denko Corp. (07/16/25)
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