• Associate Director, Drug Product External…

    Bristol Myers Squibb (Summit, NJ)
    …Therapy team. The Associate Director, Drug Product External Manufacturing QA provides Quality oversight to Contract Manufacturing Organizations (CMOs) ... to provide QA oversight of CMO(s) including Deviations, CAPAs, Change Controls, Batch Record Review, Lot disposition to support the clinical and commercial… more
    Bristol Myers Squibb (12/29/24)
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  • QA Associate II

    System One (Mahwah, NJ)
    Title: Quality Assurance Associate II Location: Mahwah, NJ area Schedule: Tues- Saturday 2nd shift 4 PM- 12:30 PM (some flex needed) Type: Contract to Hire ... procedures. Key responsibilities include document management, review of manufacturing batch records, quality control (QC) data, facilitating material… more
    System One (11/18/24)
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